nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A congenital muscular dystrophy quality of life and caregiver assessment survey
|
Smith-Hoban, Diane |
|
2010 |
20 |
8 |
p. 564-565 2 p. |
artikel |
2 |
Clinical and genetic characterization of manifesting carriers of DMD mutations
|
Soltanzadeh, Payam |
|
2010 |
20 |
8 |
p. 499-504 6 p. |
artikel |
3 |
Clinical characterization and genetic analysis of a possible novel type of dominant Charcot-Marie-Tooth disease
|
Lee, Yi-Chung |
|
2010 |
20 |
8 |
p. 534-539 6 p. |
artikel |
4 |
Congenital muscular dystrophy: A parent’s hopes and fears
|
Sklaroff-Van Hook, Susan |
|
2010 |
20 |
8 |
p. 566- 1 p. |
artikel |
5 |
Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern
|
Deconinck, N. |
|
2010 |
20 |
8 |
p. 517-523 7 p. |
artikel |
6 |
Editorial Board
|
|
|
2010 |
20 |
8 |
p. IFC- 1 p. |
artikel |
7 |
Erratum to ‘Cap myopathy caused by a mutation of the skeletal alpha-actin gene ACTA1’ [Neuromuscular Disorders 20 (2010) 238–240]
|
Hung, Ryan M. |
|
2010 |
20 |
8 |
p. 567- 1 p. |
artikel |
8 |
Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutation
|
Stenzel, Werner |
|
2010 |
20 |
8 |
p. 531-533 3 p. |
artikel |
9 |
Fukutin mutations in congenital muscular dystrophies with defective glycosylation of dystroglycan in Korea
|
Lim, Bung Chan |
|
2010 |
20 |
8 |
p. 524-530 7 p. |
artikel |
10 |
Hereditary muscular dystrophies and the heart
|
Hermans, M.C.E. |
|
2010 |
20 |
8 |
p. 479-492 14 p. |
artikel |
11 |
Impact of tracheostomy on swallowing performance in Duchenne muscular dystrophy
|
Terzi, Nicolas |
|
2010 |
20 |
8 |
p. 493-498 6 p. |
artikel |
12 |
Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopy
|
Wary, Claire |
|
2010 |
20 |
8 |
p. 548-558 11 p. |
artikel |
13 |
Prevalent cardiac phenotype resulting in heart transplantation in a novel LMNA gene duplication
|
Volpi, L. |
|
2010 |
20 |
8 |
p. 512-516 5 p. |
artikel |
14 |
Reduction of abnormal behavioral response to brief restraint by information from other mice in dystrophin-deficient mdx mice
|
Yamamoto, Kazuhiro |
|
2010 |
20 |
8 |
p. 505-511 7 p. |
artikel |
15 |
174th ENMC International Workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: Implications of scientific advances 19–21 March 2010, Naarden, The Netherlands
|
Poulton, J. |
|
2010 |
20 |
8 |
p. 559-563 5 p. |
artikel |
16 |
Validation of an automated computational method for skeletal muscle fibre morphometry analysis
|
Garton, Fleur |
|
2010 |
20 |
8 |
p. 540-547 8 p. |
artikel |
17 |
WMS 2010
|
|
|
2010 |
20 |
8 |
p. I- 1 p. |
artikel |
18 |
WMS News
|
|
|
2010 |
20 |
8 |
p. III-IV nvt p. |
artikel |
19 |
WMS online application form
|
|
|
2010 |
20 |
8 |
p. II- 1 p. |
artikel |