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Victor Dubowitz - Publications

Affiliations: 
Imperial College, London, London, England, United Kingdom 
Area:
Paediatric Neurology
Website:
http://en.wikipedia.org/wiki/Victor_Dubowitz
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Year Citation  Score
2005 Dubowitz V. A short history of the World Muscle Society. Neuromuscular Disorders : Nmd. 15: 642-7. PMID 16085417 DOI: 10.1016/J.Nmd.2005.07.003  0.311
2005 Dubowitz V. Prednisone for Duchenne muscular dystrophy. The Lancet. Neurology. 4: 264. PMID 15847833 DOI: 10.1016/S1474-4422(05)70050-8  0.343
2004 Dubowitz V. Therapeutic efforts in Duchenne muscular dystrophy; the need for a common language between basic scientists and clinicians. Neuromuscular Disorders : Nmd. 14: 451-5. PMID 15336684 DOI: 10.1016/J.Nmd.2004.06.002  0.307
2003 Mercuri E, Brockington M, Straub V, Quijano-Roy S, Yuva Y, Herrmann R, Brown SC, Torelli S, Dubowitz V, Blake DJ, Romero NB, Estournet B, Sewry CA, Guicheney P, Voit T, et al. Phenotypic spectrum associated with mutations in the fukutin-related protein gene. Annals of Neurology. 53: 537-42. PMID 12666124 DOI: 10.1002/Ana.10559  0.317
2002 Tonini MM, Passos-Bueno MR, Cerqueira A, Pavanello R, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? Neuromuscular Disorders : Nmd. 12: 554-7. PMID 12117479 DOI: 10.1016/S0960-8966(02)00014-7  0.331
2001 Philpot J, Counsell S, Bydder G, Sewry CA, Dubowitz V, Muntoni F. Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect? Neuromuscular Disorders : Nmd. 11: 489-93. PMID 11404123 DOI: 10.1016/S0960-8966(00)00221-2  0.361
2001 Jungbluth H, Sewry CA, Brown SC, Nowak KJ, Laing NG, Wallgren-Pettersson C, Pelin K, Manzur AY, Mercuri E, Dubowitz V, Muntoni F. Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene. Neuromuscular Disorders : Nmd. 11: 35-40. PMID 11166164 DOI: 10.1016/S0960-8966(00)00167-X  0.37
2000 Jungbluth H, Sewry C, Brown SC, Manzur AY, Mercuri E, Bushby K, Rowe P, Johnson MA, Hughes I, Kelsey A, Dubowitz V, Muntoni F. Minicore myopathy in children: a clinical and histopathological study of 19 cases. Neuromuscular Disorders : Nmd. 10: 264-73. PMID 10838253 DOI: 10.1016/S0960-8966(99)00125-X  0.346
2000 Mercuri E, Goodwin F, Sewry C, Dubowitz V, Muntoni F. Diaphragmatic spinal muscular atrophy with bulbar weakness. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 4: 69-72. PMID 10817487 DOI: 10.1053/Ejpn.1999.0265  0.353
2000 Brockington M, Sewry CA, Herrmann R, Naom I, Dearlove A, Rhodes M, Topaloglu H, Dubowitz V, Voit T, Muntoni F. Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42. American Journal of Human Genetics. 66: 428-35. PMID 10677302 DOI: 10.1086/302775  0.334
2000 Dubowitz V. Congenital muscular dystrophy: an expanding clinical syndrome. Annals of Neurology. 47: 143-4. PMID 10665483 DOI: 10.1002/1531-8249(200002)47:2<143::Aid-Ana2>3.0.Co;2-Y  0.307
1999 Dubowitz V. Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 3: 49-51. PMID 10700538 DOI: 10.1016/S1090-3798(99)80012-9  0.416
1999 D'Alessandro M, Naom I, Ferlini A, Sewry C, Dubowitz V, Muntoni F. Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy? Human Genetics. 105: 308-13. PMID 10543397 DOI: 10.1007/S004399900093  0.338
1999 Pelin K, Hilpelä P, Donner K, Sewry C, Akkari PA, Wilton SD, Wattanasirichaigoon D, Bang ML, Centner T, Hanefeld F, Odent S, Fardeau M, Urtizberea JA, Muntoni F, Dubowitz V, et al. Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy. Proceedings of the National Academy of Sciences of the United States of America. 96: 2305-10. PMID 10051637 DOI: 10.1073/Pnas.96.5.2305  0.318
1998 Naom I, D'Alessandro M, Sewry CA, Philpot J, Manzur AY, Dubowitz V, Muntoni F. Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy. Neuromuscular Disorders : Nmd. 8: 495-501. PMID 9829280 DOI: 10.1016/S0960-8966(98)00065-0  0.338
1995 Mercuri E, Muntoni F, Berardinelli A, Pennock J, Sewry C, Philpot J, Dubowitz V. Somatosensory and visual evoked potentials in congenital muscular dystrophy: Correlation with MRI changes and muscle merosin status Neuropediatrics. 26: 3-7. PMID 7791947 DOI: 10.1055/S-2007-979711  0.348
1989 Sewry CA, Voit T, Dubowitz V. Myopathy with unique ultrastructural feature in Marinesco-Sjögren syndrome. Annals of Neurology. 24: 576-80. PMID 3239958 DOI: 10.1002/Ana.410240416  0.326
1989 Dubowitz V, Connell J, Oozeer R, De Vries L, Dubowitz LMS. Clinical and EEG response to anticonvulsants in neonatal seizures Archives of Disease in Childhood. 64: 459-464. PMID 2730114 DOI: 10.1136/adc.64.4_Spec_No.459  0.405
1989 Dubowitz V, Connell J, Oozeer R, De Vries L, Dubowitz LMS. Continuous EEG monitoring of neonatal seizures: Diagnostic and prognostic considerations Archives of Disease in Childhood. 64: 452-458. PMID 2730113 DOI: 10.1136/adc.64.4_Spec_No.452  0.427
1989 Lary S, De Vries LS, Kaiser A, Dubowitz LM, Dubowitz V. Auditory brain stem responses in infants with posthaemorrhagic ventricular dilatation. Archives of Disease in Childhood. 64: 17-23. PMID 2647041  0.391
1987 De Vries LS, Connell JA, Dubowitz LM, Oozeer RC, Dubowitz V, Pennock JM. Neurological, electrophysiological and MRI abnormalities in infants with extensive cystic leukomalacia. Neuropediatrics. 18: 61-6. PMID 3600997 DOI: 10.1055/s-2008-1052453  0.464
1987 Connell J, Oozeer R, Regev R, De Vries LS, Dubowitz LM, Dubowitz V. Continuous four-channel EEG monitoring in the evaluation of echodense ultrasound lesions and cystic leucomalacia. Archives of Disease in Childhood. 62: 1019-24. PMID 3314719 DOI: 10.1136/adc.62.10.1019  0.439
1987 Regev R, de Vries LS, Heckmatt JZ, Dubowitz V. Cerebral ventricular dilation in congenital myotonic dystrophy. The Journal of Pediatrics. 111: 372-6. PMID 3305848  0.461
1986 De Vries LS, Heckmatt JZ, Burrin JM, Dubowitz LM, Dubowitz V. Low serum thyroxine concentrations and neural maturation in preterm infants. Archives of Disease in Childhood. 61: 862-6. PMID 3767414  0.418
1985 Lary S, Briassoulis G, de Vries L, Dubowitz LM, Dubowitz V. Hearing threshold in preterm and term infants by auditory brainstem response. The Journal of Pediatrics. 107: 593-9. PMID 4045608 DOI: 10.1016/S0022-3476(85)80030-5  0.433
1985 de Vries LS, Dubowitz LM, Dubowitz V, Kaiser A, Lary S, Silverman M, Whitelaw A, Wigglesworth JS. Predictive value of cranial ultrasound in the newborn baby: a reappraisal. Lancet. 2: 137-40. PMID 2862328 DOI: 10.1016/S0140-6736(85)90237-5  0.407
Low-probability matches (unlikely to be authored by this person)
2002 Dubowitz V. Therapeutic possibilities in muscular dystrophy: the hope versus the hype. Neuromuscular Disorders : Nmd. 12: 113-6. PMID 11738351 DOI: 10.1016/S0960-8966(01)00319-4  0.298
1999 Morrison KE, Steers G, Dubowitz V. No evidence of association between apolipoprotein E genotype and phenotypic severity in childhood onset proximal spinal muscular atrophy. Neuromuscular Disorders : Nmd. 9: 372-5. PMID 10545039 DOI: 10.1016/S0960-8966(99)00036-X  0.296
1998 Muntoni F, Lichtarowicz-Krynska EJ, Sewry CA, Manilal S, Recan D, Llense S, Taylor J, Morris GE, Dubowitz V. Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy. Neuromuscular Disorders : Nmd. 8: 72-6. PMID 9608559 DOI: 10.1016/S0960-8966(98)00006-6  0.292
1999 Mercuri E, Gruter-Andrew J, Philpot J, Sewry C, Counsell S, Henderson S, Jensen A, Naom I, Bydder G, Dubowitz V, Muntoni F. Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status. Neuromuscular Disorders : Nmd. 9: 383-7. PMID 10545041 DOI: 10.1016/S0960-8966(99)00034-6  0.286
2000 Dubowitz DJ, Tyszka JM, Sewry CA, Moats RA, Scadeng M, Dubowitz V. High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy. Neuromuscular Disorders : Nmd. 10: 292-8. PMID 10838257 DOI: 10.1016/S0960-8966(00)00104-8  0.286
2006 Dubowitz V. Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy. Neuromuscular Disorders : Nmd. 16: 865-6. PMID 17118656 DOI: 10.1016/J.Nmd.2006.09.003  0.281
2001 Skordis LA, Dunckley MG, Burglen L, Campbell L, Talbot K, Patel S, Melki J, Davies KE, Dubowitz V, Muntoni F. Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA. Human Genetics. 108: 356-7. PMID 11379882 DOI: 10.1007/S004390100497  0.278
1999 Muntoni F, Goodwin F, Sewry C, Cox P, Cowan F, Airaksinen E, Patel S, Ignatius J, Dubowitz V. Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1. Neuropediatrics. 30: 243-8. PMID 10598835 DOI: 10.1055/s-2007-973498  0.278
1984 Johnson M, Pennock J, Bydder G, Steiner R, Thomas D, Hayward R, Bryant D, Payne J, Levene M, Whitelaw A, Dubowitz L, Dubowitz V. Clinical NMR imaging of the brain in children: Normal and neurologic disease Magnetic Resonance Imaging. 2: 151. DOI: 10.1016/0730-725X(84)90086-9  0.275
1995 Mercuri E, Dubowitz L, Berardinelli A, Pennock J, Jongmans M, Henderson S, Muntoni F, Sewry C, Philpot J, Dubowitz V. Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes. Neuropediatrics. 26: 156-62. PMID 7477754 DOI: 10.1055/S-2007-979746  0.274
2007 Dubowitz V. Erratum to “Clinical casebook: Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy” [Neuromuscular Disorders 16 (2006) 813] Neuromuscular Disorders. 17: 80. DOI: 10.1016/J.Nmd.2006.12.011  0.272
1983 Fawer CL, Dubowitz LM, Levene MI, Dubowitz V. Auditory brainstem responses in neurologically abnormal infants. Neuropediatrics. 14: 88-92. PMID 6877533 DOI: 10.1055/S-2008-1059559  0.265
1997 Tan E, Topaloglu H, Sewry C, Zorlu Y, Naom I, Erdem S, D'Alessandro M, Muntoni F, Dubowitz V. Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency. Neuromuscular Disorders : Nmd. 7: 85-9. PMID 9131648 DOI: 10.1016/S0960-8966(96)00421-X  0.26
1969 Dubowitz V, Rogers KJ. 5-hydroxyindoles in the cerebrospinal fluid of infants with Down's syndrome and muscle hypotonia Developmental Medicine and Child Neurology. 11: 730-734. PMID 4243826 DOI: 10.1111/j.1469-8749.1969.tb01516.x  0.257
1998 Muntoni F, Taylor J, Sewry CA, Naom I, Dubowitz V. An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary alpha2 laminin deficiency unlinked to the LAMA2 locus on 6q22. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 2: 19-26. PMID 10726842 DOI: 10.1016/1090-3798(98)01001-9  0.253
1984 Dubowitz LM, Dubowitz V, Palmer PG, Miller G, Fawer CL, Levene MI. Correlation of neurologic assessment in the preterm newborn infant with outcome at 1 year. The Journal of Pediatrics. 105: 452-6. PMID 6470869 DOI: 10.1016/S0022-3476(84)80028-1  0.252
1982 Heckmatt JZ, Leeman S, Dubowitz V. Ultrasound imaging in the diagnosis of muscle disease. The Journal of Pediatrics. 101: 656-60. PMID 7131136 DOI: 10.1016/S0022-3476(82)80286-2  0.252
1998 Manzur AY, Sewry CA, Ziprin J, Dubowitz V, Muntoni F. A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance. Neuromuscular Disorders : Nmd. 8: 467-73. PMID 9829276 DOI: 10.1016/S0960-8966(98)00064-9  0.251
1986 Heckmatt JZ, Sewry CA, Hodes D, Dubowitz V. Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children. Brain : a Journal of Neurology. 941-64. PMID 4075080 DOI: 10.1093/BRAIN/108.4.941  0.244
1987 Heckmatt JZ, Placzek M, Thompson AH, Dubowitz V, Watson G. An unusual case of neonatal myasthenia. Journal of Child Neurology. 2: 63-6. PMID 3305689  0.244
1988 Heckmatt JZ, Pier N, Dubowitz V. Real-time ultrasound imaging of muscles. Muscle & Nerve. 11: 56-65. PMID 3277050 DOI: 10.1002/MUS.880110110  0.243
1964 Dubowitz V. Nonprogressive Neurogenic Muscular Atrophy with ‘Voluntary Fasciculation’ Proceedings of the Royal Society of Medicine. 57: 117-118. DOI: 10.1177/003591576405700219  0.242
1996 Mercuri E, Pennock J, Goodwin F, Sewry C, Cowan F, Dubowitz L, Dubowitz V, Muntoni F. Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy. Neuromuscular Disorders : Nmd. 6: 425-9. PMID 9027850 DOI: 10.1016/S0960-8966(96)00383-5  0.239
1992 Dubowitz V. The muscular dystrophies. Postgraduate Medical Journal. 68: 500-6. PMID 1437944 DOI: 10.1136/pgmj.68.801.500  0.235
1989 Patel K, Leevers S, Abbs S, Hart KA, Heckmatt JZ, Bobrow M, Dubowitz V. Absence of dystrophin in Becker muscular dystrophy. Lancet (London, England). 1: 47. PMID 2563029 DOI: 10.1016/S0140-6736(89)91705-4  0.234
1994 Thomas NH, Heckmatt JZ, Rodillo E, Ransley YF, Dubowitz V. Continuous muscle fibre activity (Isaacs' syndrome) in infancy: a report of two cases. Neuromuscular Disorders : Nmd. 4: 147-51. PMID 8012196 DOI: 10.1016/0960-8966(94)90007-8  0.233
1982 Palmer P, Dubowitz LM, Levene MI, Dubowitz V. Developmental and neurological progress of preterm infants with intraventricular haemorrhage and ventricular dilatation. Archives of Disease in Childhood. 57: 748-53. PMID 7138063 DOI: 10.1136/adc.57.10.748  0.232
1998 Dubowitz V. What's in a name? Muscular dystrophy revisited. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 2: 279-84. PMID 10727193 DOI: 10.1016/S1090-3798(98)80001-9  0.232
