Search Results - "Mamsa, H"

A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism by Blanco-Arias, Patricia, Einholm, Anja P., Mamsa, Hafsa, Concheiro, Carla, Gutiérrez-de-Terán, Hugo, Romero, Jesús, Toustrup-Jensen, Mads S., Carracedo, Ángel, Jen, Joanna C., Vilsen, Bente, Sobrido, María-Jesús

“…The Na+/K+-ATPases are ion pumps of fundamental importance in maintaining the electrochemical gradient essential for neuronal survival and function. Mutations…”
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Prolonged hemiplegic episodes in children due to mutations in ATP1A2 by Jen, J C, Klein, A, Boltshauser, E, Cartwright, M S, Roach, E S, Mamsa, H, Baloh, R W

“…Background: Familial hemiplegic migraine (FHM) is an unusual migraine syndrome characterised by recurrent transient attacks of unilateral weakness or paralysis…”
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A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity by Lee, Hane, Jen, Joanna C., Wang, Hui, Chen, Zugen, Mamsa, Hafsa, Sabatti, Chiara, Baloh, Robert W., Nelson, Stanley F.

“…Benign recurrent vertigo (BRV) is a common disorder affecting up to 2% of the adult population and may be etiologically related to migraine because of…”
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