(Q35653693)

9 August 2017

title

Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia (English)

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9 August 2017

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R Lodi

1

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Anthony H V Schapira

7

object named as

A H Schapira

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9 August 2017

2

J M Cooper

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9 August 2017

J L Bradley

3

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9 August 2017

D Manners

4

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9 August 2017

P Styles

5

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9 August 2017

D J Taylor

6

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9 August 2017

language of work or name

English

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publication date

1 September 1999

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Proceedings of the National Academy of Sciences of the United States of America

9 August 2017

published in

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9 August 2017

volume

96

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9 August 2017

issue

20

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9 August 2017

page(s)

11492-11495

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Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Clinical and genetic abnormalities in patients with Friedreich's ataxia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Myopathy in vitamin E deficient rats: muscle fibre necrosis associated with disturbances of mitochondrial function

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Body fat assessed from total body density and its estimation from skinfold thickness: measurements on 481 men and women aged from 16 to 72 Years

12 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

12 July 2018

12 December 2020

Multiple controls of oxidative metabolism in living tissues as studied by phosphorus magnetic resonance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Glucose metabolism alterations in Friedreich's ataxia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Evidence for mitochondrial DNA damage by lipid peroxidation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Phosphorus magnetic resonance spectroscopy (31P MRS) in neuromuscular disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Substrate regulation of mitochondrial oxidative phosphorylation in hypercapnic rabbit muscle

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Cytosolic phosphorylation potential

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body myositis assessed by 31P-magnetic resonance spectroscopy.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

1H NMR spectroscopy studies of Huntington's disease: correlations with CAG repeat numbers

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Proton spectroscopy in myotonic dystrophy: correlations with CTG repeats.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Metabolic recovery after exercise and the assessment of mitochondrial function in vivo in human skeletal muscle by means of 31P NMR.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

In vivo muscle magnetic resonance spectroscopy in the clinical investigation of mitochondrial disease

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=18061

Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study

25 September 2018

1 reference

12 December 2020

Respiratory enzymes in oxidative phosphorylation. I. Kinetics of oxygen utilization

1 reference

12 December 2020

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

12 December 2020

Radical initiated alpha-tocopherol depletion and lipid peroxidation in mitochondrial membranes

1 reference

12 December 2020

Control of phosphocreatine resynthesis during recovery from exercise in human skeletal muscle

1 reference

12 December 2020

Cellular energetics of dystrophic muscle

1 reference

12 December 2020

The neurologic syndrome of vitamin E deficiency: a significant cause of ataxia

1 reference

12 December 2020

Bioenergetics of skeletal muscle in mitochondrial myopathy

1 reference

12 December 2020

Control of energy metabolism during muscle contraction

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.96.20.11492

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9 August 2017

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9 August 2017

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