<?xml version='1.0' encoding='UTF-8'?><xml><records><record><source-app name="HighWire" version="7.x">Drupal-HighWire</source-app><ref-type name="Journal Article">17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mousali, Yahya M.</style></author><author><style face="normal" font="default" size="100%">Obeid, Tahir</style></author><author><style face="normal" font="default" size="100%">Alshamy, Abdulrahman M.</style></author><author><style face="normal" font="default" size="100%">Abdullah, Layla S.</style></author></authors><secondary-authors></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Cerebellar syndromes as a late presentation of Langerhans cell histiocytosis</style></title><secondary-title><style face="normal" font="default" size="100%">Neurosciences Journal</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2004</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2004-10-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">309-311</style></pages><volume><style face="normal" font="default" size="100%">9</style></volume><issue><style face="normal" font="default" size="100%">4</style></issue><abstract><style  face="normal" font="default" size="100%">We report a patient with late onset ataxia who was initially labeled as idiopathic diabetes insipidus for many years. Pathological and radiological investigations revealed Langerhans cell histiocytosis. This case report aims to draw the attention of physicians to this delayed and rare presentation.</style></abstract></record></records></xml>