| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A MYH3 mutation identified for the first time in a Chinese family with Sheldon-Hall syndrome (DA2B)
|
Xu, Yang
|
|
2018
|
28 |
5 |
p. 456-462
|
artikel
|
| 2 |
Benign thymic enlargement in myasthenia gravis
|
Zouvelou, Vasiliki
|
|
2018
|
28 |
5 |
p. 454-455
|
artikel
|
| 3 |
Critical period of neuromuscular development: Importance for a new treatment of SMA
|
Vrbová, Gerta
|
|
2018
|
28 |
5 |
p. 385-393
|
artikel
|
| 4 |
Disruption of sleep-wake continuum in myotonic dystrophy type 1: Beyond conventional sleep staging
|
Bonanni, Enrica
|
|
2018
|
28 |
5 |
p. 414-421
|
artikel
|
| 5 |
Editorial Board
|
|
|
2018
|
28 |
5 |
p. CO2
|
artikel
|
| 6 |
From excitation to intracellular Ca2+ movements in skeletal muscle: Basic aspects and related clinical disorders
|
Allard, Bruno
|
|
2018
|
28 |
5 |
p. 394-401
|
artikel
|
| 7 |
Low dystrophin levels are insufficient to normalize the neuromuscular synaptic abnormalities of mdx mice
|
van der Pijl, Elizabeth M.
|
|
2018
|
28 |
5 |
p. 427-442
|
artikel
|
| 8 |
Muscle biopsy technical safety and quality using a self-contained, vacuum-assisted biopsy technique
|
Gallo, Antonio
|
|
2018
|
28 |
5 |
p. 450-453
|
artikel
|
| 9 |
222nd ENMC International Workshop:
|
Wood, Libby
|
|
2018
|
28 |
5 |
p. 463-469
|
artikel
|
| 10 |
Parental mosaicism in RYR1-related Central Core Disease
|
Marks, S.
|
|
2018
|
28 |
5 |
p. 422-426
|
artikel
|
| 11 |
Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands
|
Stunnenberg, B.C.
|
|
2018
|
28 |
5 |
p. 402-407
|
artikel
|
| 12 |
Progressive fat replacement of muscle contributes to the disease mechanism of patients with single, large-scale deletions of mitochondrial DNA
|
Hedermann, Gitte
|
|
2018
|
28 |
5 |
p. 408-413
|
artikel
|
| 13 |
Sporadic acute benign calf myositis: Systematic literature review
|
Capoferri, Gioele
|
|
2018
|
28 |
5 |
p. 443-449
|
artikel
|
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