| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2
|
Flanigan, Kevin M.
|
|
2013
|
23 |
2 |
p. 192-
1 p.
|
artikel
|
| 2 |
Childhood chronic inflammatory demyelinating polyradiculoneuropathy: Combined analysis of a large cohort and eleven published series
|
McMillan, Hugh J.
|
|
2013
|
23 |
2 |
p. 103-111
9 p.
|
artikel
|
| 3 |
Congenital myopathy with focal loss of cross-striations revisited
|
Voermans, N.C.
|
|
2013
|
23 |
2 |
p. 160-164
5 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2013
|
23 |
2 |
p. IFC-
1 p.
|
artikel
|
| 5 |
Electrophysiological and motor function scale association in a pre-symptomatic infant with spinal muscular atrophy type I
|
Finkel, Richard S.
|
|
2013
|
23 |
2 |
p. 112-115
4 p.
|
artikel
|
| 6 |
Innovative methods to assess upper limb strength and function in non-ambulant Duchenne patients
|
Servais, L.
|
|
2013
|
23 |
2 |
p. 139-148
10 p.
|
artikel
|
| 7 |
Myopathy in a rhesus monkey with biopsy findings similar to human sporadic inclusion body myositis
|
Skuk, Daniel
|
|
2013
|
23 |
2 |
p. 155-159
5 p.
|
artikel
|
| 8 |
Novel excitation-contraction uncoupled RYR1 mutations in patients with central core disease
|
Kraeva, Natalia
|
|
2013
|
23 |
2 |
p. 120-132
13 p.
|
artikel
|
| 9 |
Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia
|
Peyer, Anne-Kathrin
|
|
2013
|
23 |
2 |
p. 149-154
6 p.
|
artikel
|
| 10 |
Prednisolone-sparing effect of cyclosporin A therapy for very elderly patients with myasthenia gravis
|
Nakamura, Seika
|
|
2013
|
23 |
2 |
p. 176-179
4 p.
|
artikel
|
| 11 |
Pregnancy during enzyme replacement therapy for late-onset acid maltase deficiency
|
Zagnoli, Fabien
|
|
2013
|
23 |
2 |
p. 180-181
2 p.
|
artikel
|
| 12 |
Recurrent episodes of rhabdomyolysis in pontocerebellar hypoplasia type 2
|
Zafeiriou, Dimitrios I.
|
|
2013
|
23 |
2 |
p. 116-119
4 p.
|
artikel
|
| 13 |
Report on the Myomatrix Conference April 22–24, 2012, University of Nevada, Reno, Nevada, USA
|
Rutkowski, Anne
|
|
2013
|
23 |
2 |
p. 188-191
4 p.
|
artikel
|
| 14 |
Response
|
Witting, Nanna
|
|
2013
|
23 |
2 |
p. 193-
1 p.
|
artikel
|
| 15 |
Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations
|
Burke, Georgina
|
|
2013
|
23 |
2 |
p. 170-175
6 p.
|
artikel
|
| 16 |
Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota Hutterite
|
Liewluck, Teerin
|
|
2013
|
23 |
2 |
p. 133-138
6 p.
|
artikel
|
| 17 |
160th ENMC International Workshop (First ENMC practical care workshop) Exercise training in patients with muscle diseases
|
Vissing, John
|
|
2013
|
23 |
2 |
p. 182-187
6 p.
|
artikel
|
| 18 |
Whole exome sequencing in foetal akinesia expands the genotype–phenotype spectrum of GBE1 glycogen storage disease mutations
|
Ravenscroft, Gianina
|
|
2013
|
23 |
2 |
p. 165-169
5 p.
|
artikel
|
| 19 |
WMS 2013
|
|
|
2013
|
23 |
2 |
p. I-
1 p.
|
artikel
|
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