| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aberrant development of neuromuscular junctions in glycosylation-defective Largemyd mice
|
Herbst, Ruth
|
|
2009
|
19 |
5 |
p. 366-378
13 p.
|
artikel
|
| 2 |
Cap disease due to mutation of the beta-tropomyosin gene (TPM2)
|
Clarke, Nigel F.
|
|
2009
|
19 |
5 |
p. 348-351
4 p.
|
artikel
|
| 3 |
Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians
|
Dupré, Nicolas
|
|
2009
|
19 |
5 |
p. 330-334
5 p.
|
artikel
|
| 4 |
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia
|
Stojkovic, Tanya
|
|
2009
|
19 |
5 |
p. 316-323
8 p.
|
artikel
|
| 5 |
Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency
|
Laforêt, Pascal
|
|
2009
|
19 |
5 |
p. 324-329
6 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2009
|
19 |
5 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardation
|
Puckett, Rebecca L.
|
|
2009
|
19 |
5 |
p. 352-356
5 p.
|
artikel
|
| 8 |
Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene
|
Jungbluth, Heinz
|
|
2009
|
19 |
5 |
p. 344-347
4 p.
|
artikel
|
| 9 |
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy
|
Kan, Hermien E.
|
|
2009
|
19 |
5 |
p. 357-362
6 p.
|
artikel
|
| 10 |
Rare genetic disorders in certain populations
|
Emery, Alan
|
|
2009
|
19 |
5 |
p. 307-
1 p.
|
artikel
|
| 11 |
Relapse of polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome without increased level of vascular endothelial growth factor following successful autologous peripheral blood stem cell transplantation
|
Imai, Noboru
|
|
2009
|
19 |
5 |
p. 363-365
3 p.
|
artikel
|
| 12 |
Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2
|
Cardani, Rosanna
|
|
2009
|
19 |
5 |
p. 335-343
9 p.
|
artikel
|
| 13 |
148th ENMC international workshop on the scientific contributions of the EURALS consortium on amyotrophic lateral sclerosis
|
Beghi, Ettore
|
|
2009
|
19 |
5 |
p. 379-381
3 p.
|
artikel
|
| 14 |
Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia
|
Weihl, Conrad C.
|
|
2009
|
19 |
5 |
p. 308-315
8 p.
|
artikel
|
| 15 |
WMS 2009
|
|
|
2009
|
19 |
5 |
p. II-
1 p.
|
artikel
|
| 16 |
WMS News
|
|
|
2009
|
19 |
5 |
p. IV-V
nvt p.
|
artikel
|
| 17 |
WMS online application form
|
|
|
2009
|
19 |
5 |
p. III-
1 p.
|
artikel
|
Tijdschrift beschrijving