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2006, 2nd ed., ISBN 9781841844633, xxi, 370
Book
2006, 1, Neurological disease and therapy, ISBN 9780824729240, Volume 78, xxvi, 830
With cutting-edge contributions from internationally recognized experts and field pioneers, Amyotrophic Lateral Sclerosis is the definitive guide to the... 
Amyotrophic lateral sclerosis | Neurology | Neuroscience | Amyotrophic Lateral Sclerosis
Book
2005, 1st ed., ISBN 9781932603064, x, 246
ALS is not a curable disease, but it is a treatable one. Treatments are now available that can make a major difference in prolonging life and enhancing the... 
Amyotrophic lateral sclerosis | Clinical & internal medicine | HEA039140 | Popular works
Book
2014, 3rd edition., ISBN 0199686025, x, 326 pages
Amytrophic Lateral Sclerosis (ALS or motor neurone disease) is a progressive neurodegenerative disease that can cause profound suffering for both the patient... 
Palliative Care | therapy | Amyotrophic Lateral Sclerosis | Amyotrophic lateral sclerosis | Nursing & Ancillary Services | Palliative treatment
Book
1998, ISBN 0521581036, xx, 303
Amyotrophic lateral sclerosis (ALS), otherwise known as Lou Gehrig's or motor neuron disease, is one of several degenerative diseases of the ageing nervous... 
Amyotrophic lateral sclerosis
Book
eBook
1998, Contemporary neurology series, ISBN 9780803602694, Volume 49
eBook
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 | palliative medicine | neurology team | als | psychosocial care | amyotrophic lateral sclerosis | palliative care | motor neurone disease
Book
Nature, ISSN 0028-0836, 05/2010, Volume 465, Issue 7295, pp. 223 - 226
Amyotrophic lateral sclerosis (ALS) has its onset in middle age and is a progressive disorder characterized by degeneration of motor neurons of the primary... 
OPEN-ANGLE GLAUCOMA | COMPLEX | PROTEIN | GENE | MULTIDISCIPLINARY SCIENCES | EXPRESSION | NEMO | MYOSIN-VI | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Middle Aged | Transcription Factor TFIIIA - genetics | Cytoplasm - metabolism | Male | NF-kappa B - metabolism | Cytoplasm - pathology | Transcription Factor TFIIIA - metabolism | Mutation, Missense - genetics | DNA-Binding Proteins - metabolism | Young Adult | Base Sequence | Aged, 80 and over | Adult | Female | Child | Superoxide Dismutase - metabolism | NF-kappa B - agonists | Amino Acid Sequence | NF-kappa B - antagonists & inhibitors | Amyotrophic Lateral Sclerosis - genetics | Japan | Mutant Proteins - genetics | Transcription Factor TFIIIA - chemistry | Exons - genetics | Mutant Proteins - metabolism | Mutation - genetics | Transcription Factor TFIIIA - analysis | Protein Transport | Amyotrophic Lateral Sclerosis - pathology | Asian Continental Ancestry Group | Pedigree | Mutant Proteins - chemistry | Adolescent | Amyotrophic Lateral Sclerosis - metabolism | Polymorphism, Single Nucleotide - genetics | Aged | Consanguinity | Superoxide Dismutase-1 | Mutant Proteins - analysis | Codon, Nonsense - genetics | Sequence Deletion - genetics | Cellular proteins | Gene mutations | Physiological aspects | Amyotrophic lateral sclerosis | Genetic aspects | Research | Health aspects | Risk factors | Haplotypes | Studies | Genes | Genetics | Amino acids | Mutation | Family medical history | Chromosomes | Apoptosis | Index Medicus
Journal Article
1990, Progress in clinical neurologic trials., ISBN 9780939957231, Volume 1, xv, 238
Book
The New England Journal of Medicine, ISSN 0028-4793, 10/2017, Volume 377, Issue 16, pp. 1602 - 1602
The article by Brown et al. (July 13 issue)1 provides a comprehensive review of the mechanisms, pathophysiological processes, and clinical features of... 
Ostomy | Amyotrophic lateral sclerosis | Ventilation | Endoscopy | Health risk assessment | Sclerosis | Quality of life
Journal Article
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