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                             17 results found
no title author magazine year volume issue page(s) type
1 Can IgG4-related disease present as isolated myositis? Suresh, Sumatha Channapatna

33 7 p. 570-574
article
2 Clinical study on cognitive impairment in Duchenne muscular dystrophy Zhang, Xiao-fang

33 7 p. 596-604
article
3 Development of Continuum of Care for McArdle disease: A practical tool for clinicians and patients Reason, S.L.

33 7 p. 575-579
article
4 Editorial Board
33 7 p. IFC
article
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
article
6 Long-read Nanopore sequencing identified D4Z4 contractions in patients with facioscapulohumeral muscular dystrophy Yeetong, Patra

33 7 p. 551-556
article
7 Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients Zemorshidi, Fariba

33 7 p. 589-595
article
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
article
9 Prediction of respiratory impairment in myotonic dystrophies using the ‘Respiratory involvement symptom checklist’ (Respicheck) Gutschmidt, Kristina

33 7 p. 610-618
article
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
article
11 Respiratory features of centronuclear myopathy in the Netherlands Bouma, Sietse

33 7 p. 580-588
article
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
article
13 267th ENMC International workshop: psychological interventions for improving quality of life in slowly progressive neuromuscular disorders Pater, Ronne

33 7 p. 562-569
article
14 Titin related myopathy with ophthalmoplegia. A novel phenotype Alawneh, Issa

33 7 p. 605-609
article
15 WMS 2023 Congress announcement
33 7 p. III
article
16 WMS 2023 Flyer
33 7 p. II
article
17 WMS Information
33 7 p. I
article
                             17 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands