<?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%">HUNG, NGUYEN DUY</style></author><author><style face="normal" font="default" size="100%">DUC, NGUYEN MINH</style></author><author><style face="normal" font="default" size="100%">VAN, NGUYEN THANH</style></author><author><style face="normal" font="default" size="100%">DUNG, LE THANH</style></author><author><style face="normal" font="default" size="100%">HA, HOANG DUC</style></author><author><style face="normal" font="default" size="100%">HUE, NGUYEN DUY</style></author></authors><secondary-authors></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Vietnamese Case Series of Hirayama Disease</style></title><secondary-title><style face="normal" font="default" size="100%">In Vivo</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2020</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2020-07-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">2153-2157</style></pages><doi><style  face="normal" font="default" size="100%">10.21873/invivo.12022</style></doi><volume><style face="normal" font="default" size="100%">34</style></volume><issue><style face="normal" font="default" size="100%">4</style></issue><abstract><style  face="normal" font="default" size="100%">Background/Aim: Hirayama disease, a rare neurological disorder, is characterized by progressive, asymmetric muscle atrophy of the forearm and hand in young male patients. Case Report: We noted two cases of Hirayama disease that appeared in the right upper limb and identified the cervical neutral and flexion position magnetic resonance imaging (MRI) characteristics. Conclusion: In the flexion posture, the cervical MRI allows early diagnosis of Hirayama disease and should be considered in patients with the typical clinical symptoms.</style></abstract></record></records></xml>