(Q35038668)

5 August 2017

1 reference

title

Mitochondria and amyotrophic lateral sclerosis (English)

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amyotrophic lateral sclerosis

5 August 2017

0 references

2

Anthony H V Schapira

1 reference

5 August 2017

Richard W Orrell

1

1 reference

5 August 2017

1 January 2002

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International Review of Neurobiology

5 August 2017

1 reference

5 August 2017

53

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5 August 2017

411-426

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Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients

5 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Expression of a Cu,Zn superoxide dismutase typical of familial amyotrophic lateral sclerosis induces mitochondrial alteration and increase of cytosolic Ca2+ concentration in transfected neuroblastoma SH-SY5Y cells

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Amyotrophic lateral sclerosis: oxidative energy metabolism and calcium homeostasis in peripheral blood lymphocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Mitochondrial DNA deletion mutation levels are elevated in ALS brains

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Amyotrophic lateral sclerosis and Parkinsonism-dementia complex on Guam. Further pathologic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Chronic mitochondrial inhibition induces selective motoneuron death in vitro: a new model for amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Dose-ranging study of riluzole in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis/Riluzole Study Group II

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Functional and morphometric study of the liver in motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Manganese superoxide dismutase levels are elevated in a proportion of amyotrophic lateral sclerosis patient cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Cleavage, aggregation and toxicity of the expanded androgen receptor in spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Hepatic ultrastructural changes and liver dysfunction in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Differential effects of creatine depletion on the regulation of enzyme activities and on creatine-stimulated mitochondrial respiration in skeletal muscle, heart, and brain

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Clinical implications of the genetics of ALS and other motor neuron diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

An orally active anti-apoptotic molecule (CGP 3466B) preserves mitochondria and enhances survival in an animal model of motoneuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Mitochondria in sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

Motor neuron disease on Guam: geographic and familial occurrence, 1956-85.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2953015-4

7 January 2021

10.1016/S0074-7742(02)53015-4

Identifiers

DOI

1 reference

5 August 2017

1 reference

PubMed ID

12512348