AMYOTROPHIC LATERAL SCLEROSIS 1

Known as: ALS1, Amyotrophic Lateral Sclerosis, Familial, AMYOTROPHIC LATERAL SCLEROSIS 1, FAMILIAL 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1970-2018
0102019702018

Papers overview

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Highly Cited
2012
Highly Cited
2012
Amyotrophic lateral sclerosis (ALS) is a late-onset neurodegenerative disorder resulting from motor neuron death. Approximately… (More)
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Highly Cited
2012
Highly Cited
2012
BACKGROUND Amyotrophic lateral sclerosis (ALS) is incurable and characterized by progressive paralysis of the muscles of the… (More)
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Highly Cited
2011
Highly Cited
2011
Mutations in the SOD1 and TARDBP genes have been commonly identified in Amyotrophic Lateral Sclerosis (ALS). Recently, mutations… (More)
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Highly Cited
2010
Highly Cited
2010
Amyotrophic lateral sclerosis (ALS) has its onset in middle age and is a progressive disorder characterized by degeneration of… (More)
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Highly Cited
2010
Highly Cited
2010
OBJECTIVE Amyotrophic lateral sclerosis (ALS) is a fatal disorder of motor neuron degeneration. Most cases of ALS are sporadic… (More)
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Highly Cited
2007
Highly Cited
2007
OBJECTIVE Amyotrophic lateral sclerosis (ALS) is a common, fatal motor neuron disorder with no effective treatment. Approximately… (More)
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Highly Cited
2007
Highly Cited
2007
Amyotrophic lateral sclerosis (ALS) is a devastating motor neuron degenerative disease whose etiology and pathogenesis remain… (More)
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Highly Cited
2007
Highly Cited
2007
OBJECTIVE To investigate the value of objective biomarkers for upper (UMN) and lower (LMN) motor neuron involvement in ALS… (More)
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Highly Cited
2006
Highly Cited
2006
The fungal pathogen Candida albicans is frequently associated with catheter-based infections because of its ability to form… (More)
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Highly Cited
2004
Highly Cited
2004
Proteinacious intracellular aggregates in motor neurons are a key feature of both sporadic and familial amyotrophic lateral… (More)
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