| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy
|
Galassi, Giuliana
|
|
2008
|
18 |
6 |
p. 465-470
6 p.
|
artikel
|
| 2 |
Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies
|
Strach, Katharina
|
|
2008
|
18 |
6 |
p. 475-482
8 p.
|
artikel
|
| 3 |
Distal inflammatory myopathy: Unusual presentation of polymyositis or new entity?
|
Dimitri, Dalia
|
|
2008
|
18 |
6 |
p. 493-500
8 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2008
|
18 |
6 |
p. IFC-
1 p.
|
artikel
|
| 5 |
Eight years experience with enzyme replacement therapy in two children and one adult with Pompe disease
|
van Capelle, C.I.
|
|
2008
|
18 |
6 |
p. 447-452
6 p.
|
artikel
|
| 6 |
Erratum to “Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy” [Neuromuscular Disorders 17(7) (2007) 562–568]
|
Pierson, Christopher R.
|
|
2008
|
18 |
6 |
p. 519-
1 p.
|
artikel
|
| 7 |
First International “Institute of Myology Workshop” on Facioscapulohumeral Muscular Dystrophy, Paris, May 22, 2007
|
Leterrier, F.
|
|
2008
|
18 |
6 |
p. 514-518
5 p.
|
artikel
|
| 8 |
Forthcoming meetings
|
|
|
2008
|
18 |
6 |
p. III-
1 p.
|
artikel
|
| 9 |
Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster
|
Gosselin, Isabelle
|
|
2008
|
18 |
6 |
p. 483-492
10 p.
|
artikel
|
| 10 |
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene
|
Bornstein, Belén
|
|
2008
|
18 |
6 |
p. 453-459
7 p.
|
artikel
|
| 11 |
No carnitine palmitoyltransferase deficiency in skeletal muscle in 18 malignant hyperthermia susceptible individuals
|
Wieser, Thomas
|
|
2008
|
18 |
6 |
p. 471-474
4 p.
|
artikel
|
| 12 |
Severe neonatal myasthenia due to maternal anti-MuSK antibodies
|
Béhin, Anthony
|
|
2008
|
18 |
6 |
p. 443-446
4 p.
|
artikel
|
| 13 |
Transient receptor potential cation channels in normal and dystrophic mdx muscle
|
Krüger, Jana
|
|
2008
|
18 |
6 |
p. 501-513
13 p.
|
artikel
|
| 14 |
Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonism
|
Invernizzi, Federica
|
|
2008
|
18 |
6 |
p. 460-464
5 p.
|
artikel
|
| 15 |
What’s new in congenital myopathies?
|
North, Kathryn
|
|
2008
|
18 |
6 |
p. 433-442
10 p.
|
artikel
|
| 16 |
WMS online application form
|
|
|
2008
|
18 |
6 |
p. I-
1 p.
|
artikel
|
| 17 |
WMS - 13th International Congress
|
|
|
2008
|
18 |
6 |
p. II-
1 p.
|
artikel
|
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