| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy
|
Dunand, Murielle
|
|
2009
|
19 |
11 |
p. 802-
1 p.
|
article
|
| 2 |
Current advances in the development of therapies for neuromuscular disorders based on myostatin signalling, 3rd International Institute of Myology Workshop, Paris, September 12th, 2008
|
Dumonceaux, Julie
|
|
2009
|
19 |
11 |
p. 797-799
3 p.
|
article
|
| 3 |
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy
|
Flanigan, Kevin M.
|
|
2009
|
19 |
11 |
p. 743-748
6 p.
|
article
|
| 4 |
Drug screening for muscular dystrophy: From target to function toward patients, is anything lost?
|
|
|
2009
|
19 |
11 |
p. 800-
1 p.
|
article
|
| 5 |
Editorial Board
|
|
|
2009
|
19 |
11 |
p. IFC-
1 p.
|
article
|
| 6 |
Gait analysis using accelerometry in dystrophin-deficient dogs
|
Barthélémy, Inès
|
|
2009
|
19 |
11 |
p. 788-796
9 p.
|
article
|
| 7 |
Myasthenia gravis precipitated by trauma: Latent myasthenia and the concept of ‘threshold’
|
Lane, Russell
|
|
2009
|
19 |
11 |
p. 773-775
3 p.
|
article
|
| 8 |
[No title]
|
Jayatunga, Uditha
|
|
2009
|
19 |
11 |
p. 803-
1 p.
|
article
|
| 9 |
Point mutations in Czech DMD/BMD patients and their phenotypic outcome
|
Sedláčková, Jana
|
|
2009
|
19 |
11 |
p. 749-753
5 p.
|
article
|
| 10 |
Prevalence and psychosocial impact of lower urinary tract symptoms in patients with Duchenne muscular dystrophy
|
Wijk, Evaline van
|
|
2009
|
19 |
11 |
p. 754-758
5 p.
|
article
|
| 11 |
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations
|
Collins, James
|
|
2009
|
19 |
11 |
p. 784-787
4 p.
|
article
|
| 12 |
Report on the 7th Annual Scientific Meeting of the Asian and Oceanian Myology Centre, Melbourne, November 2008
|
|
|
2009
|
19 |
11 |
p. 804-
1 p.
|
article
|
| 13 |
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene
|
Catteruccia, Michela
|
|
2009
|
19 |
11 |
p. 779-783
5 p.
|
article
|
| 14 |
Scaled-down genetic analysis of myotonic dystrophy type 1 and type 2
|
Nakamori, Masayuki
|
|
2009
|
19 |
11 |
p. 759-762
4 p.
|
article
|
| 15 |
Sporadic inclusion body myositis: HLA-DRB1 allele interactions influence disease risk and clinical phenotype
|
Mastaglia, Frank L.
|
|
2009
|
19 |
11 |
p. 763-765
3 p.
|
article
|
| 16 |
Three distinguishable phenotypes in golden retriever muscular dystrophy
|
|
|
2009
|
19 |
11 |
p. 800-801
2 p.
|
article
|
| 17 |
Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene
|
Tonin, Paola
|
|
2009
|
19 |
11 |
p. 776-778
3 p.
|
article
|
| 18 |
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts
|
Vesa, Jouni
|
|
2009
|
19 |
11 |
p. 766-772
7 p.
|
article
|
| 19 |
WMS 2010
|
|
|
2009
|
19 |
11 |
p. I-
1 p.
|
article
|
| 20 |
WMS News
|
|
|
2009
|
19 |
11 |
p. III-IV
nvt p.
|
article
|
| 21 |
WMS online application form
|
|
|
2009
|
19 |
11 |
p. II-
1 p.
|
article
|
Journal description