| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy
|
Di Blasi, Claudia
|
|
2010
|
20 |
5 |
p. 326-329
4 p.
|
article
|
| 2 |
Editorial Board
|
|
|
2010
|
20 |
5 |
p. IFC-
1 p.
|
article
|
| 3 |
Episodic myoglobinuria in a primary gamma-sarcoglycanopathy
|
Pena, Loren
|
|
2010
|
20 |
5 |
p. 337-339
3 p.
|
article
|
| 4 |
Friedreich ataxia presenting as sudden cardiac death in childhood: Clinical, genetic and pathological correlation, with implications for genetic testing and counselling
|
Quercia, Nada
|
|
2010
|
20 |
5 |
p. 340-342
3 p.
|
article
|
| 5 |
Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian family
|
Stober, Andrea
|
|
2010
|
20 |
5 |
p. 335-336
2 p.
|
article
|
| 6 |
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN)
|
Cordelli, D.M.
|
|
2010
|
20 |
5 |
p. 343-345
3 p.
|
article
|
| 7 |
Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin–proteasome pathway
|
Vignaud, Alban
|
|
2010
|
20 |
5 |
p. 319-325
7 p.
|
article
|
| 8 |
Rasch-built myotonic dystrophy type 1 activity and participation scale (DM1-Activ)
|
Hermans, Mieke C.E.
|
|
2010
|
20 |
5 |
p. 310-318
9 p.
|
article
|
| 9 |
Reverse protein arrays as novel approach for protein quantification in muscular dystrophies
|
Escher, Claudia
|
|
2010
|
20 |
5 |
p. 302-309
8 p.
|
article
|
| 10 |
Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: Implication for clinical trials
|
Arechavala-Gomeza, Virginia
|
|
2010
|
20 |
5 |
p. 295-301
7 p.
|
article
|
| 11 |
The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: Report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009
|
Muntoni, F.
|
|
2010
|
20 |
5 |
p. 355-362
8 p.
|
article
|
| 12 |
166th ENMC International Workshop on Collagen type VI-related Myopathies, 22–24 May 2009, Naarden, The Netherlands
|
Allamand, Valérie
|
|
2010
|
20 |
5 |
p. 346-354
9 p.
|
article
|
| 13 |
Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings
|
Kumar, Kishore R.
|
|
2010
|
20 |
5 |
p. 330-334
5 p.
|
article
|
| 14 |
WMS 2010
|
|
|
2010
|
20 |
5 |
p. I-
1 p.
|
article
|
| 15 |
WMS News
|
|
|
2010
|
20 |
5 |
p. III-IV
nvt p.
|
article
|
| 16 |
WMS online application form
|
|
|
2010
|
20 |
5 |
p. II-
1 p.
|
article
|
Journal description