Volume 9; Issue 1

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Neuromuscular Disorders
Volume 9; Issue 1

Neuromuscular Disorders

Volume 9; Issue 1

1

Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes

Sophie Bouju, Geneviève Piétu, Martine Le Cunff, Nathalie Cros, Perrine Malzac, Jean-François Pellissier, Françoise Pons, Jean-J Léger, Charles Auffray, Claude A Dechesne

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 636 KB

english, 1999

2

IgM paraproteinemia in a patient with primary lateral sclerosis

Joy Desai, Michael Swash

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 29 KB

english, 1999

3

Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patients

Stephan M Tanner, Vreni Schneider, Nick S.T Thomas, Angus Clarke, Lazarus Lazarou, Sabina Liechti-Gallati

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 132 KB

english, 1999

4

Higher content of insulin-like growth factor-I in dystrophic mdx mouse: potential role in the spontaneous regeneration through an electrophysiological investigation of muscle function

Annamaria De Luca, Sabata Pierno, Claudia Camerino, Daniela Cocchi, Diana Conte Camerino

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 371 KB

english, 1999

5

Transforming growth factor-β1 and fibrosis in congenital muscular dystrophies

Pia Bernasconi, Claudia Di Blasi, Marina Mora, Lucia Morandi, Silvia Galbiati, Paolo Confalonieri, Ferdinando Cornelio, Renato Mantegazza

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 504 KB

english, 1999

6

Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)

John W Day, Robert Roelofs, Bonnie Leroy, Irene Pech, Kellie Benzow, Laura P.W Ranum

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 414 KB

english, 1999

7

A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease

Claudio Bruno, Lucia Tamburino, Noriko Kawashima, Antonio L. Andreu, Sara Shanske, George M. Hadjigeorgiou, Atsushi Kawashima, Salvatore DiMauro

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 203 KB

english, 1999

8

Structural congenital myopathies (excluding nemaline myopathy, myotubular myopathy and desminopathies): 56th European Neuromuscular Centre (ENMC) sponsored International Workshop December 12–14, 1997, Naarden, The Netherlands

Hans H Goebel, Janice R Anderson

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 1.42 MB

english, 1999

9

Editorial

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 36 KB

english, 1999