Neuromuscular Disorders

ISSNs: 0960-8966

Additional searchable ISSN (electronic): 1873-2364

Elsevier, Oxford [u.a.]

Scopus rating (2022): CiteScore 4.7 SJR 0.84 SNIP 0.954

Journal

Titles	Neuromuscular Disorders Neuromuscular disorders
Additional searchable titles	Neuromuscular disorders : NMD, Neuromuscul Disord
ISSNs	0960-8966
Additional searchable ISSN (electronic)	1873-2364
Publisher	Elsevier, Oxford [u.a.]
ZDB-ID	1077681-3
ZDB-ID	2008287-3

Keywords

ASJC Scopus subject areas

Pediatrics, Perinatology and Child Health
Neurology
Neurology (clinical)
Genetics (clinical)

Library keywords

610 Medicine and health

Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy

The Muscle Study Group and TREAT-NMD & von der Hagen, M., Nov 2021, In: Neuromuscular disorders. 31, 11, p. 1161-1168 8 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy – A patients’ perspective

Janisch, M., Boehme, K., Thiele, S., Bock, A., Kirschner, J., Schara, U., Walter, C., & 2 othersNolte-Buchholtz, S. & von der Hagen, M., Dec 2020, In: Neuromuscular disorders. 30, 12, p. 975-985 11 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutation

Chamova, T., Bichev, S., Todorov, T., Gospodinova, M., Taneva, A., Kastreva, K., Zlatareva, D., & 11 othersKrupev, M., Hadjiivanov, R., Guergueltcheva, V., Grozdanova, L., Tzoneva, D., Huebner, A., v. der Hagen, M., Schoser, B., Lochmüller, H., Todorova, A. & Tournev, I., Aug 2018, In: Neuromuscular disorders. 28, 8, p. 625-632 8 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria

Ravenscroft, G., Di Donato, N., Hahn, G., Davis, M. R., Craven, P. D., Poke, G., Neas, K. R., & 3 othersNeuhann, T. M., Dobyns, W. B. & Laing, N. G., 2016, In: Neuromuscular Disorders. 26, 11, p. 744-748 5 p.

Research output: Contribution to journal › Case report › Contributed › peer-review

Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK

Gallenmüller, C., Felber, W. M., Dusl, M., Stucka, R., Guergueltcheva, V., Blaschek, A., von der Hagen, M., & 4 othersHuebner, A., Müller, J. S., Lochmüller, H. & Abicht, A., Jan 2014, In: Neuromuscular Disorders. 24, 1, p. 31-35 5 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

View all research output (8)

Research Portal of the TU Dresden

Neuromuscular Disorders

Keywords

ASJC Scopus subject areas

Library keywords

Related content

Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy

Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy – A patients’ perspective

Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutation

Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria

Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK