| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Analysis of growth factor expression in affected and unaffected muscles of oculo-pharyngeal muscular dystrophy (OPMD) patients: A pilot study
|
Bouazza, Belaid
|
|
2009
|
19 |
3 |
p. 199-206
8 p.
|
artikel
|
| 2 |
Becker muscular dystrophy caused by an intronic mutation reducing the efficiency of the splice donor site of intron 26 of the dystrophin gene
|
Baskin, Berivan
|
|
2009
|
19 |
3 |
p. 189-192
4 p.
|
artikel
|
| 3 |
Does the K153R variant of the myostatin gene influence the clinical presentation of women with McArdle disease?
|
González-Freire, Marta
|
|
2009
|
19 |
3 |
p. 220-222
3 p.
|
artikel
|
| 4 |
Dysphagia is present but mild in myotonic dystrophy type 2
|
Tieleman, A.A.
|
|
2009
|
19 |
3 |
p. 196-198
3 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2009
|
19 |
3 |
p. IFC-
1 p.
|
artikel
|
| 6 |
ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
|
Liang, Wen-Chen
|
|
2009
|
19 |
3 |
p. 212-216
5 p.
|
artikel
|
| 7 |
Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype
|
Vuillaumier-Barrot, S.
|
|
2009
|
19 |
3 |
p. 182-188
7 p.
|
artikel
|
| 8 |
Glucocorticoids may trigger attacks in several types of periodic paralysis
|
Arzel-Hézode, Marianne
|
|
2009
|
19 |
3 |
p. 217-219
3 p.
|
artikel
|
| 9 |
Immune-mediated rippling muscle disease with myasthenia gravis: A report of seven patients with long-term follow-up in two
|
Schoser, Benedikt
|
|
2009
|
19 |
3 |
p. 223-228
6 p.
|
artikel
|
| 10 |
Interfamilial phenotypic heterogeneity in SMARD1
|
Joseph, S.
|
|
2009
|
19 |
3 |
p. 193-195
3 p.
|
artikel
|
| 11 |
Muscle course 2009
|
|
|
2009
|
19 |
3 |
p. I-
1 p.
|
artikel
|
| 12 |
Myopathic form of phosphoglycerate kinase (PGK) deficiency: A new case and pathogenic considerations
|
Spiegel, Ronen
|
|
2009
|
19 |
3 |
p. 207-211
5 p.
|
artikel
|
| 13 |
Nemaline myopathy: A tale of two cultures
|
Dubowitz, Victor
|
|
2009
|
19 |
3 |
p. 177-178
2 p.
|
artikel
|
| 14 |
Newcastle: From coal to muscle
|
|
|
2009
|
19 |
3 |
p. 235-239
5 p.
|
artikel
|
| 15 |
The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence
|
Lehtokari, Vilma-Lotta
|
|
2009
|
19 |
3 |
p. 179-181
3 p.
|
artikel
|
| 16 |
158th ENMC international workshop on congenital muscular dystrophy (Xth international CMD workshop) 8th–10th February 2008 Naarden, The Netherlands
|
Muntoni, F.
|
|
2009
|
19 |
3 |
p. 229-234
6 p.
|
artikel
|
| 17 |
WMS 2009
|
|
|
2009
|
19 |
3 |
p. II-
1 p.
|
artikel
|
| 18 |
WMS News
|
|
|
2009
|
19 |
3 |
p. IV-V
nvt p.
|
artikel
|
| 19 |
WMS online application form
|
|
|
2009
|
19 |
3 |
p. III-
1 p.
|
artikel
|
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