| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation
|
Tasca, Giorgio
|
|
2010
|
20 |
11 |
p. 730-734
5 p.
|
artikel
|
| 2 |
Cardiovascular magnetic resonance imaging evaluation of two families with Becker muscular dystrophy
|
Mavrogeni, Sophie
|
|
2010
|
20 |
11 |
p. 717-719
3 p.
|
artikel
|
| 3 |
Clinical and neuropathological findings in patients with TACO1 mutations
|
Seeger, Jürgen
|
|
2010
|
20 |
11 |
p. 720-724
5 p.
|
artikel
|
| 4 |
Congenital muscular dystrophy, myasthenic symptoms and epidermolysis bullosa simplex (EBS) associated with mutations in the PLEC1 gene encoding plectin
|
Forrest, Katharine
|
|
2010
|
20 |
11 |
p. 709-711
3 p.
|
artikel
|
| 5 |
Debio-025 is more effective than prednisone in reducing muscular pathology in mdx mice
|
Wissing, Erin R.
|
|
2010
|
20 |
11 |
p. 753-760
8 p.
|
artikel
|
| 6 |
Disorders of muscle lipid metabolism: Diagnostic and therapeutic challenges
|
Laforêt, Pascal
|
|
2010
|
20 |
11 |
p. 693-700
8 p.
|
artikel
|
| 7 |
Editorial Board
|
|
|
2010
|
20 |
11 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity
|
Claeys, Kristl G.
|
|
2010
|
20 |
11 |
p. 701-708
8 p.
|
artikel
|
| 9 |
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy
|
Mazzone, Elena
|
|
2010
|
20 |
11 |
p. 712-716
5 p.
|
artikel
|
| 10 |
Not waiting to live, not living to wait....
|
Moeschen, P.T.
|
|
2010
|
20 |
11 |
p. 770-771
2 p.
|
artikel
|
| 11 |
Novel MPZ mutations and congenital hypomyelinating neuropathy
|
McMillan, Hugh J.
|
|
2010
|
20 |
11 |
p. 725-729
5 p.
|
artikel
|
| 12 |
Polymyositis in African HIV-infected subjects
|
Heckmann, J.M.
|
|
2010
|
20 |
11 |
p. 735-739
5 p.
|
artikel
|
| 13 |
170th ENMC International Workshop: Bone protection for corticosteroid treated Duchenne muscular dystrophy. 27–29 November 2009, Naarden, The Netherlands
|
Quinlivan, R.
|
|
2010
|
20 |
11 |
p. 761-769
9 p.
|
artikel
|
| 14 |
Ultrastructural changes in diaphragm neuromuscular junctions in a severe mouse model for Spinal Muscular Atrophy and their prevention by bifunctional U7 snRNA correcting SMN2 splicing
|
Voigt, Tilman
|
|
2010
|
20 |
11 |
p. 744-752
9 p.
|
artikel
|
| 15 |
Using mouse cranial muscles to investigate neuromuscular pathology in vivo
|
Murray, L.M.
|
|
2010
|
20 |
11 |
p. 740-743
4 p.
|
artikel
|
| 16 |
WMS 2011
|
|
|
2010
|
20 |
11 |
p. I-
1 p.
|
artikel
|
| 17 |
WMS News
|
|
|
2010
|
20 |
11 |
p. III-IV
nvt p.
|
artikel
|
| 18 |
WMS online application form
|
|
|
2010
|
20 |
11 |
p. II-
1 p.
|
artikel
|
Tijdschrift beschrijving