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(1 - 4 of 4)
Two novel SCNIA mutations identified in families with familial hemiplegic migraine
Weller, C.M.; Pelzer, N.; Vries, B. de; Lopez, M.A.; Fabregues, O. de; Pascual, J.; ... ; Maagdenberg, A.M.J.M. van den 2014
Two novel SCNIA mutations identified in families with familial hemiplegic migraine
Article / Letter to editor
metadata only
Familial hemiplegic migraine treated by sodium valproate and lamotrigine
Pelzer, N.; Stam, A.H.; Carpay, J.A.; Vries, B. de; Maagdenberg, A.M.J.M. van den; Ferrari, M.D.; ... ; Terwindt, G.M. 2014
Familial hemiplegic migraine treated by sodium valproate and lamotrigine
Article / Letter to editor
metadata only
Presynaptic Ca(v)2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held
Inchauspe, C.G.; Urbano, F.J.; Guilmi, M.N. di; Ferrari, M.D.; Maagdenberg, A.M.J.M. van den; Forsythe, I.D.; Uchitel, O.D. 2012
Presynaptic Ca(v)2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held
Article / Letter to editor
metadata only
A long-term follow-up study of 18 patients with sporadic hemiplegic migraine
Stam, A.H.; Louter, M.A.; Haan, J.; Vries, B. de; Maagdenberg, A.M.J.M. van den; Frants, R.R.; ... ; Terwindt, G.M. 2011
A long-term follow-up study of 18 patients with sporadic hemiplegic migraine
Article / Letter to editor
metadata only