| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case
|
Kulshrestha, Richa
|
|
2018
|
28 |
12 |
p. 1016-1021
|
artikel
|
| 2 |
Editorial Board
|
|
|
2018
|
28 |
12 |
p. IFC
|
artikel
|
| 3 |
IGHMBP2 mutation associated with organ-specific autonomic dysfunction
|
Tomaselli, Pedro J.
|
|
2018
|
28 |
12 |
p. 1012-1015
|
artikel
|
| 4 |
Isokinetic assessment of trunk muscles in facioscapulohumeral muscular dystrophy type 1 patients
|
Esnault, Julien
|
|
2018
|
28 |
12 |
p. 996-1002
|
artikel
|
| 5 |
Microangiopathy and mild mixed neuromyopathic alterations in a patient with homozygous PIEZO-2 mutation
|
Quade, Annegret
|
|
2018
|
28 |
12 |
p. 1006-1011
|
artikel
|
| 6 |
Pattern of myogenesis and vascular repair in early and advanced lesions of juvenile dermatomyositis
|
Baumann, Matthias
|
|
2018
|
28 |
12 |
p. 973-985
|
artikel
|
| 7 |
Severe limb-girdle muscular dystrophy 2A in two young siblings from Guinea-Bissau associated with a novel null homozygous mutation in CAPN3 gene
|
Oliveira Santos, Miguel
|
|
2018
|
28 |
12 |
p. 1003-1005
|
artikel
|
| 8 |
Small mutation screening in the DMD gene by whole exome sequencing of an Argentine Duchenne/Becker muscular dystrophies cohort
|
Luce, Leonela N.
|
|
2018
|
28 |
12 |
p. 986-995
|
artikel
|
| 9 |
234th ENMC International Workshop: Chaperone dysfunction in muscle disease Naarden, The Netherlands, 8–10 December 2017
|
Weihl, Conrad C.
|
|
2018
|
28 |
12 |
p. 1022-1030
|
artikel
|
| 10 |
The 2019 version of the gene table of neuromuscular disorders (nuclear genome)
|
Bonne, Gisèle
|
|
2018
|
28 |
12 |
p. 1031-1063
|
artikel
|
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