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Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum DisorderGastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Unraveling the molecular signatures of oxidative phosphorylation to cope with the nutritionally changing metabolic capabilities of liver and muscle tissues in farmed fish.Mitochondrial disease: genetics and management.The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes.Adrenal Insufficiency in Mitochondrial Disease: A Rare Case of GFER-Related Mitochondrial Encephalomyopathy and Review of the Literature.Mitochondrial disease and endocrine dysfunction.Genetics of mitochondrial dysfunction and infertility.Risk factors for poor bone health in primary mitochondrial disease.Endocrine Dysfunctions in Patients with Inherited Metabolic Diseases.Low prevalence of patients with mitochondrial disease in the German/Austrian DPV diabetes registry.Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.Mutation in the nuclear-encoded mitochondrial isoleucyl-tRNA synthetase IARS2 in patients with cataracts, growth hormone deficiency with short stature, partial sensorineural deafness, and peripheral neuropathy or with Leigh syndrome.Childhood cerebral X-linked adrenoleukodystrophy with atypical neuroimaging abnormalities and a novel mutation.Reply to: Reduced Bone Mineral Density in m.3243A>G Carriers May Be Multifactorial.A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism.Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study.Endocrine Disorders in Primary Mitochondrial Disease.Mitochondrial disease: an uncommon but important cause of diabetes mellitusMitochondrial diseases caused by mtDNA mutations: a mini-review
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 13 June 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Endocrine disorders in mitochondrial disease.
@en
Endocrine disorders in mitochondrial disease.
@nl
type
label
Endocrine disorders in mitochondrial disease.
@en
Endocrine disorders in mitochondrial disease.
@nl
prefLabel
Endocrine disorders in mitochondrial disease.
@en
Endocrine disorders in mitochondrial disease.
@nl
P2860
P921
P1476
Endocrine disorders in mitochondrial disease
@en
P2093
Mark Walker
Robert W Taylor
P2860
P356
10.1016/J.MCE.2013.06.004
P5008
P577
2013-06-13T00:00:00Z