| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block
|
Kitaguchi, Tetsuo
|
|
2001
|
11 |
6-7 |
p. 542-546
5 p.
|
artikel
|
| 2 |
Author index
|
|
|
2001
|
11 |
6-7 |
p. 675-679
5 p.
|
artikel
|
| 3 |
Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy
|
Chae, Jonghee
|
|
2001
|
11 |
6-7 |
p. 547-555
9 p.
|
artikel
|
| 4 |
Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility
|
Stojkovic, T
|
|
2001
|
11 |
6-7 |
p. 538-541
4 p.
|
artikel
|
| 5 |
Do immune cells promote the pathology of dystrophin-deficient myopathies?
|
Spencer, Melissa J
|
|
2001
|
11 |
6-7 |
p. 556-564
9 p.
|
artikel
|
| 6 |
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy
|
Flanigan, Kevin M
|
|
2001
|
11 |
6-7 |
p. 525-529
5 p.
|
artikel
|
| 7 |
Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families
|
Sambuughin, Nyamkhishig
|
|
2001
|
11 |
6-7 |
p. 530-537
8 p.
|
artikel
|
| 8 |
Instructions to authors
|
|
|
2001
|
11 |
6-7 |
p. 696-697
2 p.
|
artikel
|
| 9 |
Ion channels in muscle and cardiac hereditary diseases: from gene dysfunction to pharmacological therapy
|
Desaphy, Jean-François
|
|
2001
|
11 |
6-7 |
p. 583-588
6 p.
|
artikel
|
| 10 |
Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular–eye–brain loci: report of three siblings
|
Ruggieri, V
|
|
2001
|
11 |
6-7 |
p. 570-578
9 p.
|
artikel
|
| 11 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2001
|
11 |
6-7 |
p. 690-695
6 p.
|
artikel
|
| 12 |
Neuromuscular Disorders
|
|
|
2001
|
11 |
6-7 |
p. 597-
1 p.
|
artikel
|
| 13 |
Neuromuscular disorders: gene location
|
|
|
2001
|
11 |
6-7 |
p. 680-689
10 p.
|
artikel
|
| 14 |
Nitric oxide: biologic effects on muscle and role in muscle diseases
|
Kaminski, Henry J
|
|
2001
|
11 |
6-7 |
p. 517-524
8 p.
|
artikel
|
| 15 |
Programme (Summary)
|
|
|
2001
|
11 |
6-7 |
p. 600-601
2 p.
|
artikel
|
| 16 |
Program of the 6th WMS Congress
|
|
|
2001
|
11 |
6-7 |
p. 602-613
12 p.
|
artikel
|
| 17 |
Report of the 83rd ENMC International Workshop: 4th Workshop on Nemaline Myopathy, 22–24 September 2000, Naarden, The Netherlands
|
Wallgren-Pettersson, Carina
|
|
2001
|
11 |
6-7 |
p. 589-595
7 p.
|
artikel
|
| 18 |
Respiratory chain defects in hereditary spastic paraplegias
|
Piemonte, F.
|
|
2001
|
11 |
6-7 |
p. 565-569
5 p.
|
artikel
|
| 19 |
Table of location of abstract topics
|
|
|
2001
|
11 |
6-7 |
p. 614-
1 p.
|
artikel
|
| 20 |
Tables
|
Smith, John
|
|
2001
|
11 |
6-7 |
p. 615-674
60 p.
|
artikel
|
| 21 |
Vecuronium-associated axonal motor neuropathy: a variant of critical illness polyneuropathy?
|
Geller, Thomas J
|
|
2001
|
11 |
6-7 |
p. 579-582
4 p.
|
artikel
|
| 22 |
Welcome to Utah
|
|
|
2001
|
11 |
6-7 |
p. 598-599
2 p.
|
artikel
|
Tijdschrift beschrijving