nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Brain involvement in Charcot–Marie–Tooth disease due to ganglioside-induced differentiation associated-protein 1 mutation
|
Al-Ghamdi, Fouad |
|
2017 |
27 |
9 |
p. 848-851 4 p. |
artikel |
2 |
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains
|
Harris, Elizabeth |
|
2017 |
27 |
9 |
p. 861-872 12 p. |
artikel |
3 |
Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period
|
Sframeli, Maria |
|
2017 |
27 |
9 |
p. 793-803 11 p. |
artikel |
4 |
Cystinosis distal myopathy, novel clinical, pathological and genetic features
|
Cabrera-Serrano, Macarena |
|
2017 |
27 |
9 |
p. 873-878 6 p. |
artikel |
5 |
Editorial Board
|
|
|
2017 |
27 |
9 |
p. CO2- 1 p. |
artikel |
6 |
Evaluation of coexisting polymyositis in feline myasthenia gravis: A case series
|
Mayousse, Vincent |
|
2017 |
27 |
9 |
p. 804-815 12 p. |
artikel |
7 |
Exome sequencing identifies targets in the treatment-resistant ophthalmoplegic subphenotype of myasthenia gravis
|
Nel, Melissa |
|
2017 |
27 |
9 |
p. 816-825 10 p. |
artikel |
8 |
Grand paternal inheritance of X-linked myotubular myopathy due to mosaicism, and identification of necklace fibers in an asymptomatic male
|
Hedberg-Oldfors, Carola |
|
2017 |
27 |
9 |
p. 843-847 5 p. |
artikel |
9 |
Insights from genotype–phenotype correlations by novel SPEG mutations causing centronuclear myopathy
|
Wang, Haicui |
|
2017 |
27 |
9 |
p. 836-842 7 p. |
artikel |
10 |
Long-term follow-up of motor function and muscle strength in the congenital and childhood forms of myotonic dystrophy type 1
|
Kroksmark, Anna-Karin |
|
2017 |
27 |
9 |
p. 826-835 10 p. |
artikel |
11 |
Misdiagnosis is an important factor for diagnostic delay in McArdle disease
|
Scalco, Renata Siciliani |
|
2017 |
27 |
9 |
p. 852-855 4 p. |
artikel |
12 |
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient
|
Ikenberg, Elena |
|
2017 |
27 |
9 |
p. 856-860 5 p. |
artikel |