1977 Dubowitz V. Allopurinol in Duchenne muscular dystrophy. Lancet (London, England). 1: 248-9. PMID 64767 DOI: 10.1016/S0140-6736(77)91035-2  0.23
1993 Sewry CA, Sansome A, Clerk A, Sherratt TG, Hasson N, Rodillo E, Heckmatt JZ, Strong PN, Dubowitz V. Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness. Neuromuscular Disorders : Nmd. 3: 141-8. PMID 8358239 DOI: 10.1016/0960-8966(93)90006-6  0.23
1981 Levene MI, Wigglesworth JS, Dubowitz V. Cerebral structure and intraventricular haemorrhage in the neonate: a real-time ultrasound study. Archives of Disease in Childhood. 56: 416-24. PMID 7259271 DOI: 10.1136/adc.56.6.416  0.229
2002 Dubowitz V. Special Centennial Workshop-- 101st ENMC International Workshop: Therapeutic Possibilities in Duchenne Muscular Dystrophy, 30th November-2nd December 2001, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 12: 421-31. PMID 12062262 DOI: 10.1016/S0960-8966(02)00006-8  0.228
2008 Dubowitz V. Symposium on Muscular Dystrophy Developmental Medicine & Child Neurology. 18: 527-527. DOI: 10.1111/J.1469-8749.1976.TB03694.X  0.228
1982 Levene MI, Whitelaw A, Dubowitz V, Bydder GM, Steiner RE, Randell CP, Young IR. Nuclear magnetic resonance imaging of the brain in children. British Medical Journal (Clinical Research Ed.). 285: 774-6. PMID 6810994 DOI: 10.1136/bmj.285.6344.774  0.228
1993 Clerk A, Morris GE, Dubowitz V, Davies KE, Sewry CA. Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle. The Histochemical Journal. 25: 554-61. PMID 8407365 DOI: 10.1007/BF00173053  0.226
2016 Cohn RD, Dubowitz V. Duchenne muscular dystrophy: Ringo to the rescue? Neuromuscular Disorders : Nmd. 26: 5-6. PMID 26801251 DOI: 10.1016/j.nmd.2015.12.001  0.225
1995 Philpot J, Sewry C, Pennock J, Dubowitz V. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle. Neuromuscular Disorders : Nmd. 5: 301-5. PMID 7580243 DOI: 10.1016/0960-8966(94)00069-L  0.225
1982 Morante A, Dubowitz LM, Leven M, Dubowitz V. The development of visual function in normal and neurologically abnormal preterm and fullterm infants. Developmental Medicine and Child Neurology. 24: 771-84. PMID 7152141 DOI: 10.1111/j.1469-8749.1982.tb13698.x  0.224
2000 Philpot J, Pennock J, Cowan F, Sewry CA, Dubowitz V, Bydder G, Muntoni F. Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 4: 109-14. PMID 10872105 DOI: 10.1053/ejpn.2000.0277  0.224
1987 Herva R, von Wendt L, von Wendt G, Saukkonen AL, Leisti J, Dubowitz V. A syndrome with juvenile cataract, cerebellar atrophy, mental retardation and myopathy. Neuropediatrics. 18: 164-9. PMID 3683758 DOI: 10.1055/S-2008-1052473  0.224
1985 Heckmatt JZ, Dubowitz V. Diagnostic advantage of needle muscle biopsy and ultrasound imaging in the detection of focal pathology in a girl with limb girdle dystrophy. Muscle & Nerve. 8: 705-9. PMID 3903492 DOI: 10.1002/MUS.880080813  0.222
1980 Dubowitz LM, Dubowitz V, Palmer P, Verghote M. A new approach to the neurological assessment of the preterm and full-term newborn infant. Brain & Development. 2: 3-14. PMID 7416439 DOI: 10.1016/S0387-7604(80)80003-9  0.222
1988 Patel K, Voit T, Dunn MJ, Strong PN, Dubowitz V. Dystrophin and nebulin in the muscular dystrophies. Journal of the Neurological Sciences. 87: 315-26. PMID 3062133 DOI: 10.1016/0022-510X(88)90256-0  0.222
1994 Dubowitz V. 22nd ENMC Sponsored Workshop on Congenital Muscular Dystrophy held in Baarn, The Netherlands, 14-16 May 1993 Neuromuscular Disorders. 4: 75-81. PMID 8173355 DOI: 10.1016/0960-8966(94)90051-5  0.221
1995 Philpot J, Topaloglu H, Pennock J, Dubowitz V. Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy Neuromuscular Disorders. 5: 227-231. PMID 7633188 DOI: 10.1016/0960-8966(94)00047-D  0.22
1989 Heckmatt JZ, Pier N, Dubowitz V. Assessment of quadriceps femoris muscle atrophy and hypertrophy in neuromuscular disease in children. Journal of Clinical Ultrasound : Jcu. 16: 177-81. PMID 3150399 DOI: 10.1002/JCU.1870160306  0.22
1994 Sewry CA, Sansome A, Matsumura K, Campbell KP, Dubowitz V. Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy. Neuromuscular Disorders : Nmd. 4: 121-9. PMID 8012192 DOI: 10.1016/0960-8966(94)90003-5  0.22
2012 Cullup T, Lamont PJ, Cirak S, Damian MS, Wallefeld W, Gooding R, Tan SV, Sheehan J, Muntoni F, Abbs S, Sewry CA, Dubowitz V, Laing NG, Jungbluth H. Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement. Neuromuscular Disorders : Nmd. 22: 1096-104. PMID 22784669 DOI: 10.1016/j.nmd.2012.06.007  0.219
1991 Bush A, Dubowitz V. Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy Neuromuscular Disorders. 1: 201-204. PMID 1822795 DOI: 10.1016/0960-8966(91)90025-N  0.218
1995 Muntoni F, Melis MA, Ganau A, Dubowitz V. Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathy American Journal of Human Genetics. 56: 151-157. PMID 7825571  0.218
1996 Sewry CA, Taylor J, Anderson LV, Ozawa E, Pogue R, Piccolo F, Bushby K, Dubowitz V, Muntoni F. Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy. Neuromuscular Disorders : Nmd. 6: 467-74. PMID 9027857 DOI: 10.1016/S0960-8966(96)00389-6  0.218
2002 Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy. Neuropediatrics. 33: 10-4. PMID 11930270 DOI: 10.1055/s-2002-23593  0.216
1983 Palmer PG, Dubowitz LM, Verghote M, Dubowitz V. Neurological and neurobehavioural differences between preterm infants at term and full-term newborn infants. Neuropediatrics. 13: 183-9. PMID 7155301 DOI: 10.1055/S-2008-1059620  0.216
1982 Scott OM, Hyde SA, Goddard C, Dubowitz V. Quantitation of muscle function in children: a prospective study in Duchenne muscular dystrophy. Muscle & Nerve. 5: 291-301. PMID 7099196 DOI: 10.1002/MUS.880050405  0.215
1970 Dubowitz LM, Dubowitz V, Goldberg C. Clinical assessment of gestational age in the newborn infant. The Journal of Pediatrics. 77: 1-10. PMID 5430794 DOI: 10.1016/S0022-3476(70)80038-5  0.215
1997 Goodwin F, Muntoni F, Dubowitz V. Epilepsy in Duchenne and Becker muscular dystrophies. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 1: 115-9. PMID 10728205  0.215
1999 Philpot J, Cowan F, Pennock J, Sewry C, Dubowitz V, Bydder G, Muntoni F. Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging. Neuromuscular Disorders : Nmd. 9: 81-5. PMID 10220862 DOI: 10.1016/S0960-8966(98)00110-2  0.214
2002 Jungbluth H, Müller CR, Halliger-Keller B, Brockington M, Brown SC, Feng L, Chattopadhyay A, Mercuri E, Manzur AY, Ferreiro A, Laing NG, Davis MR, Roper HP, Dubowitz V, Bydder G, et al. Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. Neurology. 59: 284-7. PMID 12136074  0.214
1977 Moosa A, Dubowitz V. Motor nerve conduction velocity in spinal muscular atrophy of childhood. Archives of Disease in Childhood. 51: 974-7. PMID 1015851 DOI: 10.1136/adc.51.12.974  0.213
1996 DUBOWITZ V. ASYMMETRICAL MORO RESPONSE IN NEUROLOGICALLY NORMAL INFANTS. Developmental Medicine and Child Neurology. 7: 244-8. PMID 14343220 DOI: 10.1111/J.1469-8749.1965.TB10928.X  0.212
1992 Sewry C, Topaloglu H, Dubowitz V. Myosin isoforms in congenital muscular dystrophy Pediatric Neurology. 8: 409. DOI: 10.1016/0887-8994(92)90348-3  0.212
1977 Schwartz MS, Moosa A, Dubowitz V. Correlation of single fibre EMG and muscle histochrmistry using an open biopsy recording technique. Journal of the Neurological Sciences. 31: 369-78. PMID 845618 DOI: 10.1016/0022-510X(77)90215-5  0.211
1997 Dubowitz V. The muscular dystrophies--clarity or chaos? The New England Journal of Medicine. 336: 650-1. PMID 9032052 DOI: 10.1056/NEJM199702273360909  0.211
1989 Rutherford MA, Heckmatt JZ, Dubowitz V. Congenital myotonic dystrophy: Respiratory function at birth determines survival Archives of Disease in Childhood. 64: 191-195. PMID 2930224 DOI: 10.1136/adc.64.2.191  0.21
1970 Dubowitz V, Roy S. Central core disease of muscle: clinical, histochemical and electron microscopic studies of an affected mother and child. Brain : a Journal of Neurology. 93: 133-46. PMID 5418397 DOI: 10.1093/BRAIN/93.1.133  0.209
1995 Muntoni F, Wilson L, Marrosu G, Marrosu MG, Cianchetti C, Mestroni L, Ganau A, Dubowitz V, Sewry C. A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart. The Journal of Clinical Investigation. 96: 693-9. PMID 7635962 DOI: 10.1172/Jci118112  0.209
1989 Voit T, Patel K, Dunn MJ, Dubowitz V, Strong PN. Distribution of dystrophin, nebulin and Ricinus communis I (RCA-I)-binding glycoprotein in tissues of normal and mdx mice. Journal of the Neurological Sciences. 89: 199-211. PMID 2647911 DOI: 10.1016/0022-510X(89)90022-1  0.209
1998 Taylor J, Sewry CA, Dubowitz V, Muntoni F. Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expression. Neurology. 51: 1116-20. PMID 9781539  0.207
1991 Dubowitz V. Prednisone in Duchenne dystrophy Neuromuscular Disorders. 1: 161-163. PMID 1822789 DOI: 10.1016/0960-8966(91)90019-O  0.206
1997 Quinlivan RM, Robb SA, Sewry C, Dubowitz V, Piccolo F, Kaplan JC. Absence of alpha-sarcoglycan and novel missense mutations in the alpha-sarcoglycan gene in a young British girl with muscular dystrophy. Developmental Medicine and Child Neurology. 39: 770-4. PMID 9393893  0.205
1996 Dubowitz V. The clinical phenotype in congenital muscular dystrophy Neuromuscular Disorders. 6: S17. DOI: 10.1016/0960-8966(96)88995-4  0.203
1997 Taylor J, Muntoni F, Robb S, Dubowitz V, Sewry C. Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1? Neuromuscular Disorders : Nmd. 7: 211-6. PMID 9196901 DOI: 10.1016/S0960-8966(97)00461-6  0.202
1987 Connell JA, Oozeer R, Dubowitz V. Continuous 4-channel EEG monitoring: A guide to interpretation, with normal values, in preterm infants Neuropediatrics. 18: 138-145. PMID 3683751 DOI: 10.1055/S-2008-1052466  0.201
1989 Heckmatt JZ, Pier N, Dubowitz V. Measurement of quadriceps muscle thickness and subcutaneous tissue thickness in normal children by real-time ultrasound imaging. Journal of Clinical Ultrasound : Jcu. 16: 171-6. PMID 3150398 DOI: 10.1002/JCU.1870160305  0.201
1981 Levene MI, Dubowitz LM, Palmer P, Fawer CL, Dubowitz V. Brain ultrasound in preterm infants. Lancet (London, England). 2: 36. PMID 6113404 DOI: 10.1016/S0140-6736(81)90265-8  0.201
1985 Capaldi MJ, Dunn MJ, Sewry CA, Dubowitz V. Lectin blotting of human muscle. Identification of a high molecular weight glycoprotein which is absent or altered in Duchenne muscular dystrophy. Journal of the Neurological Sciences. 68: 225-31. PMID 4009204 DOI: 10.1016/0022-510X(85)90103-0  0.201
1981 Dubowitz LM, Levene MI, Morante A, Palmer P, Dubowitz V. Neurologic signs in neonatal intraventricular hemorrhage: a correlation with real-time ultrasound. The Journal of Pediatrics. 99: 127-33. PMID 7252649 DOI: 10.1016/S0022-3476(81)80977-8  0.199
1989 Dubowitz V. Responses of diseased muscle to electrical and mechanical intervention. Ciba Foundation Symposium. 138: 240-55. PMID 3058432 DOI: 10.1002/9780470513675.CH15  0.199
2002 Kinali M, Mercuri E, Main M, Muntoni F, Dubowitz V. An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophy. Neuromuscular Disorders : Nmd. 12: S169-74. PMID 12206813 DOI: 10.1016/S0960-8966(02)00097-4  0.199
2000 Naom I, D'alessandro M, Sewry CA, Jardine P, Ferlini A, Moss T, Dubowitz V, Muntoni F. Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy. Brain : a Journal of Neurology. 123: 31-41. PMID 10611118  0.199
1974 Mushin AS, Dubowitz V. The Incidence of Minor Retinal Abnormalities in Premature Infants and their Relationship to Retinopathy of Prematurity Pediatric Research. 8: 908-908. DOI: 10.1203/00006450-197411000-00069  0.198
1997 Taylor J, Muntoni F, Dubowitz V, Sewry CA. The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age related. Neuropathology and Applied Neurobiology. 23: 399-405. PMID 9364465  0.198
1989 Hodgson S, Hart K, Abbs S, Heckmatt J, Rodillo E, Bobrow M, Dubowitz V. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. Journal of Medical Genetics. 26: 682-93. PMID 2585468 DOI: 10.1136/jmg.26.11.682  0.196
1987 Heckmatt JZ, Dubowitz V. Ultrasound imaging and directed needle biopsy in the diagnosis of selective involvement in muscle disease. Journal of Child Neurology. 2: 205-13. PMID 3301997 DOI: 10.1177/088307388700200307  0.196
1968 Dubowitz V, Sharrard J. Congenital Clubfoot with Central Core Disease of Muscle Proceedings of the Royal Society of Medicine. 61: 1258-1260. DOI: 10.1177/003591576806101204  0.195
2015 Dubowitz V, Cohn RD. Dystrophin and Duchenne dystrophy. Neuromuscular Disorders : Nmd. 25: 361-2. PMID 25890834 DOI: 10.1016/j.nmd.2015.03.013  0.195
1969 Dubowitz V. The “New” Myopathies Neuropediatrics. 1: 137-148. DOI: 10.1055/S-0028-1091869  0.195
1985 Dubowitz V. Evaluation and Differential Diagnosis of the Hypotonic Infant Pediatrics in Review. 6: 237-243. DOI: 10.1542/PIR.6-8-237  0.194
