| 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 |
|
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