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                             12 gevonden resultaten
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
                             12 gevonden resultaten
 
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