nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Can IgG4-related disease present as isolated myositis?
|
Suresh, Sumatha Channapatna |
|
|
33 |
7 |
p. 570-574 |
artikel |
2 |
Clinical study on cognitive impairment in Duchenne muscular dystrophy
|
Zhang, Xiao-fang |
|
|
33 |
7 |
p. 596-604 |
artikel |
3 |
Development of Continuum of Care for McArdle disease: A practical tool for clinicians and patients
|
Reason, S.L. |
|
|
33 |
7 |
p. 575-579 |
artikel |
4 |
Editorial Board
|
|
|
|
33 |
7 |
p. IFC |
artikel |
5 |
Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophy
|
Barington, Maria |
|
|
33 |
7 |
p. 539-545 |
artikel |
6 |
Long-read Nanopore sequencing identified D4Z4 contractions in patients with facioscapulohumeral muscular dystrophy
|
Yeetong, Patra |
|
|
33 |
7 |
p. 551-556 |
artikel |
7 |
Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients
|
Zemorshidi, Fariba |
|
|
33 |
7 |
p. 589-595 |
artikel |
8 |
Novel p.Asp27Glu ACTA1 variant features congenital myopathy with finger flexor weakness, cardiomyopathy, and cardiac conduction defects
|
Mulvany-Robbins, Bridget |
|
|
33 |
7 |
p. 546-550 |
artikel |
9 |
Prediction of respiratory impairment in myotonic dystrophies using the ‘Respiratory involvement symptom checklist’ (Respicheck)
|
Gutschmidt, Kristina |
|
|
33 |
7 |
p. 610-618 |
artikel |
10 |
Psychopharmaceutical treatment for neurobehavioral problems in Duchenne muscular dystrophy: a descriptive study using real-world data
|
Weerkamp, Pien M.M. |
|
|
33 |
7 |
p. 619-626 |
artikel |
11 |
Respiratory features of centronuclear myopathy in the Netherlands
|
Bouma, Sietse |
|
|
33 |
7 |
p. 580-588 |
artikel |
12 |
Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant
|
Blanco-Arias, Patricia |
|
|
33 |
7 |
p. 557-561 |
artikel |
13 |
267th ENMC International workshop: psychological interventions for improving quality of life in slowly progressive neuromuscular disorders
|
Pater, Ronne |
|
|
33 |
7 |
p. 562-569 |
artikel |
14 |
Titin related myopathy with ophthalmoplegia. A novel phenotype
|
Alawneh, Issa |
|
|
33 |
7 |
p. 605-609 |
artikel |
15 |
WMS 2023 Congress announcement
|
|
|
|
33 |
7 |
p. III |
artikel |
16 |
WMS 2023 Flyer
|
|
|
|
33 |
7 |
p. II |
artikel |
17 |
WMS Information
|
|
|
|
33 |
7 |
p. I |
artikel |