(Q50482573)

14 March 2018

title

Neonatal liver failure and Leigh syndrome possibly due to CoQ-responsive OXPHOS deficiency. (English)

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14 March 2018

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10

Lerman-Sagie T

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14 March 2018

author name string

Leshinsky-Silver E

1

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14 March 2018

Levine A

2

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14 March 2018

Nissenkorn A

3

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14 March 2018

Barash V

4

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14 March 2018

Perach M

5

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14 March 2018

Buzhaker E

6

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14 March 2018

Shahmurov M

7

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14 March 2018

Polak-Charcon S

8

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14 March 2018

Lev D

9

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14 March 2018

publication date

1 August 2003

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14 March 2018

Molecular Genetics and Metabolism

published in

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14 March 2018

volume

79

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14 March 2018

issue

4

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14 March 2018

page(s)

288-293

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14 March 2018

A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Human cultured skin fibroblasts survive profound inherited ubiquinone depletion

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https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Coenzyme Q10 depletion is comparatively less detrimental to human cultured skin fibroblasts than respiratory chain complex deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Coenzyme Q-responsive Leigh's encephalopathy in two sisters

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Ubiquinone biosynthesis in microorganisms

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Familial cerebellar ataxia with muscle coenzyme Q10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

Biochemical and molecular investigations in respiratory chain deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900097-0

7 January 2021

10.1016/S1096-7192(03)00097-0

Identifiers

DOI

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14 March 2018

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14 March 2018