Medical management of hereditary optic neuropathies. - Wikidata - awgldk - TriplyDB

Medical management of hereditary optic neuropathies.

Medical management of hereditary optic neuropathies.

http://www.wikidata.org/entity/Q33980183

about

Leber hereditary optic neuropathy: current perspectives Natural Product Screening Reveals Naphthoquinone Complex I Bypass Factors.Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.A retrospective analysis of characteristics of visual field damage in patients with Leber's hereditary optic neuropathy.Bone Marrow-Derived Cells as a Therapeutic Approach to Optic Nerve Diseases.Auditory neuropathy--neural and synaptic mechanisms.Macular nerve fibre and ganglion cell layer changes in acute Leber's hereditary optic neuropathy.Optic Nerve.Leber Hereditary Optic Neuropathy: A Mitochondrial Disease Unique in Many Ways.A Meta-analysis of the association between different genotypes (G11778A, T14484C and G3460A) of Leber hereditary optic neuropathy and visual prognosis Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy.The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress.Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathy.Apoptosis inducing factor deficiency causes retinal photoreceptor degeneration. The protective role of the redox compound methylene blue Current and Emerging Treatment Modalities for Leber's Hereditary Optic Neuropathy: A Review of the Literature

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Medical management of hereditary optic neuropathies.

http://www.wikidata.org/entity/Q33980183

description

2014 nî lūn-bûn

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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2014 թվականի հուլիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Medical management of hereditary optic neuropathies.

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Medical management of hereditary optic neuropathies.

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Medical management of hereditary optic neuropathies.

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Medical management of hereditary optic neuropathies.

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Medical management of hereditary optic neuropathies.

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Medical management of hereditary optic neuropathies.

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FNEUR.2014.00141

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Frontiers in Neurology

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Medical management of hereditary optic neuropathies.

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Alfredo Arrigo Sadun

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Michele Carbonelli

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Piero Barboni

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P2860

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews

OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophy

Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

Allotopic expression of mitochondrial-encoded genes in mammals: achieved goal, undemonstrated mechanism or impossible task?

Multi-system neurological disease is common in patients with OPA1 mutations

Safety and efficacy of gene transfer for Leber's congenital amaurosis

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141

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scholarly article

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10.3389/FNEUR.2014.00141

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5

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Valerio Carelli

Chiara La Morgia

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2014-07-31T00:00:00Z

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264866330

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