| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencing
|
Dai, Yi
|
|
2015
|
25 |
8 |
p. 617-624
8 p.
|
artikel
|
| 2 |
A missense mutation in domain III in HSPG2 in Schwartz–Jampel syndrome compromises secretion of perlecan into the extracellular space
|
Iwata, Satoshi
|
|
2015
|
25 |
8 |
p. 667-671
5 p.
|
artikel
|
| 3 |
A sporadic case of late-onset familial amyloid polyneuropathy with a monoclonal gammopathy
|
Correia, Ana Sofia
|
|
2015
|
25 |
8 |
p. 658-660
3 p.
|
artikel
|
| 4 |
Disease course and therapeutic approach in dermatomyositis: A four-center retrospective study of 100 patients
|
Johnson, Nicholas E.
|
|
2015
|
25 |
8 |
p. 625-631
7 p.
|
artikel
|
| 5 |
Dystrophinopathy mimicking metabolic myopathies
|
Liewluck, Teerin
|
|
2015
|
25 |
8 |
p. 653-657
5 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2015
|
25 |
8 |
p. CO2-
1 p.
|
artikel
|
| 7 |
Muscle imaging in fibrodysplasia ossificans progressiva: The neurologist's perspective
|
Tasca, Giorgio
|
|
2015
|
25 |
8 |
p. 672-673
2 p.
|
artikel
|
| 8 |
Myasthenia gravis with presynaptic neurophysiological signs: Two case reports and literature review
|
Alboini, Paolo Emilio
|
|
2015
|
25 |
8 |
p. 646-650
5 p.
|
artikel
|
| 9 |
Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy
|
Santos, Dante Brasil
|
|
2015
|
25 |
8 |
p. 632-639
8 p.
|
artikel
|
| 10 |
Selective response to rituximab in a young child with MuSK-associated myasthenia gravis
|
Govindarajan, Raghav
|
|
2015
|
25 |
8 |
p. 651-652
2 p.
|
artikel
|
| 11 |
The influence of somatosensory and muscular deficits on postural stabilization: Insights from an instrumented analysis of subjects affected by different types of Charcot–Marie–Tooth disease
|
Lencioni, Tiziana
|
|
2015
|
25 |
8 |
p. 640-645
6 p.
|
artikel
|
| 12 |
208th ENMC International Workshop: Formation of a European Network to develop a European data sharing model and treatment guidelines for Pompe disease Naarden, The Netherlands, 26–28 September 2014
|
Schoser, Benedikt
|
|
2015
|
25 |
8 |
p. 674-678
5 p.
|
artikel
|
| 13 |
X-linked spinal muscular atrophy (SMAX2) caused by de novo c.1731C>T substitution in the UBA1 gene
|
Jędrzejowska, Maria
|
|
2015
|
25 |
8 |
p. 661-666
6 p.
|
artikel
|
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