Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.
about
Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations.Mitochondrial myopathies and encephalomyopathies.Update on hereditary optic neuropathy.Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees.Trial end points and natural history in patients with G11778A Leber hereditary optic neuropathy : preparation for gene therapy clinical trial.Treatment of Leber hereditary optic neuropathyPedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.Molecular genetic basis of primary inherited optic neuropathies.Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.Treatment of hereditary optic neuropathies.Genetic and phenotypic variability of optic neuropathies.Identification of small molecules that improve ATP synthesis defects conferred by Leber's hereditary optic neuropathy mutationsLeber Hereditary Optic Neuropathy: Bringing the Lab to the Clinic.A Meta-analysis of the association between different genotypes (G11778A, T14484C and G3460A) of Leber hereditary optic neuropathy and visual prognosisMitochondrial DNA sequence variation in multiple sclerosis.Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.Visual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation.Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings.Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.
P2860
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P2860
Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.
description
1994 nî lūn-bûn
@nan
1994 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Leber's hereditary optic neuro ...... l genotype and visual outcome.
@ast
Leber's hereditary optic neuro ...... l genotype and visual outcome.
@en
type
label
Leber's hereditary optic neuro ...... l genotype and visual outcome.
@ast
Leber's hereditary optic neuro ...... l genotype and visual outcome.
@en
prefLabel
Leber's hereditary optic neuro ...... l genotype and visual outcome.
@ast
Leber's hereditary optic neuro ...... l genotype and visual outcome.
@en
P2093
P2860
P356
P1476
Leber's hereditary optic neuro ...... al genotype and visual outcome
@en
P2093
E M Bleeker-Wagemakers
F A Wijburg
G Zorn-Ende
P A Bolhuis
P2860
P304
P356
10.1136/JMG.31.4.280
P407
P577
1994-04-01T00:00:00Z