Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA? (Q71482569)

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18 October 2019

title

Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8786027%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

author name string

P Silvestre-Aillaud

1

1 reference

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18 October 2019

D BenDahan

2

1 reference

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18 October 2019

V Paquis-Fluckinger

3

1 reference

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18 October 2019

J Pouget

4

1 reference

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18 October 2019

J F Pelissier

5

1 reference

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18 October 2019

C Desnuelle

6

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18 October 2019

P J Cozzone

7

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18 October 2019

B Vialettes

8

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18 October 2019

publication date

1 December 1995

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18 October 2019

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18 October 2019

volume

38

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18 October 2019

issue

12

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18 October 2019

page(s)

1485-1486

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https://scigraph.springernature.com/pub.10.1007/bf00400614

18 October 2019

exact match

0 references

cites work

Heterogeneity of metabolic response to muscular exercise in humans. New criteria of invariance defined by in vivo phosphorus-31 NMR spectroscopy

1 reference

12 December 2020

Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene

1 reference

12 December 2020

Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.

1 reference

12 December 2020

Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.

1 reference

12 December 2020

Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics

1 reference

12 December 2020

Mitochondrial encephalomyopathy (MELAS): pathological study and successful therapy with coenzyme Q10 and idebenone

1 reference

12 December 2020

Long-term coenzyme Q10 therapy for a mitochondrial encephalomyopathy with cytochrome c oxidase deficiency: a 31P NMR study

1 reference

12 December 2020

Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial.

1 reference

12 December 2020

Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies.

1 reference

12 December 2020

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

12 December 2020

Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene

1 reference

12 December 2020

Mitochondrial gene defects in patients with NIDDM

1 reference

12 December 2020

A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.

1 reference

12 December 2020

31P NMR spectroscopy and ergometer exercise test as evidence for muscle oxidative performance improvement with coenzyme Q in mitochondrial myopathies

1 reference

12 December 2020

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00400614

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8786027%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference