| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Bilateral congenital lumbar hernias in a patient with central core disease – A case report
|
Lazier, Joanna
|
|
2016
|
26 |
1 |
p. 56-59
4 p.
|
artikel
|
| 2 |
Commentary from the Editor
|
Dubowitz, Victor
|
|
2016
|
26 |
1 |
p. 1-4
4 p.
|
artikel
|
| 3 |
Duchenne muscular dystrophy: Ringo to the rescue?
|
Cohn, Ronald D.
|
|
2016
|
26 |
1 |
p. 5-6
2 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2016
|
26 |
1 |
p. CO2-
1 p.
|
artikel
|
| 5 |
Electromechanical delay components during skeletal muscle contraction and relaxation in patients with myotonic dystrophy type 1
|
Esposito, Fabio
|
|
2016
|
26 |
1 |
p. 60-72
13 p.
|
artikel
|
| 6 |
Epidemiology of myasthenia gravis in Ontario, Canada
|
Breiner, Ari
|
|
2016
|
26 |
1 |
p. 41-46
6 p.
|
artikel
|
| 7 |
Evaluation of muscle oxygenation by near infrared spectroscopy in patients with facioscapulohumeral muscular dystrophy
|
Olivier, N.
|
|
2016
|
26 |
1 |
p. 47-55
9 p.
|
artikel
|
| 8 |
Functional characterization of the RYR1 mutation p.Arg4737Trp associated with susceptibility to malignant hyperthermia
|
Johannsen, Stephan
|
|
2016
|
26 |
1 |
p. 21-25
5 p.
|
artikel
|
| 9 |
GDAP1 mutations in Italian axonal Charcot–Marie–Tooth patients: Phenotypic features and clinical course
|
Pezzini, I.
|
|
2016
|
26 |
1 |
p. 26-32
7 p.
|
artikel
|
| 10 |
Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1
|
Akman, H. Orhan
|
|
2016
|
26 |
1 |
p. 16-20
5 p.
|
artikel
|
| 11 |
Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes
|
Díaz-Manera, Jordi
|
|
2016
|
26 |
1 |
p. 33-40
8 p.
|
artikel
|
| 12 |
Positive effects of bisphosphonates on bone and muscle in a mouse model of Duchenne muscular dystrophy
|
Yoon, Sung-Hee
|
|
2016
|
26 |
1 |
p. 73-84
12 p.
|
artikel
|
| 13 |
Sarcocystis fayeri in skeletal muscle of horses with neuromuscular disease
|
Aleman, Monica
|
|
2016
|
26 |
1 |
p. 85-93
9 p.
|
artikel
|
| 14 |
Targeted next-generation sequencing assay for detection of mutations in primary myopathies
|
Evilä, Anni
|
|
2016
|
26 |
1 |
p. 7-15
9 p.
|
artikel
|
| 15 |
20th Anniversary Congress of the World Muscle Society, Brighton 2015
|
Miller, Jane
|
|
2016
|
26 |
1 |
p. 104-110
7 p.
|
artikel
|
| 16 |
The Meryon Lecture at the 18th Annual Meeting of the Meryon Society Wolfson College, Oxford, UK, 12th September 2014
|
Tournev, Ivailo
|
|
2016
|
26 |
1 |
p. 94-103
10 p.
|
artikel
|
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