1998 Campbell L, Daniels RJ, Dubowitz V, Davies KE. Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family. American Journal of Human Genetics. 63: 37-44. PMID 9634516 DOI: 10.1086/301918  0.194
1999 Haataja L, Mercuri E, Regev R, Cowan F, Rutherford M, Dubowitz V, Dubowitz L. Optimality score for the neurologic examination of the infant at 12 and 18 months of age. The Journal of Pediatrics. 135: 153-61. PMID 10431108 DOI: 10.1016/S0022-3476(99)70016-8  0.193
1982 Dunn MJ, Sewry CA, Dubowitz V. Cytochemical studies of lectin binding by diseased human muscle. Journal of the Neurological Sciences. 55: 147-59. PMID 7131029 DOI: 10.1016/0022-510X(82)90096-X  0.193
1979 Vanasse M, Dubowitz V. Hereditary Motor and Sensory Neuropathy Type I in Infancy and Childhood: A Clinical, Electrodiagnostic, Genetic and Muscle Biopsy Study Neuropediatrics. 10: 454-455. DOI: 10.1055/S-0028-1085400  0.193
1994 Bush A, Dubowitz V. Becker muscular dystrophy: An unusual presentation [4] Archives of Disease in Childhood. 70: 71. PMID 8110014 DOI: 10.1136/adc.70.1.71-c  0.192
1994 Wilson LA, Cooper BJ, Dux L, Dubowitz V, Sewry CA. Expression of utrophin (dystrophin-related protein) during regeneration and maturation of skeletal muscle in canine X-linked muscular dystrophy Neuropathology and Applied Neurobiology. 20: 359-367. PMID 7808586  0.191
1980 Dubowitz LM, Dubowitz V, Morante A. Visual function in the newborn: a study of preterm and full-term infants. Brain & Development. 2: 15-29. PMID 7416438 DOI: 10.1016/S0387-7604(80)80004-0  0.191
1999 Mercuri E, Manzur A, Jungbluth H, Bonne G, Muchir A, Sewry C, Schwartz K, Dubowitz V, Muntoni F. 297 Early presentation of autosomal dominant Emery-Dreifuss muscular dystrophy European Journal of Paediatric Neurology. 3: A117. DOI: 10.1016/S1090-3798(99)91296-5  0.191
1995 Wallgren-Pettersson C, Clarke A, Samson F, Fardeau M, Dubowitz V, Moser H, Grimm T, Barohn RJ, Barth PG. The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies. Journal of Medical Genetics. 32: 673-9. PMID 8544184 DOI: 10.1136/jmg.32.9.673  0.191
1995 Muntoni F, Sewry C, Wilson L, Angelini C, Trevisan C, Brambati B, Dubowitz V. Prenatal diagnosis in congenital muscular dystrophy The Lancet. 345: 591. PMID 7776805 DOI: 10.1016/S0140-6736(95)90504-9  0.191
1967 Dubowitz V. Pathology of experimentally re-innervated skeletal muscle. Journal of Neurology, Neurosurgery, and Psychiatry. 30: 99-110. PMID 4226750 DOI: 10.1136/jnnp.30.2.99  0.191
1990 Munsat TL, Skerry L, Korf B, Pober B, Schapira Y, Gascon GG, Al-Rajeh SM, Dubowitz V, Davies K, Brzustowicz LM, Penchaszadeh GK, Gilliam TC. Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA 5q) Neurology. 40: 1831-1836. PMID 2247230 DOI: 10.1212/WNL.40.12.1831  0.191
1984 Heckmatt JZ, Moosa A, Hutson C, Maunder-Sewry CA, Dubowitz V. Diagnostic needle muscle biopsy. A practical and reliable alternative to open biopsy. Archives of Disease in Childhood. 59: 528-32. PMID 6742872 DOI: 10.1136/adc.59.6.528  0.191
1977 Hosking JP, Bhat US, Dubowitz V, Edwards RH. Measurements of muscle strength and performance in children with normal and diseased muscle. Archives of Disease in Childhood. 51: 957-63. PMID 1015849 DOI: 10.1136/adc.51.12.957  0.19
1998 Lamont PJ, Dubowitz V, Landon DN, Davis M, Morgan-Hughes JA. Fifty year follow-up of a patient with central core disease shows slow but definite progression. Neuromuscular Disorders : Nmd. 8: 385-91. PMID 9713855 DOI: 10.1016/S0960-8966(98)00043-1  0.19
1993 Dux L, Cooper BJ, Sewry CA, Dubowitz V. Notechis scutatus venom increases the yield of proliferating muscle cells from biopsies of normal and dystrophic canine muscle-A possible source for myoblast transfer studies Neuromuscular Disorders. 3: 23-29. PMID 8329886 DOI: 10.1016/0960-8966(93)90038-L  0.19
2010 Dubowitz V. Cross-innervated mammalian skeletal muscle: histochemical, physiological and biochemical observations. The Journal of Physiology. 193: 481-496.3. PMID 16992291 DOI: 10.1113/jphysiol.1967.sp008373  0.189
1997 Sewry CA, Naom I, D'Alessandro M, Sorokin L, Bruno S, Wilson LA, Dubowitz V, Muntoni F. Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain. Neuromuscular Disorders : Nmd. 7: 169-75. PMID 9185180 DOI: 10.1016/S0960-8966(97)00425-2  0.189
1996 DUBOWITZ V. INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY. Brain : a Journal of Neurology. 87: 707-18. PMID 14236013 DOI: 10.1093/BRAIN/87.4.707  0.189
1993 Dubowitz V. Duchenne muscular dystrophy, 2nd edn. Neuromuscular Disorders. 3: 181. DOI: 10.1016/0960-8966(93)90016-D  0.189
1994 Thomas NH, Dubowitz V. The natural history of type I (severe) spinal muscular atrophy. Neuromuscular Disorders : Nmd. 4: 497-502. PMID 7881295 DOI: 10.1016/0960-8966(94)90090-6  0.189
1994 Wilson LA, Dux L, Cooper BJ, Dubowitz V, Sewry CA. Experimental regeneration in canine muscular dystrophy-2. Expression of myosin heavy chain isoforms Neuromuscular Disorders. 4: 25-37. PMID 7513568 DOI: 10.1016/0960-8966(94)90045-0  0.189
1987 Scott OM, Vrbová G, Hyde SA, Dubowitz V. Responses of muscles of patients with Duchenne muscular dystrophy to chronic electrical stimulation. Journal of Neurology, Neurosurgery, and Psychiatry. 49: 1427-34. PMID 3492592 DOI: 10.1136/jnnp.49.12.1427  0.187
1978 Hosking GP, Young A, Dubowitz V, Edwards RH. Tests of skeletal muscle function in children. Archives of Disease in Childhood. 53: 224-9. PMID 646431 DOI: 10.1136/adc.53.3.224  0.187
1963 DUBOWITZ V. Enzymatic Maturation of Skeletal Muscle Nature. 197: 1215-1215. DOI: 10.1038/1971215A0  0.186
1971 Roy S, Dubowitz V, Wolman L. Ultrastructure of muscle in infantile spinal muscular atrophy. Journal of the Neurological Sciences. 12: 219-32. PMID 5544805 DOI: 10.1016/0022-510X(71)90050-5  0.186
1994 Murdoch Eaton DG, Wertheim D, Oozeer R, Dubowitz LM, Dubowitz V. Reversible changes in cerebral activity associated with acidosis in preterm neonates Acta Paediatrica, International Journal of Paediatrics. 83: 486-492. PMID 8086724  0.186
1981 Maunder-Sewry CA, Dubowitz V. Needle muscle biopsy for carrier detection in Duchenne muscular dystrophy. Part 1. Light microscopy--histology, histochemistry and quantitation. Journal of the Neurological Sciences. 49: 305-24. PMID 6452514 DOI: 10.1016/0022-510X(81)90087-3  0.185
1997 Philpot J, Brockinton M, Sewry C, Dubowitz V, Muntoni F. Clinical presentation in merosin-positive congenital muscular dystrophy Neuromuscular Disorders. 7: 434. DOI: 10.1016/S0960-8966(97)87192-1  0.184
1989 Thomas NH, Dubowitz V. Muscular dystrophy and other muscle disorders Current Opinion in Pediatrics. 1: 296-300. DOI: 10.1097/00008480-198912000-00007  0.183
1996 DUBOWITZ V. THE REFLEXES IN PROGRESSIVE MUSCULAR DYSTROPHY. Developmental Medicine and Child Neurology. 6: 621-2. PMID 14248482 DOI: 10.1111/j.1469-8749.1964.tb02803.x  0.183
1985 Scott OM, Vrbová G, Hyde SA, Dubowitz V. Effects of chronic low frequency electrical stimulation on normal human tibialis anterior muscle. Journal of Neurology, Neurosurgery, and Psychiatry. 48: 774-81. PMID 4031929 DOI: 10.1136/jnnp.48.8.774  0.183
1990 Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D, Dubowitz V, Zerres K, Hausmanowa-Petrusewicz I, Ott J, Munsat TL, et al. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2-13.3 Nature. 344: 540-541. PMID 2320125 DOI: 10.1038/344540A0  0.183
2001 Mercuri E, Rutherford M, De Vile C, Counsell S, Sewry C, Brown S, Bydder G, Dubowitz V, Muntoni F. Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophy. Neuromuscular Disorders : Nmd. 11: 297-9. PMID 11297945 DOI: 10.1016/S0960-8966(00)00190-5  0.183
1985 Appleyard ST, Dunn MJ, Dubowitz V, Rose ML. Increased expression of HLA ABC class I antigens by muscle fibres in Duchenne muscular dystrophy, inflammatory myopathy, and other neuromuscular disorders. Lancet (London, England). 1: 361-3. PMID 2857418 DOI: 10.1016/S0140-6736(85)91384-4  0.183
1998 Barth PG, Dubowitz V. X-linked myotubular myopathy--a long-term follow-up study. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 2: 49-56. PMID 10726846 DOI: 10.1016/1090-3798(98)01004-9  0.182
1970 Dubowitz V. The infant cry. A spectrographic and auditory analysis Journal of the Neurological Sciences. 10: 607-608. DOI: 10.1016/0022-510X(70)90194-2  0.181
1980 Dubowitz LM, Dubowitz V, Morante A, Verghote M. Visual function in the preterm and fullterm newborn infant. Developmental Medicine and Child Neurology. 22: 465-75. PMID 7409338 DOI: 10.1111/j.1469-8749.1980.tb04351.x  0.181
1966 Dubowitz V, Platts M. Central core disease of muscle with focal wasting. Journal of Neurology, Neurosurgery, and Psychiatry. 28: 432-7. PMID 5838477 DOI: 10.1136/jnnp.28.5.432  0.181
1981 Dubowitz V. Muscular dystrophy and other inherited diseases of skeletal muscle in animals, annals of the New York Academy of Sciences Journal of the Neurological Sciences. 50: 160. DOI: 10.1016/0022-510X(81)90052-6  0.18
1981 Heckmatt JZ, Dubowitz V, Leeman S. Ultrasound Imaging in the Diagnosis of Muscle Disease Clinical Science. 60: 19P-19P. DOI: 10.1042/Cs060019P  0.18
1999 Philpot J, Bagnall A, King C, Dubowitz V, Muntoni F. Feeding problems in merosin deficient congenital muscular dystrophy. Archives of Disease in Childhood. 80: 542-7. PMID 10332004  0.18
1972 Moosa A, Dubowitz V. Postnatal maturation of peripheral nerves in preterm and full-term infants. The Journal of Pediatrics. 79: 915-22. PMID 5132304 DOI: 10.1016/S0022-3476(71)80184-1  0.18
2011 Dubowitz V. Muscle cramps and coffee. Neuromuscular Disorders : Nmd. 21: 235. PMID 21310614 DOI: 10.1016/j.nmd.2011.01.004  0.18
1967 Dubowitz V. Muscle glycogenosis. Developmental Medicine and Child Neurology. 8: 432-6. PMID 4226180 DOI: 10.1111/j.1469-8749.1966.tb01777.x  0.18
1976 Witkowski JA, Dubowitz V. Growth of diseased human muscle in combined cultures with normal mouse embryonic spinal cord. Journal of the Neurological Sciences. 26: 203-20. PMID 126304 DOI: 10.1016/0022-510X(75)90033-7  0.179
1999 Wallgren-Pettersson C, Pelin K, Hilpelä P, Donner K, Porfirio B, Graziano C, Swoboda KJ, Fardeau M, Urtizberea JA, Muntoni F, Sewry C, Dubowitz V, Iannaccone S, Minetti C, Pedemonte M, et al. Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy. Neuromuscular Disorders : Nmd. 9: 564-72. PMID 10619714 DOI: 10.1016/S0960-8966(99)00061-9  0.178
1988 Voit T, Sewry CA, Dunn MJ, Dubowitz V. Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus. Journal of the Neurological Sciences. 84: 301-14. PMID 3379448 DOI: 10.1016/0022-510X(88)90134-7  0.178
1996 Dubowitz V. 41st ENMC International Workshop on Congenital Muscular Dystrophy 8-10 March 1996, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 6: 295-306. PMID 8887959 DOI: 10.1016/0960-8966(96)00358-6  0.178
1979 Dubowitz V. Involvement of the nervous system in muscular dystrophies in man. Annals of the New York Academy of Sciences. 317: 431-9. PMID 289322 DOI: 10.1111/j.1749-6632.1979.tb56558.x  0.177
1962 Dubowitz V. VIRILISATION AND MALFORMATION OF A FEMALE INFANT The Lancet. 280: 405-406. DOI: 10.1016/S0140-6736(62)90267-2  0.177
2002 Dubowitz V, Kinali M, Main M, Mercuri E, Muntoni F. Remission of clinical signs in early duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 6: 153-9. PMID 12363102 DOI: 10.1053/ejpn.2002.0583  0.176
1968 Dubowitz V, Whittaker GF, Brown BH, Robinson A. Nerve conduction velocity--an index of neurological maturity of the newborn infant Developmental Medicine and Child Neurology. 10: 741-749. PMID 5752101 DOI: 10.1111/j.1469-8749.1968.tb02972.x  0.176
1966 Dubowitz V. Enzyme histochemistry of skeletal muscle. 3. Neurogenic muscular atrophies. Journal of Neurology, Neurosurgery, and Psychiatry. 29: 23-8. PMID 4379649 DOI: 10.1136/jnnp.29.1.23  0.176
1991 Davies KE, Thomas NH, Daniels RJ, Dubowitz V. Molecular studies of spinal muscular atrophy. Neuromuscular Disorders : Nmd. 1: 83-5. PMID 1822785 DOI: 10.1016/0960-8966(91)90053-U  0.174
1988 Patel K, Strong PN, Dubowitz V, Dunn MJ. Calmodulin-binding profiles for nebulin and dystrophin in human skeletal muscle. Febs Letters. 234: 267-71. PMID 3292289 DOI: 10.1016/0014-5793(88)80095-4  0.174
1997 Muntoni F, Taylor J, Dubowitz V, Sewry C. An early-onset autosomal recessive muscular dystrophy with distal wasting and rigidity of the spine Neuromuscular Disorders. 7: 445. DOI: 10.1016/S0960-8966(97)87236-7  0.174
1994 Sewry CA, Matsumura K, Campbell KP, Dubowitz V. Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 4: 401-9. PMID 7881285 DOI: 10.1016/0960-8966(94)90079-5  0.174
1987 Voit T, Sewry CA, Dunn MJ, Dubowitz V. Ultrastructural Localisation Of Ricinus Communis-I Lectin To Skeletal Muscle From Foetuses At High Risk For Duchenne Muscular Dystrophy Pediatric Research. 22: 222-222. DOI: 10.1203/00006450-198708000-00053  0.172
