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Final Programme - iuphar

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FC12 Ion channelopathies:<br />

New windows on complex disease and therapy<br />

Leader: William A Catterall, (USA)<br />

FC12.1 Ion channelopathies in the brain: inherited epilepsy and migraine<br />

Chairs: William A Catterall, (USA) & Daniela Pietrobon, (Italy)<br />

09:30 - 09:55 FC12.1.1 Sodium channelopathies and epilepsy<br />

Ingrid Scheffer, (Australia)<br />

09:55 - 10:20 FC12.1.2 Mechanisms of hyperexcitability, febrile seizure, and ataxia in a mouse model of severe<br />

myoclonic epilepsy of infancy<br />

William A Catterall, (USA)<br />

10:20 - 10:45 FC12.1.3 Functional effects of sodium channel mutations in inherited epilepsy and migraine<br />

Massimo Mantegazza, (Italy)<br />

10:45 - 11:15 COFFEE BREAK<br />

11:15 - 11:40 FC12.1.4 Gain-of-function mutations of calcium channels in familial hemiplegic migraine<br />

Daniela Pietrobon, (Italy)<br />

11:40 - 11:55 FC12.1.5 Free Communication Presentation:<br />

Tyrosine nitration of voltage-dependent calcium channels in experimental colitis.<br />

Hamid Akbarali, (USA), G Ross, M Kang<br />

11:55 - 12:10 FC12.1.6 Free Communication Presentation:<br />

L-type calcium channels dominate the quantal catecholamine release in rat embryo<br />

cromafín cells stimulated with potassium or hypoxia<br />

Antonio MG de Diego, (Spain), JC Fernandez-Morales, AG Garcia<br />

94 Wednesday 21 July ■ 09:30 - 12:15 ■ Meeting Room 20

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