| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of amyotrophic lateral sclerosis with a very slow progression over 44 years
|
Grohme, K.
|
|
2001
|
11 |
4 |
p. 414-416
3 p.
|
artikel
|
| 2 |
A mutation in the X-linked Emery–Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy
|
Vohanka, Stanislav
|
|
2001
|
11 |
4 |
p. 411-413
3 p.
|
artikel
|
| 3 |
A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies
|
Meuleman, J
|
|
2001
|
11 |
4 |
p. 400-403
4 p.
|
artikel
|
| 4 |
ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle’s disease
|
Löfberg, Mervi
|
|
2001
|
11 |
4 |
p. 370-375
6 p.
|
artikel
|
| 5 |
Efficient non-viral DNA-mediated gene transfer to human primary myoblasts using electroporation
|
Espinos, E
|
|
2001
|
11 |
4 |
p. 341-349
9 p.
|
artikel
|
| 6 |
Inherited early onset severe axonal polyneuropathy with respiratory failure and autonomic involvement
|
Mohan, U.
|
|
2001
|
11 |
4 |
p. 395-399
5 p.
|
artikel
|
| 7 |
Instructions to authors
|
|
|
2001
|
11 |
4 |
p. 438-439
2 p.
|
artikel
|
| 8 |
Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy
|
Hayashi, Yukiko K
|
|
2001
|
11 |
4 |
p. 350-359
10 p.
|
artikel
|
| 9 |
Mitochondrial encephalomyopathies: gene mutation
|
|
|
2001
|
11 |
4 |
p. 432-437
6 p.
|
artikel
|
| 10 |
Neuromuscular disorders: gene location
|
|
|
2001
|
11 |
4 |
p. 423-431
9 p.
|
artikel
|
| 11 |
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria
|
Cagliani, R.
|
|
2001
|
11 |
4 |
p. 389-394
6 p.
|
artikel
|
| 12 |
Regulation of α7 integrin by mechanical stress during skeletal muscle regeneration
|
Kääriäinen, Minna
|
|
2001
|
11 |
4 |
p. 360-369
10 p.
|
artikel
|
| 13 |
81st ENMC International Workshop: 4th Meeting on Emery–Dreifuss Muscular Dystrophy 7th and 8th July 2000, Naarden, The Netherlands
|
Ellis, Juliet A
|
|
2001
|
11 |
4 |
p. 417-420
4 p.
|
artikel
|
| 14 |
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations
|
Gellera, C.
|
|
2001
|
11 |
4 |
p. 404-410
7 p.
|
artikel
|
| 15 |
UPDATE IN NEUROMUSCULAR DISORDERS
|
|
|
2001
|
11 |
4 |
p. 422-
1 p.
|
artikel
|
| 16 |
Why did the heated discussion arise between Erb and Landouzy–Dejerine concerning the priority in describing the facio-scapulo-humeral muscular dystrophy and what is the main reason for this famous discussion?
|
Kazakov, V
|
|
2001
|
11 |
4 |
p. 421-
1 p.
|
artikel
|
| 17 |
X-linked myopathy with excessive autophagy: a clinicopathological study of five new families
|
Chabrol, B.
|
|
2001
|
11 |
4 |
p. 376-388
13 p.
|
artikel
|
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