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                             14 results found
no title author magazine year volume issue page(s) type
1 Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy Amouri, R.
2005
15 5 p. 361-363
3 p.
article
2 A rapid PCR method for genotyping the Largemyd mouse, a model of glycosylation-deficient congenital muscular dystrophy Browning, Claudia A.
2005
15 5 p. 331-335
5 p.
article
3 Congenital muscular dystrophy with glycosylation defects of α-dystroglycan in Japan Matsumoto, Hiroshi
2005
15 5 p. 342-348
7 p.
article
4 Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation Müller, T.
2005
15 5 p. 372-376
5 p.
article
5 IFC: Editorial Board 2005
15 5 p. co2-
1 p.
article
6 Instructions to Authors 2005
15 5 p. 396-397
2 p.
article
7 Multifocal motor neuropathy, type 1 diabetes and asymptomatic Hashimoto's thyroiditis: an unusual association Reisin, Ricardo C.
2005
15 5 p. 358-360
3 p.
article
8 New phenotypic diversity associated with the mitochondrial tRNASer(UCN) gene mutation Pulkes, T.
2005
15 5 p. 364-371
8 p.
article
9 [No title] Lecky, Bryan
2005
15 5 p. 395-
1 p.
article
10 Preservation of in vitro muscle fiber function in dermatomyositis and inclusion body myositis: a single fiber study Krivickas, Lisa S.
2005
15 5 p. 349-354
6 p.
article
11 Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis Atkin, Julie D.
2005
15 5 p. 377-388
12 p.
article
12 Proteolysis of β-dystroglycan in muscular diseases Matsumura, Kiichiro
2005
15 5 p. 336-341
6 p.
article
13 123rd ENMC International Workshop: Management and Therapy in Myotonic Dystrophy, 6–8 February 2004, Naarden, The Netherlands van Engelen, Baziel G.M.
2005
15 5 p. 389-394
6 p.
article
14 Serological follow-up in juvenile myasthenia: clinical and acetylcholine receptor antibody status of patients followed for at least 2 years Anlar, Banu
2005
15 5 p. 355-357
3 p.
article
                             14 results found
 
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