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Muscle and nerve, ISSN 0148-639X
Journal
2006, 2nd ed., ISBN 0199212937, x, 352
Amyotrophic lateral sclerosis (or motor neurone disease) is a rare disease but one that can cause profound suffering for both the patient and their family... 
Amyotrophic lateral sclerosis | Palliative Care | Palliative treatment | therapy | Patient Care and End-of-Life Decision Making | Palliative Medicine Research | neurology team | als | psychosocial care | amyotrophic lateral sclerosis | palliative care | motor neurone disease
Book
eJournal
Journal of clinical neuromuscular disease, ISSN 1522-0443, 1999
Journal
Annals of the Rheumatic Diseases, ISSN 0003-4967, 04/2016, Volume 75, Issue 4, pp. 696 - 701
Journal Article
2005, Supportive care series, ISBN 9780192631411, xvii, 540
Book
Neurogenetics, ISSN 1364-6753, 1997
Journal
Neuromuscular disorders, ISSN 0960-8966, 1991
Journal
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2485 - 2506
Hereditary muscular diseases commonly involve the heart. Cardiac manifestations encompass a spectrum of phenotypes, including both cardiomyopathies and rhythm disorders... 
arrhythmias | dystrophy | skeletal muscle | myopathy | cardiomyopathies | CARDIAC & CARDIOVASCULAR SYSTEMS | RESTRICTIVE CARDIOMYOPATHY | FRIEDREICHS-ATAXIA | CLINICAL SPECTRUM | BARTH-SYNDROME | LINKED DILATED CARDIOMYOPATHY | LIMB-GIRDLE | LEFT-VENTRICULAR NONCOMPACTION | DIAGNOSTIC WORK-UP | HYPERTROPHIC CARDIOMYOPATHY | DUCHENNE MUSCULAR-DYSTROPHY | Glycogen Storage Disease Type II - genetics | Muscular Diseases - epidemiology | Humans | Muscular Dystrophy, Duchenne - epidemiology | Glycogen Storage Disease Type II - diagnostic imaging | Muscular Dystrophies - genetics | Muscular Dystrophy, Duchenne - diagnostic imaging | Phenotype | Heart Diseases - epidemiology | Muscular Dystrophies - epidemiology | Pedigree | Review Literature as Topic | Glycogen Storage Disease Type II - epidemiology | Heart Diseases - diagnostic imaging | Muscular Diseases - genetics | Muscular Dystrophies - diagnostic imaging | Muscular Dystrophy, Duchenne - genetics | Heart Diseases - genetics | Muscular Diseases - diagnostic imaging | Heart | Arrhythmia | Creatine kinase | Glycogen | Muscles | Genetic aspects | Lactic acid | Cardiology | Creatine | Fatty acids | Genetic screening | Pediatrics | Conduction | Cardiac arrhythmia | Disease | Muscular diseases | Cardiomyopathy | Disorders | Kinases | Muscular dystrophy | Defects | Eutrophication | Genotype & phenotype | Mitochondria | Glycogenosis | Ataxia | Oxidation | Bioindicators | Heart diseases | Age | Heart failure | Phenotypes | Neuromuscular diseases | Genetic disorders | Patients | Coronary artery disease | Skeletal muscle | Diseases | Storage diseases | Friedreich's ataxia | Musculoskeletal system | Medical prognosis | Family studies | Biomarkers | Ventricle | Mutation
Journal Article
Seminars in Neurology, ISSN 0271-8235, 10/2016, Volume 36, Issue 5, pp. 409 - 418
Abstract Neuromuscular diseases are a broadly defined group of disorders that all involve injury or dysfunction of peripheral nerves or muscle... 
Review Article | neuropathy | radiculopathy | myopathy | amyotrophic lateral sclerosis | ganglionopathy | electromyography | Amyotrophic Lateral Sclerosis | Humans | Electromyography | Neuromuscular Diseases - diagnosis | Lambert-Eaton Myasthenic Syndrome | Myasthenia Gravis | Neuromuscular Diseases - therapy
Journal Article
Journal of autoimmunity, ISSN 0896-8411, 2014, Volume 48-49, pp. 143 - 148
Journal Article
Journal Article