Victor Dubowitz - Publications

Affiliations: 
Imperial College, London, London, England, United Kingdom 
Area:
Paediatric Neurology
Website:
http://en.wikipedia.org/wiki/Victor_Dubowitz

166 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.36
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  0.36
2013 Dubowitz V. Response. Neuromuscular Disorders : Nmd. 23: 697. PMID 23850237 DOI: 10.1016/j.nmd.2013.07.001  0.36
2013 Dubowitz V. Steroids in Duchenne dystrophy. Neuromuscular Disorders : Nmd. 23: 527-8. PMID 23743333 DOI: 10.1016/j.nmd.2013.05.004  0.36
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  0.36
2011 Dubowitz V. Muscle cramps and coffee. Neuromuscular Disorders : Nmd. 21: 235. PMID 21310614 DOI: 10.1016/j.nmd.2011.01.004  0.36
2010 Dubowitz V. Deformities in Duchenne dystrophy. Neuromuscular Disorders : Nmd. 20: 282. PMID 20371091 DOI: 10.1016/j.nmd.2010.03.013  0.36
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  0.36
2010 Dubowitz V. Letter 7 Neuromuscular Disorders. 20: 219. DOI: 10.1016/j.nmd.2010.02.011  0.36
2006 Dubowitz V. Clinical Casebook Neuromuscular Disorders. 16: 813. DOI: 10.1016/j.nmd.2006.09.005  0.36
2005 Dubowitz V. Prednisone for Duchenne muscular dystrophy. The Lancet. Neurology. 4: 264. PMID 15847833 DOI: 10.1016/S1474-4422(05)70050-8  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
2003 Dubowitz V, Casaer P. Editorial comment European Journal of Paediatric Neurology. 7: 1-2. DOI: 10.1016/S1090-3798(02)00147-2  0.36
2003 Dubowitz V. Editorial farewell European Journal of Paediatric Neurology. 7: 2.  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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.  0.36
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: 10.1053/ejpn.1999.0181  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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/s004390051106  0.36
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  0.36
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  0.36
1999 Dubowitz V. Forty years of neuromuscular disease: a historical perspective. Journal of Child Neurology. 14: 26-8. PMID 10223844  0.36
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  0.36
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  0.36
1999 Dubowitz V. Editorial comment: European Journal of Paediatric Neurology European Journal of Paediatric Neurology. 3: 1-2. DOI: 10.1053/ejpn.1999.0171  0.36
1999 Dubowitz V. Commentary from the Editor: Editorial Neuromuscular Disorders. 9: 1-2. DOI: 10.1016/S0960-8966(98)00122-9  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
1997 Dubowitz V. Utrophin euphoria. Neuromuscular Disorders : Nmd. 7: 5-6. PMID 9132140 DOI: 10.1016/S0960-8966(96)00432-4  0.36
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  0.36
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  0.36
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  0.36
1997 Dubowitz V. The muscular dystrophies--clarity or chaos? The New England Journal of Medicine. 336: 650-1. PMID 9032052 DOI: 10.1056/NEJM199702273360909  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
1996 Dubowitz V. New developments in congenital muscular dystrophy Neuromuscular Disorders. 6: 228. DOI: 10.1016/0960-8966(96)84617-7  0.36
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  0.36
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'AcadéMie Des Sciences. SéRie Iii, Sciences De La Vie. 318: 1245-52. PMID 8745640  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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.  0.36
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.  0.36
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  0.36
1994 Bush A, Dubowitz V. Becker muscular dystrophy: An unusual presentation [4] Archives of Disease in Childhood. 70: 71. PMID 8110014  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
1994 Muntoni F, Gobbi P, Sewry C, Sherratt T, Taylor J, Sandhu SK, Abbs S, Roberts R, Hodgson SV, Bobrow M. Deletions in the 5' region of dystrophin and resulting phenotypes. Journal of Medical Genetics. 31: 843-7. PMID 7853367  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
1993 Dubowitz V. Editorial. Selected proceedings of Strasbourg Meeting Neuromuscular Disorders. 3: 351.  0.36
1993 Dubowitz V. Meryon's disease Neuromuscular Disorders. 3: 261.  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
1992 Dubowitz V. Transferring myoblasts in Duchenne dystrophy British Medical Journal. 305: 844-845. PMID 1422391  0.36
1992 Dubowitz V. Genetic counselling Neuromuscular Disorders. 2: 85-86. PMID 1422202 DOI: 10.1016/0960-8966(92)90039-9  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
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  0.36
1991 Dubowitz V. Prednisone in Duchenne dystrophy Neuromuscular Disorders. 1: 161-163. PMID 1822789 DOI: 10.1016/0960-8966(91)90019-O  0.36
1991 Dubowitz V. Neuromuscular disorders: gene location Neuromuscular Disorders : Nmd. 1: 75-76. PMID 1822779 DOI: 10.1016/0960-8966(91)90050-3  0.36
1991 Dubowitz V. A new muscle journal for the nineties Neuromuscular Disorders. 1: 1-2. PMID 1822773  0.36
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  0.36
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  0.36
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  0.4
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  0.36
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  0.36
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  0.4
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  0.4
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  0.4
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