Results 51 to 60 of about 234,110 (135)

Coexisting typical migraine in familial hemiplegic migraine

, 2010
In contrast to patients with migraine with aura (MA) and migraine without aura (MO), most patients with familial hemiplegic migraine (FHM) do not report migraine-like attacks after pharmacologic provocation with glyceryl trinitrate (GTN), a donor of ...
Hansen, Jakob Møller, Ashina, Messoud, Thomsen, Lise Lykke, Olesen, Jes   +3 more
core   +1 more source

Aura and Stroke: relationship and what we have learnt from preclinical models

The Journal of Headache and Pain, 2019
Background Population-based studies have highlighted a close relationship between migraine and stroke. Migraine, especially with aura, is a risk factor for both ischemic and hemorrhagic stroke.
Muge Yemisci, Katharina Eikermann-Haerter   +1 more
doaj   +1 more source

Trigeminal neuralgia, migraine and sympathetic hyperactivity in a patient with Parry–Romberg syndrome [PDF]

, 2006
Parry–Romberg syndrome is a rare disorder of unknown aetiology that involves slowly progressive but self-limited wasting of subcutaneous tissues on one side of the face, usually in the distribution of a branch of the trigeminal nerve.
Drummond, P.D., Finch, P.M., Hassard, S.
core  

Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: A Fos protein study

Neurobiology of Disease, 2014
Familial hemiplegic migraine type 1 (FHM-1) is a monogenic subtype of migraine with aura caused by missense mutations in the CACNA1A gene, which encodes the pore-forming α1 subunit of voltage-gated neuronal CaV2.1 (P/Q-type) calcium channels.
JungWook Park, HeuiSoo Moon, Simon Akerman, Philip R. Holland, Michele P. Lasalandra, Anna P. Andreou, Michel D. Ferrari, Arn M.J.M. van den Maagdenberg, Peter J. Goadsby   +8 more
doaj   +1 more source

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

Cerebellar Atrophy and Changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family

Frontiers in Cellular Neuroscience, 2017
Background: Immune mechanisms recently emerged as important contributors to migraine pathology with cytokines affecting neuronal excitation. Therefore, elucidating the profile of cytokines activated in various forms of migraine, including those with a ...
Svetlana F. Khaiboullina, Elena G. Mendelevich, Leyla H. Shigapova, Elena Shagimardanova, Guzel Gazizova, Alexey Nikitin, Ekaterina Martynova, Yuriy N. Davidyuk, Enver I. Bogdanov, Oleg Gusev, Oleg Gusev, Oleg Gusev, Arn M. J. M. van den Maagdenberg, Rashid A. Giniatullin, Rashid A. Giniatullin, Albert A. Rizvanov   +15 more
doaj   +1 more source

Astrocytes in Atp1a2‐deficient heterozygous mice exhibit hyperactivity after induction of cortical spreading depression

FEBS Open Bio, 2020
The ATP1A2 coding α2 subunit of Na,K‐ATPase, which is predominantly located in astrocytes, is a causative gene of familial hemiplegic migraine type 2 (FHM2).
Hiroki Sugimoto, Masaaki Sato, Junichi Nakai, Kiyoshi Kawakami   +3 more
doaj   +1 more source

Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant

BMC Neurology, 2020
Background To investigate the genetic and environmental factors responsible for phenotype variability in a family carrying a novel CACNA1A missense mutation.
Rosaria Nardello, Giorgia Plicato, Giuseppe Donato Mangano, Elena Gennaro, Salvatore Mangano, Filippo Brighina, Vincenzo Raieli, Antonina Fontana   +7 more
doaj   +1 more source

Variable manifestations of familial hemiplegic migraine associated with reversible cerebral edema in children

, 2012
Three children with familial hemiplegic migraine presented with right-sided weakness, speech difficulty, altered mental status, and gait abnormalities.
Sharp, Gregory B, Asghar, Sheila J, Glasier, Charles, Milesi-Hallé, Alessandra, Kaushik, Chavvi   +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