Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination. - Wikidata - awgldk - TriplyDB

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

http://www.wikidata.org/entity/Q37561288

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Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.Gastro-intestinal Involvement in m.3243A>G-associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.

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Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

http://www.wikidata.org/entity/Q37561288

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 25 July 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

@en

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

@nl

type

label

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

@en

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

@nl

prefLabel

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

@en

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.

@nl

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Annals of Neurology

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Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination

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Alexandra Bright

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Carol Ellen Holmes

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Catherine Feeney

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Charlotte L Alston

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Mark Roberts

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Mellisa Maguire

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Paula Hynd

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Robert W Taylor

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Yan Yiannakou

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Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy

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

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock, 2012

Dysphagia, malnutrition and gastrointestinal problems in patients with mitochondrial disease caused by the m3243A>G mutation.

Emerging drugs for the treatment of gastroparesis.

Neuroimaging of mitochondrial disease.

Ischemic colitis: clinical practice in diagnosis and treatment.

Characteristics of intestinal pseudo-obstruction in patients with mitochondrial diseases

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.

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686-692

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10.1002/ANA.24736

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5

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80

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Andrew M Schaefer

Doug M Turnbull

Robert McFarland

Gráinne S. Gorman

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2016-09-19T00:00:00Z

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27453452

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