Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q24562797

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A neurodegenerative perspective on mitochondrial optic neuropathies Axonal degeneration in peripheral nerves in a case of Leber hereditary optic neuropathy Mitochondrial myopathies and encephalomyopathies.Extra-visual functional and structural connection abnormalities in Leber's hereditary optic neuropathy.Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?Medical management of hereditary optic neuropathies.Interferons, signal transduction pathways, and the central nervous system.Leber hereditary optic neuropathy Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside.Neuroimaging of mitochondrial disease.Leber's Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited LHON: Mitochondrial Mutations and More.Magnetic resonance imaging, magnetisation transfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy.Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system?Inherited mitochondrial optic neuropathies.POLG1-related and other "mitochondrial Parkinsonisms": an overview.Neurodegeneration as a consequence of failed mitochondrial maintenance.Peripheral neuropathy associated with mitochondrial disease in children.Genetic and phenotypic variability of optic neuropathies.Parkinsonism and inborn errors of metabolism.Impairment of central and peripheral myelin in mitochondrial diseases.Bilateral progressive visual loss in an epileptic, mentally retarded boy.Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA.Leber's 'Plus' in a Korean Patient with 14484/ND6 Mutation.Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation.Auditory function in individuals within Leber's hereditary optic neuropathy pedigrees.Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus.Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy.Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.Patterns of white matter diffusivity abnormalities in Leber's hereditary optic neuropathy: a tract-based spatial statistics study.Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature child.Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis.Movement disorders in mitochondrial disease.Involvement of the Spinal Cord in Mitochondrial Disorders.Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects.Lebersche Optikusneuropathie Mother's curse neutralizes natural selection against a human genetic disease over three centuries

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

http://www.wikidata.org/entity/Q24562797

description

1995 nî lūn-bûn

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1995 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1995 թվականի օգոստոսին հրատարակված գիտական հոդված

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1995年の論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年论文

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Leber's "plus": neurological a ...... 's hereditary optic neuropathy

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Leber's "plus": neurological a ...... 's hereditary optic neuropathy

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Leber's "plus": neurological a ...... 's hereditary optic neuropathy

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Journal of Neurology, Neurosurgery and Psychiatry

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Leber's "plus": neurological a ...... 's hereditary optic neuropathy

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E K Nikoskelainen

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K Huoponen

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M L Savontaus

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P Sonninen

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R J Marttila

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T Lamminen

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V Juvonen

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P2860

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation

An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

Melas: an original case and clinical criteria for diagnosis

Familial dystonia and visual failure with striatal CT lucencies

Leber's hereditary optic neuropathy masquerading as tobacco-alcohol amblyopia.

A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.

Bilateral striatal necrosis, dystonia and optic atrophy in two siblings

LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS

Leber's hereditary optic neuropathy. New genetic considerations.

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160-4

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3248856

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10.1136/JNNP.59.2.160

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2

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59

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7629530

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