nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F
|
Dinçer, P |
|
2000 |
10 |
4-5 |
p. 247-250 4 p. |
artikel |
2 |
‘An artefact gone awry’: Identification of the first case of nemaline myopathy by Dr R.D.K. Reye
|
Schnell, Christina |
|
2000 |
10 |
4-5 |
p. 307-312 6 p. |
artikel |
3 |
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
|
Driss, A. |
|
2000 |
10 |
4-5 |
p. 240-246 7 p. |
artikel |
4 |
A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy
|
Hyde, Sylvia A. |
|
2000 |
10 |
4-5 |
p. 257-263 7 p. |
artikel |
5 |
Book review
|
Emery, Alan |
|
2000 |
10 |
4-5 |
p. 324-325 2 p. |
artikel |
6 |
Book review
|
Palace, Dr.Jackie |
|
2000 |
10 |
4-5 |
p. 324- 1 p. |
artikel |
7 |
Calpain3 expression during human cardiogenesis
|
Fougerousse, Françoise |
|
2000 |
10 |
4-5 |
p. 251-256 6 p. |
artikel |
8 |
Copies of the survival motor neuron gene in spinal muscular atrophy: the more, the better
|
Brahe, Christina |
|
2000 |
10 |
4-5 |
p. 274-275 2 p. |
artikel |
9 |
Emery–Dreifuss muscular dystrophy – a 40 year retrospective
|
Emery, Alan E.H |
|
2000 |
10 |
4-5 |
p. 228-232 5 p. |
artikel |
10 |
High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy
|
Dubowitz, David J |
|
2000 |
10 |
4-5 |
p. 292-298 7 p. |
artikel |
11 |
Human Molecular Genetics 2
|
Emery, Alan |
|
2000 |
10 |
4-5 |
p. 326- 1 p. |
artikel |
12 |
Index
|
|
|
2000 |
10 |
4-5 |
p. 385-389 5 p. |
artikel |
13 |
Minicore myopathy in children: a clinical and histopathological study of 19 cases
|
Jungbluth, H |
|
2000 |
10 |
4-5 |
p. 264-273 10 p. |
artikel |
14 |
Modulation of disease severity in mice with targeted disruption of the acid α-glucosidase gene
|
Raben, Nina |
|
2000 |
10 |
4-5 |
p. 283-291 9 p. |
artikel |
15 |
Neurologic Complications in Organ Transplant Recipients
|
Cartlidge, N.E.F |
|
2000 |
10 |
4-5 |
p. 325- 1 p. |
artikel |
16 |
Nuclear proteins and cell death in inherited neuromuscular disease
|
Morris, G.E |
|
2000 |
10 |
4-5 |
p. 217-227 11 p. |
artikel |
17 |
Pre-clinical screening of drugs using the mdx mouse
|
Granchelli, Joseph A |
|
2000 |
10 |
4-5 |
p. 235-239 5 p. |
artikel |
18 |
Regenerative capacity and the number of satellite cells in soleus muscles of normal and mdx mice
|
Reimann, J. |
|
2000 |
10 |
4-5 |
p. 276-282 7 p. |
artikel |
19 |
Report of the 70th ENMC International Workshop: Nemaline myopathy, 11–13 June 1999, Naarden, The Netherlands
|
Wallgren-Pettersson, Carina |
|
2000 |
10 |
4-5 |
p. 299-306 8 p. |
artikel |
20 |
Therapeutic screening in the mdx mouse
|
Conte Camerino, Diana |
|
2000 |
10 |
4-5 |
p. 233-234 2 p. |
artikel |
21 |
75th European Neuromuscular Centre International Workshop: 2nd Workshop on the Treatment of Muscular Dystrophy 10–12 December, 1999, Naarden, The Netherlands
|
Dubowitz, Victor |
|
2000 |
10 |
4-5 |
p. 313-320 8 p. |
artikel |