| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abstracts
|
|
|
2002
|
12 |
7-8 |
p. 718-783
66 p.
|
artikel
|
| 2 |
Amyotrophic lateral sclerosis with very slow progression
|
Finsterer, Josef
|
|
2002
|
12 |
7-8 |
p. 694-695
2 p.
|
artikel
|
| 3 |
A novel mitochondrial DNA tRNAIle (A4267G) mutation in a sporadic patient with mitochondrial myopathy
|
Taylor, Robert W.
|
|
2002
|
12 |
7-8 |
p. 659-664
6 p.
|
artikel
|
| 4 |
Apoptosis and muscle fibre loss in neuromuscular disorders
|
Tews, D.S.
|
|
2002
|
12 |
7-8 |
p. 613-622
10 p.
|
artikel
|
| 5 |
Author index
|
|
|
2002
|
12 |
7-8 |
p. 784-789
6 p.
|
artikel
|
| 6 |
Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes
|
Street, V.A.
|
|
2002
|
12 |
7-8 |
p. 643-650
8 p.
|
artikel
|
| 7 |
Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)
|
Mercuri, Eugenio
|
|
2002
|
12 |
7-8 |
p. 631-638
8 p.
|
artikel
|
| 8 |
Cognitive function in children with spinal muscular atrophy
|
Sieratzki, Jechil S
|
|
2002
|
12 |
7-8 |
p. 693-694
2 p.
|
artikel
|
| 9 |
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMD
|
Voit, Th
|
|
2002
|
12 |
7-8 |
p. 623-630
8 p.
|
artikel
|
| 10 |
Congenital myasthenic syndromes: gene mutations
|
|
|
2002
|
12 |
7-8 |
p. 807-811
5 p.
|
artikel
|
| 11 |
Desmin – Protein Surplus Myopathies, 96th European Neuromuscular Centre (ENMC)-sponsored International Workshop held 14–16 September 2001, Naarden, The Netherlands
|
Goebel, Hans H
|
|
2002
|
12 |
7-8 |
p. 687-692
6 p.
|
artikel
|
| 12 |
Editorial Board
|
|
|
2002
|
12 |
7-8 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy
|
Dawkins, Jennifer L
|
|
2002
|
12 |
7-8 |
p. 656-658
3 p.
|
artikel
|
| 14 |
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene
|
van de Wetering, R.A.C
|
|
2002
|
12 |
7-8 |
p. 651-655
5 p.
|
artikel
|
| 15 |
Instructions to authors
|
|
|
2002
|
12 |
7-8 |
p. 812-813
2 p.
|
artikel
|
| 16 |
MESSAGE FROM THE PRESIDENT OF WMS
|
|
|
2002
|
12 |
7-8 |
p. 699-
1 p.
|
artikel
|
| 17 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2002
|
12 |
7-8 |
p. 801-806
6 p.
|
artikel
|
| 18 |
Mutations in the nebulin gene can cause severe congenital nemaline myopathy
|
Wallgren-Pettersson, Carina
|
|
2002
|
12 |
7-8 |
p. 674-679
6 p.
|
artikel
|
| 19 |
Na+/Ca2+ exchange in human myotubes: intracellular calcium rises in response to external sodium depletion are enhanced in DMD
|
Deval, Emmanuel
|
|
2002
|
12 |
7-8 |
p. 665-673
9 p.
|
artikel
|
| 20 |
Nebulin mutations in autosomal recessive nemaline myopathy: an update
|
Pelin, Katarina
|
|
2002
|
12 |
7-8 |
p. 680-686
7 p.
|
artikel
|
| 21 |
Neuromuscular Disorders
|
|
|
2002
|
12 |
7-8 |
p. 697-
1 p.
|
artikel
|
| 22 |
Neuromuscular disorders: gene location
|
|
|
2002
|
12 |
7-8 |
p. 790-800
11 p.
|
artikel
|
| 23 |
Programme (Summary)
|
|
|
2002
|
12 |
7-8 |
p. 700-701
2 p.
|
artikel
|
| 24 |
Program of the 7th WMS Congress
|
|
|
2002
|
12 |
7-8 |
p. 702-716
15 p.
|
artikel
|
| 25 |
Quantitative assessment of calf circumference in Duchenne muscular dystrophy patients
|
Beenakker, E.A.C.
|
|
2002
|
12 |
7-8 |
p. 639-642
4 p.
|
artikel
|
| 26 |
Response to comments by J. Finsterer: Amyotrophic lateral sclerosis with very slow progression
|
Borasio, G.D
|
|
2002
|
12 |
7-8 |
p. 695-696
2 p.
|
artikel
|
| 27 |
Response to comments by J.S. Sieratzki and B. Woll: Cognitive function in children with spinal muscular atrophy
|
von Gontard, A
|
|
2002
|
12 |
7-8 |
p. 694-
1 p.
|
artikel
|
| 28 |
Table of location of abstract topics
|
|
|
2002
|
12 |
7-8 |
p. 717-
1 p.
|
artikel
|
| 29 |
WELCOME TO THE NETHERLANDS
|
|
|
2002
|
12 |
7-8 |
p. 698-
1 p.
|
artikel
|
Tijdschrift beschrijving