Sewry CA - Search Results

1

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.

Sewry CA, Naom I, D'Alessandro M, Sorokin L, Bruno S, Wilson LA, Dubowitz V, Muntoni F. Sewry CA, et al. Neuromuscul Disord. 1997 May;7(3):169-75. doi: 10.1016/s0960-8966(97)00425-2. Neuromuscul Disord. 1997. PMID: 9185180

2

Experimental regeneration in canine muscular dystrophy--1. Immunocytochemical evaluation of dystrophin and beta-spectrin expression.

Sewry CA, Wilson LA, Dux L, Dubowitz V, Cooper BJ. Sewry CA, et al. Neuromuscul Disord. 1992;2(5-6):331-42. doi: 10.1016/s0960-8966(06)80004-0. Neuromuscul Disord. 1992. PMID: 1300182

3

Characterisation of dystrophin in fetuses at risk for Duchenne muscular dystrophy.

Clerk A, Sewry CA, Dubowitz V, Strong PN. Clerk A, et al. Among authors: sewry ca. J Neurol Sci. 1992 Aug;111(1):82-91. doi: 10.1016/0022-510x(92)90116-3. J Neurol Sci. 1992. PMID: 1403002

4

Characterisation of dystrophin during development of human skeletal muscle.

Clerk A, Strong PN, Sewry CA. Clerk A, et al. Among authors: sewry ca. Development. 1992 Feb;114(2):395-402. doi: 10.1242/dev.114.2.395. Development. 1992. PMID: 1592000

5

Dystrophin abnormalities in polymyositis and dermatomyositis.

Sewry CA, Clerk A, Heckmatt JZ, Vyse T, Dubowitz V, Strong PN. Sewry CA, et al. Neuromuscul Disord. 1991;1(5):333-9. doi: 10.1016/0960-8966(91)90119-d. Neuromuscul Disord. 1991. PMID: 1822343

6

Rhabdomyolysis after intramuscular iron-dextran in malabsorption.

Foulkes WD, Sewry C, Calam J, Hodgson HJ. Foulkes WD, et al. Ann Rheum Dis. 1991 Mar;50(3):184-6. doi: 10.1136/ard.50.3.184. Ann Rheum Dis. 1991. PMID: 2015014 Free PMC article.

7

Characterisation of dystrophin in carriers of Duchenne muscular dystrophy.

Clerk A, Rodillo E, Heckmatt JZ, Dubowitz V, Strong PN, Sewry CA. Clerk A, et al. Among authors: sewry ca. J Neurol Sci. 1991 Apr;102(2):197-205. doi: 10.1016/0022-510x(91)90069-j. J Neurol Sci. 1991. PMID: 2072119

8

[Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin].

Voit T, Patel K, Sewry CA, Strong PN, Dubowitz V, Dunn MJ. Voit T, et al. Among authors: sewry ca. Monatsschr Kinderheilkd. 1989 Jan;137(1):20-7. Monatsschr Kinderheilkd. 1989. PMID: 2646527 German.

9

Myopathy with unique ultrastructural feature in Marinesco-Sjögren syndrome.

Sewry CA, Voit T, Dubowitz V. Sewry CA, et al. Ann Neurol. 1988 Oct;24(4):576-80. doi: 10.1002/ana.410240416. Ann Neurol. 1988. PMID: 3239958

10

Binding of Ricinus communis I lectin to developing dystrophic muscle in human fetus.

Voit T, Sewry CA, Dunn MJ, Dubowitz V. Voit T, et al. Among authors: sewry ca. J Neurol Sci. 1988 Apr;84(2-3):301-14. doi: 10.1016/0022-510x(88)90134-7. J Neurol Sci. 1988. PMID: 3379448

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