Neuropathies optiques héréditaires

Forskning

Neuropathies optiques héréditaires

Research output: Contribution to journal › Journal article › Research › peer-review

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Neuropathies optiques héréditaires. / Milea, D; Verny, C.

In: Revue Neurologique, Vol. 168, No. 10, 2012, p. 706-9.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Milea, D & Verny, C 2012, 'Neuropathies optiques héréditaires', Revue Neurologique, vol. 168, no. 10, pp. 706-9. https://doi.org/10.1016/j.neurol.2012.08.005

APA

Milea, D., & Verny, C. (2012). Neuropathies optiques héréditaires. Revue Neurologique, 168(10), 706-9. https://doi.org/10.1016/j.neurol.2012.08.005

Vancouver

Milea D, Verny C. Neuropathies optiques héréditaires. Revue Neurologique. 2012;168(10):706-9. https://doi.org/10.1016/j.neurol.2012.08.005

Author

Milea, D ; Verny, C. / Neuropathies optiques héréditaires. In: Revue Neurologique. 2012 ; Vol. 168, No. 10. pp. 706-9.

Bibtex

@article{904bcef0fd8f447eabd9e8f1e272da0b,

title = "Neuropathies optiques h{\'e}r{\'e}ditaires",

abstract = "Hereditary optic neuropathies are a group of heterogeneous conditions affecting both optic nerves, with an autosomal dominant, autosomal recessive, X-related or mitochondrial transmission. The two most common non-syndromic hereditary optic neuropathies (Leber's hereditary optic neuropathy and autosomal dominant optic atrophy) are very different in their clinical presentation and their genetic transmission, leading however to a common, non-specific optic nerve atrophy. Beyond the optic atrophy-related visual loss, which is the clinical hallmark of this group of diseases, other associated neurological signs are increasingly recognized.",

author = "D Milea and C Verny",

note = "Copyright {\textcopyright} 2012. Published by Elsevier Masson SAS.",

year = "2012",

doi = "10.1016/j.neurol.2012.08.005",

language = "Fransk",

volume = "168",

pages = "706--9",

journal = "Revue Neurologique",

issn = "0035-3787",

publisher = "Elsevier Masson",

number = "10",

}

RIS

TY - JOUR

T1 - Neuropathies optiques héréditaires

AU - Milea, D

AU - Verny, C

PY - 2012

Y1 - 2012

N2 - Hereditary optic neuropathies are a group of heterogeneous conditions affecting both optic nerves, with an autosomal dominant, autosomal recessive, X-related or mitochondrial transmission. The two most common non-syndromic hereditary optic neuropathies (Leber's hereditary optic neuropathy and autosomal dominant optic atrophy) are very different in their clinical presentation and their genetic transmission, leading however to a common, non-specific optic nerve atrophy. Beyond the optic atrophy-related visual loss, which is the clinical hallmark of this group of diseases, other associated neurological signs are increasingly recognized.

AB - Hereditary optic neuropathies are a group of heterogeneous conditions affecting both optic nerves, with an autosomal dominant, autosomal recessive, X-related or mitochondrial transmission. The two most common non-syndromic hereditary optic neuropathies (Leber's hereditary optic neuropathy and autosomal dominant optic atrophy) are very different in their clinical presentation and their genetic transmission, leading however to a common, non-specific optic nerve atrophy. Beyond the optic atrophy-related visual loss, which is the clinical hallmark of this group of diseases, other associated neurological signs are increasingly recognized.

U2 - 10.1016/j.neurol.2012.08.005

DO - 10.1016/j.neurol.2012.08.005

M3 - Tidsskriftartikel

VL - 168

SP - 706

EP - 709

JO - Revue Neurologique

JF - Revue Neurologique

SN - 0035-3787

IS - 10

ER -

ID: 48527091