ISSN: 1522-0443

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Journal of Clinical Neuromuscular Disease Q3 Unclaimed

Lippincott Williams and Wilkins Ltd. United States

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Journal of Clinical Neuromuscular Disease is a journal indexed in SJR in Medicine (miscellaneous) and Neurology (clinical) with an H index of 36. It has a price of 2480 €. It has an SJR impact factor of 0,394 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,394.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Medicine (miscellaneous) (Q3) Neurology (Q3) Neurology (clinical) (Q3) Neurology (clinical) (Q3)

Price

2480 €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

Journal of Clinical Neuromuscular Disease

0,394

SJR Impact factor

36

H Index

42

Total Docs (Last Year)

141

Total Docs (3 years)

565

Total Refs

120

Total Cites (3 years)

91

Citable Docs (3 years)

0.81

Cites/Doc (2 years)

13.45

Ref/Doc

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Aims and Scope

Best articles by citations

A Novel Clinical Phenotype of Myopathy, Sensorimotor Neuropathy, Infertility, and Hypogonadism With Multiple Mitochondrial DNA Deletions

Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss Syndrome) Presenting With Polyneuropathy - A Case Series

Respiratory Failure in Lambert-Eaton Myasthenic Syndrome Precipitated by Calcium-Channel Blockers: Report of a Case and Literature Review

On the Concept of Myasthenic Crisis

Peripheral Neurology: Case Studies

Peripheral Neuropathy After Hair Dye Exposure

Necrotizing Myopathies

Sensory Nerve Action Potential Abnormalities in Neuralgic Amyotrophy: A Report of 18 Cases

Sensory Neuronopathy in Spinal Muscular Atrophy

An Adult Male With Progressive Spastic Paraparesis and Gait Instability

The Electromyographic Features of Acute Rhabdomyolysis

Chronic Myopathy Associated With Anti-Signal Recognition Particle Antibodies Can Be Misdiagnosed As Facioscapulohumeral Muscular Dystrophy

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Pathology of Skeletal Muscle

Clinical Improvement of Monomelic Amyotrophy After Avoidance of Sustained Neck Flexion

Inflammatory Myopathy Associated With Imatinib Mesylate Therapy

Amyotrophic Lateral Sclerosis: A Guide for Patients and Families

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Treatment of Painful Peripheral Neuropathy

Prednisone Eliminates the Electrophysiological Decrement of Myotonia Congenita

Motor Neuron Disease With Selective Degeneration of Anterior Horn Cells Associated With Non-Hodgkin Lymphoma

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Neuromuscular Function and Disease: Basic, Clinical, and Electrodiagnostic Aspects