(Q57252205)

https://api.crossref.org/works/10.1038%2FEYE.1994.102

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

A SEX-LINKED HEREDO-DEGENERATIVE NEUROLOGICAL DISORDER, ASSOCIATED WITH LEBER'S OPTIC ATROPHY. I. CLINICAL STUDIES.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Neurological studies in families with Leber's optic atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Leber hereditary optic neuropathy in Australia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Finger prick blood testing in Leber hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Ocular Fundus in Acute Leber Optic Neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Sensorineural deafness inherited as a tissue specific mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Genetic aspects of antibiotic induced deafness: mitochondrial inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Leber's optic atrophy: VEP and BAEP changes in 16 asymptomatic subjects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Familial dystonia and visual failure with striatal CT lucencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Cardiac arrhythmia and Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

Leber's disease and dystonia: a mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

Bilateral optic neuropathy with remission in young men. Variation on a theme by Leber?

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

THE SIGNIFICANCE OF HEREDITY IN OPHTHALMOLOGY. PRELIMINARY SURVEY OF HEREDITARY EYE DISEASES IN TASMANIA

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

The clinical profile of optic neuritis. Experience of the Optic Neuritis Treatment Trial. Optic Neuritis Study Group

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

Leber's hereditary optic neuropathy in women

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021

Charcot-Marie-Tooth disease with Leber optic atrophy

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1994.102

7 January 2021