| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy
|
Melacini, P.
|
|
1996
|
6 |
5 |
p. 367-376
10 p.
|
artikel
|
| 2 |
Chronic inflammatory demyelinating polyneuropathy
|
Briani, Chiara
|
|
1996
|
6 |
5 |
p. 311-325
15 p.
|
artikel
|
| 3 |
Familial desmin-related myopathies and cardiomyopathies — from myopathology to molecular and clinical genetics
|
Goebel, H.H.
|
|
1996
|
6 |
5 |
p. 383-388
6 p.
|
artikel
|
| 4 |
Genes V
|
Emery, Alan
|
|
1996
|
6 |
5 |
p. 395-
1 p.
|
artikel
|
| 5 |
Hypoosmotic shocks induce elevation of resting calcium level in duchenne muscular dystrophy myotubes contracting in vitro
|
Imbert, Nathalie
|
|
1996
|
6 |
5 |
p. 351-360
10 p.
|
artikel
|
| 6 |
Letter to the editor
|
Bellen, P.
|
|
1996
|
6 |
5 |
p. 393-
1 p.
|
artikel
|
| 7 |
Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities
|
Mora, Marina
|
|
1996
|
6 |
5 |
p. 377-381
5 p.
|
artikel
|
| 8 |
Mitochondrial encephalomyopathies: Gene mutation
|
|
|
1996
|
6 |
5 |
p. XI-XV
nvt p.
|
artikel
|
| 9 |
Neuromuscular disorders: Gene location
|
|
|
1996
|
6 |
5 |
p. I-X
nvt p.
|
artikel
|
| 10 |
Parkinson's disease (advances in neurology, volume 69
|
Pentland, Brian
|
|
1996
|
6 |
5 |
p. 396-
1 p.
|
artikel
|
| 11 |
Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-coa dehydrogenase deficiency with the G1528C mutation
|
Tyni, Tiina
|
|
1996
|
6 |
5 |
p. 327-337
11 p.
|
artikel
|
| 12 |
Patterns of abnormal protein expression in target formations and unstructured cores
|
de Bleecker, Jan L.
|
|
1996
|
6 |
5 |
p. 339-349
11 p.
|
artikel
|
| 13 |
Pediatric clinical electromyography
|
Mills, K.R.
|
|
1996
|
6 |
5 |
p. 395-396
2 p.
|
artikel
|
| 14 |
40th ENMC sponsored international workshop: Nemaline myopathy 2–4 February 1996, Naarden, The Netherlands
|
Wallgren-Pettersson, Carina
|
|
1996
|
6 |
5 |
p. 389-391
3 p.
|
artikel
|
| 15 |
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis
|
Hosler, Betsy A.
|
|
1996
|
6 |
5 |
p. 361-366
6 p.
|
artikel
|
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