(Q34101152)

31 July 2017

1 reference

title

Friedreich's ataxia and iron metabolism (English)

1 reference

31 July 2017

1 reference

Gordon N

1

1 reference

31 July 2017

1 December 2000

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31 July 2017

Brain and Development

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31 July 2017

22

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31 July 2017

465-468

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31 July 2017

8

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A study of iron metabolism in neuropsychiatric patients. Hallervorden-Spatz disease.

31 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical features

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Frataxin gene of Friedreich's ataxia is targeted to mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

The yeast frataxin homologue mediates mitochondrial iron efflux. Evidence for a mitochondrial iron cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Deletion of the yeast homologue of the human gene associated with Friedreich's ataxia elicits iron accumulation in mitochondria.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Increased serum transferrin receptor concentrations in Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Recent advances in the molecular pathogenesis of Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Early onset of Friedreich's ataxia in a compound heterozygote

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Effect of idebenone on cardiomyopathy in Friedreich's ataxia: a preliminary study

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Normal serum iron and ferritin concentrations in patients with Friedreich's ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Serum transferrin receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Molecular pathogenesis of Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Mitochondrial dysfunction in neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

A mutation in a mitochondrial ABC transporter results in mitochondrial dysfunction through oxidative damage of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Genetic disorders affecting proteins of iron metabolism: clinical implications

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Deciphering the cause of Friedreich ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Increased iron in the dentate nucleus of patients with Friedrich's ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

The importance of selenium to human health

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

Friedreich ataxia: an overview

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900175-3

7 January 2021

10.1016/S0387-7604(00)00175-3

Identifiers

DOI

1 reference

31 July 2017

1 reference

PubMed ID

11111058