1979 Neville HE, Maunder-Sewry CA, McDougall J, Sewell JR, Dubowitz V. Chloroquine-induced cytosomes with curvilinear profiles in muscle. Muscle & Nerve. 2: 376-81. PMID 492214 DOI: 10.1002/mus.880020509  0.172
1991 Sewry CA, Clerk A, Heckmatt JZ, Vyse T, Dubowitz V, Strong PN. Dystrophin abnormalities in polymyositis and dermatomyositis. Neuromuscular Disorders : Nmd. 1: 333-9. PMID 1822343 DOI: 10.1016/0960-8966(91)90119-D  0.172
1999 Dubowitz V. 352 Therapeutic possibilities in muscular dystrophies European Journal of Paediatric Neurology. 3: A112-A113. DOI: 10.1016/S1090-3798(99)91283-7  0.172
1997 Topaloglu H, Muntoni F, Dubowitz V, Sewry C. Expression of HLA class I antigens in skeletal muscle is a diagnostic marker in juvenile dermatomyositis. Journal of Child Neurology. 12: 60-3. PMID 9010797  0.172
1998 Dubowitz L, Mercuri E, Dubowitz V. An optimality score for the neurologic examination of the term newborn. The Journal of Pediatrics. 133: 406-16. PMID 9738726 DOI: 10.1016/S0022-3476(98)70279-3  0.171
1996 Dubowitz V. Happy birthday, world muscle society Neuromuscular Disorders. 6: 227. DOI: 10.1016/0960-8966(96)84616-5  0.171
1995 Philpot J, Muntoni F, Skellett S, Dubowitz V. Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: A possible sequel of drug toxicity in first trimester of pregnancy? Neuromuscular Disorders. 5: 67-69. PMID 7719144 DOI: 10.1016/0960-8966(94)E0028-7  0.171
1972 Moosa A, Dubowitz V. Assessment of gestational age in newborn infants: nerve conduction velocity versus maturity score. Developmental Medicine and Child Neurology. 14: 290-5. PMID 5033815 DOI: 10.1111/j.1469-8749.1972.tb02592.x  0.171
1983 Dubowitz V. Neonatal Neurology Trends in Neurosciences. 6: 72. DOI: 10.1016/0166-2236(83)90039-5  0.17
1982 Dubowitz V. Neonatal neurology Early Human Development. 6: 381-383. DOI: 10.1016/0378-3782(82)90077-9  0.17
1981 Dubowitz V. Neonatal Neurology Journal of Neurology, Neurosurgery & Psychiatry. 44: 191-192. DOI: 10.1136/jnnp.44.2.191-c  0.17
1996 Merlini L, Dubowitz V. World Muscle Society (WMS) Neuromuscular Disorders. 6: XVII-XIX. DOI: 10.1016/S0960-8966(96)90036-X  0.17
1991 Dubowitz V. A new muscle journal for the nineties Neuromuscular Disorders. 1: 1-2. PMID 1822773  0.17
2016 Dubowitz V. Welcome to the World Muscle Society Congress in Granada Neuromuscular Disorders. 26: S50-S51. DOI: 10.1016/j.nmd.2016.07.009  0.169
2015 Muntoni F, Quinlivan R, Dubowitz V. Welcome to the World Muscle Society Congress in Brighton Neuromuscular Disorders. 25: S146-S148. DOI: 10.1016/j.nmd.2015.08.003  0.168
1995 Wallgren-Pettersson C, Avela K, Marchand S, Kolehmainen J, Tahvanainen E, Hansen FJ, Muntoni F, Dubowitz V, De Visser M, Van Langen IM. A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis. Neuromuscular Disorders : Nmd. 5: 441-3. PMID 8580725 DOI: 10.1016/0960-8966(95)00022-F  0.168
1980 Neerunjun JS, Allsop J, Dubowitz V. Hypoxanthine-guanine phosphoribosyltransferase activity of blood and muscle in Duchenne dystrophy. Muscle & Nerve. 2: 19-23. PMID 545141 DOI: 10.1002/MUS.880020104  0.167
1984 Appleyard ST, Dunn MJ, Dubowitz V, Scott ML, Pittman SJ, Shotton DM. Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscle. Proceedings of the National Academy of Sciences of the United States of America. 81: 776-80. PMID 6583676 DOI: 10.1073/PNAS.81.3.776  0.167
1998 Mercuri E, Anker S, Philpot J, Sewry C, Dubowitz V, Muntoni F. Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy. Pediatric Neurology. 18: 399-401. PMID 9650678 DOI: 10.1016/S0887-8994(97)00222-1  0.167
1990 Scott OM, Hyde SA, Vrbová G, Dubowitz V. Therapeutic possibilities of chronic low frequency electrical stimulation in children with Duchenne muscular dystrophy. Journal of the Neurological Sciences. 95: 171-82. PMID 2324768 DOI: 10.1016/0022-510X(90)90240-N  0.166
1986 Heckmatt J, Dubowitz V. Ultrasound Imaging and Needle Biopsy in Detecting Selective Pathology within the Quadriceps Muscles Clinical Science. 71: 24P-25P. DOI: 10.1042/CS071024PA  0.166
1992 Murdoch Eaton DG, Wertheim D, Oozeer R, Royston P, Dubowitz L, Dubowitz V. The effect of pethidine on the neonatal EEG Developmental Medicine and Child Neurology. 34: 155-163. PMID 1733821 DOI: 10.1111/J.1469-8749.1992.Tb14982.X  0.166
1984 Skouteli H, Dubowitz V. Fasciculation of the eyelids: an additional clue to clinical diagnosis in spinal muscular atrophy. Neuropediatrics. 15: 145-6. PMID 6483112 DOI: 10.1055/S-2008-1052358  0.165
2004 Dubowitz V. Current and future therapy in muscular dystrophy; need for a common language between basic scientists and clinicians. Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology / Edited by the Gaetano Conte Academy For the Study of Striated Muscle Diseases. 23: V-IX. PMID 15605947  0.164
1995 Helbling-Leclerc A, Topaloglu H, Tomé FM, Sewry C, Gyapay G, Naom I, Muntoni F, Dubowitz V, Barois A, Estournet B. Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2. Comptes Rendus De L'Acadã©Mie Des Sciences. Sã©Rie Iii, Sciences De La Vie. 318: 1245-52. PMID 8745640  0.164
1996 Rodrigues NR, Owen N, Talbot K, Patel S, Muntoni F, Ignatius J, Dubowitz V, Davies KE. Gene deletions in spinal muscular atrophy. Journal of Medical Genetics. 33: 93-6. PMID 8929942 DOI: 10.1136/Jmg.33.2.93  0.164
1992 Clerk A, Sewry CA, Dubowitz V, Strong PN. Characterisation of dystrophin in fetuses at risk for Duchenne muscular dystrophy. Journal of the Neurological Sciences. 111: 82-91. PMID 1403002 DOI: 10.1016/0022-510X(92)90116-3  0.164
1974 Dubowitz V. A Modern Approach to Muscle Disease Pediatric Research. 8: 907-907. DOI: 10.1203/00006450-197411000-00063  0.164
1980 Heckmatt JZ, Dubowitz V, Leeman S. Detection of pathological change in dystrophic muscle with B-scan ultrasound imaging. Lancet. 1: 1389-90. PMID 6104175 DOI: 10.1016/S0140-6736(80)92656-2  0.163
1996 Lerche H, Mitrovic N, Dubowitz V, Lehmann-Horn F. Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle. Annals of Neurology. 39: 599-608. PMID 8619545 DOI: 10.1002/ana.410390509  0.163
1979 Neerunjun JS, Dubowitz V, Peters TJ. Analytical subcellular fractionation and enzymic analysis of dystrophic mouse skeletal muscle [proceedings]. Biochemical Society Transactions. 6: 1266-8. PMID 369917 DOI: 10.1042/BST0061266  0.163
1983 Miller G, Heckmatt JZ, Dubowitz LM, Dubowitz V. Use of nerve conduction velocity to determine gestational age in infants at risk and in very-low-birth-weight infants. The Journal of Pediatrics. 103: 109-12. PMID 6864374 DOI: 10.1016/S0022-3476(83)80792-6  0.163
1995 Rodrigues NR, Owen N, Talbot K, Ignatius J, Dubowitz V, Davies KE. Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy. Human Molecular Genetics. 4: 631-4. PMID 7633412 DOI: 10.1093/Hmg/4.4.631  0.163
1972 Bishop A, Gallup B, Skeate Y, Dubowitz V. Morphological studies on normal and diseased human muscle in culture. Journal of the Neurological Sciences. 13: 333-50. PMID 5119447 DOI: 10.1016/0022-510X(71)90037-2  0.162
1995 Shorer Z, Philpot J, Muntoni F, Sewry C, Dubowitz V. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy. Journal of Child Neurology. 10: 472-5. PMID 8576559  0.162
1982 Haas RH, Dyck RF, Dubowitz V, Pepys MB. C-reactive protein in childhood dermatomyositis. Annals of the Rheumatic Diseases. 41: 483-5. PMID 7125717 DOI: 10.1136/ard.41.5.483  0.162
1973 Dubowitz V. Rigid Spine Syndrome: A Muscle Syndrome in Search of a Name Proceedings of the Royal Society of Medicine. 66: 219-220. DOI: 10.1177/003591577306600304  0.161
1966 Dubowitz V. Nerve conduction velocities in premature and full-term infants. Developmental Medicine and Child Neurology. 7: 426-7. PMID 5862045 DOI: 10.1111/j.1469-8749.1965.tb08234.x  0.161
1977 Maunder CA, Yarom R, Dubowitz V. Electron-microscopic X-ray microanalysis of normal and diseased human muscle. Journal of the Neurological Sciences. 33: 323-34. PMID 915520 DOI: 10.1016/0022-510X(77)90129-0  0.161
1966 Dubowitz V. Enzyme histochemistry of skeletal muscle. Journal of Neurology, Neurosurgery, and Psychiatry. 28: 516-24. PMID 4222370 DOI: 10.1136/jnnp.28.6.516  0.16
1977 Neerunjun JS, Dubowitz V. Concomitance of basophilia, ribonucleic acid and acid phosphatase activity in regenerating muscle fibres. Journal of the Neurological Sciences. 33: 95-109. PMID 903792 DOI: 10.1016/0022-510X(77)90185-X  0.16
1995 Le Thiet Thanh, Nguyen Thi Man, Hori S, Sewry CA, Dubowitz V, Morris GE. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin. American Journal of Medical Genetics. 58: 177-86. PMID 8533812 DOI: 10.1002/ajmg.1320580217  0.159
1991 Clerk A, Rodillo E, Heckmatt JZ, Dubowitz V, Strong PN, Sewry CA. Characterisation of dystrophin in carriers of Duchenne muscular dystrophy. Journal of the Neurological Sciences. 102: 197-205. PMID 2072119 DOI: 10.1016/0022-510X(91)90069-J  0.159
1969 Dubowitz V. The floppy infant--a practical approach to classification. Developmental Medicine and Child Neurology. 10: 706-10. PMID 5715647 DOI: 10.1111/j.1469-8749.1968.tb02967.x  0.157
1984 Capaldi MJ, Dunn MJ, Sewry CA, Dubowitz V. Altered binding of Ricinus communis I lectin by muscle membranes in Duchenne muscular dystrophy. Journal of the Neurological Sciences. 63: 129-41. PMID 6699652 DOI: 10.1016/0022-510X(84)90114-X  0.156
1988 Heckmatt JZ, Hyde SA, Gabain A, Dubowitz V. Therapeutic trial of isaxonine in Duchenne muscular dystrophy. Muscle & Nerve. 11: 836-47. PMID 3050510 DOI: 10.1002/MUS.880110807  0.156
1979 Stern CM, Kahan MC, Dubowitz V. Lymphocyte capping in Duchenne muscular dystrophy. Lancet. 1: 1300. PMID 87766 DOI: 10.1016/S0140-6736(79)92264-5  0.156
1973 Dubowitz V. Morphological studies on transplanted muscle between normal and dystrophic animals. Clinical Science. 44: 14P. PMID 4699298 DOI: 10.1042/CS044014PA  0.155
1979 Neerunjun JS, Allsop J, Dubowitz V. Hypoxanthine--guanine phosphoribosyltransferase activity in blood and skeletal muscles of normal and dystrophic mice. Clinical Science and Molecular Medicine. Supplement. 55: 573-6. PMID 282949 DOI: 10.1042/CS0550573  0.155
2005 Dubowitz V. Influenzal encephalopathy. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 9: 43. PMID 15701566 DOI: 10.1016/j.ejpn.2004.10.006  0.154
1986 Hodgson SV, Barber JC, Dowie A, Dubowitz V. A de novo X;13 translocation with abnormal phenotype. Journal of Medical Genetics. 23: 477-8. PMID 3783628 DOI: 10.1136/jmg.23.5.477  0.154
1961 Dubowitz V, Pearse AGE. Enzymic activity of normal and dystrophic human muscle: A histochemical study The Journal of Pathology and Bacteriology. 81: 365-378. DOI: 10.1002/PATH.1700810208  0.153
1984 Capaldi MJ, Dunn MJ, Sewry CA, Dubowitz V. Binding of Ricinus communis I lectin to the muscle cell plasma membrane in diseased muscle. Journal of the Neurological Sciences. 64: 315-24. PMID 6470742 DOI: 10.1016/0022-510X(84)90179-5  0.153
1989 McDouall RM, Dunn MJ, Dubowitz V. Expression of class I and class II MHC antigens in neuromuscular diseases. Journal of the Neurological Sciences. 89: 213-26. PMID 2926449 DOI: 10.1016/0022-510X(89)90023-3  0.153
1981 Thompson BJ, Burghes AHM, Dunn MJ, Dubowitz V. The application of direct tissue isoelectric focusing to the study of human skeletal muscle Electrophoresis. 2: 251-258. DOI: 10.1002/ELPS.1150020410  0.152
1974 Neerunjun JS, Dubowitz V. Isoenzyme studies in the identification of transplanted muscle in the mouse. Clinical Science and Molecular Medicine. 46: 555-8. PMID 4829864 DOI: 10.1042/CS0460555  0.151
1975 NEERUNJUN JS, DUBOWITZ V. MUSCLE TRANSPLANTATION BETWEEN NORMAL AND DYSTROPHIC MICE. 1. HISTOLOGICAL STUDIES Neuropathology and Applied Neurobiology. 1: 111-124. DOI: 10.1111/j.1365-2990.1975.tb00383.x  0.151
1987 Hart KA, Hodgson S, Walker A, Cole CG, Johnson L, Dubowitz V, Bobrow M. DNA deletions in mild and severe Becker muscular dystrophy. Human Genetics. 75: 281-5. PMID 3030926 DOI: 10.1007/BF00281075  0.15
1975 Neerunjun JS, Dubowitz V. Muscle transplantation and regeneration in the dystrophic hamster. Part 1. Histological studies. Journal of the Neurological Sciences. 23: 505-19. PMID 4443823 DOI: 10.1016/0022-510x(74)90023-9  0.15
1970 Dubowitz V, Crome L. The central nervous system in Duchenne muscular dystrophy. Brain : a Journal of Neurology. 92: 805-8. PMID 5364010 DOI: 10.1093/BRAIN/92.4.805  0.149
2015 Dubowitz V. Unnatural natural history of Duchenne muscular dystrophy. Neuromuscular Disorders : Nmd. 25: 936. PMID 26653026 DOI: 10.1016/j.nmd.2015.11.005  0.149
1996 Sewry CA, Philpot J, Sorokin LM, Wilson LA, Naom I, Goodwin F, D'Alessandro M, Dubowitz V, Muntoni F. Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy. Lancet. 347: 582-4. PMID 8596321 DOI: 10.1016/S0140-6736(96)91274-X  0.148
