Dominant optic atrophy

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Standard

Dominant optic atrophy. / Lenaers, Guy; Hamel, Christian; Delettre, Cécile; Amati-Bonneau, Patrizia; Procaccio, Vincent; Bonneau, Dominique; Reynier, Pascal; Milea, Dan.

I: Orphanet Journal of Rare Diseases, Bind 7, 2012, s. 46.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Lenaers, G, Hamel, C, Delettre, C, Amati-Bonneau, P, Procaccio, V, Bonneau, D, Reynier, P & Milea, D 2012, 'Dominant optic atrophy', Orphanet Journal of Rare Diseases, bind 7, s. 46. https://doi.org/10.1186/1750-1172-7-46

APA

Lenaers, G., Hamel, C., Delettre, C., Amati-Bonneau, P., Procaccio, V., Bonneau, D., Reynier, P., & Milea, D. (2012). Dominant optic atrophy. Orphanet Journal of Rare Diseases, 7, 46. https://doi.org/10.1186/1750-1172-7-46

Vancouver

Lenaers G, Hamel C, Delettre C, Amati-Bonneau P, Procaccio V, Bonneau D o.a. Dominant optic atrophy. Orphanet Journal of Rare Diseases. 2012;7:46. https://doi.org/10.1186/1750-1172-7-46

Author

Lenaers, Guy ; Hamel, Christian ; Delettre, Cécile ; Amati-Bonneau, Patrizia ; Procaccio, Vincent ; Bonneau, Dominique ; Reynier, Pascal ; Milea, Dan. / Dominant optic atrophy. I: Orphanet Journal of Rare Diseases. 2012 ; Bind 7. s. 46.

Bibtex

@article{14e99cfa48a8430eac6d4774b027a3bf,
title = "Dominant optic atrophy",
abstract = "DEFINITION OF THE DISEASE: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic condition characterized by a bilateral degeneration of the optic nerves, causing insidious visual loss, typically starting during the first decade of life. The disease affects primary the retinal ganglion cells (RGC) and their axons forming the optic nerve, which transfer the visual information from the photoreceptors to the lateral geniculus in the brain.",
author = "Guy Lenaers and Christian Hamel and C{\'e}cile Delettre and Patrizia Amati-Bonneau and Vincent Procaccio and Dominique Bonneau and Pascal Reynier and Dan Milea",
year = "2012",
doi = "10.1186/1750-1172-7-46",
language = "English",
volume = "7",
pages = "46",
journal = "Orphanet Journal of Rare Diseases",
issn = "1750-1172",
publisher = "BioMed Central",

}

RIS

TY - JOUR

T1 - Dominant optic atrophy

AU - Lenaers, Guy

AU - Hamel, Christian

AU - Delettre, Cécile

AU - Amati-Bonneau, Patrizia

AU - Procaccio, Vincent

AU - Bonneau, Dominique

AU - Reynier, Pascal

AU - Milea, Dan

PY - 2012

Y1 - 2012

N2 - DEFINITION OF THE DISEASE: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic condition characterized by a bilateral degeneration of the optic nerves, causing insidious visual loss, typically starting during the first decade of life. The disease affects primary the retinal ganglion cells (RGC) and their axons forming the optic nerve, which transfer the visual information from the photoreceptors to the lateral geniculus in the brain.

AB - DEFINITION OF THE DISEASE: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic condition characterized by a bilateral degeneration of the optic nerves, causing insidious visual loss, typically starting during the first decade of life. The disease affects primary the retinal ganglion cells (RGC) and their axons forming the optic nerve, which transfer the visual information from the photoreceptors to the lateral geniculus in the brain.

U2 - 10.1186/1750-1172-7-46

DO - 10.1186/1750-1172-7-46

M3 - Journal article

C2 - 22776096

VL - 7

SP - 46

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

SN - 1750-1172

ER -

ID: 48527053