(Q48787948)

English

Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10.

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10. (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

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Regina S Moisés

4

object named as

Regina S Moisés

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

author name string

Carla S Bergamin

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

Luiz Clemente Rolim

2

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

Sergio A Dib

3

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

publication date

1 November 2008

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

Arquivos Brasileiros de Endocrinologia e Metabologia

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

52

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

8

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

1345-1349

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

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

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Mitochondrial respiratory-chain diseases

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Mitochondrial diabetes: molecular mechanisms and clinical presentation

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

UKPDS 21: low prevalence of the mitochondrial transfer RNA gene (tRNA(Leu(UUR))) mutation at position 3243bp in UK Caucasian type 2 diabetic patients.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

[Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation].

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

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/10.1590%2FS0004-27302008000800023

21 January 2018

Diabetes mellitus associated with 3243 mitochondrial tRNA(Leu(UUR)) mutation: clinical features and coenzyme Q10 treatment

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Maternally inherited diabetes and deafness: a multicenter study

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control study

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Intestinal pseudo-obstruction in a diabetic man: role of the mitochondrial A3243G mutation.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Chronic intestinal pseudo-obstruction

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tract

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302008000800023

21 January 2018

Identifiers

10.1590/S0004-27302008000800023

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/19169492

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