1988 Sewry CA, Dubowitz V, Abraha A, Luzio JP, Campbell AK. Immunocytochemical localisation of complement components C8 and C9 in human diseased muscle. The role of complement in muscle fibre damage. Journal of the Neurological Sciences. 81: 141-53. PMID 3694223 DOI: 10.1016/0022-510X(87)90091-8  0.148
1992 Manzur AY, Hyde SA, Rodillo E, Heckmatt JZ, Bentley G, Dubowitz V. A randomized controlled trial of early surgery in duchenne muscular dystrophy Neuromuscular Disorders. 2: 379-387. PMID 1300186 DOI: 10.1016/S0960-8966(06)80009-X  0.148
1967 Dubowitz V. Enzyme histochemistry of developing human muscle. Nature. 211: 884-5. PMID 4226185 DOI: 10.1038/211884A0  0.148
1993 Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN. Exon skipping and translation in patients with frameshift deletions in the dystrophin gene. American Journal of Human Genetics. 53: 1007-15. PMID 8213828  0.147
1984 Dubowitz V. Illustrated Guide to Malformations of the Central Nervous System at Birth Journal of Neurology, Neurosurgery & Psychiatry. 47: 332-332. DOI: 10.1136/JNNP.47.3.332-A  0.147
1973 Moosa A, Dubowitz V. Spinal muscular atrophy in childhood. Two clues to clinical diagnosis. Archives of Disease in Childhood. 48: 386-8. PMID 4703068 DOI: 10.1136/adc.48.5.386  0.147
1975 NEERUNJUN JS, DUBOWITZ V. MUSCLE TRANSPLANTATION BETWEEN NORMAL AND DYSTROPHIC MICE. 2. HISTOCHEMICAL STUDIES Neuropathology and Applied Neurobiology. 1: 125-140. DOI: 10.1111/j.1365-2990.1975.tb00384.x  0.147
1976 NEERUNJUN JS, DUBOWITZ V. QUANTITATIVE STUDIES OF MUSCLES TRANSPLANTED BETWEEN NORMAL AND DYSTROPHIC MICE Neuropathology and Applied Neurobiology. 2: 279-292. DOI: 10.1111/j.1365-2990.1976.tb00503.x  0.147
1975 GALLUP B, DUBOWITZ V. REGENERATION AND INNERVATION OF NORMAL AND DYSTROPHIC MUSCLE CULTURED WITH NORMAL AND DYSTROPHIC SPINAL CORD Neuropathology and Applied Neurobiology. 1: 205-229. DOI: 10.1111/j.1365-2990.1975.tb00649.x  0.147
1992 Hodgson SV, Abbs S, Clark S, Manzur A, Heckmatt JZH, Dubowitz V, Bobrow M. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability Neuromuscular Disorders. 2: 269-276. PMID 1483053 DOI: 10.1016/0960-8966(92)90059-F  0.147
1997 Naom I, Sewry C, D'Alessandro M, Topaloglu H, Ferlini A, Wilson L, Dubowitz V, Muntoni F. Prenatal diagnosis in merosin-deficient congenital muscular dystrophy. Neuromuscular Disorders : Nmd. 7: 176-9. PMID 9185181 DOI: 10.1016/S0960-8966(97)00448-3  0.146
1979 Neerunjun JS, Dubowitz V. Increased calcium-activated neutral protease activity in muscles of dystrophic hamsters and mice. Journal of the Neurological Sciences. 40: 105-11. PMID 430097 DOI: 10.1016/0022-510X(79)90196-5  0.146
1967 Dubowitz V, Newman DL. Change in enzyme pattern after cross-innervation of fast and slow skeletal muscle [46] Nature. 214: 840-841. PMID 4293137 DOI: 10.1038/214840a0  0.146
1975 Neerunjun JS, Dubowitz V. Muscle transplantation and regeneration in the dystrophic hamster. Part 2. Histochemical studies. Journal of the Neurological Sciences. 23: 521-36. PMID 4155428 DOI: 10.1016/0022-510X(74)90024-0  0.146
1975 Neerunjun JS, Dubowitz V. Identification of regenerated dystrophic minced muscle transplanted in normal mice. Journal of the Neurological Sciences. 24: 33-8. PMID 1110372 DOI: 10.1016/0022-510X(75)90005-2  0.145
1969 Skeate Y, Bishop A, Dubowitz V. DIFFERENTIATION OF DISEASED HUMAN MUSCLE IN CULTURE Cell Proliferation. 2: 307-310. DOI: 10.1111/j.1365-2184.1969.tb00240.x  0.145
1997 Campbell L, Potter A, Ignatius J, Dubowitz V, Davies K. Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype. American Journal of Human Genetics. 61: 40-50. PMID 9245983 DOI: 10.1086/513886  0.145
1976 Somer H, Dubowitz V, Donner M. Creatine kinase isoenzymes in neuromuscular diseases. Journal of the Neurological Sciences. 29: 129-36. PMID 978205 DOI: 10.1016/0022-510X(76)90165-9  0.145
1989 Rodillo E, Marini ML, Heckmatt JZ, Dubowitz V. Scoliosis in spinal muscular atrophy: review of 63 cases. Journal of Child Neurology. 4: 118-23. PMID 2785548 DOI: 10.1177/088307388900400208  0.145
1972 Gallup B, Strugalska-Cynowska H, Dubowitz V. Histochemical studies on normal and diseased human and chick muscle in tissue culture. Journal of the Neurological Sciences. 17: 109-25. PMID 4340931 DOI: 10.1016/0022-510X(72)90134-7  0.144
1998 DUBOWITZ V, PEARSE AG. Reciprocal relationship of phosphorylase and oxidative enzymes in skeletal muscle. Nature. 185: 701-2. PMID 13818366 DOI: 10.1038/185701A0  0.144
1981 Haas RH, Robinson A, Evans K, Lascelles PT, Dubowitz V. An X-linked disease of the nervous system with disordered copper metabolism and features differing from Menkes disease. Neurology. 31: 852-9. PMID 7195507 DOI: 10.1212/WNL.31.7.852  0.142
1973 DUBOWITZ V. Neonatal Anatomy Nature. 246: 233-234. DOI: 10.1038/246233c0  0.142
2000 Dubowitz V. What is muscular dystrophy? Forty years of progressive ignorance. Journal of the Royal College of Physicians of London. 34: 464-8. PMID 11077661  0.142
1996 Dubowitz V. New developments in congenital muscular dystrophy Neuromuscular Disorders. 6: 228. DOI: 10.1016/0960-8966(96)84617-7  0.141
1976 Witkowski JA, Durbidge M, Dubowitz V. Growth of human muscle in tissue culture. An improved technique. In Vitro. 12: 98-106. PMID 1248854 DOI: 10.1007/BF02796355  0.141
1998 DUBOWITZ V, PEARSE AG. A comparative histochemical study of oxidative enzyme and phosphorylase activity in skeletal muscle. Zeitschrift Fur Zellforschung Und Mikroskopische Anatomie. Abteilung Histochemie. 2: 105-17. PMID 13724667 DOI: 10.1007/BF00744575  0.14
1970 Dubowitz V, Rogers K. 5-Hydroxyindoles in mongolism and hydrocephalus. Archives of Disease in Childhood. 44: 783. PMID 4243060 DOI: 10.1136/adc.44.238.783  0.14
1997 Sewry CA, D'Alessandro M, Wilson LA, Sorokin LM, Naom I, Bruno S, Ferlini A, Dubowitz V, Muntoni F. Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy. Neuropediatrics. 28: 217-22. PMID 9309712 DOI: 10.1055/s-2007-973703  0.14
1992 Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, Ray PN, Strong PN, Worton RG. Dystrophin in frameshift deletion patients with Becker muscular dystrophy. American Journal of Human Genetics. 51: 562-70. PMID 1496988  0.138
1977 Neerunjun JS, Dubowitz V. Comparison of gamma-glutamyl transpeptidase activity in tissues of normal and dystrophic hamsters and mice. Journal of the Neurological Sciences. 33: 335-40. PMID 21230 DOI: 10.1016/0022-510X(77)90130-7  0.137
1989 Rodillo E, Noble-Jamieson CM, Aber V, Heckmatt JZ, Muntoni F, Dubowitz V. Respiratory muscle training in Duchenne muscular dystrophy. Archives of Disease in Childhood. 64: 736-8. PMID 2658856 DOI: 10.1136/adc.64.5.736  0.137
1978 Dubowitz V, van Iddekinge B, Rodeck CH, Campbell S, Singer JD, Scheuerbrandt G, Moss DW. Prenatal diagnosis in Duchenne muscular dystrophy: Salvage of normal male fetus. Lancet (London, England). 1: 90. PMID 74582 DOI: 10.1016/S0140-6736(78)90021-1  0.137
1976 Neerunjun JS, Jones DA, Dubowitz V. Functional properties of muscle transplanted between normal and dystrophic mice. Experimental Neurology. 52: 556-64. PMID 954923 DOI: 10.1016/0014-4886(76)90226-0  0.137
1997 Naom I, D'Alessandro M, Sewry C, Ferlini A, Topaloglu H, Helbling-Leclerc A, Guicheney P, Schwartz K, Akcoren Z, Dubowitz V, Muntoni F. The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy. Human Genetics. 99: 535-40. PMID 9099847 DOI: 10.1007/s004390050402  0.136
2003 Nevo Y, Muntoni F, Sewry C, Legum C, Kutai M, Harel S, Dubowitz V. Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype. The Israel Medical Association Journal : Imaj. 5: 94-7. PMID 12674656  0.136
1998 DUBOWITZ V, PEARSE AG. Oxidative enzymes and phosphorylase in central-core disease of muscle. Lancet (London, England). 2: 23-4. PMID 13818365 DOI: 10.1016/S0140-6736(60)92665-9  0.136
1995 Daniels RJ, Campbell L, Rodrigues NR, Francis MJ, Morrison KE, McLean M, MacKenzie A, Ignatius J, Dubowitz V, Davies KE. Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele. Journal of Medical Genetics. 32: 93-6. PMID 7760328 DOI: 10.1136/Jmg.32.2.93  0.136
1992 Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V. Prenatal prediction of spinal muscular atrophy. Journal of Medical Genetics. 29: 165-70. PMID 1348091  0.135
1981 Maunder-Sewry CA, Dubowitz V. Increased calcium in dystrophic muscle. British Medical Journal. 280: 1147. PMID 7427122 DOI: 10.1136/bmj.280.6223.1147  0.134
1960 Dubowitz V, Lawson D. Myotonia Congenita with “Delayed Myotonia.” Proceedings of the Royal Society of Medicine. 53: 786-787. DOI: 10.1177/003591576005300917  0.134
1990 Heckmatt J, Rodillo E, Dubowitz V. Management of children: pharmacological and physical. British Medical Bulletin. 45: 788-801. PMID 2688829 DOI: 10.1093/OXFORDJOURNALS.BMB.A072358  0.134
1989 Heckmatt J, Hasson N, Saunders C, Thompson N, Peters AM, Cambridge G, Rose M, Hyde SA, Dubowitz V. Cyclosporin in juvenile dermatomyositis. Lancet (London, England). 1: 1063-6. PMID 2566009 DOI: 10.1016/S0140-6736(89)92456-2  0.133
1977 Neerunjun JS, Dubowitz V. Effect of pentobarbitone sodium on serum creatine kinase of normal and dystrophic hamsters. Clinical Science and Molecular Medicine. 52: 137-42. PMID 844246 DOI: 10.1042/CS0520137  0.133
1997 Naom IS, D'Alessandro M, Topaloglu H, Sewry C, Ferlini A, Helbling-Leclerc A, Guicheney P, Weissenbach J, Schwartz K, Bushby K, Philpot J, Dubowitz V, Muntoni F. Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy. Journal of Medical Genetics. 34: 99-104. PMID 9039983  0.133
1973 Gallup B, Dubowitz V. Letter: Failure of "dystrophic" neurones to support functional regeneration of normal or dystrophic muscle in culture. Nature. 243: 287-9. PMID 4743214 DOI: 10.1038/243287A0  0.132
1987 Hart K, Cole C, Walker A, Hodgson S, Johnson L, Dubowitz V, Ray P, Worton R, Bobrow M. The screening of Duchenne muscular dystrophy patients for submicroscopic deletions. Journal of Medical Genetics. 23: 516-20. PMID 3806637 DOI: 10.1136/jmg.23.6.516  0.132
2000 Naom I, D'Alessandro M, Sewry CA, Jardine P, Ferlini A, Moss T, Dubowitz V, Muntoni F. Mutations in the laminin α2-chain gene in two children with early-onset muscular dystrophy Brain. 123: 31-41.  0.132
1979 Emery AE, Burt D, Dubowitz V, Rocker I, Donnai D, Harris R, Donnai P. Antenatal diagnosis of Duchenne muscular dystrophy. Lancet (London, England). 1: 847-9. PMID 86094 DOI: 10.1016/S0140-6736(79)91264-9  0.132
1994 Eaton DGM, Wertheim D, Oozeer R, Dubowitz L, Dubowitz V. THE EFFECT OF INOTROPIC THERAPY ON THE VERY PRETERM NEONATAL ELECTROENCEPHALOGRAM (EEG) Pediatric Research. 35: 275-275. DOI: 10.1203/00006450-199402000-00127  0.131
2013 Dubowitz V. Steroids in Duchenne dystrophy. Neuromuscular Disorders : Nmd. 23: 527-8. PMID 23743333 DOI: 10.1016/j.nmd.2013.05.004  0.13
1990 Gilliam TC, Brzustowicz LM, Castilla LH, Lehner T, Penchaszadeh GK, Daniels RJ, Byth BC, Knowles J, Hislop JE, Shapira Y, Dubowitz V, Munsat TL, Ott J, Davies KE. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy Nature. 345: 823-825. PMID 1972783 DOI: 10.1038/345823A0  0.13
1992 Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K. Linkage analysis of spinal muscular atrophy. Genomics. 12: 335-9. PMID 1346777 DOI: 10.1016/0888-7543(92)90382-3  0.13
1995 Sansome A, Dubowitz V. Intravenous immunoglobulin in juvenile dermatomyositis - Four year review of nine cases Archives of Disease in Childhood. 72: 25-28. PMID 7717731  0.129
1976 Dubowitz V. Neurological fragility in the newborn: Influence of medication in labour. British Journal of Anaesthesia. 47: 1005-10. PMID 1191462 DOI: 10.1093/BJA/47.9.1005  0.126
1995 Dubowitz V, Daniels RJ, Davies KE. Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q. Neuromuscular Disorders : Nmd. 5: 25-9. PMID 7719137 DOI: 10.1016/0960-8966(94)00043-9  0.126
1994 Hillaire D, Leclerc A, Fauré S, Topaloglu H, Chiannilkulchaï N, Guicheney P, Grinas L, Legos P, Philpot J, Evangelista T, Routon MC, Mayer M, Pellissier JF, Estournet B, Barois A, ... ... Dubowitz V, et al. Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping Human Molecular Genetics. 3: 1657-1661. PMID 7833925 DOI: 10.1093/Hmg/3.9.1657  0.125
1995 Rapisarda R, Muntoni F, Gobbi P, Dubowitz V. Duchenne muscular dystrophy presenting with failure to thrive Archives of Disease in Childhood. 72: 437-438. PMID 7618913  0.124
1992 Sewry CA, Wilson LA, Dux L, Dubowitz V, Cooper BJ. Experimental regeneration in canine muscular dystrophy-1. Immunocytochemical evaluation of dystrophin and β-spectrin expression Neuromuscular Disorders. 2: 331-342. PMID 1300182 DOI: 10.1016/S0960-8966(06)80004-0  0.121
1988 Voit T, Sewry C, Dunn M, Dubowitz V. Binding of Five Lectins to the Muscle Cell Plasma Membrane in Duchenne Dystrophy Clinical Science. 74: 25P-25P. DOI: 10.1042/cs074025pa  0.121
