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1. Palliative care in amyotrophic lateral sclerosis
: from diagnosis to bereavement
by Oliver, David, 1954 and Borasio, Gian Domenico and Walsh, Declan
2006, 2nd ed., ISBN 0199212937, x, 352
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
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2. Muscle & nerve
and American Association of Electrodiagnostic MedicineAmerican Association of Electromyography and Electrodiagnosis
Muscle & nerve, ISSN 0148-639X, 1978
Muscles | Periodicals | Neuromuscular diseases | Nerves
Journal
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3. Medically unexplained illness
: gender and biopsychosocial implications
by Johnson, Susan K
2008, 1st ed., ISBN 9780979212581, x, 271
Book
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4. Full Text Developmental Medicine Child Neurology
eJournal
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5. Journal of clinical neuromuscular disease
Journal of clinical neuromuscular disease, ISSN 1522-0443, 1999
Musculoskeletal system | Neuromuscular diseases | Diseases
Journal
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6. Full Text Disease specificity of autoantibodies to cytosolic 5′-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases
by Herbert, Megan K and Stammen-Vogelzangs, Judith and Verbeek, Marcel M and Rietveld, Anke and Lundberg, Ingrid E and Chinoy, Hector and Lamb, Janine A and Cooper, Robert G and Roberts, Mark and Badrising, Umesh A and De Bleecker, Jan L and Machado, Pedro M and Hanna, Michael G and Plestilova, Lenka and Vencovsky, Jiri and van Engelen, Baziel G and Pruijn, Ger J M
Annals of the rheumatic diseases, ISSN 0003-4967, 04/2016, Volume 75, Issue 4, pp. 696 - 701
Life Sciences & Biomedicine | Rheumatology | Science & Technology | Humans | Middle Aged | Myositis, Inclusion Body - immunology | Sjogren's Syndrome - immunology | Male | Case-Control Studies | Myositis, Inclusion Body - diagnosis | Dermatomyositis - immunology | Sensitivity and Specificity | 5'-Nucleotidase - immunology | Lupus Erythematosus, Systemic - immunology | Polymyositis - diagnosis | Adult | Female | Diabetes Mellitus, Type 1 - immunology | Neuromuscular Diseases - immunology | Polymyositis - immunology | Autoimmune Diseases - immunology | Dermatomyositis - diagnosis | Scleroderma, Systemic - immunology | Autoantibodies - immunology | Multiple Sclerosis - immunology | ROC Curve | Aged | Arthritis, Rheumatoid - immunology | Inclusion body myositis | Care and treatment | Dosage and administration | Autoantibodies | Antigenic determinants | Studies | Antigens | Musculoskeletal system | Immunoglobulins | Neuromuscular diseases | Disease | Peptides | Autoimmune diseases | Scleroderma | Patients | Dementia | Index Medicus | Idiopathic inflammatory myopathy | Disease-specificity | Cytosolic 5’-nucleotidase 1A (cN-1A) | ELISA | Medicin och hälsovetenskap
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7. Supportive care in respiratory disease
by Ahmedzai, Sam, 1950 and Muers, Martin F
2005, Supportive care series, ISBN 9780192631411, xvii, 540
Respiratory organs | Palliative treatment | Diseases | Patient Care and End-of-Life Decision Making | Pain Management and Palliative Pharmacology | Pulmonary disease | Breathlessness | Cardiac disease | Respiratory symptoms | Advancing disease | Incurable disease | Neuromuscular disorders | Patients | Cough | Cancer
Book
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8. Amyotrophic lateral sclerosis
: official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
by Swash, Michael and Hardiman, Orla and World Federation of Neurology. Research Group on Motor Neuron Diseases and World Federation of Neurology and Research Group on Motor Neuron Diseases
Amyotrophic lateral sclerosis, ISSN 1748-2968, 2006
Motor neurons | Amyotrophic lateral sclerosis | Diseases | periodicals
Journal
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9. Peripheral neuropathy
by Dyck, Peter James, 1927 and Thomas, P. K. 1926-2008 (Peter Kynaston)
2005, 4th ed., ISBN 9780721694917, Volume 1-2, 2 v. (xxiv, 2753, xcii p.)
