| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1
|
Hoffjan, Sabine
|
|
2006
|
16 |
11 |
p. 749-753
5 p.
|
artikel
|
| 2 |
Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes
|
Mastaglia, Frank
|
|
2006
|
16 |
11 |
p. 754-758
5 p.
|
artikel
|
| 3 |
Forthcoming meetings
|
|
|
2006
|
16 |
11 |
p. V-
1 p.
|
artikel
|
| 4 |
IFC: Ed Board
|
|
|
2006
|
16 |
11 |
p. CO2-
1 p.
|
artikel
|
| 5 |
Instructions to Authors
|
|
|
2006
|
16 |
11 |
p. 811-812
2 p.
|
artikel
|
| 6 |
Isaacs’ syndrome associated with myasthenia gravis, showing remission after cytoreductive surgery of pleural recurrence of thymoma
|
Fukushima, Kazuhiro
|
|
2006
|
16 |
11 |
p. 763-765
3 p.
|
artikel
|
| 7 |
Muscle cell and motor protein function in patients with a IIa myosin missense mutation (Glu-706 to Lys)
|
Li, M.
|
|
2006
|
16 |
11 |
p. 782-791
10 p.
|
artikel
|
| 8 |
Muscle protein analysis in the detection of heterozygotes for recessive limb girdle muscular dystrophy type 2B and 2E
|
Fanin, Marina
|
|
2006
|
16 |
11 |
p. 792-799
8 p.
|
artikel
|
| 9 |
Myofibrillar myopathy with congenital cataract and skeletal anomalies without mutations in the desmin, αB-crystallin, myotilin, LMNA or SEPN1 genes
|
Kostera-Pruszczyk, Anna
|
|
2006
|
16 |
11 |
p. 759-762
4 p.
|
artikel
|
| 10 |
Myopathy in horses with pituitary pars intermedia dysfunction (Cushing’s disease)
|
Aleman, M.
|
|
2006
|
16 |
11 |
p. 737-744
8 p.
|
artikel
|
| 11 |
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy
|
van der Kooi, E.L.
|
|
2006
|
16 |
11 |
p. 766-769
4 p.
|
artikel
|
| 12 |
[No title]
|
Graves, Tracey
|
|
2006
|
16 |
11 |
p. 809-
1 p.
|
artikel
|
| 13 |
[No title]
|
Stewart, John
|
|
2006
|
16 |
11 |
p. 809-810
2 p.
|
artikel
|
| 14 |
Outpatient continuous inotrope infusion as an adjunct to heart failure therapy in Duchenne muscular dystrophy
|
Cripe, Linda H.
|
|
2006
|
16 |
11 |
p. 745-748
4 p.
|
artikel
|
| 15 |
Premature proliferative arrest of cricopharyngeal myoblasts in oculo-pharyngeal muscular dystrophy: Therapeutic perspectives of autologous myoblast transplantation
|
Périé, Sophie
|
|
2006
|
16 |
11 |
p. 770-781
12 p.
|
artikel
|
| 16 |
Ramblings announcement
|
|
|
2006
|
16 |
11 |
p. VI-VII
nvt p.
|
artikel
|
| 17 |
Refsum’s disease may mimic familial Guillain Barre syndrome
|
Verny, Christophe
|
|
2006
|
16 |
11 |
p. 805-808
4 p.
|
artikel
|
| 18 |
SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)
|
Corrado, L.
|
|
2006
|
16 |
11 |
p. 800-804
5 p.
|
artikel
|
| 19 |
12th International WMS Congress, 17-20 October 2007
|
|
|
2006
|
16 |
11 |
p. III-
1 p.
|
artikel
|
| 20 |
WMS application form
|
|
|
2006
|
16 |
11 |
p. I-
1 p.
|
artikel
|
| 21 |
WMS Call for Topics
|
|
|
2006
|
16 |
11 |
p. IV-
1 p.
|
artikel
|
| 22 |
WMS web addresses
|
|
|
2006
|
16 |
11 |
p. II-
1 p.
|
artikel
|
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