Victor Dubowitz
Affiliations: | Imperial College, London, London, England, United Kingdom |
Area:
Paediatric NeurologyWebsite:
http://en.wikipedia.org/wiki/Victor_DubowitzGoogle:
"Victor Dubowitz"Mean distance: 29.89 (cluster 44)
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Publications
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Dubowitz V. (2005) A short history of the World Muscle Society. Neuromuscular Disorders : Nmd. 15: 642-7 |
Dubowitz V. (2005) Prednisone for Duchenne muscular dystrophy. The Lancet. Neurology. 4: 264 |
Dubowitz V. (2004) Therapeutic efforts in Duchenne muscular dystrophy; the need for a common language between basic scientists and clinicians. Neuromuscular Disorders : Nmd. 14: 451-5 |
Mercuri E, Brockington M, Straub V, et al. (2003) Phenotypic spectrum associated with mutations in the fukutin-related protein gene. Annals of Neurology. 53: 537-42 |
Tonini MM, Passos-Bueno MR, Cerqueira A, et al. (2002) 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 |
Philpot J, Counsell S, Bydder G, et al. (2001) Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect? Neuromuscular Disorders : Nmd. 11: 489-93 |
Jungbluth H, Sewry CA, Brown SC, et al. (2001) 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 |
Jungbluth H, Sewry C, Brown SC, et al. (2000) Minicore myopathy in children: a clinical and histopathological study of 19 cases. Neuromuscular Disorders : Nmd. 10: 264-73 |
Mercuri E, Goodwin F, Sewry C, et al. (2000) Diaphragmatic spinal muscular atrophy with bulbar weakness. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 4: 69-72 |
Brockington M, Sewry CA, Herrmann R, et al. (2000) Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42. American Journal of Human Genetics. 66: 428-35 |