Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study-Reference-Cited by-同舟云学术

Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study

Published:2016-07-29 Issue:1 Volume:11 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Wente Sarah,Schröder Simone,Buckard Johannes,Büttel Hans-Martin,von Deimling Florian,Diener Wilfried,Häussler Martin,Hübschle Susanne,Kinder Silvia,Kurlemann Gerhard,Kretzschmar Christoph,Lingen Michael,Maroske Wiebke,Mundt Dirk,Sánchez-Albisua Iciar,Seeger Jürgen,Toelle Sandra P.,Boltshauser Eugen,Brockmann Knut^ORCID

Funder

Niedersächsisches Ministerium für Wissenschaft und Kultur

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-016-0486-z

Reference28 articles.

1. Cogan DG. A type of congenital ocular motor apraxia presenting jerky head movements. Trans Am Acad Ophthal Otolaryng. 1952;56:853–62.

2. Harris CM, Shawkat F, Russell-Eggitt I, Wilson J, Taylor D. Intermittent horizontal saccade failure ('ocular motor apraxia') in children. Br J Ophthalmol. 1996;80:151–8.

3. Zee DS, Yee RD, Singer HS. Congenital ocular motor apraxia. Brain. 1977;100:581–99.