Neuromuscular Disorders
Research Hotspot & Research Scope

Research Hotspot & Research Scope
Neuromuscular Disorders

Research Scope

Dystrophy Muscular Disease Muscle Patient Mutation Duchenne Myopathy Type Mitochondrial Neuromuscular Clinical Myotonic 1 Gene Treatment Novel Skeletal Therapy Case Congenital Model Syndrome Study New Myasthenic Analysis Neuropathy Outcome Dysfunction Human Report Genetic Variant Measure Function Review Cell Mtdna Disorder Cause Phenotype Dmd Effect Use Sequencing Limb Mri Mouse Literature Associated Netherlands Charcot-marie-tooth Test International Workshop Sma Spinal Atrophy Onset Junction Dystrophin Protein Body Zebrafish Related Development Respiratory Cardiomyopathy Care Monitoring Metabolic Assessment Family Natural History Cohort Expression Activity Myositis Dna Correlation Deficiency Sporadic Evaluation Enmc Spectrum Ii Adult Generation Complex Walk Uk 2017 Longitudinal Health Girdle Progressive 2 Recessive Imaging Approach Registry Motor Facioscapulohumeral Deltae50-md Dog Therapeutic Early Child Progression Severity Mitophagy Myostatin Modelling Stem Inflammatory Inclusion Finding Diagnosis Diagnostics Chain Serum Single Developing Biomarkers Correlate Severe People Mild Mcardle Diagnostic Method Naarden Mechanism Genomic Molecular Investigation Tool Pompe Next Role Predict Causing Homozygous Compound Limb-girdle DMD Pregnancy Rna Ryr1 Autosomal Response Phenotypic Data Whole Exome Mtm1 Female Quantitative Involvement Charcot–marie–tooth Potential Channelopathies Functional Level / Loss-of-function Mortality Systematic Discovery Into Centre Ataluren Nonsense Necrotizing Anti-3-hydroxy-3-methylglutaryl-coenzyme Reductase Vitro Pluripotent Comparison Factor March 2018 Caused 4 Flow Cytometry Genetics Due Biallelic Combined Biomarker Characterization 1a European Consortium 1-2 July 2016 Alpha-dystroglycanopathy dystrophy DM1 Acute Non-invasive Pressure Ventilation Artificial Neuro-muscular Evidence Lower Brain Abnormality London Challenge Copy Number Revisited Reported 6-minute Alternative Trial Threshold Delivery Translation Transmission Advance First Targeted Screening Late Symptom Pulmonary Compared World Bone Network Neuronal Becker Possible Year Individual Physical Myh2 Mimicking Dominant Juvenile Dermatomyositis Heterozygous

Popular Journals

Neuromuscular Disorders
Journal Profile & Journal Metrics
Neuromuscular Disorders | Academic Accelerator - About the Journal

About

This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies).The Editors welcome original articles from all areas of the field:• Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery).• Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics.• Studies of animal models relevant to the human diseases.The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders. Neuromuscular Disorders is a peer-reviewed medical journal that focuses on neuromuscular disease, including muscular dystrophy, spinal muscular atrophy, and myasthenia. It is the official journal of the World Muscle Society. It was established in 1991 and is published by Elsevier.

ISSN

0960-8966

ISSN

The ISSN of Neuromuscular Disorders is 0960-8966 . An ISSN is an 8-digit code used to identify newspapers, journals, magazines and periodicals of all kinds and on all media–print and electronic.

ISSN (Online)

1873-2364

ISSN (Online)

The ISSN (Online) of Neuromuscular Disorders is 1873-2364 . An ISSN is an 8-digit code used to identify newspapers, journals, magazines and periodicals of all kinds and on all media–print and electronic.

Publisher

Elsevier Ltd.

Publisher

Neuromuscular Disorders is published by Elsevier Ltd. .

Publication Frequency

-

Publication Frequency

Neuromuscular Disorders publishes reports - .

Coverage

1991 - Present

Coverage

The Publication History of Neuromuscular Disorders covers 1991 - Present .

Open Access

NO

Open Access

Neuromuscular Disorders is Subscription-based (non-OA) Journal. Publishers own the rights to the articles in their journals. Anyone who wants to read the articles should pay by individual or institution to access the articles. Anyone who wants to use the articles in any way must obtain permission from the publishers.

Publication Fee

Publication Fee

There is no publication fee for submiting manuscript to Neuromuscular Disorders. Neuromuscular Disorders is Subscription-based (non-OA) Journal. Publishers own the rights to the articles in their journals. Anyone who wants to read the articles should pay by individual or institution to access the articles.

Language

-

Language

The language of Neuromuscular Disorders is - .

Country/Region

United Kingdom

Country/Region

The publisher of Neuromuscular Disorders is Elsevier Ltd. , which locates in United Kingdom .