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Browsing by Author Stam, A.H.

Full Text	Issue Date	Title	Author(s)
	2009	Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.	Vries, B. de; Stam, A.H.; Kirkpatrick, M.; Molkot, K.R. van; Koenderink, J.B., et al
	2008	CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.	Stam, A.H.; Molkot, K.R. van; Kremer, H.P.H.; Gartner, J.; Brown, J., et al
	2007	Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine	Vries, B. de; Freilinger, T.; Molkot, K.R. van; Koenderink, J.B.; Stam, A.H., et al
	2007	First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.	Molkot, K.R. van; Stam, A.H.; Raman, A.; Koenderink, J.B.; Vries, L.B.A. de, et al
	2007	Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.	Castro, M.J.; Stam, A.H.; Lemos, C.; Barros, J.; Gouveia, R.G., et al
	2006	Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.	Molkot, K.R. van; Stroink, H.; Koenderink, J.B.; Kors, E.E.; Heuvel, J.J.M.W. van den, et al