| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adult-onset Satoyoshi syndrome in a young male
|
Montanaro, Vinícius Viana Abreu
|
|
2017
|
27 |
4 |
p. 382-384
3 p.
|
artikel
|
| 2 |
Anatomical and mesoscopic characterization of the dystrophic diaphragm: An in vivo nuclear magnetic resonance imaging study in the Golden retriever muscular dystrophy dog
|
Thibaud, J.L.
|
|
2017
|
27 |
4 |
p. 315-325
11 p.
|
artikel
|
| 3 |
Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy
|
Meier, Thomas
|
|
2017
|
27 |
4 |
p. 307-314
8 p.
|
artikel
|
| 4 |
Clinical follow-up of pregnancy in myasthenia gravis patients
|
Ducci, Renata D.
|
|
2017
|
27 |
4 |
p. 352-357
6 p.
|
artikel
|
| 5 |
Corrigendum to “Response to: Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both” [Neuromuscular Disorders 26/8 (2016) 549]
|
Mancuso, Michelangelo
|
|
2017
|
27 |
4 |
p. e1-
1 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2017
|
27 |
4 |
p. CO2-
1 p.
|
artikel
|
| 7 |
Fist sign in inclusion body myositis
|
Kobayashi, Zen
|
|
2017
|
27 |
4 |
p. 385-386
2 p.
|
artikel
|
| 8 |
Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathy
|
Prahm, Kira Philipsen
|
|
2017
|
27 |
4 |
p. 358-362
5 p.
|
artikel
|
| 9 |
Immunohistochemistry on a panel of Emery–Dreifuss muscular dystrophy samples reveals nuclear envelope proteins as inconsistent markers for pathology
|
Le Thanh, Phu
|
|
2017
|
27 |
4 |
p. 338-351
14 p.
|
artikel
|
| 10 |
Low bone mineral density and fractures are highly prevalent in pediatric patients with spinal muscular atrophy regardless of disease severity
|
Wasserman, Halley M.
|
|
2017
|
27 |
4 |
p. 331-337
7 p.
|
artikel
|
| 11 |
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose
|
Voermans, N.C.
|
|
2017
|
27 |
4 |
p. 370-376
7 p.
|
artikel
|
| 12 |
Prognostic value of nocturnal hypoventilation in neuromuscular patients
|
Orlikowski, David
|
|
2017
|
27 |
4 |
p. 326-330
5 p.
|
artikel
|
| 13 |
219th ENMC International Workshop Titinopathies International database of titin mutations and phenotypes, Heemskerk, The Netherlands, 29 April–1 May 2016
|
Hackman, Peter
|
|
2017
|
27 |
4 |
p. 396-407
12 p.
|
artikel
|
| 14 |
220th ENMC workshop: Dystroglycan and the dystroglycanopathies Naarden, The Netherlands, 27–29 May 2016
|
Brown, Susan C.
|
|
2017
|
27 |
4 |
p. 387-395
9 p.
|
artikel
|
| 15 |
The role of p62/SQSTM1 in sporadic inclusion body myositis
|
Nakano, Satoshi
|
|
2017
|
27 |
4 |
p. 363-369
7 p.
|
artikel
|
| 16 |
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance
|
Geroldi, Alessandro
|
|
2017
|
27 |
4 |
p. 377-381
5 p.
|
artikel
|
| 17 |
Update in NMD Announcement
|
|
|
2017
|
27 |
4 |
p. IV-
1 p.
|
artikel
|
Tijdschrift beschrijving