| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel PYGM mutation in a Korean patient with McArdle disease: The role of nonsense-mediated mRNA decay
|
Sohn, Eun Hee
|
|
2008
|
18 |
11 |
p. 886-889
4 p.
|
artikel
|
| 2 |
Becker’s muscular dystrophy aggravating facioscapulohumeral muscular dystrophy – double trouble as an explanation for an atypical phenotype
|
Rudnik-Schöneborn, S.
|
|
2008
|
18 |
11 |
p. 881-885
5 p.
|
artikel
|
| 3 |
Clinical and molecular overlap between myopathies and inherited connective tissue diseases
|
Voermans, N.C.
|
|
2008
|
18 |
11 |
p. 843-856
14 p.
|
artikel
|
| 4 |
Differential diagnosis of muscular hypotonia in infants: The kyphoscoliotic type of Ehlers–Danlos syndrome (EDS VI)
|
Voermans, N.C.
|
|
2008
|
18 |
11 |
p. 906-907
2 p.
|
artikel
|
| 5 |
Dystrophin knockdown mice suggest that early, transient dystrophin expression might be enough to prevent later pathology
|
Duan, Dongsheng
|
|
2008
|
18 |
11 |
p. 904-905
2 p.
|
artikel
|
| 6 |
Erratum to “Response to ‘Outcome measure for SMA II and III patients’” [Neuromuscul Disord 18 (2008) 594–595]
|
O’Hagen, J.
|
|
2008
|
18 |
11 |
p. 911-
1 p.
|
artikel
|
| 7 |
IFC: Ed Board
|
|
|
2008
|
18 |
11 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita
|
Fialho, Doreen
|
|
2008
|
18 |
11 |
p. 869-872
4 p.
|
artikel
|
| 9 |
[No title]
|
Metcalfe, Richard
|
|
2008
|
18 |
11 |
p. 909-
1 p.
|
artikel
|
| 10 |
[No title]
|
Burke, Georgina
|
|
2008
|
18 |
11 |
p. 910-
1 p.
|
artikel
|
| 11 |
[No title]
|
Poulton, Jo
|
|
2008
|
18 |
11 |
p. 908-909
2 p.
|
artikel
|
| 12 |
[No title]
|
Gow, David
|
|
2008
|
18 |
11 |
p. 908-
1 p.
|
artikel
|
| 13 |
Prevention of muscle fibrosis and improvement in muscle performance in the mdx mouse by halofuginone
|
Turgeman, Tidhar
|
|
2008
|
18 |
11 |
p. 857-868
12 p.
|
artikel
|
| 14 |
Response
|
Giunta, Cecilia
|
|
2008
|
18 |
11 |
p. 907-
1 p.
|
artikel
|
| 15 |
Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength
|
Ambrósio, C.E.
|
|
2008
|
18 |
11 |
p. 892-893
2 p.
|
artikel
|
| 16 |
Sarcoidosis in a case of MuSK-positive myasthenia gravis
|
Spengos, Konstantinos
|
|
2008
|
18 |
11 |
p. 890-891
2 p.
|
artikel
|
| 17 |
The relationship between regional body composition and quantitative strength in facioscapulohumeral muscular dystrophy (FSHD)
|
Skalsky, Andrew J.
|
|
2008
|
18 |
11 |
p. 873-880
8 p.
|
artikel
|
| 18 |
Towards harmonisation of outcome measures for DMD and SMA within TREAT-NMD; Report of three expert workshops: TREAT-NMD/ENMC Workshop on outcome measures, 12th–13th May 2007, Naarden, The Netherlands; TREAT-NMD Workshop on outcome measures in experimental trials for DMD, 30th June–1st July 2007, Naarden, The Netherlands; Conjoint Institute of Myology TREAT-NMD Meeting on physical activity monitoring in neuromuscular disorders, 11th July 2007, Paris, France
|
Mercuri, E.
|
|
2008
|
18 |
11 |
p. 894-903
10 p.
|
artikel
|
| 19 |
WMS online application form
|
|
|
2008
|
18 |
11 |
p. I-
1 p.
|
artikel
|
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