Peripheral Nervous System Diseases | Peripheral Nerves | pathology
Book
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10. Molecular mechanisms of muscular dystrophies
2006, ISBN 158706264X, 233
Book
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11. Full Text Chronic Diseases, Chromosomal Abnormalities, and Congenital Malformations as Risk Factors for Respiratory Syncytial Virus Hospitalization: A Population-Based Cohort Study
by Kim Kristensen and Thomas Hjuler and Henrik Ravn and Eric A. F. Simões and Lone G. Stensballe
Clinical infectious diseases, ISSN 1058-4838, 3/2012, Volume 54, Issue 6, pp. 810 - 817
Human respiratory syncytial virus | Neuromuscular diseases | Predisposing factors | Respiratory syncytial viruses | Chronic diseases | Disease risk | Hospitalization | Children | Down syndrome | ARTICLES AND COMMENTARIES | Heart diseases | Infectious Diseases | Immunology | Life Sciences & Biomedicine | Microbiology | Science & Technology | Biological and medical sciences | Viral diseases of the respiratory system and ent viral diseases | Infectious diseases | Medical sciences | Human viral diseases | Viral diseases | Length of Stay | Severity of Illness Index | Humans | Risk Factors | Proportional Hazards Models | Hospitalization - statistics & numerical data | Infant | Immune System Diseases - complications | Lung Diseases, Interstitial - complications | Incidence | Immune System Diseases - congenital | Respiratory Syncytial Viruses | Neuromuscular Diseases - complications | Chromosome Aberrations | Denmark | Liver Diseases - complications | Registries | Respiratory Syncytial Virus Infections - virology | Chronic Disease | Infant, Newborn | Metabolism, Inborn Errors - complications | Respiratory Syncytial Virus Infections - complications | Cohort Studies | Respiratory syncytial virus infection | Research | Demographic aspects | Risk factors | Pediatrics | Respiratory syncytial virus | Congenital diseases | Chronic illnesses | Congenital defects | Respiratory diseases | Surgery | Metabolism | Chromosome aberrations | Siblings | Index Medicus
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12. Neuromuscular disease
: a case-based approach
by Wokke, John H. J and van Doorn, Pieter A and Hoogendijk, Jessica E and de Visser, Marianne
2013, ISBN 0521171857, 184
Case studies | Neuromuscular diseases | Diagnosis
Book
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13. Full Text Chronic fatigue syndrome
by Moss-Morris, Rona, 1962 and Petrie, Keith J
2000, Experience of illness series, ISBN 0415202396, 160
Chronic fatigue syndrome | Primary Health Care & Family Practice | Medical Sociology | Nursing
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14. Dysphagia in neuromuscular diseases
by Miller, Robert M. 1946- (Robert Michael) and Britton, Deanna, 1962- author
2011, Clinical dysphagia series, ISBN 9781597563697, xi, 196
Neuromuscular diseases | Treatment | Complications | therapy | diagnosis | Deglutition disorders | etiology
Book
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15. Full Text Augmentation of phenotype in a transgenic Parkinson mouse heterozygous for a Gaucher mutation
by Fishbein, Ianai and Kuo, Yien-Ming and Giasson, Benoit I and Nussbaum, Robert L
Brain (London, England : 1878), ISSN 0006-8950, 12/2014, Volume 137, Issue 12, pp. 3235 - 3247
Lysosomal protein degradation | Mouse model | Gaucher disease | Parkinson's disease | Alpha-synuclein | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Errors of metabolism | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Metabolic diseases | Nervous system as a whole | Medical sciences | Diseases of striated muscles. Neuromuscular diseases | Nervous system (semeiology, syndromes) | Lipids (lysosomal enzyme disorders, storage diseases) | Parkinson Disease - complications | Gene Expression | Glucosylceramidase - genetics | Genotype | Mice, Transgenic | Gaucher Disease - complications | Mice, 129 Strain | Parkinson Disease - genetics | Mutation - genetics | Phenotype | Animals | Gaucher Disease - genetics | Heterozygote | alpha-Synuclein - genetics | alpha-Synuclein - metabolism | Disease Models, Animal | Index Medicus | Abridged Index Medicus | mouse model | alpha-synuclein | Original | lysosomal protein degradation | Parkinson’s disease
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16. Understanding chronic fatigue syndrome
: an empirical guide to assessment and treatment
by Friedberg, Fred and Jason, Leonard
1998, 1st ed., ISBN 9781557985118, xvii, 266
diagnosis | Fatigue Syndrome, Chronic | therapy | Chronic fatigue syndrome
Book
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17. Cardiac Phenotypes in Hereditary Muscle Disorders: JACC State-of-the-Art Review
by Arbustini, Eloisa and Di Toro, Alessandro and Giuliani, Lorenzo and Favalli, Valentina and Narula, Nupoor and Grasso, Maurizia
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2485 - 2506
arrhythmias | dystrophy | skeletal muscle | myopathy | cardiomyopathies | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | 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 | Pediatrics | Conduction | Cardiac arrhythmia | Disease | Muscular diseases | Creatine kinase | Cardiomyopathy | Disorders | Kinases | Creatine | Muscular dystrophy | Genetic screening | Defects | Eutrophication | Genotype & phenotype | Mitochondria | Glycogenosis | Ataxia | Oxidation | Bioindicators | Cardiology | Heart diseases | Age | Heart failure | Phenotypes | Neuromuscular diseases | Genetic disorders | Glycogen | Muscles | Fatty acids | Patients | Coronary artery disease | Skeletal muscle | Diseases | Storage diseases | Friedreich's ataxia | Musculoskeletal system | Medical prognosis | Family studies | Biomarkers | Lactic acid | Ventricle | Mutation
Journal Article
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