| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An evaluation of leukaemia inhibitory factor as a potential therapeutic agent in the treatment of muscle disease
|
White, Jason D.
|
|
2002
|
12 |
10 |
p. 909-916
8 p.
|
artikel
|
| 2 |
Author Index
|
|
|
2002
|
12 |
10 |
p. IX-XIV
nvt p.
|
artikel
|
| 3 |
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC International Workshop, 23–24 November 2001, Naarden, The Netherlands
|
Pepe, Guglielmina
|
|
2002
|
12 |
10 |
p. 984-993
10 p.
|
artikel
|
| 4 |
Clinical Neurophysiology of the Vestibular System, 3rd ed.
|
Lueck, Christian J
|
|
2002
|
12 |
10 |
p. 995-
1 p.
|
artikel
|
| 5 |
Clinical Trials in Neurologic Practice
|
Marson, Tony
|
|
2002
|
12 |
10 |
p. 995-
1 p.
|
artikel
|
| 6 |
Congenital myasthenic syndromes: gene mutations
|
|
|
2002
|
12 |
10 |
p. 1015-1017
3 p.
|
artikel
|
| 7 |
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy
|
Durling, H.J
|
|
2002
|
12 |
10 |
p. 947-951
5 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2002
|
12 |
10 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Erratum to “T.O.1 Randomized trial on the additional effect of methylprednisolone on standard treatment with intravenous immunoglobulin in Guillain-Barré syndrome” [Neuromuscul Disord 12 (2002) 781]
|
van Koningsveld, R
|
|
2002
|
12 |
10 |
p. 997-
1 p.
|
artikel
|
| 10 |
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy
|
Vytopil, Michal
|
|
2002
|
12 |
10 |
p. 958-963
6 p.
|
artikel
|
| 11 |
Genes, Girls and Gamow
|
Emery, Alan E.H
|
|
2002
|
12 |
10 |
p. 994-
1 p.
|
artikel
|
| 12 |
Genotype–phenotype correlations in X-linked myotubular myopathy
|
McEntagart, Meriel
|
|
2002
|
12 |
10 |
p. 939-946
8 p.
|
artikel
|
| 13 |
High dose weekly oral prednisone improves strength in boys with Duchenne muscular dystrophy
|
Connolly, Anne M.
|
|
2002
|
12 |
10 |
p. 917-925
9 p.
|
artikel
|
| 14 |
In Memoriam: Guglielmo Scarlato (1931–2002)
|
Moggio, M
|
|
2002
|
12 |
10 |
p. 996-
1 p.
|
artikel
|
| 15 |
Instructions to authors
|
|
|
2002
|
12 |
10 |
p. 1018-1019
2 p.
|
artikel
|
| 16 |
Keyword Index
|
|
|
2002
|
12 |
10 |
p. XV-XVIII
nvt p.
|
artikel
|
| 17 |
Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases
|
Rodolico, C
|
|
2002
|
12 |
10 |
p. 964-969
6 p.
|
artikel
|
| 18 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2002
|
12 |
10 |
p. 1009-1014
6 p.
|
artikel
|
| 19 |
Neuromuscular disorders: gene location
|
|
|
2002
|
12 |
10 |
p. 998-1008
11 p.
|
artikel
|
| 20 |
Report on the Muscular Dystrophy Campaign workshop: Exercise in neuromuscular diseases Newcastle, January 2002
|
Eagle, Michelle
|
|
2002
|
12 |
10 |
p. 975-983
9 p.
|
artikel
|
| 21 |
Skeletal muscle of mice with a mutation in slow α-tropomyosin is weaker at lower lengths
|
de Haan, A
|
|
2002
|
12 |
10 |
p. 952-957
6 p.
|
artikel
|
| 22 |
Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation
|
Eagle, Michelle
|
|
2002
|
12 |
10 |
p. 926-929
4 p.
|
artikel
|
| 23 |
The spectrum of pathology in central core disease
|
Sewry, C.A
|
|
2002
|
12 |
10 |
p. 930-938
9 p.
|
artikel
|
| 24 |
Volume contents
|
|
|
2002
|
12 |
10 |
p. I-VIII
nvt p.
|
artikel
|
| 25 |
WMS Application Form
|
|
|
2002
|
12 |
10 |
p. XIX-
1 p.
|
artikel
|
| 26 |
Workshop: Management of adults and children with feeding difficulties secondary to chronic muscle disease, 22nd March 2002, Sheffield, UK
|
Hill, Marguerite
|
|
2002
|
12 |
10 |
p. 970-974
5 p.
|
artikel
|
| 27 |
World Muscle Society (WMS) and Neuromuscular Disorders on the Web
|
|
|
2002
|
12 |
10 |
p. XX-
1 p.
|
artikel
|
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