1995 Sewry CA, Philpot J, Mahony D, Wilson LA, Muntoni F, Dubowitz V. Expression of laminin subunits in congenital muscular dystrophy. Neuromuscular Disorders : Nmd. 5: 307-16. PMID 7580244 DOI: 10.1016/0960-8966(94)00072-H  0.121
1976 Dubowitz V. Treatment of dermatomyositis in childhood. Archives of Disease in Childhood. 51: 494-500. PMID 962360 DOI: 10.1136/adc.51.7.494  0.121
1982 Dubowitz V. An Introduction to Paediatric Neurology Postgraduate Medical Journal. 58: 670-670. DOI: 10.1136/PGMJ.58.684.670-A  0.121
1986 Noble-Jamieson CM, Heckmatt JZ, Dubowitz V, Silverman M. Effects of posture and spinal bracing on respiratory function in neuromuscular disease. Archives of Disease in Childhood. 61: 178-81. PMID 3954442 DOI: 10.1136/adc.61.2.178  0.121
1983 Miller G, Heckmatt JZ, Dubowitz V. Drug treatment of juvenile dermatomyositis. Archives of Disease in Childhood. 58: 445-50. PMID 6859938 DOI: 10.1136/Adc.58.6.445  0.121
1987 Hodgson S, Boswinkel E, Cole C, Walker A, Dubowitz V, Granata C, Merlini L, Bobrow M. A linkage study of Emery-Dreifuss muscular dystrophy. Human Genetics. 74: 409-16. PMID 3466853 DOI: 10.1007/BF00280495  0.12
1991 McDouall RM, Dunn MJ, Dubowitz V. Nature of the mononuclear infiltrate and the mechanism of muscle damage in juvenile dermatomyositis and Duchenne muscular dystrophy. Journal of the Neurological Sciences. 99: 199-217. PMID 1982294 DOI: 10.1016/0022-510X(90)90156-H  0.12
1985 Fear CN, Mutton DE, Berry AC, Heckmatt JZ, Dubowitz V. Chromosome 15 in Prader-Willi syndrome Developmental Medicine and Child Neurology. 27: 305-311. PMID 4018424 DOI: 10.1111/j.1469-8749.1985.tb04540.x  0.12
1985 Capaldi MJ, Dunn MJ, Sewry CA, Dubowitz V. Lectin binding in human skeletal muscle: a comparison of 15 different lectins. The Histochemical Journal. 17: 81-92. PMID 3988549 DOI: 10.1007/BF01003405  0.119
1982 Lloyd BW, Dubowitz V. Progressive neurological disorder associated with obstructive jaundice and vitamin E deficiency. Neuropediatrics. 13: 155-7. PMID 7133335 DOI: 10.1055/S-2008-1059615  0.119
1980 Maunder-Sewry CA, Dubowitz V. Myonuclear calcium in carriers of Duchenne muscular dystrophy. An X-ray microanalysis study. Journal of the Neurological Sciences. 42: 337-47. PMID 512671 DOI: 10.1016/0022-510X(79)90167-9  0.118
1995 Dubowitz V, Fardeau M. Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands. Neuromuscular Disorders : Nmd. 5: 253-8. PMID 10712013 DOI: 10.1016/0960-8966(95)90011-X  0.118
1982 Stephens HR, Duance VC, Dunn MJ, Bailey AJ, Dubowitz V. Collagen types in neuromuscular diseases. Journal of the Neurological Sciences. 53: 45-62. PMID 7057201 DOI: 10.1016/0022-510X(82)90079-X  0.118
1963 Dubowitz V. HISTOLOGICAL CHANGES IN MUSCULAR-DYSTROPHY CARRIERS The Lancet. 281: 224. DOI: 10.1016/S0140-6736(63)91245-5  0.117
1985 Heckmatt JZ, Dubowitz V, Hyde SA, Florence J, Gabain AC, Thompson N. Prolongation of walking in Duchenne muscular dystrophy with lightweight orthoses: review of 57 cases. Developmental Medicine and Child Neurology. 27: 149-54. PMID 3996772 DOI: 10.1111/j.1469-8749.1985.tb03763.x  0.116
1992 Steare SE, Dubowitz V, Benatar A. Subclinical cardiomyopathy in Becker muscular dystrophy Heart. 68: 304-308. PMID 1389764 DOI: 10.1136/hrt.68.9.304  0.116
1990 Oozeer R, Wertheim D, Murdoch-Eaton D, Connell J, Dubowitz V. Computerised neonatal EEG monitoring and analysis Electroencephalography and Clinical Neurophysiology. 75: S111-S112. DOI: 10.1016/0013-4694(90)92124-F  0.115
1997 Dubowitz V. 50th ENMC International Workshop: congenital muscular dystrophy. 28 February 1997 to 2 March 1997, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 7: 539-47. PMID 10712016  0.114
1993 Sansome A, Royston P, Dubowitz V. Steroids in Duchenne muscular dystrophy; Pilot study of a new low-dosage schedule Neuromuscular Disorders. 3: 567-569. PMID 8186713 DOI: 10.1016/0960-8966(93)90117-3  0.114
1975 Yarom R, Maunder CA, Hall TA, Dubowitz V. X-ray microanalysis of mast cells in rat's muscle Experientia. 31: 1339-1340. PMID 812729 DOI: 10.1007/BF01945815  0.113
1996 Sewry CA, Naom I, D'Alessandro M, Ferlini A, Philpot J, Mercuri E, Dubowitz V, Muntoni F. The protein defect in congenital muscular dystrophy. Biochemical Society Transactions. 24: 281S. PMID 8736939  0.113
1981 Vanasse M, Dubowitz V. Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood. Muscle & Nerve. 4: 26-30. PMID 7231442 DOI: 10.1002/MUS.880040106  0.113
2011 Dubowitz V. Intellectual Impairment in Muscular Dystrophy. Archives of Disease in Childhood. 40: 296-301. PMID 21032424 DOI: 10.1136/adc.40.211.296  0.112
1992 Dubowitz V. Recent advances in neuromuscular disorders in childhood. Acta Paediatrica Japonica : Overseas Edition. 33: 198-205. PMID 1957646 DOI: 10.1111/j.1442-200X.1991.tb01544.x  0.112
1986 Hodgson SV, Heckmatt JZ, Hughes E, Crolla JA, Dubowitz V, Bobrow M. A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome. American Journal of Medical Genetics. 23: 837-47. PMID 3953680 DOI: 10.1002/AJMG.1320230311  0.111
1977 Dubowitz LM, Dubowitz V, Goldberg C, Keith I. Rapid assessment of gestational age at birth. Archives of Disease in Childhood. 51: 986-7. PMID 1015855 DOI: 10.1136/adc.51.12.986-a  0.11
1979 Jones R, Khan R, Hughes S, Dubowitz V. Congenital muscular dystrophy: the importance of early diagnosis and orthopaedic management in the long-term prognosis. The Journal of Bone and Joint Surgery. British Volume. 61: 13-7. PMID 422630 DOI: 10.1302/0301-620X.61B1.422630  0.11
1985 Guerard MJ, Sewry CA, Dubowitz V. Lobulated fibers in neuromuscular diseases. Journal of the Neurological Sciences. 69: 345-56. PMID 3162002 DOI: 10.1016/0022-510X(85)90145-5  0.109
1969 Dubowitz V. Neurological assessment of gestational age in newborn. Archives of Disease in Childhood. 44: 135. PMID 5765984 DOI: 10.1136/adc.44.233.135-a  0.109
1987 Hodgson S, Walker A, Cole C, Hart K, Johnson L, Heckmatt J, Dubowitz V, Bobrow M. The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy. Journal of Medical Genetics. 24: 152-9. PMID 3572997 DOI: 10.1136/jmg.24.3.152  0.108
1999 Mercuri E, Naom I, King M, Sewry C, Dubowitz V, Muntoni F. 298 Mutations in the lamin a2 chain gene in children with merosin-deficient CMD and cortical dysplasia European Journal of Paediatric Neurology. 3: A117. DOI: 10.1016/S1090-3798(99)91297-7  0.107
1996 DUBOWITZ V. MYOPATHIC CHANGES IN A MUSCULAR DYSTROPHY CARRIER. Journal of Neurology, Neurosurgery, and Psychiatry. 26: 322-5. PMID 14043046 DOI: 10.1136/jnnp.26.4.322  0.107
1963 Dubowitz V. Myopathic Changes in Muscular Dystrophy Carriers Proceedings of the Royal Society of Medicine. 56: 810-812. DOI: 10.1177/003591576305600923  0.107
1976 Yarom R, Maunder C, Scripps M, Hall TA, Dubowitz V. A simplified method of specimen preparation for X-ray microanalysis of muscle and blood cells. Histochemistry. 45: 49-59. PMID 811631 DOI: 10.1007/BF00508050  0.107
1982 Dubowitz V. New approaches to nerve and muscle disorders: Basic and applied contributions. Edited by A. D. Kidman, J. K. Tomkins, R. A. Westerman, 418 pp, excerpta medica, Amsterdam, The Netherlands, 1981. $63.75 Muscle & Nerve. 5: 348-348. DOI: 10.1002/MUS.880050416  0.107
2010 Dubowitz V. Clinical myology at the crossroads; the gospel truth. Neuromuscular Disorders : Nmd. 20: 95-6. PMID 20142012 DOI: 10.1016/j.nmd.2010.01.007  0.106
2006 Dubowitz V. Clinical Casebook Neuromuscular Disorders. 16: 813. DOI: 10.1016/j.nmd.2006.09.005  0.105
1989 Barrett R, Hyde SA, Scott OM, Dubowitz V. Changes in center of gravity in boys with Duchenne muscular dystrophy. Muscle & Nerve. 11: 1157-63. PMID 3226433 DOI: 10.1002/MUS.880111109  0.104
1993 Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V. Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA). Human Genetics. 92: 133-8. PMID 8370578 DOI: 10.1007/BF00219680  0.103
1977 Dubowitz L, Dubowitz V. Neurological Assessment of the Newborn Neuropediatrics. 8: 505-506. DOI: 10.1055/S-0028-1091557  0.102
1981 Leibowitz D, Dubowitz V. Intellect and behaviour in Duchenne muscular dystrophy. Developmental Medicine and Child Neurology. 23: 577-90. PMID 7286451 DOI: 10.1111/j.1469-8749.1981.tb02039.x  0.102
1976 Dubowitz V, Hersov L. Management of children with non-organic (hysterical) disorders of motor function. Developmental Medicine and Child Neurology. 18: 358-68. PMID 939349 DOI: 10.1111/j.1469-8749.1976.tb03658.x  0.102
1992 Cole CG, Abbs SJ, Dubowitz V, Hodgson SV, Warner J, Merlini L, Bobrow M. Linkage of emery-dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIII Neuromuscular Disorders. 2: 51-57. PMID 1525559 DOI: 10.1016/0960-8966(92)90027-4  0.101
1972 Gallup B, Bishop A, Dubowitz V. Autoradiographic studies of RNA and DNA synthesis during myogenesis in cultures of human, chick and rat muscle. Journal of the Neurological Sciences. 17: 127-40. PMID 5053921 DOI: 10.1016/0022-510X(72)90135-9  0.1
2009 Dubowitz V. Ramblings in the history of spinal muscular atrophy. Neuromuscular Disorders : Nmd. 19: 69-73. PMID 18951794 DOI: 10.1016/j.nmd.2008.10.004  0.099
1997 Manzur A, Muntoni F, Sewry C, Ziprin J, Dubowitz V. Dystrophic central core disease or muscular dystrophy with central cores? A possible new autosomal recessive disorder with central core disease Neuromuscular Disorders. 7: 428. DOI: 10.1016/S0960-8966(97)87166-0  0.099
1966 Dubowitz V. Hereditary Proximal Spinal Muscular Atrophy Bmj. 2: 173-174. DOI: 10.1136/bmj.2.5506.173-c  0.098
1989 Dubowitz V. The Duchenne dystrophy story: from phenotype to gene and potential treatment. Journal of Child Neurology. 4: 240-50. PMID 2677113 DOI: 10.1177/088307388900400402  0.098
1995 Dubowitz V. The history of a genetic disease, Duchenne Muscular Dystrophy or Meryon's disease Neuromuscular Disorders. 5: 524-525. DOI: 10.1016/0960-8966(95)90020-9  0.098
1981 Maunder-Sewry CA, Gorodetsky R, Yarom R, Dubowitz V. Element analysis of skeletal muscle in Duchenne muscular dystrophy using x-ray fluorescence spectrometry. Muscle & Nerve. 3: 502-8. PMID 7453715 DOI: 10.1002/MUS.880030607  0.098
1975 Dubowitz V. Benign infantile spinal muscular atrophy. Developmental Medicine and Child Neurology. 16: 672-5. PMID 4420627 DOI: 10.1111/j.1469-8749.1974.tb04188.x  0.098
1971 Dubowitz V, Cooke P, Colver D, Harris F. Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases. Journal of Medical Genetics. 8: 195-201. PMID 4328883 DOI: 10.1136/jmg.8.2.195  0.097
1987 Bowles NE, Dubowitz V, Sewry CA, Archard LC. Dermatomyositis, polymyositis, and Coxsackie-B-virus infection. Lancet (London, England). 1: 1004-7. PMID 2883345 DOI: 10.1016/S0140-6736(87)92271-9  0.096
1982 Dubowitz V. Sensory Ganglio-neuropathy in Infantile Spinal Muscular Atrophy Neuropediatrics. 13: 51-51. DOI: 10.1055/S-2008-1059596  0.095
1989 Rodillo EB, Fernandez-Bermejo E, Heckmatt JZ, Dubowitz V. Prevention of rapidly progressive scoliosis in Duchenne muscular dystrophy by prolongation of walking with orthoses. Journal of Child Neurology. 3: 269-74. PMID 3198893 DOI: 10.1177/088307388800300407  0.093
1987 Walker A, Hart K, Cole C, Hodgson S, Johnson L, Dubowitz V, Bobrow M. Linkage studies in Duchenne and Becker muscular dystrophies. Journal of Medical Genetics. 23: 538-47. PMID 2879925 DOI: 10.1136/jmg.23.6.538  0.093
1991 Dubowitz V. Chaos in classification of the spinal muscular atrophies of childhood Neuromuscular Disorders. 1: 77-80. PMID 1845352 DOI: 10.1016/0960-8966(91)90051-S  0.091
1980 Duance VC, Stephens HR, Dunn M, Bailey AJ, Dubowitz V. A role for collagen in the pathogenesis of muscular dystrophy? Nature. 284: 470-2. PMID 7360283 DOI: 10.1038/284470A0  0.09
1980 Dunn MJ, Burghes AH, Dubowitz V. Erythrocyte ghost Na+,K+-adenosine triphosphatase in Duchenne muscular dystrophy. Journal of the Neurological Sciences. 46: 209-20. PMID 6247454 DOI: 10.1016/0022-510X(80)90079-9  0.089
1968 Corkery JJ, Dubowitz V, Lister J, Moosa A. Colonic perforation after exchange transfusion. British Medical Journal. 4: 345-9. PMID 5303083 DOI: 10.1136/bmj.4.5627.345  0.088
1975 Cunningham M, Dubowitz V, Godfrey S. RESPIRATORY FUNCTION IN CHILDREN WITH NEUROMUSCULAR DISORDERS Pediatric Research. 9: 861-861. DOI: 10.1203/00006450-197511000-00058  0.087
1995 Zerres K, Rudnik-Schoneborn S, Dubowitz V, Emery AEH, Forst R, Granata C, Haverkamp F, Merlini L, Mielke U, Mokrusch T, Mortier W, Nix WA, Rudel R, Voit T, Wollinsky KH, et al. Guidelines for symptomatic therapy in spinal muscular atrophy (SMA) Acta Cardiomiologica. 7: 61-66.  0.086
1992 Quinlivan RM, Dubowitz V. Cardiac transplantation in Becker muscular dystrophy Neuromuscular Disorders. 2: 165-167. PMID 1483041 DOI: 10.1016/0960-8966(92)90002-N  0.086
1976 Dubowitz V. Neuromuscular disorders in childhood. Old dogmas, new concepts. Archives of Disease in Childhood. 50: 335-46. PMID 1103747 DOI: 10.1136/adc.50.5.335  0.086
