| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Absence of β-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy
|
Monnier, Nicole
|
|
2009
|
19 |
2 |
p. 118-123
6 p.
|
artikel
|
| 2 |
Activity limitations in patients with neuromuscular disorders: A responsiveness study of the ACTIVLIM questionnaire
|
Vandervelde, Laure
|
|
2009
|
19 |
2 |
p. 99-103
5 p.
|
artikel
|
| 3 |
A novel homozygous RRM2B missense mutation in association with severe mtDNA depletion
|
Kollberg, Gittan
|
|
2009
|
19 |
2 |
p. 147-150
4 p.
|
artikel
|
| 4 |
An unusual complication of immunosuppression in myasthenia gravis: Progressive multifocal leukoencephalopathy
|
Gedizlioglu, Muhteşem
|
|
2009
|
19 |
2 |
p. 155-157
3 p.
|
artikel
|
| 5 |
Canine inflammatory myopathy associated with Leishmania Infantum infection
|
Paciello, Orlando
|
|
2009
|
19 |
2 |
p. 124-130
7 p.
|
artikel
|
| 6 |
Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
|
Taanman, Jan-Willem
|
|
2009
|
19 |
2 |
p. 151-154
4 p.
|
artikel
|
| 7 |
Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families – Detection of carrier status in symptomatic and asymptomatic female relatives
|
Pikó, Henriett
|
|
2009
|
19 |
2 |
p. 108-112
5 p.
|
artikel
|
| 8 |
Editorial Board
|
|
|
2009
|
19 |
2 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Eosinophilic myositis as presenting symptom in γ-sarcoglycanopathy
|
Baumeister, Sarah K.
|
|
2009
|
19 |
2 |
p. 167-171
5 p.
|
artikel
|
| 10 |
Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: A case study
|
Tsuji, Masahiro
|
|
2009
|
19 |
2 |
p. 140-142
3 p.
|
artikel
|
| 11 |
Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient
|
Blázquez, Alberto
|
|
2009
|
19 |
2 |
p. 143-146
4 p.
|
artikel
|
| 12 |
Novel activation domain derived from Che-1 cofactor coupled with the artificial protein Jazz drives utrophin upregulation
|
Desantis, Agata
|
|
2009
|
19 |
2 |
p. 158-162
5 p.
|
artikel
|
| 13 |
Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity
|
Baets, Jonathan
|
|
2009
|
19 |
2 |
p. 172-175
4 p.
|
artikel
|
| 14 |
Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease
|
Van der Beek, N.A.M.E.
|
|
2009
|
19 |
2 |
p. 113-117
5 p.
|
artikel
|
| 15 |
Relationship between foot strength and motor function in preschool-age children
|
Rose, Kristy J.
|
|
2009
|
19 |
2 |
p. 104-107
4 p.
|
artikel
|
| 16 |
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation
|
Uro-Coste, Emmanuelle
|
|
2009
|
19 |
2 |
p. 163-166
4 p.
|
artikel
|
| 17 |
Treatment with inhibitors of the NF-κB pathway improves whole body tension development in the mdx mouse
|
Siegel, Ashley L.
|
|
2009
|
19 |
2 |
p. 131-139
9 p.
|
artikel
|
| 18 |
WMS 2009
|
|
|
2009
|
19 |
2 |
p. I-
1 p.
|
artikel
|
| 19 |
WMS News
|
|
|
2009
|
19 |
2 |
p. III-IV
nvt p.
|
artikel
|
| 20 |
WMS online application form
|
|
|
2009
|
19 |
2 |
p. II-
1 p.
|
artikel
|
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