| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease
|
Bruno, Claudio
|
|
1999
|
9 |
1 |
p. 34-37
4 p.
|
artikel
|
| 2 |
Characterization of 34 novel and six known MTM1 gene mutations in 47 unrelated X-linked myotubular myopathy patients
|
Tanner, Stephan M
|
|
1999
|
9 |
1 |
p. 41-49
9 p.
|
artikel
|
| 3 |
Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)
|
Day, John W
|
|
1999
|
9 |
1 |
p. 19-27
9 p.
|
artikel
|
| 4 |
Editorial
|
|
|
1999
|
9 |
1 |
p. 1-2
2 p.
|
artikel
|
| 5 |
Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genes
|
Bouju, Sophie
|
|
1999
|
9 |
1 |
p. 3-10
8 p.
|
artikel
|
| 6 |
Higher content of insulin-like growth factor-I in dystrophic mdx mouse: potential role in the spontaneous regeneration through an electrophysiological investigation of muscle function
|
De Luca, Annamaria
|
|
1999
|
9 |
1 |
p. 11-18
8 p.
|
artikel
|
| 7 |
IgM paraproteinemia in a patient with primary lateral sclerosis
|
Desai, Joy
|
|
1999
|
9 |
1 |
p. 38-40
3 p.
|
artikel
|
| 8 |
Structural congenital myopathies (excluding nemaline myopathy, myotubular myopathy and desminopathies): 56th European Neuromuscular Centre (ENMC) sponsored International Workshop December 12–14, 1997, Naarden, The Netherlands
|
Goebel, Hans H
|
|
1999
|
9 |
1 |
p. 50-57
8 p.
|
artikel
|
| 9 |
Transforming growth factor-β1 and fibrosis in congenital muscular dystrophies
|
Bernasconi, Pia
|
|
1999
|
9 |
1 |
p. 28-33
6 p.
|
artikel
|
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