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                             14 results found
no title author magazine year volume issue page(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
article
2 Clinical and neuroradiological correlates of sleep in myotonic dystrophy type 1 Hamilton, Mark J

32 5 p. 377-389
article
3 Editorial Board
32 5 p. IFC
article
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
article
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
article
6 Identification of a novel mutation and genotype–phenotype relationship in MEGF10 myopathy Fujii, Kanako

32 5 p. 436-440
article
7 Leveraging cardiac magnetic resonance imaging to assess skeletal muscle progression in Duchenne muscular dystrophy Kaslow, Jacob A.

32 5 p. 390-398
article
8 Mitochondrial dysfunction in anti-3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) immune-mediated necrotising myopathy Acosta, Ignacio Javier

32 5 p. 441-444
article
9 Professor Isabel Illa (1952 - 2022) Olivé, Montse

32 5 p. 450
article
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
article
11 Upper body involvement in GNE myopathy assessed by muscle imaging Torchia, E.

32 5 p. 410-418
article
12 WMS 2022 Congress announcement
32 5 p. III
article
13 WMS 2022 Flyer
32 5 p. II
article
14 WMS Information
32 5 p. I
article
                             14 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands