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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
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2. Full Text Amyotrophic Lateral Sclerosis
by Brown, Robert H and Al-Chalabi, Ammar
The New England journal of medicine, ISSN 0028-4793, 07/2017, Volume 377, Issue 2, pp. 162 - 172
Genetic Variation | Amyotrophic Lateral Sclerosis - physiopathology | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Humans | Survival Analysis | Amyotrophic Lateral Sclerosis - epidemiology | Pathology | Motor neuron diseases | Neurons | Genes | Amyotrophic lateral sclerosis | Mutation | Motor task performance | Index Medicus | Abridged Index Medicus
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3. Full Text Amyotrophic lateral sclerosis
by van Es, Michael A, MD and Hardiman, Orla, Prof and Chio, Adriano, Prof and Al-Chalabi, Ammar, Prof and Pasterkamp, R Jeroen, Prof and Veldink, Jan H, Prof and van den Berg, Leonard H, Prof
The Lancet (British edition), ISSN 0140-6736, 11/2017, Volume 390, Issue 10107, pp. 2084 - 2098
Internal Medicine | Medicine(all) | Journal Article | Review | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genetic Predisposition to Disease | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Humans | Amyotrophic Lateral Sclerosis - diagnosis | Male | Survival Rate | TDP-43 Proteinopathies | DNA-Binding Proteins - genetics | Cause of Death | Disease Progression | Female | Chronic Disease | Amyotrophic Lateral Sclerosis - epidemiology | Amyotrophic lateral sclerosis | Medical research | Neurosciences | Neurons | Analysis | Medicine, Experimental | Research institutes | Dementia | Brain | Motor neurons | Spinal cord | Neuromuscular diseases | Medical imaging | Neuropathology | Patients | Studies | Neurology | Medical prognosis | Dementia disorders | Biomarkers | Genetics | Bioindicators | Diagnostic systems | Frontotemporal dementia | Age | Index Medicus | Abridged Index Medicus
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4. Full Text Amyotrophic lateral sclerosis
by Kiernan, Matthew C, Prof and Vucic, Steve, PhD and Cheah, Benjamin C, MBiostat and Turner, Martin R, PhD and Eisen, Andrew, Prof and Hardiman, Orla, Prof and Burrell, James R, MBBS and Zoing, Margaret C, BNurs
The Lancet (British edition), ISSN 0140-6736, 2011, Volume 377, Issue 9769, pp. 942 - 955
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Neurology | General aspects | Cerebrospinal fluid. Meninges. Spinal cord | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Medical sciences | Nervous system (semeiology, syndromes) | Amyotrophic Lateral Sclerosis - diagnosis | Amyotrophic Lateral Sclerosis - etiology | Amyotrophic Lateral Sclerosis - physiopathology | Amyotrophic Lateral Sclerosis - therapy | Humans | Amyotrophic lateral sclerosis | Care and treatment | Diagnosis | Research | Medical research | Genetics | Womens health | Motor systems | Clinical trials | Reviews | Longevity | Neurodegenerative diseases | Index Medicus | Abridged Index Medicus
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5. Full Text Amyotrophic lateral sclerosis
by Wijesekera, Lokesh C and Leigh, P Nigel
Orphanet journal of rare diseases, ISSN 1750-1172, 2009, Volume 4, Issue 1, pp. 3 - 3
Genetics & Heredity | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Superoxide Dismutase - genetics | Prognosis | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Amyotrophic Lateral Sclerosis - diagnosis | Male | DNA-Binding Proteins - genetics | Motor Neurons - pathology | Young Adult | Amyotrophic Lateral Sclerosis - pathology | Adult | Female | Aged | Mutation | Superoxide Dismutase-1 | Amyotrophic Lateral Sclerosis - epidemiology | Care and treatment | Demographic aspects | Patient outcomes | Amyotrophic lateral sclerosis | Development and progression | Genetic aspects | Diagnosis | Research | Nervous system agents | Index Medicus
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6. Full Text A comprehensive review of amyotrophic lateral sclerosis
by Zarei, Sara and Carr, Karen and Reiley, Luz and Diaz, Kelvin and Guerra, Orleiquis and Altamirano, Pablo Fernandez and Pagani, Wilfredo and Lodin, Daud and Orozco, Gloria and Chinea, Angel
Surgical neurology international, ISSN 2152-7806, 01/2015, Volume 6, Issue 1, p. 171
Amyotrophic lateral sclerosis | superoxide dismutase | sporadic and familial ALS
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