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Transient hemiplegia in a patient with migraine: A case of sporadic hemiplegic migraine [PDF]

open access: yesSAGE Open Medical Case Reports
Hemiplegic migraine is a rare form of migraine characterized by aura with unilateral paralysis; however, studies on its treatment are limited. A 39-year-old man with migraine headaches and myofascial pain syndrome was referred to our hospital with ...
Hiroki Maita   +4 more
doaj   +3 more sources

Identification of Copy Number Variations in Familial Hemiplegic Migraine Genes in Suspected Hemiplegic Migraine Patients [PDF]

open access: yesBiomedicines
Background: Familial hemiplegic migraine (FHM) is a rare and severe form of migraine disorder featuring aura symptoms that include hemiplegia during attacks.
Thais Zielke   +4 more
doaj   +2 more sources

Disappearance of aura symptoms in patients with hemiplegic migraine after patent foramen ovale closure: a case report and literature review [PDF]

open access: yesFrontiers in Neurology, 2023
Hemiplegic migraine (HM) can cause significant functional impairment and negatively affect the quality of life of affected individuals. Emerging evidence suggests an association between migraines and congenital patent foramen ovale (PFO), which is a ...
Pian Wang   +4 more
doaj   +2 more sources

Case report When Hemiplegic Migraine Defies Expectations: Diagnostic Complexity in a Rare Genetic Disorder [PDF]

open access: yesCase Reports in Neurology
This case describes a diagnostically challenging presentation of familial hemiplegic migraine, combining prolonged hemiparesis, severe headaches, altered consciousness and fever.
Amandine Goossens   +4 more
doaj   +2 more sources

Reduced Frequency of Prolonged Sporadic Hemiplegic Migraine Attacks Following Fremanezumab Treatment-A Case Report. [PDF]

open access: yesEur J Neurol
A 64‐year‐old man was admitted to the stroke unit with acute aphasia and right‐sided hemiplegia, but imaging showed no signs of acute stroke. Symptoms gradually improved and fully resolved by Day 21, following the onset of a hemicranial headache. A diagnosis of sporadic hemiplegic migraine was made, and no further attacks occurred under fremanezumab ...
Hotz JF   +9 more
europepmc   +2 more sources

A Case Report of Hemiplegic Migraine with Mutation in the ATP1A2 Gene [PDF]

open access: yesPharmacogenomics and Personalized Medicine
Dong-Mei Guan,1,* Yuan-Zhuang Shan,1,* Hao-Tian Zhao,2 Ying Meng,2 Zhong-Rui Yan,2 Hai-Lin Zhang2 1Shandong University of Tradition Chinese Medicine, Jinan, Shandong, People’s Republic of China; 2Department of Neurology, Jining No.1 People’s ...
Guan DM   +5 more
doaj   +2 more sources

Efficacy of anti-calcitonin gene-related peptide monoclonal antibodies in hemiplegic migraine: a case report and review of literature [PDF]

open access: yesFrontiers in Neurology
Hemiplegic migraine (HM) is a rare subtype of migraine with aura characterized by transient unilateral motor weakness during attacks. Although monoclonal antibodies (mABs) targeting the calcitonin gene-related peptide (CGRP) pathway have shown efficacy ...
Máté Héja, László Oláh
doaj   +2 more sources

Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine [PDF]

open access: yesFrontiers in Molecular Neuroscience, 2022
Familial hemiplegic migraine (FHM) is a severe neurogenetic disorder for which three causal genes, CACNA1A, SCN1A, and ATP1A2, have been implicated. However, more than 80% of referred diagnostic cases of hemiplegic migraine (HM) are negative for exonic ...
Neven Maksemous   +12 more
doaj   +2 more sources

Dissociated neurovascular dynamics in ATP1A2-related familial hemiplegic migraine mimicking acute ischemic stroke [PDF]

open access: yesBMC Neurology
Background Hemiplegic migraine (HM) is a rare migraine subtype with motor aura. Familial hemiplegic migraine type 2 (FHM2), caused by ATP1A2 mutations, often mimics acute stroke, making early neuroimaging differentiation critical. While dynamic perfusion
Gha-hyun Lee, Jiyoung Kim, Jae Wook Cho
doaj   +2 more sources

Familial hemiplegic migraine type 2: a case report of an adolescent with ATP1A2 mutation [PDF]

open access: yesFrontiers in Neurology
This study presents a case report of a male adolescent diagnosed with familial hemiplegic migraine type 2 (FHM2), an autosomal dominant inheritance disorder caused by ATP1A2 mutation.
Hui Zhang   +7 more
doaj   +2 more sources

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