Molecular approaches to amyotrophic lateral sclerosis

R. Glenn Smith; Stanley H. Appel

doi:10.1146/annurev.med.46.1.133

Molecular approaches to amyotrophic lateral sclerosis

R. Glenn Smith, Stanley H. Appel

Research output: Contribution to journal › Review article › peer-review

34 Scopus citations

Abstract

New discoveries are expanding our knowledge of mechanisms involved in amyotrophic lateral sclerosis (ALS) pathogenesis. Some recent advances in our understanding of motoneuron death in familial ALS (fALS) and sporadic ALS (sALS) are reviewed, with emphasis on molecular similarities that may further unite these phenotypically linked diseases.

Original language	English (US)
Pages (from-to)	133-145
Number of pages	13
Journal	Annual Review of Medicine
Volume	46
DOIs	https://doi.org/10.1146/annurev.med.46.1.133
State	Published - 1995

Keywords

Autoimmune motoneuron injury
Calcium channel
Excitotoxicity
Oxidative injury
Superoxide dismutase deficiency

ASJC Scopus subject areas

Cell Biology
General Medicine

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10.1146/annurev.med.46.1.133

Cite this

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title = "Molecular approaches to amyotrophic lateral sclerosis",

abstract = "New discoveries are expanding our knowledge of mechanisms involved in amyotrophic lateral sclerosis (ALS) pathogenesis. Some recent advances in our understanding of motoneuron death in familial ALS (fALS) and sporadic ALS (sALS) are reviewed, with emphasis on molecular similarities that may further unite these phenotypically linked diseases.",

keywords = "Autoimmune motoneuron injury, Calcium channel, Excitotoxicity, Oxidative injury, Superoxide dismutase deficiency",

author = "Smith, {R. Glenn} and Appel, {Stanley H.}",

year = "1995",

doi = "10.1146/annurev.med.46.1.133",

language = "English (US)",

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journal = "Annual Review of Medicine",

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T1 - Molecular approaches to amyotrophic lateral sclerosis

AU - Smith, R. Glenn

AU - Appel, Stanley H.

PY - 1995

Y1 - 1995

N2 - New discoveries are expanding our knowledge of mechanisms involved in amyotrophic lateral sclerosis (ALS) pathogenesis. Some recent advances in our understanding of motoneuron death in familial ALS (fALS) and sporadic ALS (sALS) are reviewed, with emphasis on molecular similarities that may further unite these phenotypically linked diseases.

AB - New discoveries are expanding our knowledge of mechanisms involved in amyotrophic lateral sclerosis (ALS) pathogenesis. Some recent advances in our understanding of motoneuron death in familial ALS (fALS) and sporadic ALS (sALS) are reviewed, with emphasis on molecular similarities that may further unite these phenotypically linked diseases.

KW - Autoimmune motoneuron injury

KW - Calcium channel

KW - Excitotoxicity

KW - Oxidative injury

KW - Superoxide dismutase deficiency

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UR - http://www.scopus.com/inward/citedby.url?scp=0028924368&partnerID=8YFLogxK

U2 - 10.1146/annurev.med.46.1.133

DO - 10.1146/annurev.med.46.1.133

M3 - Review article

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AN - SCOPUS:0028924368

SN - 0066-4219

VL - 46

SP - 133

EP - 145

JO - Annual Review of Medicine

JF - Annual Review of Medicine

ER -

Molecular approaches to amyotrophic lateral sclerosis

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

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