Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient. (Q38932064)

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7 December 2019

title

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient (English)

1 reference

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hereditary optic neuropathy

7 December 2019

main subject

1 reference

1

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7 December 2019

Rocco Liguori

7

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7 December 2019

author name string

P Barboni

2

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7 December 2019

A Zacchini

3

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7 December 2019

R Mancini

4

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7 December 2019

L Monari

5

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7 December 2019

S Cevoli

6

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7 December 2019

M Sensi

8

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7 December 2019

E Lugaresi

9

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7 December 2019

P Montagna

10

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7 December 2019

publication date

1 October 1998

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Journal of the Neurological Sciences

7 December 2019

number of pages

6

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based on heuristic

inferred from page(s)

published in

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7 December 2019

volume

160

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7 December 2019

issue

2

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7 December 2019

page(s)

183-188

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Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

7 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

The Interaction of Q Analogs, Particularly Hydroxydecyl Benzoquinone (Idebenone), with the Respiratory Complexes of Heart Mitochondria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Remission of Leber's hereditary optic neuropathy with idebenone

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Leber's hereditary optic neuropathy. New genetic considerations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Benzodiazepine sensitivity in Leber's hereditary optic neuroretinopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1

Adenosine triphosphate deficiency: a genre of optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-510X(98)00239-1