| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Blockade of TNF in vivo using cV1q antibody reduces contractile dysfunction of skeletal muscle in response to eccentric exercise in dystrophic mdx and normal mice
|
Piers, A.T.
|
|
2011
|
21 |
2 |
p. 132-141
10 p.
|
artikel
|
| 2 |
Co-occurrence of amyotrophic lateral sclerosis and Charcot-Marie-Tooth disease type 2A in a patient with a novel mutation in the mitofusin-2 gene
|
Marchesi, Chiara
|
|
2011
|
21 |
2 |
p. 129-131
3 p.
|
artikel
|
| 3 |
Dysregulation and cellular mislocalization of specific miRNAs in myotonic dystrophy type 1
|
Perbellini, Riccardo
|
|
2011
|
21 |
2 |
p. 81-88
8 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2011
|
21 |
2 |
p. IFC-
1 p.
|
artikel
|
| 5 |
Effects of long-term treatment and combination therapeutics for neuromuscular disorders
|
|
|
2011
|
21 |
2 |
p. 151-156
6 p.
|
artikel
|
| 6 |
ENMC
|
|
|
2011
|
21 |
2 |
p. I-
1 p.
|
artikel
|
| 7 |
Isolated dysphagia due to paraneoplastic myasthenic syndrome with anti-P/Q-type voltage-gated calcium-channel and anti-acetylcholine receptor antibodies
|
Fernandez-Torron, Roberto
|
|
2011
|
21 |
2 |
p. 126-128
3 p.
|
artikel
|
| 8 |
Muscle course
|
|
|
2011
|
21 |
2 |
p. II-
1 p.
|
artikel
|
| 9 |
New Directions in Biology and Disease of Skeletal Muscle, Meeting Report, 5–8 May 2010, Ottawa, Canada
|
Ferrier, Andrew
|
|
2011
|
21 |
2 |
p. 157-159
3 p.
|
artikel
|
| 10 |
Novel GNE mutations in two phenotypically distinct HIBM2 patients
|
Weihl, Conrad C.
|
|
2011
|
21 |
2 |
p. 102-105
4 p.
|
artikel
|
| 11 |
Oculopharyngodistal myopathy – A possible association with cardiomyopathy
|
Thevathasan, Wesley
|
|
2011
|
21 |
2 |
p. 121-125
5 p.
|
artikel
|
| 12 |
Report on the 9th Annual Scientific Meeting of the Asian and Oceanian Myology Centre, Seoul, Korea, March 2010
|
|
|
2011
|
21 |
2 |
p. 150-
1 p.
|
artikel
|
| 13 |
Response
|
Liewluck, Teerin
|
|
2011
|
21 |
2 |
p. 148-149
2 p.
|
artikel
|
| 14 |
Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibres due to a DNM2 mutation
|
Romero, Norma Beatriz
|
|
2011
|
21 |
2 |
p. 148-
1 p.
|
artikel
|
| 15 |
175th ENMC International Workshop: Mitochondrial protein synthesis in health and disease, 25–27th June 2010, Naarden, The Netherlands
|
Chrzanowska-Lightowlers, Z.M.A.
|
|
2011
|
21 |
2 |
p. 142-147
6 p.
|
artikel
|
| 16 |
Transient restoration of succinate dehydrogenase activity after rhabdomyolysis in iron–sulphur cluster deficiency myopathy
|
Kollberg, Gittan
|
|
2011
|
21 |
2 |
p. 115-120
6 p.
|
artikel
|
| 17 |
Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy
|
Parra, Juan
|
|
2011
|
21 |
2 |
p. 97-101
5 p.
|
artikel
|
| 18 |
Variable phenotypes are associated with PMP22 missense mutations
|
Russo, M.
|
|
2011
|
21 |
2 |
p. 106-114
9 p.
|
artikel
|
| 19 |
White matter abnormalities and neurocognitive correlates in children and adolescents with myotonic dystrophy type 1: A diffusion tensor imaging study
|
Wozniak, Jeffrey R.
|
|
2011
|
21 |
2 |
p. 89-96
8 p.
|
artikel
|
| 20 |
WMS 2011
|
|
|
2011
|
21 |
2 |
p. III-
1 p.
|
artikel
|
| 21 |
WMS News
|
|
|
2011
|
21 |
2 |
p. V-VI
nvt p.
|
artikel
|
| 22 |
WMS online application form
|
|
|
2011
|
21 |
2 |
p. IV-
1 p.
|
artikel
|
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