Results 101 to 110 of about 234,110 (135)

Familial hemiplegic migraine in a child with seizure disorder: clinical history is the key to diagnosis. [PDF]

BMJ Case Rep, 2019
Balakrishnan P, Katakam PK, Hegde AP.
europepmc   +1 more source

Familial Hemiplegic Migraine (FHM) with Transient Psychotic Symptoms: A Case Report and Literature Review. [PDF]

Turk Psikiyatri Derg
Öz T, Gürel ŞC.
europepmc   +1 more source

A structural analysis of the splice-specific functional impact of the pathogenic familial hemiplegic migraine type 1 S218L mutation on Ca_v2.1 P/Q-type channel gating. [PDF]

Mol Brain
Sack AS, Samera GJ, Hissen A, Wester RJ, Garcia E, Adams PJ, Snutch TP.   +6 more
europepmc   +1 more source

Relief Following Chronic Stress Augments Spreading Depolarization Susceptibility in Familial Hemiplegic Migraine Mice. [PDF]

Neuroscience, 2019
Balkaya M, Seidel JL, Sadeghian H, Qin T, Chung DY, Eikermann-Haerter K, van den Maagdenberg AMJM, Ferrari MD, Ayata C.   +8 more
europepmc   +1 more source

Late sodium current blocker GS967 inhibits persistent currents induced by familial hemiplegic migraine type 3 mutations of the SCN1A gene. [PDF]

J Headache Pain, 2019
Barbieri R, Bertelli S, Pusch M, Gavazzo P.   +3 more
europepmc   +1 more source

Cortical spreading depression and familial hemiplegic migraine 2015. [PDF]

J Headache Pain, 2015
Pietrobon D.
europepmc   +1 more source

A Migraine-Associated Na/K-ATPase Mutation Disrupts Hepatic Glucose Uptake and Peripheral Metabolism in Mice. [PDF]

Acta Physiol (Oxf)
Pessoa MT, Sidarala V, Pierre SV.
europepmc   +1 more source

Early-onset familial hemiplegic migraine due to a novel SCN1A mutation. [PDF]

Cephalalgia, 2016
Fan C, Wolking S, Lehmann-Horn F, Hedrich UB, Freilinger T, Lerche H, Borck G, Kubisch C, Jurkat-Rott K.   +8 more
europepmc   +1 more source

Migraine in children and adolescents. [PDF]

Dev Med Child Neurol
Abu-Arafeh I.
europepmc   +1 more source

Impaired Hepatic Glucose Metabolism Is Associated With Glucose Intolerance in Mice Carrying α₂ Isoform Na,K-ATPase Mutation. [PDF]

Acta Physiol (Oxf)
Staehr C, Nguyen TD, Pedersen TM, Vendelbo M, Beck HC, Kjolby M, Rajanathan R, Bouzinova EV, Jessen N, Jeppesen PB, Chibalin AV, Matchkov VV.   +11 more
europepmc   +1 more source