about
Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model.The many faces of paediatric mitochondrial disease on neuroimaging.Hypoxia as a therapy for mitochondrial disease.Alterations in the E3 ligases Parkin and CHIP result in unique metabolic signaling defects and mitochondrial quality control issues.Leigh syndrome: One disorder, more than 75 monogenic causes.Effects of Tributyltin Chloride on Cybrids with or without an ATP Synthase Pathologic Mutation.Inherited and acquired disorders of myelin: The underlying myelin pathology.The Emerging Role of Mitochondrial Targeting in Kidney Disease.Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque.Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy.Mitochondrial diseases: the contribution of organelle stress responses to pathology.Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a Drosophila Model of Leigh Syndrome.Revealing the Complexity of Mitochondrial DNA-Related Disorders.Spasticity secondary to Leigh syndrome managed with selective dorsal rhizotomy: a case report.
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Leigh syndrome: neuropathology and pathogenesis.
@en
type
label
Leigh syndrome: neuropathology and pathogenesis.
@en
prefLabel
Leigh syndrome: neuropathology and pathogenesis.
@en
P2093
P2860
P1476
Leigh syndrome: neuropathology and pathogenesis
@en
P2093
Anders Paetau
Matthew J Bird
Pirjo Isohanni
P2860
P304
P356
10.1097/NEN.0000000000000195
P577
2015-06-01T00:00:00Z