| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Characterization of dystrophic muscle in golden retriever muscular dystrophy dogs by nuclear magnetic resonance imaging
|
Thibaud, J.-L.
|
|
2007
|
17 |
7 |
p. 575-584
10 p.
|
artikel
|
| 2 |
Cytoplasmic γ-actin expression in diverse animal models of muscular dystrophy
|
Hanft, Laurin M.
|
|
2007
|
17 |
7 |
p. 569-574
6 p.
|
artikel
|
| 3 |
Editorial Board
|
|
|
2007
|
17 |
7 |
p. IFC-
1 p.
|
artikel
|
| 4 |
Forthcoming Meetings
|
|
|
2007
|
17 |
7 |
p. IV-
1 p.
|
artikel
|
| 5 |
Hand versus mouth for call–bell activation by DMD and Becker patients
|
Pellegrini, Nadine
|
|
2007
|
17 |
7 |
p. 532-536
5 p.
|
artikel
|
| 6 |
Impact of late-onset Pompe disease on participation in daily life activities: Evaluation of the Rotterdam Handicap Scale
|
Hagemans, M.L.C.
|
|
2007
|
17 |
7 |
p. 537-543
7 p.
|
artikel
|
| 7 |
Isokinetic muscle testing for weak patients suffering from neuromuscular disorders: A reliability study
|
Tiffreau, Vincent
|
|
2007
|
17 |
7 |
p. 524-531
8 p.
|
artikel
|
| 8 |
Musk-antibody positive myasthenia gravis presenting with isolated neck extensor weakness
|
Casasnovas, C.
|
|
2007
|
17 |
7 |
p. 544-546
3 p.
|
artikel
|
| 9 |
Myofiber size correlates with MTM1 mutation type and outcome in X-linked myotubular myopathy
|
Pierson, Christopher R.
|
|
2007
|
17 |
7 |
p. 562-568
7 p.
|
artikel
|
| 10 |
[No title]
|
Hillier, Charles
|
|
2007
|
17 |
7 |
p. 585-
1 p.
|
artikel
|
| 11 |
Novel homozygous mutation of the caveolin-3 gene in rippling muscle disease with extraocular muscle paresis
|
Ueyama, H.
|
|
2007
|
17 |
7 |
p. 558-561
4 p.
|
artikel
|
| 12 |
Quantitative skeletal muscle ultrasound: Diagnostic value in childhood neuromuscular disease
|
Pillen, S.
|
|
2007
|
17 |
7 |
p. 509-516
8 p.
|
artikel
|
| 13 |
Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood
|
Brockmann, Knut
|
|
2007
|
17 |
7 |
p. 517-523
7 p.
|
artikel
|
| 14 |
Variable penetrance of COL6A1 null mutations: Implications for prenatal diagnosis and genetic counselling in Ullrich congenital muscular dystrophy families
|
Peat, Rachel A.
|
|
2007
|
17 |
7 |
p. 547-557
11 p.
|
artikel
|
| 15 |
WMS12 Announcement
|
|
|
2007
|
17 |
7 |
p. II-
1 p.
|
artikel
|
| 16 |
WMS: Application form
|
|
|
2007
|
17 |
7 |
p. I-
1 p.
|
artikel
|
| 17 |
WMS: Executive Board Announcement
|
|
|
2007
|
17 |
7 |
p. III-
1 p.
|
artikel
|
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