1967 Dubowitz V. A Syndrome of Benign Congenital Hypotonia, Gross Obesity, Delayed Intellectual Development, Retarded Bone Age, and Unusual Facies Proceedings of the Royal Society of Medicine. 60: 1006-1008. DOI: 10.1177/003591576706001036  0.086
1990 Cameron PD, Dubowitz V, Besley GT, Fensom AH. Sialic acid storage disease. Archives of Disease in Childhood. 65: 314-5. PMID 2334213 DOI: 10.1136/ADC.65.3.314  0.085
2011 Dubowitz V. Muscular Dystrophy and Related Disorders. Postgraduate Medical Journal. 41: 332-46. PMID 21313711 DOI: 10.1136/pgmj.41.476.332  0.085
2019 Dubowitz V. Spinal Muscular Atrophy Revisited. Neuromuscular Disorders : Nmd. 29: 413-414. PMID 31227066 DOI: 10.1016/j.nmd.2019.06.008  0.085
1971 Moosa A, Dubowitz V. Peripheral neuropathy in Cockayne's syndrome. Archives of Disease in Childhood. 45: 674-7. PMID 4320535 DOI: 10.1136/adc.45.243.674  0.085
1996 DUBOWITZ V. PROGRESSIVE MUSCULAR DYSTROPHY: PREVENTION OF DEFORMITIES. Clinical Pediatrics. 3: 323-8. PMID 14154319 DOI: 10.1177/000992286400300520  0.084
1992 Dubowitz V. Neuromuscular Disorders Affecting the Lower Extremities Journal of Pediatric Orthopaedics B. 1: 168. DOI: 10.1097/01202412-199201020-00026  0.083
1981 DUNN M, STATHAM H, DUANCE V, STEPHENS H, DUBOWITZ V. Collagen synthesis in Duchenne muscular dystrophy Cell Biology International Reports. 5: 14. DOI: 10.1016/0309-1651(81)90060-6  0.082
1991 Peters AM, Heckmatt JZ, Hasson N, Henderson BL, el-Meleigy D, Rose ML, Dubowitz V. Renal haemodynamics of cyclosporin A nephrotoxicity in children with juvenile dermatomyositis. Clinical Science (London, England : 1979). 81: 153-9. PMID 1653658  0.082
1980 Duance VC, Black CM, Dubowitz V, Hughes GR, Bailey AJ. Polymyositis--an immunofluorescence study on the distribution of collagen types. Muscle & Nerve. 3: 487-90. PMID 7005670 DOI: 10.1002/mus.880030605  0.081
1996 Al Rajeh S, Brooke M, Cobben JM, Dubowitz V, Shapira Y, Estournet B, Finison L, Fuller C, Hausmanowa-Petrusewicz I, Ignatius J, Jacob P, Melki J, Merlini L, Munsat T, Muntoni F, et al. 38th ENMC International Workshop Spinal Muscular Atrophy Trial Group 10-12 December 1995, Naarden, The Netherlands Neuromuscular Disorders. 6: 293-294. PMID 10712015 DOI: 10.1016/S0960-8966(96)90032-2  0.081
1991 Dubowitz V. Neuromuscular disorders: gene location Neuromuscular Disorders : Nmd. 1: 75-76. PMID 1822779 DOI: 10.1016/0960-8966(91)90050-3  0.08
1984 LeVene M, Whitelaw A, Dubowitz V, Bydder G, Steiner R, Randell C, Young J. Nuclear magnetic resonance imaging of the brain in children Magnetic Resonance Imaging. 2: 65. DOI: 10.1016/0730-725X(84)90128-0  0.08
1972 Dubowitz V. Dystrophia myotonica in infancy and childhood. Archives of Disease in Childhood. 47: 671-2. PMID 5046787 DOI: 10.1136/adc.47.254.671-c  0.08
1976 Dubowitz V. Letter: Genetic miscounselling in muscular dystrophy. Archives of Disease in Childhood. 51: 325. PMID 1275548 DOI: 10.1136/adc.51.4.325  0.079
1981 Dubowitz V. DERMATOLOGICAL NON-DISEASE: A LOUSY DIAGNOSIS? The Lancet. 318: 480. DOI: 10.1016/S0140-6736(81)90824-2  0.079
1990 Heckmatt JZ, Loh L, Dubowitz V. Night-time nasal ventilation in neuromuscular disease. Lancet (London, England). 335: 579-82. PMID 1968582 DOI: 10.1016/0140-6736(90)90357-B  0.079
1999 Dubowitz V. Editorial comment: European Journal of Paediatric Neurology European Journal of Paediatric Neurology. 3: 1-2. DOI: 10.1053/ejpn.1999.0171  0.078
1972 Moosa A, Brown BH, Dubowitz V. Quantitative electromyography: carrier detection in Duchenne type muscular dystrophy using a new automatic technique Journal of Neurology Neurosurgery and Psychiatry. 35: 841-844. PMID 4647857 DOI: 10.1136/jnnp.35.6.841  0.077
1972 Dubowitz V. Diagnostic advances in neuromuscular disorders. Archives of Disease in Childhood. 47: 149-50. PMID 5018639 DOI: 10.1136/adc.47.251.149-c  0.077
1994 Poulton J, Morten K, Freeman-Emmerson C, Potter C, Sewry C, Dubowitz V, Kidd H, Stephenson J, Whitehouse W, Hansen FJ, Parisi M, Brown G. Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion Human Molecular Genetics. 3: 1763-1769. PMID 7849699  0.076
1997 Ferlini A, Sewry C, Dubowitz V, Muntoni F. Multiple transcripts in the exons 47–53 region of the dystrophin gene: does this influence dystrophin expression in normal and dystrophic tissues? Neuromuscular Disorders. 7: 438. DOI: 10.1016/S0960-8966(97)87209-4  0.076
2000 Dubowitz V. 75th European Neuromuscular Centre International Workshop: 2nd workshop on the treatment of muscular dystrophy 10-12 December, 1999, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 10: 313-20. PMID 10838260 DOI: 10.1016/S0960-8966(00)00126-7  0.076
1999 Dubowitz V. Forty years of neuromuscular disease: a historical perspective. Journal of Child Neurology. 14: 26-8. PMID 10223844  0.076
1985 Hillier J, Jones GE, Statham HE, Witkowski JA, Dubowitz V. Cell surface abnormality in clones of skin fibroblasts from a carrier of Duchenne muscular dystrophy. Journal of Medical Genetics. 22: 100-3. PMID 3989823 DOI: 10.1136/jmg.22.2.100  0.075
1992 Dubowitz V. Myoblast transfer in muscular dystrophy: Panacea or pie in the sky? Neuromuscular Disorders. 2: 305-310. PMID 1300179 DOI: 10.1016/S0960-8966(06)80001-5  0.075
1978 Ahmad M, Sanderson JE, Dubowitz V, Hallidie-Smith KA. Echocardiographic assessment of left ventricular function in Duchenne's muscular dystrophy. British Heart Journal. 40: 734-40. PMID 687470 DOI: 10.1136/hrt.40.7.734  0.075
1994 Quinlivan RM, Robb SA, Hall SM, Honavar M, Hughes RA, Dubowitz V. Infantile axonal neuropathy in two siblings. Neuromuscular Disorders : Nmd. 4: 227-32. PMID 7919970 DOI: 10.1016/0960-8966(94)90023-X  0.075
1976 Dubowitz V. Carrier detection and genetic counselling in Duchenne dystrophy. Developmental Medicine and Child Neurology. 17: 352-6. PMID 1107098 DOI: 10.1111/j.1469-8749.1975.tb04674.x  0.075
1994 Dubowitz V. Diagnostic criteria for neuromuscular disorders Neuromuscular Disorders. 4: 292-293. DOI: 10.1016/0960-8966(94)90038-8  0.074
1982 Dubowitz V. The female carrier of Duchenne muscular dystrophy. British Medical Journal (Clinical Research Ed.). 284: 1423-4. PMID 6805547 DOI: 10.1136/bmj.284.6327.1423  0.073
1978 Dubowitz V. A Clinician's View of Neuromuscular Diseases Journal of Neurology, Neurosurgery & Psychiatry. 41: 861-861. DOI: 10.1136/jnnp.41.9.861  0.073
1971 Dubowitz V. Muscular dystrophy--where is the lesion? Developmental Medicine and Child Neurology. 13: 238-40. PMID 5562866 DOI: 10.1111/J.1469-8749.1971.TB03251.X  0.073
1986 Dubowitz V. X;autosome translocations in females with Duchenne or Becker muscular dystrophy. Nature. 322: 291-2. PMID 3461282 DOI: 10.1038/322291B0  0.072
1994 Cambridge G, Ovadia E, Isenberg DA, Dubowitz V, Sperling J, Sperling R. Juvenile dermatomyositis: Serial studies of circulating autoantibodies to a 56kD nuclear protein Clinical and Experimental Rheumatology. 12: 451-457. PMID 7955614  0.072
1963 Dubowitz V. TREATMENT OF MUSCULAR DYSTROPHY The Lancet. 281: 1376. DOI: 10.1016/S0140-6736(63)91956-1  0.072
1969 Dubowitz V. Nerve conduction velocity-an index of neurological maturity of the newborn. Archives of Disease in Childhood. 43: 746. PMID 5702242 DOI: 10.1136/adc.43.232.746  0.07
1996 Dubowitz V. Alan E H Emery and Marcia L H Emery, The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease, London, Royal Society of Medicine Press, 1995, pp. xvi, 248, illus., £20.00, $40.00 (1-85315-249-8). Medical History. 40: 409-410. DOI: 10.1017/S0025727300061627  0.07
1996 Khan Y, Heckmatt JZ, Dubowitz V. Sleep studies and supportive ventilatory treatment in patients with congenital muscle disorders. Archives of Disease in Childhood. 74: 195-200. PMID 8787421  0.07
1980 DUNN M, STATHAM H, BURGHES A, RICEEVANS C, DUBOWITZ V. Erythrocyte membrane studies in duchenne muscular dystrophy Cell Biology International Reports. 4: 782. DOI: 10.1016/0309-1651(80)90135-6  0.07
1999 Dubowitz V. 68th ENMC international workshop (5th international workshop): On congenital muscular dystrophy, 9-11 April 1999, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 9: 446-54. PMID 10545052 DOI: 10.1016/S0960-8966(99)00074-7  0.069
1998 SHEDDEN WI, POTTER CW, DUBOWITZ V, WOOD M. An epidemic of gastroenteritis due to an uncommon variant of Escherichia coli 0.128. Journal of Clinical Pathology. 15: 482-3. PMID 13977020 DOI: 10.1136/jcp.15.5.482  0.069
1968 Shafiq SA, Dubowitz V, Peterson Hde C, Milhorat AT. Nemaline myopathy: report of a fatal case, with histochemical and electron microscopic studies. Brain : a Journal of Neurology. 90: 817-28. PMID 4169453 DOI: 10.1093/BRAIN/90.4.817  0.069
1980 Peters TJ, Jenkins W, Dubowitz V. Subcellular fractionation studies on hepatic tissue from a patient with Pompe's disease (type II glycogen-storage disease) Clinical Science. 59: 7-12. PMID 7009026 DOI: 10.1042/CS0590007  0.068
1998 DUBOWITZ V. Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance. Brain : a Journal of Neurology. 83: 432-9. PMID 13724668 DOI: 10.1093/BRAIN/83.3.432  0.068
1971 Dubowitz V. Recent advances in neuromuscular disorders. Rheumatology and Physical Medicine. 11: 126-30 passim. PMID 5572021 DOI: 10.1093/RHEUMATOLOGY/11.3.126  0.068
2000 DUBOWITZ V. Influenzal encephalitis. Lancet (London, England). 1: 140-1. PMID 13503234 DOI: 10.1016/s0140-6736(58)90617-2  0.066
1960 Dubowitz V. INFLUENZAL ENCEPHALITIS The Lancet. 275: 61. DOI: 10.1016/s0140-6736(60)92761-6  0.066
1982 Moss DW, Whitaker KB, Parmar C, Heckmatt J, Wikowski J, Sewry C, Dubowitz V. Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activation. Clinica Chimica Acta; International Journal of Clinical Chemistry. 116: 209-16. PMID 6794955 DOI: 10.1016/0009-8981(81)90024-3  0.066
1976 Dubowitz V. Screening for Duchenne muscular dystrophy. Archives of Disease in Childhood. 51: 249-51. PMID 776092 DOI: 10.1136/adc.51.4.249  0.065
1988 Robb SA, Fielder AH, Saunders CE, Davey NJ, Burley MW, Lord DH, Batchelor JR, Dubowitz V. C4 complement allotypes in juvenile dermatomyositis. Human Immunology. 22: 31-8. PMID 3260584 DOI: 10.1016/0198-8859(88)90049-3  0.065
1990 Cunningham L, Bowles NE, Lane RJ, Dubowitz V, Archard LC. Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA. The Journal of General Virology. 1399-402. PMID 2161907 DOI: 10.1099/0022-1317-71-6-1399  0.065
1997 Dubowitz V. A new journal in paediatric neurology for the next millennium European Journal of Paediatric Neurology. 1: 1-2. DOI: 10.1016/S1090-3798(97)80002-5  0.065
2006 Dubowitz V. THERAPEUTIC INNOVATIONS IN THE NEUROMUSCULAR DISORDERS Neuropediatrics. 37. DOI: 10.1055/s-2006-945743  0.064
1991 Khan Y, Hasson N, Manzur A, Heckmatt J, Dubowitz V. Effect of Nasal Ventilation on Nocturnal Hypoxia in Neuromuscular Patients Clinical Science. 81: 1P-1P. DOI: 10.1042/CS081001P  0.063
1997 Dubowitz V. 47th ENMC International Workshop: Treatment of muscular dystrophy. 13-15 December 1996, Naarden, The Netherlands Neuromuscular Disorders. 7: 261-267. PMID 9196909  0.063
1965 Blyth H, Carter CO, Dubowitz V, Emery AEH, Gavin J, Johnston HA, McKusick VA, Race RR, Sanger R, Tippett P. Duchenne's Muscular Dystrophy and the Xg Blood Groups: a Search for Linkage Journal of Medical Genetics. 2: 157-160. DOI: 10.1136/jmg.2.3.157  0.063
1996 SANGER R, RACE RR, TIPPETT P, GAVIN J, HARDISTY RM, DUBOWITZ V. UNEXPLAINED INHERITANCE OF THE XG GROUPS IN TWO FAMILIES. Lancet (London, England). 1: 955-6. PMID 14121353 DOI: 10.1016/S0140-6736(64)91744-1  0.062
1982 Dunn MJ, Burghes AH, Dubowitz V. Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophy. The Biochemical Journal. 201: 445-53. PMID 6124239 DOI: 10.1042/BJ2010445  0.061
1978 LITTY D, DUBOWITZ V. Film review: The Dubowitz assessment of newborn gestational age Journal of Nurse-Midwifery. 23: 12. DOI: 10.1016/0091-2182(78)90014-9  0.06
2020 Dubowitz V. Neuromuscular Disorders at 30. Neuromuscular Disorders : Nmd. PMID 32912715 DOI: 10.1016/j.nmd.2020.08.363  0.06
2002 Dubowitz V. Neuromuscular Disorders: Foreword Neuromuscular Disorders. 12: S1-S2. DOI: 10.1016/S0960-8966(02)00073-1  0.06
1992 Dubowitz V. Neuromuscular Disorders Journal of Pediatric Orthopaedics B. 1: 166. DOI: 10.1097/01202412-199201020-00020  0.06
1981 Burghes AH, Dunn MJ, Witkowski JA, Dubowitz V. Polyacrylamide-gel-electrophoretic analysis of cultured skin fibroblasts from patients with Duchenne muscular dystrophy. Biochemical Society Transactions. 9: 118-9. PMID 7215634 DOI: 10.1042/BST0090118  0.06
1996 DUBOWITZ V. FAMILIAL LOW BIRTHWEIGHT DWARFISM WITH AN UNUSUAL FACIES AND A SKIN ERUPTION. Journal of Medical Genetics. 2: 12-7. PMID 14296916 DOI: 10.1136/jmg.2.1.12  0.058
