Dubowitz V - Search Results

1

Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy.

Naom I, D'Alessandro M, Sewry CA, Philpot J, Manzur AY, Dubowitz V, Muntoni F. Naom I, et al. Among authors: dubowitz v. Neuromuscul Disord. 1998 Oct;8(7):495-501. doi: 10.1016/s0960-8966(98)00065-0. Neuromuscul Disord. 1998. PMID: 9829280

2

Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes.

Mercuri E, Dubowitz L, Berardinelli A, Pennock J, Jongmans M, Henderson S, Muntoni F, Sewry C, Philpot J, Dubowitz V. Mercuri E, et al. Among authors: dubowitz v, dubowitz l. Neuropediatrics. 1995 Jun;26(3):156-62. doi: 10.1055/s-2007-979746. Neuropediatrics. 1995. PMID: 7477754

3

Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoforms.

Wilson LA, Dux L, Cooper BJ, Dubowitz V, Sewry CA. Wilson LA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1994 Jan;4(1):25-37. doi: 10.1016/0960-8966(94)90045-0. Neuromuscul Disord. 1994. PMID: 7513568

4

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle.

Philpot J, Sewry C, Pennock J, Dubowitz V. Philpot J, et al. Among authors: dubowitz v. Neuromuscul Disord. 1995 Jul;5(4):301-5. doi: 10.1016/0960-8966(94)00069-l. Neuromuscul Disord. 1995. PMID: 7580243

5

Expression of laminin subunits in congenital muscular dystrophy.

Sewry CA, Philpot J, Mahony D, Wilson LA, Muntoni F, Dubowitz V. Sewry CA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1995 Jul;5(4):307-16. doi: 10.1016/0960-8966(94)00072-h. Neuromuscul Disord. 1995. PMID: 7580244

6

Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy.

Philpot J, Topaloglu H, Pennock J, Dubowitz V. Philpot J, et al. Among authors: dubowitz v. Neuromuscul Disord. 1995 May;5(3):227-31. doi: 10.1016/0960-8966(94)00047-d. Neuromuscul Disord. 1995. PMID: 7633188

7

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.

Mercuri E, Muntoni F, Berardinelli A, Pennock J, Sewry C, Philpot J, Dubowitz V. Mercuri E, et al. Among authors: dubowitz v. Neuropediatrics. 1995 Feb;26(1):3-7. doi: 10.1055/s-2007-979711. Neuropediatrics. 1995. PMID: 7791947

8

Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy.

Sewry CA, Matsumura K, Campbell KP, Dubowitz V. Sewry CA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):401-9. doi: 10.1016/0960-8966(94)90079-5. Neuromuscul Disord. 1994. PMID: 7881285 Clinical Trial.

9

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.

Sewry CA, Sansome A, Matsumura K, Campbell KP, Dubowitz V. Sewry CA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1994 Mar;4(2):121-9. doi: 10.1016/0960-8966(94)90003-5. Neuromuscul Disord. 1994. PMID: 8012192

10

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.

Dux L, Cooper BJ, Sewry CA, Dubowitz V. Dux L, et al. Among authors: dubowitz v. Neuromuscul Disord. 1993 Jan;3(1):23-9. doi: 10.1016/0960-8966(93)90038-l. Neuromuscul Disord. 1993. PMID: 8329886

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