ISSN: 0960-8966
Journal Home
Journal Guideline
Neuromuscular Disorders Q1 Unclaimed
Neuromuscular Disorders is a journal indexed in SJR in Genetics (clinical) and Neurology (clinical) with an H index of 112. It has an SJR impact factor of 0,824 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 0,824.
Neuromuscular Disorders focuses its scope in these topics and keywords: muscular, congenital, myasthenia, dystrophy, biopsy, disease, gravis, genebeneficial, gene, fibrosis, ...
Type: Journal
Type of Copyright:
Languages: English
Open Access Policy:
Type of publications:
Publication frecuency: -


- €
Inmediate OANPD
Embargoed OA- €
Non OAMetrics
0,824
SJR Impact factor112
H Index136
Total Docs (Last Year)421
Total Docs (3 years)4888
Total Refs1104
Total Cites (3 years)405
Citable Docs (3 years)2.44
Cites/Doc (2 years)35.94
Ref/DocOther journals with similar parameters
Genome Medicine Q1
American Journal of Human Genetics Q1
Genome Research Q1
Annual Review of Genomics and Human Genetics Q1
Genetics in Medicine Q1
Compare this journals
Aims and Scope
Best articles by citations
Introduction to Clinical Neurology, 2nd editionDouglas J. Gelb, May 2000, 416 pages, Butterworth Heinemann: London. ISBN 0750672021, £22.50
View moreWelander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies
View morePerineurial cell hyperplasia in early-onset polyneuropathy with multiple cranial neuropathies
View moreNew developments in congenital muscular dystrophy
View moreManagement 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
View moreVery-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria
View moreReversible severe myopathy of respiratory muscles due to adult-onset type III glycogenosis
View moreNumb Toes and Aching Soles: Coping with Peripheral Neuropathy.
View moreSuperoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations
View moreExpression and mitochondrial localisation of frataxin, the Friedreich's ataxia gene product
View more61st ENMC-Sponsored International Workshop:
View moreAlpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy
View moreLockhart Clarke (1817-1880): his role in the early history of muscular dystrophy
View moreAbnormal expression of heparan sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency
View moreProgress in genetic counselling and prenatal diagnosis of maternally inherited mtDNA diseases
View moreMcArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patient
View moreNeonatal carnitine palmitoyltransferase-2 deficiency: a case presenting with myopathy
View moreBlue Books of Practical Neurology: Muscle Diseases. A.H.V. Schapiro, R.C. Griggs, editors. Butterworth Heinemann, 408 pages, 1999, ISBN 07506 670852
View moreHereditary motor and sensory neuropathy -Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
View moreHereditary Motor and Sensory Neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies
View moreFriedreich ataxia: clinical and genetic aspects
View moreMuscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic
View moreA new dysferlin gene mutation in two Japanese families with limb-girdle muscular dystrophy 2B and Miyoshi myopathy
View moreATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's disease
View more
Comments