Mitochondrial dysfunction in ALS-Reference-Cited by-同舟云学术

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Mitochondrial dysfunction in ALS

Published:2012-05 Issue:2 Volume:97 Page:54-66
ISSN:0301-0082
Container-title:Progress in Neurobiology
language:en
Short-container-title:Progress in Neurobiology

Author:

Cozzolino Mauro,Carrì Maria Teresa

Funder

ALS Association

Telethon

MIUR (PRIN)

IMI-San Paolo

Fondation Thierry-Latran

ERA-Net Neuron

Association Française contre les Myopathies

AriSLA

Publisher

Elsevier BV

Subject

General Neuroscience

Reference195 articles.

1. Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis;Afifi;Neurology,1966

2. N-acetyl-l-cysteine improves survival and preserves motor performance in an animal model of familial amyotrophic lateral sclerosis;Andreassen;Neuroreport,2000

3. Increases in cortical glutamate concentrations in transgenic amyotrophic lateral sclerosis mice are attenuated by creatine supplementation;Andreassen;J. Neurochem.,2001

4. Protein oxidative damage in a transgenic mouse model of familial amyotrophic lateral sclerosis;Andrus;J. Neurochem.,1998

5. Mitochondrial damage due to SOD1 deficiency in SH-SY5Y neuroblastoma cells: a rationale for the redundancy of SOD1;Aquilano;FASEB J.,2006

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