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Vol. 63, No. 4, 2010
Issue release date: April 2010
Section title: Neurological Vignette
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Eur Neurol 2010;63:253

Heterochromia Iridis in Congenital Horner’s Syndrome

Renard D.a · Jeanjean L.b · Labauge P.a
Departments of aNeurology and bOphthalmology, CHU Nîmes, Hôpital Caremeau, Nîmes, France

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Abstract of Neurological Vignette


Author Contacts

Dimitri Renard, MD
Department of Neurology, CHU Nîmes, Hôpital Caremeau
Place du Professeur-Debré
FR–30029 Nîmes Cedex 4 (France)
Tel. +33 4 66 68 32 61, Fax +33 4 66 68 40 16, E-Mail


Article Information

Received: January 5, 2010
Accepted: January 6, 2010
Published online: April 7, 2010
Number of Print Pages : 1


Publication Details

European Neurology

Vol. 63, No. 4, Year 2010 (Cover Date: April 2010)

Journal Editor: Bogousslavsky J. (Montreux)
ISSN: 0014-3022 (Print), eISSN: 1421-9913 (Online)

For additional information:

Article / Publication Details

Received: 1/5/2010
Accepted: 1/6/2010
Published online: 4/7/2010
Issue release date: April 2010

Number of Print Pages: 1
Number of Figures: 1
Number of Tables: 0

ISSN: 0014-3022 (Print)
eISSN: 1421-9913 (Online)

For additional information:

Copyright / Drug Dosage

Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher or, in the case of photocopying, direct payment of a specified fee to the Copyright Clearance Center.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in goverment regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
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