<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="6.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">de Vries, B</style></author><author><style face="normal" font="default" size="100%">Freilinger, T</style></author><author><style face="normal" font="default" size="100%">Vanmolkot, K R J</style></author><author><style face="normal" font="default" size="100%">Koenderink, J B</style></author><author><style face="normal" font="default" size="100%">Stam, A H</style></author><author><style face="normal" font="default" size="100%">Terwindt, G M</style></author><author><style face="normal" font="default" size="100%">Babini, E</style></author><author><style face="normal" font="default" size="100%">van den Boogerd, E H</style></author><author><style face="normal" font="default" size="100%">van den Heuvel, J J M W</style></author><author><style face="normal" font="default" size="100%">Frants, R R</style></author><author><style face="normal" font="default" size="100%">Haan, J</style></author><author><style face="normal" font="default" size="100%">Pusch, M</style></author><author><style face="normal" font="default" size="100%">van den Maagdenberg, A M J M</style></author><author><style face="normal" font="default" size="100%">Ferrari, M D</style></author><author><style face="normal" font="default" size="100%">Dichgans, M</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.</style></title><secondary-title><style face="normal" font="default" size="100%">Neurology</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Neurology</style></alt-title></titles><dates><year><style  face="normal" font="default" size="100%">2007</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2007 Dec 4</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">69</style></volume><pages><style face="normal" font="default" size="100%">2170-6</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Familial (FHM) and sporadic (SHM) hemiplegic migraine are severe subtypes of migraine associated with transient hemiparesis. For FHM, three genes have been identified encoding subunits of a calcium channel (CACNA1A), a sodium-potassium pump (ATP1A2), and a sodium channel (SCN1A). Their role in SHM is unknown. Establishing a genetic basis for SHM may further the understanding of its pathophysiology and relationship with common types of migraine. It will also facilitate the often difficult differential diagnosis from other causes of transient hemiparesis.</style></abstract><issue><style face="normal" font="default" size="100%">23</style></issue><custom1><style face="normal" font="default" size="100%">http://www.ncbi.nlm.nih.gov/pubmed/18056581?dopt=Abstract</style></custom1></record></records></xml>