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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
2015, Contemporary neurology series, ISBN 019978311X, Volume 88, xxviii, 336
Book
The Lancet (British edition), ISSN 0140-6736, 08/2016, Volume 388, Issue 10047, pp. 919 - 931
Journal Article
Lancet neurology, ISSN 1474-4422, 12/2018, Volume 17, Issue 12, pp. 1083 - 1097
Understanding how prevalence, incidence, and mortality of motor neuron diseases change over time and by location is crucial for understanding the causes of these disorders and for health-care planning... 
Medical research | Nervous system diseases | Neurons | Analysis | Mortality | Medicine, Experimental | Risk factors | Amyotrophic lateral sclerosis | Epidemiology | Spinal muscular atrophy | Studies | Hereditary spastic paraplegia | Paraplegia | Motor neuron diseases | Cell death | Paralysis | Spastic paraplegia | Health risk assessment | Bayesian analysis | Age | Life Sciences | Santé publique et épidémiologie
Journal Article
Journal Article
2016, Fourth edition., ISBN 9780781778176, xlii, 975 pages
.... Then we take a close look at the structure and function of individual neurons, how they communicate... 
Brain | Neurosciences | Cerveau
Book
2017, ISBN 9780128022573, 337
Motor Neuron Diseases (MND) are a group of neurological disorders that affect motor neurons in adults and in children... 
Motor neurons | Treatment | Diseases | Amyotrophic lateral sclerosis | Cellular therapy
eBook
Nature neuroscience, ISSN 1546-1726, 10/2008, Volume 11, Issue 11, pp. 1294 - 1301
.... GRPs also extended survival and disease duration, attenuated motor neuron loss and slowed declines in forelimb motor and respiratory physiological functions... 
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Superoxide Dismutase - genetics | Phrenic Nerve - physiopathology | Humans | Glial Fibrillary Acidic Protein - metabolism | Cell Movement - physiology | Hindlimb - physiopathology | Motor Neuron Disease - therapy | Spinal Cord - pathology | Motor Neuron Disease - physiopathology | Cell Differentiation - physiology | Cell Survival - physiology | Disease Models, Animal | Calcium-Binding Proteins - metabolism | Neural Conduction - genetics | Animals, Genetically Modified | Excitatory Amino Acid Transporter 2 - deficiency | Rats | Cell Transplantation | Spinal Cord - surgery | Motor Neuron Disease - pathology | Action Potentials - physiology | Astrocytes - physiology | Animals | Green Fluorescent Proteins - biosynthesis | Microfilament Proteins | Muscle, Skeletal - physiopathology | Stem Cells - physiology | Spinal Cord - physiopathology | Physiological aspects | Motor neurons | Nervous system | Care and treatment | Degeneration | Astrocytes | astroglia | grafting | neurodegeneration | ALS | neural precursor cell | progenitor | amyotrophic lateral sclerosis | SOD1 | non-cell autonomous | stem cell | motor neuron | neuroprotection | transplantation | lineage-restricted precursor | glial precursor | replacement | astrocyte
Journal Article