| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse
|
Rae, Caroline
|
|
2002
|
12 |
2 |
p. 121-129
9 p.
|
artikel
|
| 2 |
Bodies Politic: Disease, Death and Doctors in Britain, 1650–1900 Roy Porter, Reaktion Books Ltd., London, 2001, 328 pages, ISBN 1 86189 094 X (Hardback), £25
|
Emery, Alan E.H.
|
|
2002
|
12 |
2 |
p. 212-
1 p.
|
artikel
|
| 3 |
Creatine supplementation reduces skeletal muscle degeneration and enhances mitochondrial function in mdx mice
|
Passaquin, Anne-Catherine
|
|
2002
|
12 |
2 |
p. 174-182
9 p.
|
artikel
|
| 4 |
Deficiency of a 180-kDa extracellular matrix protein in Fukuyama type congenital muscular dystrophy skeletal muscle
|
Sunada, Yoshihide
|
|
2002
|
12 |
2 |
p. 117-120
4 p.
|
artikel
|
| 5 |
Disorders of Voluntary Muscle 7th edition, Karpati G, Hilton-Jones D, Griggs R, Cambridge University Press, June 2001, 200 Half-tones, 105 line drawings, 96 tables, 7 colour illustrations, 754 pages, ISBN: Hardback 0-521-65062-3, £160.00.
|
de Visser, Marianne
|
|
2002
|
12 |
2 |
p. 211-212
2 p.
|
artikel
|
| 6 |
Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice
|
Leriche-Guérin, K
|
|
2002
|
12 |
2 |
p. 167-173
7 p.
|
artikel
|
| 7 |
Expression of IL-17B in neurons and evaluation of its possible role in the chromosome 5q-linked form of Charcot–Marie–Tooth disease
|
Moore, Emma E.
|
|
2002
|
12 |
2 |
p. 141-150
10 p.
|
artikel
|
| 8 |
Identification of six novel mutations in the acid alpha-glucosidase gene in three Spanish patients with infantile onset glycogen storage disease type II (Pompe disease)
|
Fernandez-Hojas, Roberto
|
|
2002
|
12 |
2 |
p. 159-166
8 p.
|
artikel
|
| 9 |
Instructions to authors
|
|
|
2002
|
12 |
2 |
p. 230-231
2 p.
|
artikel
|
| 10 |
Intelligence and cognitive function in children and adolescents with spinal muscular atrophy
|
von Gontard, A.
|
|
2002
|
12 |
2 |
p. 130-136
7 p.
|
artikel
|
| 11 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2002
|
12 |
2 |
p. 224-229
6 p.
|
artikel
|
| 12 |
Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy
|
Donner, Kati
|
|
2002
|
12 |
2 |
p. 151-158
8 p.
|
artikel
|
| 13 |
82nd ENMC international workshop, 5th international Emery–Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15–16 September 2000, Naarden, The Netherlands
|
Bonne, Gisèle
|
|
2002
|
12 |
2 |
p. 187-194
8 p.
|
artikel
|
| 14 |
Neuromuscular disorders: gene location
|
|
|
2002
|
12 |
2 |
p. 214-223
10 p.
|
artikel
|
| 15 |
Pathology of Skeletal Muscle, 2nd edition, S. Carpenter and G. Karpati, Oxford University Press Oxford 2001. IBSN 0-19-506364-3 £140.00
|
Sewry, Caroline
|
|
2002
|
12 |
2 |
p. 213-
1 p.
|
artikel
|
| 16 |
Stable motor and lung function throughout pregnancy in a patient with infantile spinal muscular atrophy type II
|
Rudnik-Schöneborn, Sabine
|
|
2002
|
12 |
2 |
p. 137-140
4 p.
|
artikel
|
| 17 |
The Cerebral Palsies, G. Miller &, G. Clark, 1998, 400 pp. £60. ISBN 0 7506 9964 7
|
Squier, W.
|
|
2002
|
12 |
2 |
p. 212-213
2 p.
|
artikel
|
| 18 |
The muscle-specific marker desmin is expressed in a proportion of human dermal fibroblasts after their exposure to galectin-1
|
Goldring, K
|
|
2002
|
12 |
2 |
p. 183-186
4 p.
|
artikel
|
| 19 |
88th ENMC International Workshop: Childhood chronic inflammatory demyelinating polyneuropathy (including revised diagnostic criteria), Naarden, The Netherlands, December 8–10, 2000
|
Nevo, Yoram
|
|
2002
|
12 |
2 |
p. 195-200
6 p.
|
artikel
|
| 20 |
90th ENMC International Workshop: European Spinal Muscular Atrophy Randomised Trial (EuroSMART) 9–10 February 2001, Naarden, The Netherlands
|
Merlini, Luciano
|
|
2002
|
12 |
2 |
p. 201-210
10 p.
|
artikel
|
| 21 |
Therapeutic possibilities in muscular dystrophy: the hope versus the hype
|
Dubowitz, Victor
|
|
2002
|
12 |
2 |
p. 113-116
4 p.
|
artikel
|
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