| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An analysis of the entire SOD1 gene in sporadic ALS
|
Luquin, Natasha
|
|
2008
|
18 |
7 |
p. 545-552
8 p.
|
artikel
|
| 2 |
Autosomal dominant congenital spinal muscular atrophy – A possible developmental deficiency of motor neurones?
|
Reddel, S.
|
|
2008
|
18 |
7 |
p. 530-535
6 p.
|
artikel
|
| 3 |
Caveolinopathy – New mutations and additional symptoms
|
Aboumousa, Ahmed
|
|
2008
|
18 |
7 |
p. 572-578
7 p.
|
artikel
|
| 4 |
Daily salbutamol in young patients with SMA type II
|
Pane, Marika
|
|
2008
|
18 |
7 |
p. 536-540
5 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2008
|
18 |
7 |
p. IFC-
1 p.
|
artikel
|
| 6 |
Forthcoming meetings
|
|
|
2008
|
18 |
7 |
p. III-
1 p.
|
artikel
|
| 7 |
Lysosomal myopathies: An excessive build-up in autophagosomes is too much to handle
|
Malicdan, May Christine
|
|
2008
|
18 |
7 |
p. 521-529
9 p.
|
artikel
|
| 8 |
Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathy
|
Blakely, Emma
|
|
2008
|
18 |
7 |
p. 557-560
4 p.
|
artikel
|
| 9 |
Outcome measure for SMA II and III patients
|
Bérard, Carole
|
|
2008
|
18 |
7 |
p. 593-594
2 p.
|
artikel
|
| 10 |
Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy
|
Korngut, Lawrence
|
|
2008
|
18 |
7 |
p. 579-582
4 p.
|
artikel
|
| 11 |
POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study
|
Messina, S.
|
|
2008
|
18 |
7 |
p. 565-571
7 p.
|
artikel
|
| 12 |
Response
|
O’Hagen, Jessica
|
|
2008
|
18 |
7 |
p. 594-595
2 p.
|
artikel
|
| 13 |
Survival in SMA type I: A prospective analysis of 34 consecutive cases
|
Cobben, J.M.
|
|
2008
|
18 |
7 |
p. 541-544
4 p.
|
artikel
|
| 14 |
Symptomatic nephrolithiasis in prolonged survivors of Duchenne muscular dystrophy
|
Shumyatcher, Yana
|
|
2008
|
18 |
7 |
p. 561-564
4 p.
|
artikel
|
| 15 |
156th ENMC International Workshop: Desmin and protein aggregate myopathies, 9–11 November 2007, Naarden, The Netherlands
|
Goebel, Hans H.
|
|
2008
|
18 |
7 |
p. 583-592
10 p.
|
artikel
|
| 16 |
The role of complex I genes in MELAS: A novel heteroplasmic mutation 3380G>A in ND1 of mtDNA
|
Horváth, Rita
|
|
2008
|
18 |
7 |
p. 553-556
4 p.
|
artikel
|
| 17 |
WMS online application form
|
|
|
2008
|
18 |
7 |
p. I-
1 p.
|
artikel
|
| 18 |
WMS - 13th International Congress
|
|
|
2008
|
18 |
7 |
p. II-
1 p.
|
artikel
|
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