| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
‘Amish Nemaline Myopathy’ in 2 Italian siblings harbouring a novel homozygous mutation in Troponin-I gene
|
D'Amico, Adele
|
|
|
29 |
10 |
p. 766-770
|
artikel
|
| 2 |
A novel case of inclusion body myositis and myasthenia gravis
|
Lambrianides, Sakis
|
|
|
29 |
10 |
p. 771-775
|
artikel
|
| 3 |
Changes detected in swallowing function in Friedreich ataxia over 12 months
|
Keage, Megan
|
|
|
29 |
10 |
p. 786-793
|
artikel
|
| 4 |
Development of an academic disease registry for spinal muscular atrophy
|
Mercuri, Eugenio
|
|
|
29 |
10 |
p. 794-799
|
artikel
|
| 5 |
Editorial Board
|
|
|
|
29 |
10 |
p. IFC
|
artikel
|
| 6 |
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre
|
Bugiardini, Enrico
|
|
|
29 |
10 |
p. 747-757
|
artikel
|
| 7 |
High incidence of falls in patients with myotonic dystrophy type 1 and 2: A prospective study
|
Berends, Joost
|
|
|
29 |
10 |
p. 758-765
|
artikel
|
| 8 |
Intrathecal administration of nusinersen in adult and adolescent patients with spinal muscular atrophy and scoliosis: Transforaminal versus conventional approach
|
Bortolani, Sara
|
|
|
29 |
10 |
p. 742-746
|
artikel
|
| 9 |
Meeting on data sharing for Duchenne 21–22 March 2019 Amsterdam, the Netherlands
|
Verhaart, Ingrid E.C.
|
|
|
29 |
10 |
p. 800-810
|
artikel
|
| 10 |
Membrane recruitment of nNOSµ in microdystrophin gene transfer to enhance durability
|
Boehler, Jessica F.
|
|
|
29 |
10 |
p. 735-741
|
artikel
|
| 11 |
Report of a novel ATP7A mutation causing distal motor neuropathy
|
Gualandi, Francesca
|
|
|
29 |
10 |
p. 776-785
|
artikel
|
| 12 |
26th Annual Facioscapulohumeral Dystrophy International Research Congress Marseille, France, 19–20 June 2019
|
Kinoshita, June
|
|
|
29 |
10 |
p. 811-817
|
artikel
|
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