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 |