<?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%">Buckley, Rita</style></author></authors><secondary-authors><author><style face="normal" font="default" size="100%">Clarke, Bart L.</style></author></secondary-authors></contributors><titles><title><style face="normal" font="default" size="100%">Hypoparathyroidism: Working toward Effective Treatment</style></title><secondary-title><style face="normal" font="default" size="100%">MD Conference Express</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2013</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2013-10-01 00:00:00</style></date></pub-dates></dates><pages><style  face="normal" font="default" size="100%">20-21</style></pages><abstract><style  face="normal" font="default" size="100%">Hypoparathyroidism is a rare endocrine disorder with a wide range of etiologies, including surgery and radioactive iodine therapy. It can be acquired or genetic; curable or permanent. This article describes the differential diagnosis of the disease, summarizes the latest knowledge about the various causes of acquired hypoparathyroidism, and reviews recognized genetic mutations. The article also discusses skeletal and nonskeletal hypoparathyroidism.</style></abstract><number><style face="normal" font="default" size="100%">10</style></number><volume><style face="normal" font="default" size="100%">13</style></volume></record></records></xml>