(Q71968996)

English

Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation

scientific article published on 01 May 1995

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scholarly article

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22 October 2019

Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation (English)

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22 October 2019

Leber hereditary optic neuropathy

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multiple sclerosis

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based on heuristic

inferred from title

DNA mutational analysis

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4 July 2024

author name string

N. K. Olsen

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4 July 2024

A. W. Hansen

2

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4 July 2024

S. Nørby

3

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4 July 2024

A. L. Edal

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4 July 2024

J. R. Jørgensen

5

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4 July 2024

T. Rosenberg

6

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4 July 2024

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publication date

1 May 1995

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22 October 2019

full work available at URL

https://doi.org/10.1111/j.1600-0404.1995.tb07016.x

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4 July 2024

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1600-0404.1995.tb07016.x

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10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1995.tb07016.x/fullpdf

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Acta Neurologica Scandinavica

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22 October 2019

91

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22 October 2019

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22 October 2019

326-329

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22 October 2019

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1

1 reference

10.1111/J.1600-0404.1995.TB07016.X

https://api.crossref.org/works/10.1111/J.1600-0404.1995.TB07016.X

4 July 2024

The inheritance of Leber's disease. A genealogical follow-up study

2

1 reference

10.1111/J.1600-0404.1995.TB07016.X

https://api.crossref.org/works/10.1111/J.1600-0404.1995.TB07016.X

4 July 2024

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

3

1 reference

10.1111/J.1600-0404.1995.TB07016.X

https://api.crossref.org/works/10.1111/J.1600-0404.1995.TB07016.X

4 July 2024

Diseases of the mitochondrial DNA.

4

1 reference

10.1111/J.1600-0404.1995.TB07016.X

https://api.crossref.org/works/10.1111/J.1600-0404.1995.TB07016.X

4 July 2024

Sequence and organization of the human mitochondrial genome

5

1 reference

10.1111/J.1600-0404.1995.TB07016.X

https://api.crossref.org/works/10.1111/J.1600-0404.1995.TB07016.X

4 July 2024

The elucidation of the human mitochondrial genome: a historical perspective

6

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

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

9

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

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

10

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Leber's hereditary optic neuropathy. New genetic considerations

11

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy

12

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

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

13

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

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

14

1 reference

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4 July 2024

Mutation-specific PCR: a rapid and inexpensive diagnostic method, as exemplified by mitochondrial DNA analysis in Leber's hereditary optic neuropathy

15

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Leber's disease. V

17

1 reference

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4 July 2024

Neurological studies in families with Leber's optic atrophy

18

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

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

19

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Association of the 11778 mitochondrial DNA mutation and demyelinating disease

20

1 reference

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4 July 2024

Mitochondrial encephalomyopathies

21

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Magnetic resonance imaging in Leber's optic neuropathy

22

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Leber's hereditary optic neuropathy and complex I deficiency in muscle.

23

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

24

1 reference

10.1111/J.1600-0404.1995.TB07016.X

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4 July 2024

Identifiers

10.1111/J.1600-0404.1995.TB07016.X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7639060%20AND%20SRC:MED&resulttype=core&format=json

22 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:7639060%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

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