about
Alpers-Huttenlocher syndrome: the role of a multidisciplinary health care teamEpilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review.Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Oxidative stress and mitochondrial dysfunction across broad-ranging pathologies: toward mitochondria-targeted clinical strategies.Co-occurrence of four nucleotide changes associated with an adult mitochondrial ataxia phenotype.Zebrafish lacking functional DNA polymerase gamma survive to juvenile stage, despite rapid and sustained mitochondrial DNA depletion, altered energetics and growthInherited mitochondrial genomic instability and chemical exposures.When to Suspect and How to Diagnose Mitochondrial Disorders?Mitochondrial hepatopathies: advances in genetics, therapeutic approaches, and outcomes.Clinical effects of chemical exposures on mitochondrial function.The spectrum of epilepsy caused by POLG mutations.Alpers-Huttenlocher Syndrome First Presented with Hepatic Failure: Can Liver Transplantation Be Considered as Treatment Option?Late-onset of Alpers-Huttenlocher syndrome: an unusual cause of refractory epilepsy and liver failure.
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մարտին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Alpers-Huttenlocher syndrome
@ast
Alpers-Huttenlocher syndrome
@en
Alpers-Huttenlocher syndrome
@nl
type
label
Alpers-Huttenlocher syndrome
@ast
Alpers-Huttenlocher syndrome
@en
Alpers-Huttenlocher syndrome
@nl
prefLabel
Alpers-Huttenlocher syndrome
@ast
Alpers-Huttenlocher syndrome
@en
Alpers-Huttenlocher syndrome
@nl
P2093
P2860
P3181
P1433
P1476
Alpers-Huttenlocher syndrome
@en
P2093
Bruce H Cohen
Robert K Naviaux
Russell P Saneto
P2860
P304
P3181
P356
10.1016/J.PEDIATRNEUROL.2012.09.014
P407
P577
2013-03-01T00:00:00Z