| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Bi-allelic MYH3 loss-of-function variants cause a lethal form of contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B
|
Kamien, Benjamin
|
|
|
32 |
5 |
p. 445-449
|
artikel
|
| 2 |
Clinical and neuroradiological correlates of sleep in myotonic dystrophy type 1
|
Hamilton, Mark J
|
|
|
32 |
5 |
p. 377-389
|
artikel
|
| 3 |
Editorial Board
|
|
|
|
32 |
5 |
p. IFC
|
artikel
|
| 4 |
Evaluation of real-life outcome data of patients with spinal muscular atrophy treated with nusinersen in Switzerland
|
Tscherter, Anne
|
|
|
32 |
5 |
p. 399-409
|
artikel
|
| 5 |
Genitourinary and lower gastrointestinal conditions in patients with myotonic dystrophy type 1: A systematic review of evidence and implications for clinical practice
|
Fisette-Paulhus, Isabelle
|
|
|
32 |
5 |
p. 361-376
|
artikel
|
| 6 |
Identification of a novel mutation and genotype–phenotype relationship in MEGF10 myopathy
|
Fujii, Kanako
|
|
|
32 |
5 |
p. 436-440
|
artikel
|
| 7 |
Leveraging cardiac magnetic resonance imaging to assess skeletal muscle progression in Duchenne muscular dystrophy
|
Kaslow, Jacob A.
|
|
|
32 |
5 |
p. 390-398
|
artikel
|
| 8 |
Mitochondrial dysfunction in anti-3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) immune-mediated necrotising myopathy
|
Acosta, Ignacio Javier
|
|
|
32 |
5 |
p. 441-444
|
artikel
|
| 9 |
Professor Isabel Illa (1952 - 2022)
|
Olivé, Montse
|
|
|
32 |
5 |
p. 450
|
artikel
|
| 10 |
The therapeutic potential of soluble activin type IIB receptor treatment in a limb girdle muscular dystrophy type 2D mouse model
|
Alqallaf, Ali
|
|
|
32 |
5 |
p. 419-435
|
artikel
|
| 11 |
Upper body involvement in GNE myopathy assessed by muscle imaging
|
Torchia, E.
|
|
|
32 |
5 |
p. 410-418
|
artikel
|
| 12 |
WMS 2022 Congress announcement
|
|
|
|
32 |
5 |
p. III
|
artikel
|
| 13 |
WMS 2022 Flyer
|
|
|
|
32 |
5 |
p. II
|
artikel
|
| 14 |
WMS Information
|
|
|
|
32 |
5 |
p. I
|
artikel
|
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