Gastrointestinal manifestations of mitochondrial disorders: a systematic review. - Test2 - elhamkhani - TriplyDB

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

http://www.wikidata.org/entity/Q37671957

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Mitochondrial myopathy, dysmorphism, exercise-induced vomiting and tachycardia the mutation m.4831G > A Functional Mitochondria in Health and Disease.Gastrointestinal Involvement in m.3243A>G-associated MELAS.Maxwell's demon at work: Mitochondria, the organelles that convert information into energy?Mitochondrial disease: an uncommon but important cause of diabetes mellitus Advanced Biventricular Heart Failure due to Left Ventricular Noncompaction Cardiomyopathy Leading to the Formation of a Gastric Bezoar: The Implications of Heart Failure on the Gastrointestinal Tract

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Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

http://www.wikidata.org/entity/Q37671957

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 06 October 2016

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

@en

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

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type

label

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

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Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

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prefLabel

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

@en

Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

@nl

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Therapeutic Advances in Gastroenterology

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Gastrointestinal manifestations of mitochondrial disorders: a systematic review.

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Josef Finsterer

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Marlies Frank

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P2860

Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions

Mitochondrial encephalomyopathy: variable clinical expression within a single kindred.

Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

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

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance

Mitochondrial DNA polymerase editing mutation, PolgD257A, reduces the diabetic phenotype of Akita male mice by suppressing appetite.

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).

Natural course of pontocerebellar hypoplasia type 2A.

RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy

Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.

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