1970 Roy S, Dubowitz V. Carrier detection in Duchenne muscular dystrophy. A comparative study of electron microscopy, light microscopy and serum enzymes. Journal of the Neurological Sciences. 11: 65-79. PMID 5451354 DOI: 10.1016/0022-510X(70)90041-9  0.057
1982 Burghes AHM, Dunn MJ, Statham HE, Dubowitz V. Analysis of skin fibroblast proteins in Duchenne muscular dystrophy: 1. Sodium dodecyl sulphate polyacrylamide gel electrophoresis Electrophoresis. 3: 177-185. DOI: 10.1002/ELPS.1150030402  0.057
1965 DUBOWITZ V, LORBER J, ZACHARY RB. LIPOMA OF THE CAUDA EQUINA. Archives of Disease in Childhood. 40: 207-13. PMID 14288045 DOI: 10.1136/adc.40.210.207  0.056
1984 Heckmatt JZ, Dubowitz V. Detecting the Duchenne carrier by ultrasound and computerized tomography. Lancet (London, England). 2: 1364. PMID 6139695 DOI: 10.1016/S0140-6736(83)91119-4  0.055
2011 Dubowitz V. Current concerns in the therapy of neuromuscular disorders. Neuromuscular Disorders : Nmd. 21: 3. PMID 21130653 DOI: 10.1016/j.nmd.2010.11.005  0.055
1993 Dubowitz V. BOOK REVIEWS: Textbook of Child Neurology. 4th Edition. Journal of Neurology, Neurosurgery & Psychiatry. 56: 227-228. DOI: 10.1136/jnnp.56.2.227-c  0.054
1992 Dubowitz V. Transferring myoblasts in Duchenne dystrophy British Medical Journal. 305: 844-845. PMID 1422391  0.054
1969 Dubowitz V. Dermatoglyphics of leukaemic children. Lancet (London, England). 1: 1213. PMID 4181863 DOI: 10.1016/S0140-6736(69)92193-X  0.054
1974 König P, Godfrey S, Dubowitz V. Proceedings: Genetics of wheezy children assessed by exercise-induced bronchial lability. Archives of Disease in Childhood. 49: 242. PMID 4825633 DOI: 10.1136/adc.49.3.242-b  0.054
1982 Burghes AHM, Dunn MJ, Statham HE, Dubowitz V. Analysis of skin fibroblast proteins in Duchenne muscular dystrophy: 2. Isoelectric focusing under dissociating conditions Electrophoresis. 3: 185-196. DOI: 10.1002/ELPS.1150030403  0.053
1996 DUBOWITZ LM, DUBOWITZ V. ACUTE DERMATOMYOSITIS PRESENTING WITH PULMONARY MANIFESTATIONS. Archives of Disease in Childhood. 39: 293-6. PMID 14169463 DOI: 10.1136/adc.39.205.293  0.053
1997 Dubowitz V. How primitive is the Moro reflex? European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 1: 191. PMID 10728219  0.052
1993 Dubowitz V. Meryon's disease Neuromuscular Disorders. 3: 261.  0.052
1992 Hamill G, Saunders C, Heckmatt J, Dubowitz V, Stanhope R. "Catch-up" growth in steroid dependent dermatomyositis treated with cyclosporin-A The European Journal of Medicine. 1: 16-18. PMID 1341971  0.051
1998 Dubowitz V. Closed spinal dysraphism. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 2: 324-6. PMID 10727201 DOI: 10.1016/S1090-3798(98)80009-3  0.05
1981 Dunn MJ, Burghes AH, Dubowitz V. Erythrocyte membrane (Ca/+ + Mg/+)-activated adenosine triphosphatase in Duchenne muscular dystrophy. Biochemical Society Transactions. 9: 81-2. PMID 6111509 DOI: 10.1042/BST0090081  0.05
1996 MULLAN D, DUBOWITZ V. SERUM ENZYMES IN DIAGNOSIS OF TETANUS. Lancet (London, England). 2: 505-7. PMID 14172921 DOI: 10.1016/S0140-6736(64)90457-X  0.047
1982 Statham HE, Witkowski JA, Dubowitz V. Protein degradation in skin fibroblasts from patients with Duchenne muscular dystrophy. The Biochemical Journal. 192: 257-62. PMID 7305898 DOI: 10.1042/BJ1920257  0.047
1981 Dubowitz V, Heckmatt J. Management of muscular dystrophy. Pharmacological and physical aspects. British Medical Bulletin. 36: 139-44. PMID 7020840 DOI: 10.1093/OXFORDJOURNALS.BMB.A071629  0.046
1996 DUBOWITZ V. OCULAR INVOLVEMENT IN JUVENILE RHEUMATOID ARTHRITIS, (STILL'S DISEASE). Clinical Pediatrics. 3: 274-8. PMID 14124879 DOI: 10.1177/000992286400300507  0.046
2010 Dubowitz V. Deformities in Duchenne dystrophy. Neuromuscular Disorders : Nmd. 20: 282. PMID 20371091 DOI: 10.1016/j.nmd.2010.03.013  0.045
1977 Dubowitz V. Fetal movements in utero. Developmental Medicine and Child Neurology. 19: 239-40. PMID 858450 DOI: 10.1111/J.1469-8749.1977.TB07975.X  0.044
1979 Statham HE, Dubowitz V. Duchenne muscular dystrophy: 45Ca exchange in cultured skin fibroblasts and the effect of calcium ionophore A23187. Clinica Chimica Acta; International Journal of Clinical Chemistry. 96: 225-31. PMID 385173 DOI: 10.1016/0009-8981(79)90432-7  0.044
1992 Dubowitz V. Genetic counselling Neuromuscular Disorders. 2: 85-86. PMID 1422202 DOI: 10.1016/0960-8966(92)90039-9  0.043
1973 Dubowitz V. Plasma Digoxin Concentration in Children with Heart Failure Bmj. 2: 118-119. DOI: 10.1136/bmj.2.5858.118-c  0.041
1970 Rogers KJ, Dubowitz V. 5-hydroxyindoles in hydrocephalus. A comparative study of cerebrospinal fluid and blood levels Developmental Medicine and Child Neurology. 12: 461-466. PMID 4917606 DOI: 10.1111/j.1469-8749.1970.tb01940.x  0.041
1995 Dubowitz V. Chaos in the classification of SMA: A possible resolution Neuromuscular Disorders. 5: 3-5. PMID 7719138 DOI: 10.1016/0960-8966(94)00075-K  0.04
1984 Witkowski JA, Statham HE, Dubowitz V. Rotation-mediated aggregation of skin fibroblasts in Duchenne muscular dystrophy. Effects of monensin. Journal of the Neurological Sciences. 61: 425-33. PMID 6655491 DOI: 10.1016/0022-510X(83)90175-2  0.04
1997 North KN, Laing NG, Wallgren-Pettersson C, Akkari A, Barohn R, Barth P, Beggs A, De La Chapelle A, De Visser M, Dubowitz V, Fiszman M, Goebel H, Iannaccone S, Jasani B, Labeit S, et al. Nemaline myopathy: Current concepts Journal of Medical Genetics. 34: 705-713. PMID 9321754 DOI: 10.1136/Jmg.34.9.705  0.039
1979 Dubowitz L, Morante de Romero A, Dubowitz V. A Study of Visual Function in the Newborn by the Brazelton Behavioural Scale and Fantz Box Method Neuropediatrics. 10: 417-417. DOI: 10.1055/S-0028-1085351  0.039
2010 Constantini S, Rosman NP, Evrard P, Velickovic Perat M, Stumpf DA, Dubowitz V. A tribute and toast on the occasion of the retirement of Professor Shaul Harel, MD. Journal of Child Neurology. 25: 637-43. PMID 20207614 DOI: 10.1177/0883073809357470  0.035
1994 Mac Naughton MC, Chalmers IG, Dubowitz V, Dunn PM, Grant AM, Mc Pherson K, Pearson JF, Peto R, Turnbull AC. Final report of the medical research council/royal college of obstetricians and gynaecologists multicentre randomised trial of cervical cerclage Obstetrical and Gynecological Survey. 49: 3-5. DOI: 10.1097/00006254-199401000-00002  0.033
2000 Dubowitz V. Volume contents European Journal of Paediatric Neurology. 4: 299-304. DOI: 10.1053/ejpn.2000.0390  0.032
1972 Moosa A, Dubowitz V. Slow nerve conduction velocity in cretins. Archives of Disease in Childhood. 46: 852-4. PMID 4331578 DOI: 10.1136/adc.46.250.852  0.032
1995 Wang J, Dubowitz V, Lehmann-Horn F, Ricker K, Ptacek L, Hoffman EP. In vivo sodium channel structure/function studies: Consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4 Journal of General Physiology. 77-88.  0.029
2009 Dubowitz V. Nemaline myopathy: a tale of two cultures. Neuromuscular Disorders : Nmd. 19: 177-8. PMID 19231186 DOI: 10.1016/j.nmd.2009.01.004  0.028
2007 Dubowitz V. Veterinary Myology Neuromuscular Disorders. 17: 275. DOI: 10.1016/j.nmd.2007.03.005  0.028
2008 Coleman M, Dubowitz V, Rogers KJ. 5-HFAA in Cerebrospinal Fluid Developmental Medicine & Child Neurology. 12: 539-541. DOI: 10.1111/j.1469-8749.1970.tb01957.x  0.028
1976 Maunder CA, Dubowitz V, Yarom R. Electron Microscopic X-Ray Analysis as a Potential Tool in the Localization and Quantitation of Intracellular Elements Clinical Science. 50: 14P-14P. DOI: 10.1042/CS050014P  0.026
1979 Dubowitz V, Pennington RJ. GENERAL DISCUSSION Annals of the New York Academy of Sciences. 317: 221-223. DOI: 10.1111/j.1749-6632.1979.tb56530.x  0.025
1983 Pier N, Dubowitz V. Chronic graft versus host disease presenting with polymyositis. British Medical Journal (Clinical Research Ed.). 286: 2024. PMID 6409214 DOI: 10.1136/bmj.286.6383.2024  0.024
1976 Tyrrell DA, Ryman BE, Keeton BR, Dubowitz V. Use of liposomes in treating type II glycogenosis. British Medical Journal. 2: 88. PMID 1064464 DOI: 10.1136/bmj.2.6027.88  0.023
2013 Dubowitz V. Response. Neuromuscular Disorders : Nmd. 23: 697. PMID 23850237 DOI: 10.1016/j.nmd.2013.07.001  0.021
1997 Dubowitz V. Utrophin euphoria. Neuromuscular Disorders : Nmd. 7: 5-6. PMID 9132140 DOI: 10.1016/S0960-8966(96)00432-4  0.021
1996 DUBOWITZ V. ACUTE MONOCYTIC LEUKAEMIA WITH RESPONSE TO METHOTREXATE. Archives of Disease in Childhood. 39: 289-92. PMID 14169462 DOI: 10.1136/ADC.39.205.289  0.02
1982 Thompson BJ, Dunn MJ, Burghes AHM, Dubowitz V. Improvements of isoelectric focusing in agarose for direct tissue isoelectric focusing Electrophoresis. 3: 307-314. DOI: 10.1002/ELPS.1150030602  0.02
1982 Burghes AHM, Dunn MJ, Dubowitz V. Enhancement of resolution in two-dimensional gel electrophoresis and simultaneous resolution of acidic and basic proteins Electrophoresis. 3: 354-363. DOI: 10.1002/ELPS.1150030611  0.019
2020 Dubowitz V. Commentary from the Editor. Neuromuscular Disorders : Nmd. 30: 1-4. PMID 32111347 DOI: 10.1016/j.nmd.2020.01.005  0.018
2019 Dubowitz V. Commentary from the Editor. Neuromuscular Disorders : Nmd. 29: 1-4. PMID 30717916 DOI: 10.1016/j.nmd.2019.01.005  0.018
2018 Dubowitz V. Commentary from the Editor. Neuromuscular Disorders : Nmd. 28: 1-3. PMID 29332703 DOI: 10.1016/j.nmd.2017.12.007  0.018
2017 Dubowitz V. Commentary from the Editor. Neuromuscular Disorders : Nmd. 27: 1-3. PMID 28087000 DOI: 10.1016/j.nmd.2016.12.013  0.018
2016 Dubowitz V. Commentary from the Editor. Neuromuscular Disorders : Nmd. 26: 1-4. PMID 26801250 DOI: 10.1016/j.nmd.2015.12.005  0.018
2015 Dubowitz V. Commentary from the editor. Neuromuscular Disorders : Nmd. 25: 1-4. PMID 25543197 DOI: 10.1016/j.nmd.2014.12.003  0.018
2010 Dubowitz V. Commentary from the editor. Neuromuscular Disorders : Nmd. 20: 1-5. PMID 20122643 DOI: 10.1016/j.nmd.2009.12.007  0.018
2007 Dubowitz V. Commentary from the editor. Neuromuscular Disorders : Nmd. 17: 1-5. PMID 17276884 DOI: 10.1016/j.nmd.2006.12.005  0.018
1999 Dubowitz V. Commentary from the Editor: Editorial Neuromuscular Disorders. 9: 1-2. DOI: 10.1016/S0960-8966(98)00122-9  0.017
1976 Dubowitz V. Professor Dubowitz comments Archives of Disease in Childhood. 51: 983-983. DOI: 10.1136/ADC.51.12.983  0.016
1971 Moosa A, Dubowitz V. Late infantile metachromatic leucodystrophy. Effect of low vitamin A diet. Archives of Disease in Childhood. 46: 381-3. PMID 5556636 DOI: 10.1136/adc.46.247.381  0.014
1964 Black J, Dubowitz V, Gordon RR, Holt KS, Illingworth RS, Lorber J. Management of Meningitis Bmj. 1: 1251-1252. DOI: 10.1136/bmj.1.5392.1251-a  0.012
2002 Dubowitz V, Casaer P. Forthcoming meetings European Journal of Paediatric Neurology. 6: 239. DOI: 10.1053/ejpn.2002.0604  0.012
2002 Dubowitz V. The Journal: A crisis of space and time Neuromuscular Disorders. 12: 437. DOI: 10.1016/S0960-8966(02)00063-9  0.012
2003 Dubowitz V. Editorial farewell European Journal of Paediatric Neurology. 7: 2.  0.011
2002 DUBOWITZ V, CASAER P. Index of keywords European Journal of Paediatric Neurology. 6: 350. DOI: 10.1053/EJPN.2002.0630  0.011
2021 Dubowitz V. Fools rush in where angels fear to tread. Neuromuscular Disorders : Nmd. 31: 921-924. PMID 34736632 DOI: 10.1016/j.nmd.2021.09.001  0.01
2019 Dubowitz V. Critical Review Ahead of Publication. Neuromuscular Disorders : Nmd. 29: 412. PMID 31227065 DOI: 10.1016/j.nmd.2019.06.007  0.01
2019 Dubowitz V. The World Wide Web (WWW): For better or for worse. Neuromuscular Disorders : Nmd. 29: 411. PMID 31227064 DOI: 10.1016/j.nmd.2019.06.006  0.01
2010 Dubowitz V. Letter 7 Neuromuscular Disorders. 20: 219. DOI: 10.1016/j.nmd.2010.02.011  0.01
2010 Dubowitz V. Richard H.T. Edwards PhD, FRCP (1939–2009) Neuromuscular Disorders. 20: 220-221. DOI: 10.1016/j.nmd.2010.01.009  0.01
2003 Dubowitz V, Casaer P. Editorial comment European Journal of Paediatric Neurology. 7: 1-2. DOI: 10.1016/S1090-3798(02)00147-2  0.01
2002 Dubowitz V, Casaer P. EJPN 2001: Referees consulted European Journal of Paediatric Neurology. 6: 3. DOI: 10.1053/ejpn.2001.0536  0.01
2001 Dubowitz V, Casaer P. Key word index European Journal of Paediatric Neurology. 5: 280. DOI: 10.1053/ejpn.2001.0534  0.01
2001 Dubowitz V, Casaer P. EJPN 2000: Referees consulted European Journal of Paediatric Neurology. 5: 2. DOI: 10.1053/EJPN.2001.0396  0.01
2000 Dubowitz V. Abstracts for the Jubilaeum Congresses European Journal of Paediatric Neurology. 4: 251-281. DOI: 10.1053/ejpn.2000.0318  0.01
2000 Dubowitz V, Casaer P. Editorial comment/Referees consulted European Journal of Paediatric Neurology. 4: 2. DOI: 10.1053/EJPN.1999.0252  0.01
2000 Dubowitz V, Casaer P. Editorial comment/Referees consulted European Journal of Paediatric Neurology. 4: 1-2. DOI: 10.1053/ejpn.1999.0251  0.01
1995 Dubowitz V. Anita Harding (1952 – 1995) Neuromuscular Disorders. 5: 519-520. DOI: 10.1016/0960-8966(95)90017-9  0.01
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