| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Commentary from the Editor
|
Oldfors, Anders
|
|
|
31 |
1 |
p. 1-4
|
artikel
|
| 2 |
Dysphagia in adult myopathies
|
Argov, Zohar
|
|
|
31 |
1 |
p. 5-20
|
artikel
|
| 3 |
Early onset neutral lipid storage disease with myopathy presenting as congenital hypotonia and hepatomegaly
|
Avila-Smirnow, Daniela
|
|
|
31 |
1 |
p. 52-55
|
artikel
|
| 4 |
Editorial Board
|
|
|
|
31 |
1 |
p. IFC
|
artikel
|
| 5 |
Erratum to “Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCR” [Neuromuscular Disorders, 30(3) 2020, 219-226]
|
Xu, Yan
|
|
|
31 |
1 |
p. e1
|
artikel
|
| 6 |
Gene therapy in Duchenne muscular dystrophy: Identifying and preparing for the challenges ahead
|
Heslop, Emma
|
|
|
31 |
1 |
p. 69-78
|
artikel
|
| 7 |
Impaired NDRG1 functions in Schwann cells cause demyelinating neuropathy in a dog model of Charcot-Marie-Tooth type 4D
|
Skedsmo, Fredrik S.
|
|
|
31 |
1 |
p. 56-68
|
artikel
|
| 8 |
Impaired secretion of platelet granules in patients with Duchenne muscular dystrophy – results of a prospective diagnostic study
|
Schorling, D.C.
|
|
|
31 |
1 |
p. 35-43
|
artikel
|
| 9 |
Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter
|
Rodríguez Cruz, Pedro M.
|
|
|
31 |
1 |
p. 21-28
|
artikel
|
| 10 |
Protein aggregates and autophagy involvement in a family with a mutation in Z-band alternatively spliced PDZ-motif protein
|
Cassandrini, Denise
|
|
|
31 |
1 |
p. 44-51
|
artikel
|
| 11 |
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients
|
Okhovat, Ali Asghar
|
|
|
31 |
1 |
p. 29-34
|
artikel
|
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