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                             14 results found
no title author magazine year volume issue page(s) type
1 A novel case of MSTO1 gene related congenital muscular dystrophy with progressive neurological involvement Ardicli, Didem

29 6 p. 448-455
article
2 Central drive and ventilatory failure in late-onset Pompe disease: At the gates of a new phenotype De Vito, EL

29 6 p. 444-447
article
3 Critical Review Ahead of Publication Dubowitz, Victor

29 6 p. 412
article
4 Editorial Board
29 6 p. IFC
article
5 Muscle fiber dysfunction contributes to weakness in inclusion body myositis Lassche, Saskia

29 6 p. 468-476
article
6 PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variability Kawarai, Toshitaka

29 6 p. 422-426
article
7 Polyradiculoneuropathy in dourine-affected horses Mungun-Ochir, Bayasgalan

29 6 p. 437-443
article
8 Recessive MYH7-related myopathy in two families Beecroft, Sarah J.

29 6 p. 456-467
article
9 Severe distal muscle involvement and mild sensory neuropathy in a boy with infantile onset Pompe disease treated with enzyme replacement therapy for 6 years Schänzer, Anne

29 6 p. 477-482
article
10 Spinal Muscular Atrophy Revisited Dubowitz, Victor

29 6 p. 413-414
article
11 1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018 Udd, Bjarne

29 6 p. 483-485
article
12 Surgical outcomes of cavovarus foot deformity in children with Charcot-Marie-Tooth disease Lin, Ting

29 6 p. 427-436
article
13 The World Wide Web (WWW): For better or for worse Dubowitz, Victor

29 6 p. 411
article
14 Thoracic circumference: A new outcome measure in spinal muscular atrophy type 1? Ropars, Juliette

29 6 p. 415-421
article
                             14 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands