(Q72113598)

English

Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team

scientific article published on 01 August 1994

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference

based on heuristic

inferred from title

0 references

hereditary optic neuropathy

1 reference

based on heuristic

inferred from title

author name string

N J Newman

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

A Torroni

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

M D Brown

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

M T Lott

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

M M Fernandez

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

D C Wallace

6

1 reference

Europe PubMed Central

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23 October 2019

language of work or name

0 references

publication date

1 August 1994

1 reference

Europe PubMed Central

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23 October 2019

American Journal of Ophthalmology

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

118

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Europe PubMed Central

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23 October 2019

2

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23 October 2019

158-168

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

describes a project that uses

mitochondrial DNA

1 reference

based on heuristic

inferred from title

LEBER'S DISEASE IN THE NETHERLANDS.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Leber's hereditary optic neuropathy. New genetic considerations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Cytochrome b mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Tobacco amblyopia

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Tobacco-alcohol amblyopia: a proposed biochemical basis for pathogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Tobacco amblyopia: a clinical manifestation of vitamin-B12 deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Cyanide in human disease: A review of clinical and laboratory evidence

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Whole blood cyanide levels in patients with tobacco amblyopia

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Neurological conditions resulting from prolonged and severe dietary restriction; case reports in prisoners-of-war, and general review

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Fundus changes in acute malnutritional optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Neuropathology of experimental vitamin B12 deficiency in monkeys

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Leber's hereditary optic atrophy: further evidence for a defect of cyanide metabolism?

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

Neurologic Aspects of Cobalamin Deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972895-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0002-9394(14)72895-8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8053461%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

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