nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy
|
Di Blasi, Claudia |
|
2010 |
20 |
5 |
p. 326-329 4 p. |
artikel |
2 |
Editorial Board
|
|
|
2010 |
20 |
5 |
p. IFC- 1 p. |
artikel |
3 |
Episodic myoglobinuria in a primary gamma-sarcoglycanopathy
|
Pena, Loren |
|
2010 |
20 |
5 |
p. 337-339 3 p. |
artikel |
4 |
Friedreich ataxia presenting as sudden cardiac death in childhood: Clinical, genetic and pathological correlation, with implications for genetic testing and counselling
|
Quercia, Nada |
|
2010 |
20 |
5 |
p. 340-342 3 p. |
artikel |
5 |
Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian family
|
Stober, Andrea |
|
2010 |
20 |
5 |
p. 335-336 2 p. |
artikel |
6 |
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN)
|
Cordelli, D.M. |
|
2010 |
20 |
5 |
p. 343-345 3 p. |
artikel |
7 |
Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin–proteasome pathway
|
Vignaud, Alban |
|
2010 |
20 |
5 |
p. 319-325 7 p. |
artikel |
8 |
Rasch-built myotonic dystrophy type 1 activity and participation scale (DM1-Activ)
|
Hermans, Mieke C.E. |
|
2010 |
20 |
5 |
p. 310-318 9 p. |
artikel |
9 |
Reverse protein arrays as novel approach for protein quantification in muscular dystrophies
|
Escher, Claudia |
|
2010 |
20 |
5 |
p. 302-309 8 p. |
artikel |
10 |
Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: Implication for clinical trials
|
Arechavala-Gomeza, Virginia |
|
2010 |
20 |
5 |
p. 295-301 7 p. |
artikel |
11 |
The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: Report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009
|
Muntoni, F. |
|
2010 |
20 |
5 |
p. 355-362 8 p. |
artikel |
12 |
166th ENMC International Workshop on Collagen type VI-related Myopathies, 22–24 May 2009, Naarden, The Netherlands
|
Allamand, Valérie |
|
2010 |
20 |
5 |
p. 346-354 9 p. |
artikel |
13 |
Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings
|
Kumar, Kishore R. |
|
2010 |
20 |
5 |
p. 330-334 5 p. |
artikel |
14 |
WMS 2010
|
|
|
2010 |
20 |
5 |
p. I- 1 p. |
artikel |
15 |
WMS News
|
|
|
2010 |
20 |
5 |
p. III-IV nvt p. |
artikel |
16 |
WMS online application form
|
|
|
2010 |
20 |
5 |
p. II- 1 p. |
artikel |