Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD) (Q79794045)

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25 December 2019

title

Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD) (English)

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25 December 2019

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H Narbonne

1

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25 December 2019

V Paquis-Fluckinger

2

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25 December 2019

R Valero

3

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25 December 2019

L Heyries

4

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25 December 2019

J F Pellissier

5

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25 December 2019

B Vialettes

6

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25 December 2019

publication date

1 February 2004

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25 December 2019

published in

Diabetes and Metabolism

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25 December 2019

volume

30

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25 December 2019

issue

1

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25 December 2019

page(s)

61-66

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

25 December 2019

cites work

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7 January 2021

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

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7 January 2021

Maternally inherited diabetes and deafness: a multicenter study

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7 January 2021

Prevalence of gastrointestinal symptoms associated with diabetes mellitus: a population-based survey of 15,000 adults

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7 January 2021

Gastrointestinal tract symptoms among persons with diabetes mellitus in the community.

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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.

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7 January 2021

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration

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7 January 2021

Mitochondrial myopathies with necrotizing encephalopathy of the Leigh type.

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7 January 2021

Mitochondrial encephalomyopathy showing prominent microvacuolation and necrosis of intestinal smooth muscle cells: a case diagnosed by rectal biopsy

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7 January 2021

Familial occurrence of intestinal obstruction in children with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS)

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Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes

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7 January 2021

De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring

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7 January 2021

[Intestinal pseudoobstructions and gastric necrosis in mitochondrial myopathy]

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7 January 2021

Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes.

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7 January 2021

Mitochondrial encephalomyopathy with lactic acidosis and stroke like episodes (MELAS) with prominent degeneration of the intestinal wall and cactus-like cerebellar pathology.

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7 January 2021

Mitochondrial mutation in diabetic patient with gastrointestinal symptoms

1 reference

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7 January 2021

Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis

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7 January 2021

Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging

1 reference

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7 January 2021

10.1016/S1262-3636(07)70090-3

Identifiers

DOI

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25 December 2019

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