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JAMA Neurology, ISSN 2168-6149, 03/2016, Volume 73, Issue 3, pp. 329 - 336
Journal Article
Neuroepidemiology, ISSN 0251-5350, 08/2018, Volume 51, Issue 1-2, pp. 96 - 103
Background: The International Classification of Disease, 10th Revision (ICD-10) did not include a code specific for Amyotrophic lateral sclerosis (ALS) until... 
Original Paper | Amyotrophic lateral sclerosis | Mortality | Motor neuron disease | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | ALS | PREVALENCE | EPIDEMIOLOGY | CLINICAL NEUROLOGY
Journal Article
JAMA Neurology, ISSN 2168-6149, 03/2016, Volume 73, Issue 3, p. 329
  Amyotrophic lateral sclerosis (ALS) is a progressive, fatal disease with no known cause. Case studies primarily of athletes and several case-control studies... 
Women | Exercise | Mortality | Menopause | Amyotrophic lateral sclerosis | Risk factors
Journal Article
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 07/2019, Volume 20, Issue 5-6, pp. 404 - 412
Current evidence suggests heterogeneity of amyotrophic lateral sclerosis (ALS) among geographic areas and populations. Lower mortality rates have been reported... 
mortality | Amyotrophic lateral sclerosis | risk | ethnicity | admixed population | population-based study | Life Sciences | Santé publique et épidémiologie
Journal Article
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, ISSN 2167-8421, 08/2015, Volume 16, Issue 5-6, pp. 372 - 377
Journal Article
Annals of Neurology, ISSN 0364-5134, 02/2014, Volume 75, Issue 2, pp. 287 - 297
Journal Article
Neuron, ISSN 0896-6273, 12/2015, Volume 88, Issue 5, pp. 902 - 909
A non-coding hexanucleotide repeat expansion in the gene is the most common mutation associated with familial amyotrophic lateral sclerosis (ALS) and... 
RAN translation | transgenic mice | Amyotrophic lateral sclerosis (ALS) | frontotemporal dementia (FTD) | neurodegeneration | microRNA | repeat expansions | C9ORF72 | RNA foci | Repeat expansions | MicroRNA | Neurodegeneration | Transgenic mice | Frontotemporal dementia (FTD) | DEMENTIA | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | SPECTRUM | MODEL | FRONTOTEMPORAL LOBAR DEGENERATION | TRANSLATION | SENSE | NEUROSCIENCES | PATHOLOGICAL FEATURES | Age Factors | Amyotrophic Lateral Sclerosis - physiopathology | DNA Repeat Expansion - genetics | Humans | MicroRNAs - metabolism | Frontotemporal Dementia - mortality | Cerebral Cortex - cytology | Brain - metabolism | Chromosomes, Artificial, Bacterial - genetics | Chromosomes, Artificial, Bacterial - metabolism | Neurons - physiology | C9orf72 Protein | Dipeptides - metabolism | Neurons - drug effects | Disease Models, Animal | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Frontotemporal Dementia - physiopathology | Gene Expression Regulation - genetics | Amyotrophic Lateral Sclerosis - genetics | Cells, Cultured | Genotype | Mice, Transgenic | Amyotrophic Lateral Sclerosis - mortality | Nerve Tissue Proteins - metabolism | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Animals | Brain - pathology | In Vitro Techniques | Dipeptides - genetics | Proteins | Neurosciences | Proline | Genetic engineering | Glycine | Dementia | Analysis | Genetic translation | Plasmids | Neurons | Rodents | Cloning | Amyotrophic lateral sclerosis | Behavior | Artificial chromosomes | Expansion | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 02/2013, Volume 80, Issue 9, pp. 829 - 838
Journal Article
Journal Article