| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Basement membrane remodelling and segmental fibrosis in sporadic inclusion body myositis
|
Doppler, K.
|
|
2009
|
19 |
6 |
p. 406-411
6 p.
|
artikel
|
| 2 |
Cranial nerves palsy as an initial feature of an early onset distal hereditary motor neuropathy – A new distal hereditary motor neuropathy phenotype
|
Haberlová, J.
|
|
2009
|
19 |
6 |
p. 427-428
2 p.
|
artikel
|
| 3 |
Editorial Board
|
|
|
2009
|
19 |
6 |
p. IFC-
1 p.
|
artikel
|
| 4 |
Expression of apoptosis related proteins in normal and diseased muscle: A possible role for Bcl-2 in protection of striated muscle
|
Danielsson, Olof
|
|
2009
|
19 |
6 |
p. 412-417
6 p.
|
artikel
|
| 5 |
Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1: To lump or split?
|
Laberge, Luc
|
|
2009
|
19 |
6 |
p. 397-402
6 p.
|
artikel
|
| 6 |
Genetically-engineered chemotherapy resistance in muscle stem cells enables selective enrichment and engraftment after transplantation
|
|
|
2009
|
19 |
6 |
p. 446-
1 p.
|
artikel
|
| 7 |
Increased fat mass and high incidence of overweight despite low body mass index in patients with spinal muscular atrophy
|
Sproule, Douglas M.
|
|
2009
|
19 |
6 |
p. 391-396
6 p.
|
artikel
|
| 8 |
Is there post-natal muscle growth in amyoplasia? A sequential MRI study
|
Mercuri, Eugenio
|
|
2009
|
19 |
6 |
p. 444-445
2 p.
|
artikel
|
| 9 |
Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia
|
Negro, Roberto
|
|
2009
|
19 |
6 |
p. 423-426
4 p.
|
artikel
|
| 10 |
Outcome measures in Duchenne muscular dystrophy: Are we ready for the new therapeutic era?
|
Merkies, Ingemar S.J.
|
|
2009
|
19 |
6 |
p. 447-
1 p.
|
artikel
|
| 11 |
Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis
|
Almomani, Rowida
|
|
2009
|
19 |
6 |
p. 383-390
8 p.
|
artikel
|
| 12 |
163rd ENMC International Workshop: Nucleoid and nucleotide biology in syndromes of mitochondrial DNA depletion myopathy 12–14 December 2008, Naarden, The Netherlands
|
Poulton, Joanna
|
|
2009
|
19 |
6 |
p. 439-443
5 p.
|
artikel
|
| 13 |
Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin
|
Piñol-Ripoll, Gerard
|
|
2009
|
19 |
6 |
p. 418-422
5 p.
|
artikel
|
| 14 |
165th ENMC International Workshop: Distal myopathies 6–8th February 2009 Naarden, The Netherlands
|
Udd, B.
|
|
2009
|
19 |
6 |
p. 429-438
10 p.
|
artikel
|
| 15 |
The second wind phenomenon in very young McArdle’s patients
|
Pérez, Margarita
|
|
2009
|
19 |
6 |
p. 403-405
3 p.
|
artikel
|
| 16 |
WMS 2009
|
|
|
2009
|
19 |
6 |
p. I-
1 p.
|
artikel
|
| 17 |
WMS News
|
|
|
2009
|
19 |
6 |
p. III-IV
nvt p.
|
artikel
|
| 18 |
WMS online application form
|
|
|
2009
|
19 |
6 |
p. II-
1 p.
|
artikel
|
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