ISSN: 0960-8966

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Neuromuscular Disorders Q1 Unclaimed

Elsevier Ltd United Kingdom

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Neuromuscular Disorders is a journal indexed in SJR in Genetics (clinical) and Neurology (clinical) with an H index of 116. It has an SJR impact factor of 0,885 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 0,885.

Neuromuscular Disorders focuses its scope in these topics and keywords: muscular, biopsy, disease, dystrophy, congenital, myasthenia, deficiency, decreased, chromosome, expression, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Pediatrics, Perinatology and Child Health (Q1) Genetics (clinical) (Q2) Neurology (Q2) Neurology (clinical) (Q2) Neurology (clinical) (Q2)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,885

SJR Impact factor

116

H Index

107

Total Docs (Last Year)

424

Total Docs (3 years)

3392

Total Refs

1050

Total Cites (3 years)

410

Citable Docs (3 years)

2.25

Cites/Doc (2 years)

31.7

Ref/Doc

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Aims and Scope

Best articles by citations

Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic

Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies

Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene

Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy

Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations

Sleep Disorders and Neurological Disease Antonio Culebras, editor, Marcel Dekker, New York, Basel, 2000, 422 pages, Price ¬£116.26, ISBN 0-8247-7605-4

Valproic acid triggers acute rhabdomyolysis in a patient with carnitine palmitoyltransferase type II deficiency

Normal calcium homeostasis in dystrophin-expressing facioscapulohumeral muscular dystrophy myotubes

No evidence of association between apolipoprotein E genotype and phenotypic severity in childhood onset proximal spinal muscular atrophy

New developments in congenital muscular dystrophy

Neonatal carnitine palmitoyltransferase-2 deficiency: a case presenting with myopathy

Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient

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Numb Toes and Aching Soles: Coping with Peripheral Neuropathy.

MTMI gene mutations in Japanese patients with X-linked myotubular myopathy

Mitochondrial DNA variants in inclusion body myositis

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci

Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study

Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter

McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient

Management Of Persons With Chronic Neurologic Illness Ozer, Mark.352 pp, 254?o178 mm: 15 line illustrations: Butterworth, Heinemann, Hardcover: March 2000 ¬£45 ISBN 0 7506 7005 3

Longitudinal data analysis: an application to construction of a natural history profile of Duchenne muscular dystrophy

Lockhart Clarke (1817-1880): his role in the early history of muscular dystrophy

Introduction to Clinical Neurology, 2nd editionDouglas J. Gelb, May 2000, 416 pages, Butterworth Heinemann: London. ISBN 0750672021, ¬£22.50

Inherited early onset severe axonal polyneuropathy with respiratory failure and autonomic involvement