| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Assessing disease progression in spinal muscular atrophy, current gaps, and opportunities: a narrative review
|
Muni-Lofra, R
|
|
|
49 |
C |
p.
|
artikel
|
| 2 |
Editorial Board
|
|
|
|
49 |
C |
p.
|
artikel
|
| 3 |
ENMC Mid-Career Mentoring Programme
|
|
|
|
49 |
C |
p.
|
artikel
|
| 4 |
Fluoroscopic guidance for intrathecal delivery of nusinersen in pediatric patients with spinal muscular atrophy and complex spines
|
Lando - Dotan, Shany
|
|
|
49 |
C |
p.
|
artikel
|
| 5 |
Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian families
|
Gharebaghian, Hadi
|
|
|
49 |
C |
p.
|
artikel
|
| 6 |
Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of Scotland
|
Watson-Fargie, Taylor
|
|
|
49 |
C |
p.
|
artikel
|
| 7 |
Mortality of symptomatic children with spinal muscular atrophy in the era of disease-modifying therapies
|
Finnegan, R
|
|
|
49 |
C |
p.
|
artikel
|
| 8 |
Obstetric and gynaecological features in females carrying variants in the skeletal muscle ryanodine receptor type 1 (RYR1) gene: a questionnaire study
|
Mistry, Arti M
|
|
|
49 |
C |
p.
|
artikel
|
| 9 |
281st ENMC international workshop: 2nd ENMC workshop on exercise training in muscle diseases; towards consensus-based recommendations on exercise prescription and outcome measures. Hoofddorp, The Netherlands, 4-6 October 2024
|
Voorn, Eric Lukas
|
|
|
49 |
C |
p.
|
artikel
|
| 10 |
The widening genetic and myopathologic spectrum of congenital myopathies (CMYOs): a narrative review
|
Onnée, Marion
|
|
|
49 |
C |
p.
|
artikel
|
| 11 |
UPDATE IN NEUROMUSCULAR DISORDERS
|
|
|
|
49 |
C |
p.
|
artikel
|
| 12 |
WMS CONGRESS TEXT page edits for April 2025
|
|
|
|
49 |
C |
p.
|
artikel
|
| 13 |
WMS 2025 Vienna Congress Flyer
|
|
|
|
49 |
C |
p.
|
artikel
|
| 14 |
WMS 2025 Vienna Congress Information
|
|
|
|
49 |
C |
p.
|
artikel
|
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