Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case (Q73211661)

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2 November 2019

title

Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case (English)

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2 November 2019

author name string

J B Kerrison

1

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2 November 2019

N Howell

2

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2 November 2019

N R Miller

3

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2 November 2019

L Hirst

4

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2 November 2019

W R Green

5

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2 November 2019

publication date

1 October 1995

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2 November 2019

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2 November 2019

volume

102

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2 November 2019

issue

10

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2 November 2019

page(s)

1509-1516

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Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation

2 November 2019

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

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Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

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Leber's hereditary optic atrophy: some clinical and aetiological considerations.

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Further clinical and pathological observations on Leber's optic atrophy

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Hereditary spastic dystonia with Leber's hereditary optic neuropathy: neuropathological findings

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A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

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7 January 2021

Leber hereditary optic neuropathy in Australia

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7 January 2021

Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy

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7 January 2021

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

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The effect of formalin fixation on DNA and the extraction of high-molecular-weight DNA from fixed and embedded tissues

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Molecular genetic analyses of the Tyrolean Ice Man

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Nutritional amblyopia. A histopathologic study with retrospective clinical correlation

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Tobacco-alcohol amblyopia. Further comments on its pathology

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Ocular Fundus in Acute Leber Optic Neuropathy

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7 January 2021

The early phase in Leber hereditary optic atrophy

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Fundus changes in acute malnutritional optic neuropathy

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Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

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Leber's disease and dystonia: a mitochondrial disease

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Studies on the pathogenesis of ischemic cell injury. VI. Mitochondrial flocculent densities in autolysis

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Light- and electron-microscopic studies of intracytoplasmic acidophilic granules in the human locus ceruleus and substantia nigra

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Pigment, abnormal mitochondria and laminar bodies in human sympathetic neurons. An electron microscopical study

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Mitochondrial alterations in the spinal ganglion neurons in ageing rats

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7 January 2021

10.1016/S0161-6420(95)30838-X

Identifiers

DOI

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2 November 2019

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