Volume 20; Issue 6

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Neuromuscular Disorders
Volume 20; Issue 6

Neuromuscular Disorders

Volume 20; Issue 6

1

Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin gene

Sarah E. Haigh, Sheetal S. Salvi, Maria Sevdali, Meg Stark, David Goulding, Jonathan D. Clayton, Belinda Bullard, John C. Sparrow, Upendra Nongthomba

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 2.40 MB

english, 2010

2

A novel heterozygous deletion–insertion mutation (2695–2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family

Xinghua Luan, Daojun Hong, Wei Zhang, Zhaoxia Wang, Yun Yuan

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 1.10 MB

english, 2010

3

Oral dexamethasone pulse therapy versus daily prednisolone in sub-acute onset myositis, a randomised clinical trial

J. van de Vlekkert, J.E. Hoogendijk, R.J. de Haan, A. Algra, I. van der Tweel, W.L. van der Pol, E.V. Uijtendaal, M. de Visser

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 217 KB

english, 2010

4

International Workshop on Inclusion Body Myositis held at the Institute of Myology, Paris, on 29 May 2009

Olivier Benveniste, David Hilton-Jones

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 193 KB

english, 2010

5

Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations

Valérie Tosch, Nasim Vasli, Christine Kretz, Anne-Sophie Nicot, Claire Gasnier, Nicolas Dondaine, Denis Oriot, Magalie Barth, Hugues Puissant, Norma B. Romero, Carsten G. Bönnemann, Betty Heller, Gill

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 460 KB

english, 2010

6

Nephrogenic systemic fibrosis presenting as myopathy: A case report with histopathologic correlation

Eric Edgar, Randy Woltjer, Ruth Whitham, S. Humayun Gultekin, Suzanne Watnick, Edward J. Cupler

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 396 KB

english, 2010

7

The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotype

Charlotte L. Alston, Andreas Bender, Iain P. Hargreaves, Helen Mundy, Charulata Deshpande, Thomas Klopstock, Robert McFarland, Rita Horvath, Robert W. Taylor

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 757 KB

english, 2010

8

Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene

Hasan O. Akman, Guido Davidzon, Kurenai Tanji, Emma J. MacDermott, Louann Larsen, Mercy M. Davidson, Ronald G. Haller, Lidia S. Szczepaniak, Thomas J.A. Lehman, Michio Hirano, Salvatore DiMauro

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 2.27 MB

english, 2010

9

Best Practice Guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies

Stephen Abbs, Sylvie Tuffery-Giraud, Egbert Bakker, Alessandra Ferlini, Thomas Sejersen, Clemens R. Mueller

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 198 KB

english, 2010

10

Calpainopathy presenting as foot drop in a 41 year old

G. Burke, C. Hillier, J. Cole, M. Sampson, L. Bridges, K. Bushby, R. Barresi, S.R. Hammans

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 265 KB

english, 2010

11

WMS 2010

Journal:

Neuromuscular Disorders

Year:

2010

File:

PDF, 284 KB

2010

12

WMS online application form

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 85 KB

english, 2010

13

WMS News

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 58 KB

english, 2010

14

Editorial Board

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 47 KB

english, 2010

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