(Q52109992)

22 April 2018

title

Statistical analysis of mitochondrial pathologies in childhood: identification of deficiencies using principal component analysis. (English)

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22 April 2018

principal component analysis

main subject

statistics

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author name string

Letellier T

1

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22 April 2018

Durrieu G

2

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22 April 2018

Malgat M

3

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22 April 2018

Rossignol R

4

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22 April 2018

Antoch J

5

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22 April 2018

Deshouillers JM

6

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22 April 2018

Coquet M

7

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22 April 2018

Lacombe D

8

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22 April 2018

Netter JC

9

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22 April 2018

Pedespan JM

10

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22 April 2018

Redonnet-Vernhet I

11

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22 April 2018

Mazat JP

12

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22 April 2018

publication date

1 July 2000

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22 April 2018

published in

Laboratory Investigation

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22 April 2018

volume

80

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22 April 2018

issue

7

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22 April 2018

page(s)

1019-1030

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22 April 2018

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene

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Principal component analysis and exploratory factor analysis

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Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases

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KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION

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The kinetic basis of threshold effects observed in mitochondrial diseases: a systemic approach

21 January 2018

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Control of oxidative phosphorylation in rat muscle mitochondria: implications for mitochondrial myopathies.

21 January 2018

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A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

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1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3780107

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

21 January 2018

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https://api.crossref.org/works/10.1038%2FLABINVEST.3780107

MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROME

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https://api.crossref.org/works/10.1038%2FLABINVEST.3780107

Aconitase and mitochondrial iron–sulphur protein deficiency in Friedreich ataxia

21 January 2018

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

21 January 2018

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Diseases of the mitochondrial DNA.

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Mitochondrial diseases: genotype versus phenotype

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

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Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chain

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7 January 2021

Mitochondrial myopathies

1 reference

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7 January 2021

Differential investigation of the capacity of succinate oxidation in human skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FLABINVEST.3780107

7 January 2021

Mitochondrial Myopathy Studies on Permeabilized Muscle Fibers1

1 reference

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7 January 2021

Menkes disease: study of the mitochondrial respiratory chain in three cases

1 reference

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7 January 2021

Threshold effect and tissue specificity. Implication for mitochondrial cytopathies

1 reference

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7 January 2021

10.1038/LABINVEST.3780107

Identifiers

DOI

1 reference

22 April 2018

1 reference

22 April 2018