Results 91 to 100 of about 54,391 (157)

Familial Hemiplegic Migraine and Recurrent Episodes of Psychosis:A Case Report

, 2015
Familial hemiplegic migraine (FHM) is a rare autosomal dominant form of migraine with motor aura. We present a case report of a father and son with very similar attacks of hemiplegic migraine and recurrent episodes of accompanying psychoses.
Baandrup, Lone, Bendtsen, Lars, van den Maagdenberg, Arn M J M, Bendtsen, L., LaBianca, S., Maagdenberg, A.M.J.M. van den, Baandrup, L., Jensen, Rigmor, LaBianca, Sonja, Jensen, R.   +9 more
core   +1 more source

Mutation analysis of CACNA1A gene in Iranian migrainous and review literatures

Journal of Research in Medical Sciences, 2013
Background: There are contrary results about the role of CACNA1A gene in the causation of common migraine in different populations. However, migraine may be genetically heterogeneous and more studies in different families and populations are required for
Rokhsareh Meamar, Maryam Ostadsharif, Mohammad Saadatnia, Abbas Ghorbani, Nayereh Nouri, Leila Dehghani, Mansoor Salehi   +6 more
doaj  

ePoster

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

ePosters Virtual

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

Mechanisms of increased sensitivity to noise and light in migraine headache [PDF]

, 1993
To determine whether phonophobia is a manifestation of loudness recruitment, the hearing and auditory discomfort thresholds to an 8000 Hz tone were measured during the headache-free interval and again during an attack of migraine in 16 migraine sufferers.
Woodhouse, A., Drummond, P.D.
core  

Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L

, 2017
Background Familial hemiplegic migraine type 3 is a monogenic subtype of migraine caused by missense mutations in the neuronal voltage-gated sodium channel gene SCN1A, with 10 different mutations reported so far.
Eva Auffenberg, Victoria Schubert, Tobias Freilinger, Saskia Biskup, Karin Jurkat-Rott   +4 more
core   +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

Motion sickness and migraine: optokinetic stimulation increases scalp tenderness, pain sensitivity in the fingers and photophobia [PDF]

, 2002
The aim of this study was to determine whether scalp tenderness and photophobia, two well-recognized symptoms of migraine, develop during the motion sickness induced by optokinetic stimulation.
Drummond, P.D.
core  

RHOBTB2-related paroxysmal hemiparesis: From alternating hemiplegia to hemiplegic migraine

: We report a young patient harboring a RHOBTB2 likely pathogenic variant with recurrent episodes of headache, dysautonomia and hemiplegia consistent with hemiplegic migraine. Such episodes were responsive to flunarizine prophylaxis.
Valeriani, Massimiliano, Rossi Espagnet, Camilla, Carboni, Alessia, Innocenti, Alice, Garone, Giacomo, Papetti, Laura, Parisi, Pasquale, Specchio, Nicola   +7 more
core   +1 more source

Sporadic Hemiplegic Migraine. [PDF]

Cureus, 2023
Kana T, Mehjabeen S, Patel N, Kawamj A, Shamim Z.   +4 more
europepmc   +1 more source