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1. Full Text Major advances in amyotrophic lateral sclerosis in 2020
by Hardiman, Orla
Lancet neurology, ISSN 1474-4422, 01/2021, Volume 20, Issue 1, pp. 14 - 15
Taurochenodeoxycholic Acid - pharmacology | Oligonucleotides - pharmacology | Humans | Amyotrophic Lateral Sclerosis - diagnosis | Phenylbutyrates - pharmacology | Clinical Trials as Topic | Amyotrophic Lateral Sclerosis - drug therapy | Drug Combinations | Superoxide Dismutase-1 - drug effects | Neuroimaging | Statistical analysis | Medical imaging | Pandemics | Neurodegenerative diseases | Clinical trials | Amyotrophic lateral sclerosis | Coronaviruses | Drug development | Biological activity | Design | COVID-19 | DNA-binding protein | Precision medicine | Neural networks | Biomarkers | Mathematical models | Index Medicus
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2. Full Text Global burden of motor neuron diseases: mind the gaps
by Hardiman, Orla
Lancet neurology, ISSN 1474-4422, 12/2018, Volume 17, Issue 12, pp. 1030 - 1031
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Geographical distribution | Phenotypes | Progressive bulbar palsy | Spastic paraparesis | Motor neurone disease | Cognitive ability | Amyotrophic lateral sclerosis | Superoxide dismutase | Data processing | Population studies | Spinal muscular atrophy | Atrophy | Genetic analysis | Dementia disorders | Population | Degeneration | Mutation | Paralysis | Frontotemporal dementia | Health risk assessment | Index Medicus
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3. Full Text Management of respiratory symptoms in ALS
by Hardiman, Orla and Hardiman, Orla
Journal of neurology, ISSN 0340-5354, 3/2011, Volume 258, Issue 3, pp. 359 - 365
Neurology | Neurosciences | Respiratory function | Medicine & Public Health | Non-invasive ventilation | ALS | Neuroradiology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer | Psychology. Psychoanalysis. Psychiatry | Psychopharmacology | Pharmacology. Drug treatments | Biological and medical sciences | Medical sciences | Neuropharmacology | Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) | Respiratory Insufficiency - physiopathology | Respiration, Artificial - methods | Amyotrophic Lateral Sclerosis - physiopathology | Amyotrophic Lateral Sclerosis - therapy | Humans | Respiratory Muscles - physiopathology | Respiratory Insufficiency - etiology | Respiratory Insufficiency - therapy | Amyotrophic Lateral Sclerosis - complications | Animals | Disease Management | Respiratory Mechanics - physiology | Palliative Care - methods | Complications and side effects | Care and treatment | Respiratory insufficiency | Amyotrophic lateral sclerosis | Research | Diagnosis | Health aspects | Artificial respiration | Risk factors | Index Medicus
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4. Full Text The epidemiology of ALS: A conspiracy of genes, environment and time
by Al-Chalabi, Ammar and Hardiman, Orla
Nature reviews. Neurology, ISSN 1759-4758, 2013, Volume 9, Issue 11, pp. 617 - 628
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Time | Gene-Environment Interaction | Amyotrophic Lateral Sclerosis - genetics | Humans | Risk Factors | Amyotrophic Lateral Sclerosis - epidemiology | Amyotrophic lateral sclerosis | Care and treatment | Usage | Diagnosis | Research | Epidemiology | Index Medicus
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5. Full Text End-of-life management in patients with amyotrophic lateral sclerosis
by Connolly, Sheelah, Dr and Galvin, Miriam, PhD and Hardiman, Orla, Prof
Lancet neurology, ISSN 1474-4422, 2015, Volume 14, Issue 4, pp. 435 - 442
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | United States - epidemiology | Stress, Psychological - prevention & control | Terminal Care - ethics | Hospice Care - ethics | Humans | Health Personnel - psychology | Suicide, Assisted - ethics | Cognition | Empathy | Health Personnel - ethics | Personal Autonomy | Decision Making - ethics | Palliative Care - ethics | Mental Competency | Education, Medical - standards | Palliative Care - statistics & numerical data | Hospice Care - statistics & numerical data | Communication | Health Personnel - standards | Clinical Competence | Education, Medical - trends | Caregivers - psychology | Europe - epidemiology | Amyotrophic Lateral Sclerosis - psychology | Attitude to Death | Terminal Care - statistics & numerical data | Health Personnel - education | Suicide, Assisted - statistics & numerical data | Quality of Life | Advance Directives | Stress, Psychological - etiology | Amyotrophic lateral sclerosis | Palliative care | Medical research | Decision making | Hospice care | Quality of life | Index Medicus
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6. 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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7. Full Text Cognitive impairment in amyotrophic lateral sclerosis
by Phukan, Julie, MB and Pender, Niall P, PhD and Hardiman, Orla, MD
Lancet neurology, ISSN 1474-4422, 2007, Volume 6, Issue 11, pp. 994 - 1003
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neuropsychological Tests | Cognition Disorders - diagnosis | Dementia - etiology | Prevalence | Cognition Disorders - etiology | Humans | Amyotrophic Lateral Sclerosis - psychology | Cognition Disorders - epidemiology | Cognition Disorders - psychology | Incidence | Index Medicus
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8. 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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