| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A life of Sir Francis Galton: From African exploration to the birth of eugenics, W. Gillham Nicholas; Oxford University Press, Oxford, 2001, 416 pages, ISBN 0-19-514365-5, £22.50 (cloth)
|
Emery, Alan E.H
|
|
2003
|
13 |
1 |
p. 94-
1 p.
|
artikel
|
| 2 |
Brain’s Diseases of The Nervous System, 11th edition
|
Meola, Giovanni
|
|
2003
|
13 |
1 |
p. 95-
1 p.
|
artikel
|
| 3 |
Commentary from the Editor
|
|
|
2003
|
13 |
1 |
p. 1-3
3 p.
|
artikel
|
| 4 |
Congenital myasthenic syndromes: gene mutations
|
|
|
2003
|
13 |
1 |
p. 115-119
5 p.
|
artikel
|
| 5 |
Down-regulation of an ankyrin repeat-containing protein, V-1, during skeletal muscle differentiation and its re-expression in the regenerative process of muscular dystrophy
|
Furukawa, Yuko
|
|
2003
|
13 |
1 |
p. 32-41
10 p.
|
artikel
|
| 6 |
Drug-Induced Neurological Disorders. Second Edition
|
Argov, Zohar
|
|
2003
|
13 |
1 |
p. 93-
1 p.
|
artikel
|
| 7 |
Early and severe presentation of X-linked myotubular myopathy in a girl with skewed X-inactivation
|
Jungbluth, H
|
|
2003
|
13 |
1 |
p. 55-59
5 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2003
|
13 |
1 |
p. ii-
1 p.
|
artikel
|
| 9 |
Effect of acid maltase deficiency on the endosomal/lysosomal system and glucose transporter 4
|
Orth, M
|
|
2003
|
13 |
1 |
p. 49-54
6 p.
|
artikel
|
| 10 |
Encyclopedia of Genetics
|
Emery, Alan E.H
|
|
2003
|
13 |
1 |
p. 93-94
2 p.
|
artikel
|
| 11 |
Hepatitis C virus infection and myositis: a virus localization study
|
Di Muzio, A.
|
|
2003
|
13 |
1 |
p. 68-71
4 p.
|
artikel
|
| 12 |
Instructions to authors
|
|
|
2003
|
13 |
1 |
p. 120-121
2 p.
|
artikel
|
| 13 |
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients
|
Triki, Chahnez
|
|
2003
|
13 |
1 |
p. 4-12
9 p.
|
artikel
|
| 14 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2003
|
13 |
1 |
p. 109-114
6 p.
|
artikel
|
| 15 |
Neuromuscular Diseases, Expert Clinicians Views
|
Angelini, Corrado
|
|
2003
|
13 |
1 |
p. 95-96
2 p.
|
artikel
|
| 16 |
Neuromuscular disorders: gene location
|
|
|
2003
|
13 |
1 |
p. 97-108
12 p.
|
artikel
|
| 17 |
Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle
|
Wells, Kim E
|
|
2003
|
13 |
1 |
p. 21-31
11 p.
|
artikel
|
| 18 |
Report of the 95th European Neuromuscular Centre (ENMC) sponsored International Workshop Cognitive Impairment in Neuromuscular Disorders, Naarden, The Netherlands, 13–15 July 2001
|
D'Angelo, M.G
|
|
2003
|
13 |
1 |
p. 72-79
8 p.
|
artikel
|
| 19 |
Stroke Syndromes
|
Rothwell, Peter M
|
|
2003
|
13 |
1 |
p. 96-
1 p.
|
artikel
|
| 20 |
Syncoilin accumulation in two patients with desmin-related myopathy
|
Howman, Emily V
|
|
2003
|
13 |
1 |
p. 42-48
7 p.
|
artikel
|
| 21 |
The dystrophin lymphocyte promoter revisited: 4.5-megabase intron, or artefact?
|
Wheway, Joanna M
|
|
2003
|
13 |
1 |
p. 17-20
4 p.
|
artikel
|
| 22 |
The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene
|
Chaouch, M.
|
|
2003
|
13 |
1 |
p. 60-67
8 p.
|
artikel
|
| 23 |
The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12–14, 2002
|
Bushby, K.M.D
|
|
2003
|
13 |
1 |
p. 80-90
11 p.
|
artikel
|
| 24 |
Two dystrophin proteins and transcripts in a mild dystrophinopathic patient
|
Cagliani, R
|
|
2003
|
13 |
1 |
p. 13-16
4 p.
|
artikel
|
| 25 |
What is Davidenkov's scapuloperoneal amyotrophy: is it a myopathic entity or a neurogenic syndrome? What was Davidenkov's opinion concerning this knotty problem?
|
Kazakov, Valery
|
|
2003
|
13 |
1 |
p. 91-92
2 p.
|
artikel
|
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