(Q60609066)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10485557%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

title

Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group (English)

1 reference

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13 December 2019

1 reference

4

1 reference

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13 December 2019

Sophie Caillat-Zucman

7

1 reference

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13 December 2019

Alain Gaudric

10

1 reference

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13 December 2019

author name string

P Massin

1

1 reference

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13 December 2019

M Virally-Monod

2

1 reference

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13 December 2019

B Vialettes

3

1 reference

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13 December 2019

H Gin

5

1 reference

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13 December 2019

B Porokhov

6

1 reference

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13 December 2019

P Froguel

8

1 reference

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13 December 2019

V Paquis-Fluckinger

9

1 reference

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13 December 2019

P J Guillausseau

11

1 reference

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13 December 2019

publication date

1 September 1999

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13 December 2019

1 reference

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13 December 2019

volume

106

1 reference

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13 December 2019

issue

9

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13 December 2019

page(s)

1821-1827

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

13 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Macular pattern dystrophy associated with a mutation of mitochondrial DNA.

1 reference

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7 January 2021

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Maternally inherited diabetes and deafness: a new diabetes subtype

1 reference

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7 January 2021

Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Prevalence of mitochondrial gene mutations in families with diabetes mellitus

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7 January 2021

Importance of searching for mtDNA defects in patients with diabetes and hearing deficit.

1 reference

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7 January 2021

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

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7 January 2021

Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene

1 reference

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7 January 2021

Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Macular pattern dystrophy in patients with deafness and diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation

1 reference

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7 January 2021

Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?

1 reference

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7 January 2021

Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

The Wisconsin epidemiologic study of diabetic retinopathy. III. Prevalence and risk of diabetic retinopathy when age at diagnosis is 30 or more years

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Relationship of duration and onset of diabetes to prevalence of diabetic retinopathy.

1 reference

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7 January 2021

The retinal manifestations of mitochondrial myopathy. A study of 22 cases

1 reference

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7 January 2021

Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion

1 reference

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7 January 2021

Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report.

1 reference

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7 January 2021

Retinal pathology in the Kearns-Sayre syndrome

1 reference

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7 January 2021

Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2899%2990356-1

7 January 2021

10.1016/S0161-6420(99)90356-1

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10485557%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

1 reference