Results 81 to 90 of about 34,604,755 (154)

The genetic relationship between epilepsy and hemiplegic migraine

, 2017
Yiqing Huang,1 Hai Xiao,1 Xingyue Qin,1 Yuan Nong,1 Donghua Zou,2 Yuan Wu3 1Department of Neurology, Guigang City People’s Hospital and the Eighth Affiliated Hospital of Guangxi Medical University, Guigang, People’s Republic of China ...
Huang Y, Xiao H, Qin X, Nong Y, Zou D, Wu Y   +5 more
core  

Transient nonverbal learning disorder in a child suffering from Familial Hemiplegic Migraine

, 2011
Objective: To study the link between nonverbal learning disorder and right cerebral hemisphere dysfunction due to migraine attack in a case of Familial Hemiplegic Migraine.
Barbara Podestà, Daniela Marenco, Stefano Calzolari, Eleonora Briatore, Andrea Boghi   +4 more
core   +1 more source

Mechanisms underlying the increased susceptibility to initiation of cortical spreading depression in a genetic mouse model of migraine

The Journal of Headache and Pain
Background There is evidence from human and animal studies that cortical spreading depression (CSD) is the neurophysiological correlate of migraine aura and a trigger of migraine pain mechanisms.
Marina Vitale, Angelita Tottene, Maral Zarin Zadeh, Daniela Pietrobon   +3 more
doaj   +1 more source

Clinical characterization of a novel ATP1A2 p.Gly615Glu mutation in nine family members with familial hemiplegic migraine

Familial hemiplegic migraine type 2 results from pathogenic variants in the ATP1A2 gene, which encodes for a catalytic subunit of sodium/potassium ATPase.
Calabresi, Paolo, Romozzi, Marina, Vollono, Catello, Spartano, Serena, L'Erario, Federica Francesca, Sanginario, Pasquale, Tiziano, Francesco Danilo   +6 more
core   +1 more source

ePoster

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Familial Hemiplegic Migraine

, 2007
Familial hemiplegic migraine (FHM) is a rare and genetically heterogeneous autosomal dominant subtype of migraine with aura. Mutations in the genes CACNA1A and SCAA 1A, encoding the pore-forming alpha(1) subunits of the neuronal voltage-gated Ca2 ...
PIETROBON, DANIELA
core   +1 more source

ePosters Virtual

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Calcitonin gene-related peptide does not cause migraine attacks in patients with familial hemiplegic migraine

, 2011
Calcitonin gene-related peptide (CGRP) is a key molecule in migraine pathogenesis. Intravenous CGRP triggers migraine-like attacks in patients with migraine with aura and without aura.
Jes Olesen, Ashina, Messoud, Jakob M. Hansen, Lise L. Thomsen, Thomsen, Lise L, Olesen, Jes, Messoud Ashina, Hansen, Jakob M   +7 more
core   +1 more source

Developing a pathway to clinical trials for -related epilepsies: A patient organization perspective

Therapeutic Advances in Rare Disease
CACNA1A-related disorders are rare neurodevelopmental disorders linked to variants in the CACNA1A gene. This gene encodes the α1 subunit of the P/Q-type calcium channel Cav2.1, which is globally expressed in the brain and crucial for fast synaptic ...
Pangkong M. Fox, Sunitha Malepati, Lisa Manaster, Elsa Rossignol, Jeffrey L. Noebels   +4 more
doaj   +1 more source

Voltage-gated sodium channels in the nervous system: Molecular physiology to therapeutic interventions

Neural Regeneration Research
Voltage-gated sodium channels are essential ionic-conductance pathways in the nervous system, which play an irreplaceable role in modulating neuronal excitability and signal transduction.
Ni Li, Lin Yan, Anna Peng, Xuefei Fu, Huan Qin, Kai Yao   +5 more
doaj   +1 more source