| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A 3 months mild functional test regime does not affect disease parameters in young mdx mice
|
van Putten, Maaike
|
|
2010
|
20 |
4 |
p. 273-280
8 p.
|
artikel
|
| 2 |
Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients
|
Helderman-van den Enden, A.T.J.M.
|
|
2010
|
20 |
4 |
p. 251-254
4 p.
|
artikel
|
| 3 |
Best practice in Duchenne dystrophy
|
Cohn, Ronald D.
|
|
2010
|
20 |
4 |
p. 292-
1 p.
|
artikel
|
| 4 |
Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1
|
Hung, Ryan M.
|
|
2010
|
20 |
4 |
p. 238-240
3 p.
|
artikel
|
| 5 |
Centronuclear myopathies: A widening concept
|
Romero, Norma Beatriz
|
|
2010
|
20 |
4 |
p. 223-228
6 p.
|
artikel
|
| 6 |
Deformities in Duchenne dystrophy
|
Dubowitz, Victor
|
|
2010
|
20 |
4 |
p. 282-
1 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2010
|
20 |
4 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy
|
Susman, Rachel D.
|
|
2010
|
20 |
4 |
p. 229-237
9 p.
|
artikel
|
| 9 |
Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
|
Geranmayeh, Fatemeh
|
|
2010
|
20 |
4 |
p. 241-250
10 p.
|
artikel
|
| 10 |
Improved muscle strength and mobility in the dy2J/dy2J mouse with merosin deficient congenital muscular dystrophy treated with Glatiramer acetate
|
Dadush, Oshrat
|
|
2010
|
20 |
4 |
p. 267-272
6 p.
|
artikel
|
| 11 |
162nd ENMC International Workshop: Disorders of muscle lipid metabolism in adults 28–30 November 2008, Bussum, The Netherlands
|
Laforêt, Pascal
|
|
2010
|
20 |
4 |
p. 283-289
7 p.
|
artikel
|
| 12 |
Professor Sam Perry FRS (1918–2009)
|
Dhoot, Tej
|
|
2010
|
20 |
4 |
p. 290-291
2 p.
|
artikel
|
| 13 |
Report on the 8th Asian and Oceanian Myology Center Annual Meeting, Mumbai, 2009
|
|
|
2010
|
20 |
4 |
p. 293-
1 p.
|
artikel
|
| 14 |
Serum matrix metalloproteinase-9 activity is dysregulated with disease progression in the mutant SOD1 transgenic mice
|
Soon, Cynthia P.W.
|
|
2010
|
20 |
4 |
p. 260-266
7 p.
|
artikel
|
| 15 |
Thenar and hypothenar muscle hypertrophy in Becker muscular dystrophy
|
Renard, Dimitri
|
|
2010
|
20 |
4 |
p. 281-
1 p.
|
artikel
|
| 16 |
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy
|
Reilich, Peter
|
|
2010
|
20 |
4 |
p. 255-259
5 p.
|
artikel
|
| 17 |
WMS 2010
|
|
|
2010
|
20 |
4 |
p. I-
1 p.
|
artikel
|
| 18 |
WMS News
|
|
|
2010
|
20 |
4 |
p. III-IV
nvt p.
|
artikel
|
| 19 |
WMS online application form
|
|
|
2010
|
20 |
4 |
p. II-
1 p.
|
artikel
|
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