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Browsing by Author Friedrich, T.

Full Text	Issue Date	Title	Author(s)
	2009	Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.	Tavraz, N.N.; Durr, K.L.; Koenderink, J.B.; Freilinger, T.; Bamberg, E., et al
	2008	Impaired routing of wild type FXYD2 after oligomerisation with FXYD2-G41R might explain the dominant nature of renal hypomagnesemia.	Cairo, E.R.; Friedrich, T.; Swarts, H.G.P.; Knoers, N.V.A.M.; Bindels, R.J.M., et al
	2008	Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.	Tavraz, N.N.; Friedrich, T.; Durr, K.L.; Koenderink, J.B.; Bamberg, E., et al
	2005	Rare missense variants in ATP1A2 in families with clustering of common forms of migraine.	Todt, U.; Dichgans, M.; Jurkat-Rott, K.; Heinze, A.; Zifarelli, G., et al
	2005	Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation.	Koenderink, J.B.; Zifarelli, G.; Qiu, L.; Schwarz, W.; Pont, J.J.H.H.M. de, et al
	2005	An anaerobic mitochondrion that produces hydrogen	Boxma, B.; Graaf, R.M. de; Staay, G.W.M. van der; Alen, T.A. van; Ricard, G., et al