| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acute myopathy with skin manifestations, not always idiopathic and autoimmune
|
Bevilacqua, Jorge A.
|
|
|
31 |
11 |
p. 1218-1219
|
artikel
|
| 2 |
An autopsied case of ADSSL1 myopathy
|
Motoda, Atsuko
|
|
|
31 |
11 |
p. 1220-1225
|
artikel
|
| 3 |
A novel MT-CO2 variant causing cerebellar ataxia and neuropathy: The role of muscle biopsy in diagnosis and defining pathogenicity
|
Baty, Karen
|
|
|
31 |
11 |
p. 1186-1193
|
artikel
|
| 4 |
A Novel SPEG mutation causing congenital myopathy with fiber size disproportion and dilated cardiomyopathy with heart transplantation
|
Gurgel-Giannetti, Juliana
|
|
|
31 |
11 |
p. 1199-1206
|
artikel
|
| 5 |
Congenital myopathy and epidermolysis bullosa due to PLEC variant
|
Walter, Maggie C.
|
|
|
31 |
11 |
p. 1212-1217
|
artikel
|
| 6 |
Editorial Board
|
|
|
|
31 |
11 |
p. IFC
|
artikel
|
| 7 |
Effectiveness of thymectomy in juvenile myasthenia gravis and clinical characteristics associated with better outcomes
|
Ng, Wei Chin
|
|
|
31 |
11 |
p. 1113-1123
|
artikel
|
| 8 |
Efficacy and safety of mexiletine in non-dystrophic myotonias: A randomised, double-blind, placebo-controlled, cross-over study
|
Vicart, Savine
|
|
|
31 |
11 |
p. 1124-1135
|
artikel
|
| 9 |
Facioscapulohumeral Muscular Dystrophy and Poliomyelitis followed by Multiple Sclerosis: A “triple trouble” case report and review of the literature on the association of MS and muscle disorders
|
Ziccone, Vanessa
|
|
|
31 |
11 |
p. 1179-1185
|
artikel
|
| 10 |
Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings
|
Jia, Fangzhi Frank
|
|
|
31 |
11 |
p. 1101-1112
|
artikel
|
| 11 |
Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy
|
Campbell, Craig
|
|
|
31 |
11 |
p. 1161-1168
|
artikel
|
| 12 |
High prevalence of sporadic late-onset nemaline myopathy in a cohort of whole-exome sequencing negative myopathy patients
|
De Ridder, Willem
|
|
|
31 |
11 |
p. 1154-1160
|
artikel
|
| 13 |
Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants
|
Lee, Yun Jeong
|
|
|
31 |
11 |
p. 1194-1198
|
artikel
|
| 14 |
Mild form of Danon disease: two case reports
|
Yasui, Toshio
|
|
|
31 |
11 |
p. 1207-1211
|
artikel
|
| 15 |
Muscle magnetic resonance imaging in patients with LAMA2-related muscular dystrophy
|
Tan, Dandan
|
|
|
31 |
11 |
p. 1144-1153
|
artikel
|
| 16 |
Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation
|
Shelton, G. Diane
|
|
|
31 |
11 |
p. 1169-1178
|
artikel
|
| 17 |
Treatment with L‐Citrulline in patients with post‐polio syndrome: A single center, randomized, double blind, placebo‐controlled trial
|
Putananickal, Niveditha
|
|
|
31 |
11 |
p. 1136-1143
|
artikel
|
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