Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers. - Wikidata - awgldk - TriplyDB

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

http://www.wikidata.org/entity/Q37623186

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Increased ventricular cerebrospinal fluid lactate in depressed adolescents Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.Assessment of glutamate in striatal subregions in obsessive-compulsive disorder with proton magnetic resonance spectroscopy.Effect of Milnacipran Treatment on Ventricular Lactate in Fibromyalgia: A Randomized, Double-Blind, Placebo-Controlled Trial.Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes (MELAS): A Case Report and Critical Reappraisal of Treatment Options.Imaging of MELAS.MELAS Syndrome with Cardiac Involvement: A Multimodality Imaging Approach.Elevations of Ventricular Lactate Levels Occur in Both Chronic Fatigue Syndrome and Fibromyalgia.Monitoring clinical progression with mitochondrial disease biomarkers.Biomarkers for Detecting Mitochondrial Disorders.Mitochondrial dysfunction and cerebral metabolic abnormalities in patients with mitochondrial encephalomyopathy subtypes: Evidence from proton MR spectroscopy and muscle biopsy.mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.

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Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

http://www.wikidata.org/entity/Q37623186

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 29 January 2014

@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

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

@en

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

@nl

type

label

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

@en

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

@nl

prefLabel

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

@en

Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.

@nl

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Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers

@en

P2093

Darryl De Vivo

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Kristin Marie Engelstad

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Nora Weiduschat

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Petra Kaufmann

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Salvatore DiMauro

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Xiangling Mao

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P2860

AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation.

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts

N-acetyl-L-aspartic acid: a literature review of a compound prominent in 1H-NMR spectroscopic studies of brain.

Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease.

The use of neuroimaging in the diagnosis of mitochondrial disease.

Increased mitochondrial mass in mitochondrial myopathy mice

Neuroimaging of mitochondrial disease.

Regulation of mitochondrial biogenesis in muscle by endurance exercise.

Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype

Regulation of mitochondrial proliferation in the heart: power-plant failure contributes to cardiac failure in hypertrophy.

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798-805

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10.1212/WNL.0000000000000169

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82

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Dikoma C. Shungu

Veronica J Hinton

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2014-01-29T00:00:00Z

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mitochondrial DNA

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