| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A new section for Neuromuscular Disorders: Patients’ Forum
|
|
|
2010
|
20 |
2 |
p. 97-
1 p.
|
article
|
| 2 |
A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy
|
Alston, Charlotte L.
|
|
2010
|
20 |
2 |
p. 131-135
5 p.
|
article
|
| 3 |
Ca2+ sensitizers: An emerging class of agents for counterbalancing weakness in skeletal muscle diseases?
|
Ochala, Julien
|
|
2010
|
20 |
2 |
p. 98-101
4 p.
|
article
|
| 4 |
Clinical myology at the crossroads; the gospel truth
|
|
|
2010
|
20 |
2 |
p. 95-96
2 p.
|
article
|
| 5 |
Comparative analysis of antisense oligonucleotide sequences targeting exon 53 of the human DMD gene: Implications for future clinical trials
|
Popplewell, Linda J.
|
|
2010
|
20 |
2 |
p. 102-110
9 p.
|
article
|
| 6 |
Dexamethasone induces dysferlin in myoblasts and enhances their myogenic differentiation
|
Belanto, Joseph J.
|
|
2010
|
20 |
2 |
p. 111-121
11 p.
|
article
|
| 7 |
Editorial Board
|
|
|
2010
|
20 |
2 |
p. IFC-
1 p.
|
article
|
| 8 |
ENMC Assessment
|
|
|
2010
|
20 |
2 |
p. V-
1 p.
|
article
|
| 9 |
Inclusion body myositis
|
Hilton-Jones, D.
|
|
2010
|
20 |
2 |
p. 142-147
6 p.
|
article
|
| 10 |
Incontinetia pigmenti-related myopathy or unsolved “double trouble”?
|
Huttner, H.B.
|
|
2010
|
20 |
2 |
p. 139-141
3 p.
|
article
|
| 11 |
Living with muscular dystrophy: Personal reflections
|
Munn, Michael W.
|
|
2010
|
20 |
2 |
p. 152-153
2 p.
|
article
|
| 12 |
Muscle phosphorylase b kinase deficiency revisited
|
Echaniz-Laguna, Andoni
|
|
2010
|
20 |
2 |
p. 125-127
3 p.
|
article
|
| 13 |
Myositis in Griscelli syndrome type 2 treated with hematopoietic cell transplantation
|
Born, Alfred Peter
|
|
2010
|
20 |
2 |
p. 136-138
3 p.
|
article
|
| 14 |
Parent project
|
|
|
2010
|
20 |
2 |
p. VI-
1 p.
|
article
|
| 15 |
Rigid spine syndrome revealing late-onset Pompe disease
|
Laforêt, Pascal
|
|
2010
|
20 |
2 |
p. 128-130
3 p.
|
article
|
| 16 |
The role of patient advocacy organisations in neuromuscular disease R&D – The case of the Dutch neuromuscular disease association VSN
|
Boon, Wouter
|
|
2010
|
20 |
2 |
p. 148-151
4 p.
|
article
|
| 17 |
Two siblings with limb-girdle muscular dystrophy type 2E responsive to deflazacort
|
Wong-Kisiel, Lily C.
|
|
2010
|
20 |
2 |
p. 122-124
3 p.
|
article
|
| 18 |
WMS 2010
|
|
|
2010
|
20 |
2 |
p. I-
1 p.
|
article
|
| 19 |
WMS News
|
|
|
2010
|
20 |
2 |
p. III-IV
nvt p.
|
article
|
| 20 |
WMS online application form
|
|
|
2010
|
20 |
2 |
p. II-
1 p.
|
article
|
Journal description