Disease: Hemiplegic migraine- familial type 1
- A hyperexcitability phenotype in mouse trigeminal sensory neurons expressing the R192Q Cacna1a missense mutation of familial hemiplegic migraine type-1
- A novel CACNA1A R2201W variant in a woman with hemiplegic migraine
- Activity-dependent calcium, oxygen, and vascular responses in a mouse model of familial hemiplegic migraine type 1
- Acute headache attributed to ischemic stroke: assessment of its characteristics and associated factors
- Assessing the performances of a chatbot to collect real-life data of patients suffering from primary headache disorders
- Associations between migraine and major cardiovascular events in type 2 diabetes mellitus
- Astrocytic Glutamate Transporters and Migraine
- Basal astrocyte and microglia activation in the central nervous system of Familial Hemiplegic Migraine Type I mice
- Ca<sub>V</sub>2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury
- CADASIL mutations sensitize the brain to ischemia via spreading depolarizations and abnormal extracellular potassium homeostasis
- Caffeine does not affect susceptibility to cortical spreading depolarization in mice
- Cerebrovascular function in tension-type headache and migraine with or without aura: Transcranial Doppler study
- Changes in Plasma Lipid Levels Following Cortical Spreading Depolarization in a Transgenic Mouse Model of Familial Hemiplegic Migraine
- Channeling headache: novel findings in the study of Ca(2+)-channels and FHM-1
- Characterization of persistent post-traumatic headache and management strategies in adolescents and young adults following mild traumatic brain injury
- Clinical characteristics and perfusion-computed tomography alterations in a series of patients with migraine with aura attended as stroke code
- Clinical Characteristics of Headache in Multiple Sclerosis Patients: A Cross-Sectional Study
- Complex Partial Seizure
- Concomitant Calcium Channelopathies Involving <em>CACNA1A</em> and <em>CACNA1F:</em> A Case Report and Review of the Literature
- Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A
- Cortical spreading depression can be triggered by sensory stimulation in primed wild type mouse brain: a mechanistic insight to migraine aura generation
- Cross-sectional, hospital-based analysis of headache types using ICHD-3 criteria in the Middle East, Asia, and Africa: the Head-MENAA study
- Debate: differences and similarities between tension-type headache and migraine
- Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: a Fos protein study
- Diversity of CACNA1A-related disorders
- Drosophila CaV2 channels harboring human migraine mutations cause synapse hyperexcitability that can be suppressed by inhibition of a Ca2+ store release pathway
- Effect of acupuncture treatment on nonketotic hyperglycemic hemichorea-hemiballismus: a case report
- Efficacy of contralateral acupuncture in women with migraine without aura: protocol for a randomised controlled trial
- Efficacy of Lasmiditan Across Patient and Migraine Characteristics in Japanese Patients with Migraine: A Secondary Analysis of the MONONOFU Trial
- Enlightening the association between TNF-α -308 G > A and migraine: a meta-analysis with meta-regression and trial sequential analysis
- Expression and function of calcitonin gene-related peptide (CGRP) receptors in trigeminal ganglia of R192Q Cacna1a knock-in mice
- Familial "Diplegic" Migraine - Description of a Family With a Novel CACNA1A Mutation
- Familial hemiplegic migraine type 1 mutations W1684R and V1696I alter G protein-mediated regulation of Ca(V)2.1 voltage-gated calcium channels
- Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice
- Galassi type III arachnoid cyst presenting as a migraine of weariness
- Headache in Children and Adolescents: The Association between Screen Time and Headache within a Clinical Headache Population
- Headache Worsening after COVID-19 Vaccination: An Online Questionnaire-Based Study on 841 Patients with Migraine
- Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases
- Hypercontractile Cardiac Phenotype in Mice with Migraine-Associated Mutation in the Na<sup>+</sup>,K<sup>+</sup>-ATPase α<sub>2</sub>-Isoform
- Hyperpolarization-activated current I<sub>h</sub> in mouse trigeminal sensory neurons in a transgenic mouse model of familial hemiplegic migraine type-1
- In vivo imaging reveals that pregabalin inhibits cortical spreading depression and propagation to subcortical brain structures
- Increased visinin-like protein-1, YKL-40, lipocalin-2, and IL-23 levels in patients with migraine
- Inhibition of the P2X7-PANX1 complex suppresses spreading depolarization and neuroinflammation
- Instrumented gait analysis defines the walking signature of CACNA1A disorders
- Large-scale mass spectrometry imaging investigation of consequences of cortical spreading depression in a transgenic mouse model of migraine
- Loss of inhibition by brain natriuretic peptide over P2X3 receptors contributes to enhanced spike firing of trigeminal ganglion neurons in a mouse model of familial hemiplegic migraine type-1
- Management and behavior-modifying recommendation effects in childhood headache
- mBrain: towards the continuous follow-up and headache classification of primary headache disorder patients
- Migraine (<em>Shaqeeqa</em>) and its management in Unani medicine
- Migraine headache in Sudan
- Migraine in physicians and final year medical students: A cross-sectional insight into prevalence, self-awareness, and knowledge from Pakistan
- Migraine Medications
- Migraine Type-Dependent Patterns of Brain Activation After Facial and Intranasal Trigeminal Stimulation
- Migraine with prolonged aphasic aura associated with a CACNA1A mutation: A case report and narrative review
- Migraine-Associated Mutation in the Na,K-ATPase Leads to Disturbances in Cardiac Metabolism and Reduced Cardiac Function
- Migraine-Associated Vertigo
- Next-generation sequencing identified a novel CACNA1A I1379F variant in a familial hemiplegic migraine type 1 pedigree: A case report
- Nimodipine accelerates the restoration of functional hyperemia during spreading oligemia
- Occipital bending in migraine with visual aura
- Optogenetic cortical spreading depolarization induces headache-related behaviour and neuroinflammatory responses some prolonged in familial hemiplegic migraine type 1 mice
- Pediatric vestibular migraine: Diagnosis according to ICHD-3 criteria and the effectiveness of short-term CH prophylaxis
- Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes
- Presentation, Etiology, Outcome, and Differentiation of Visual Semiology of Adult Occipital Epilepsy From Visual Aura of Migraine Headache: A Prospective Study in a Tertiary Care Center in Bangladesh
- Presynaptic CaV2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held
- Prevalence of migraine in adults with celiac disease: A case control cross-sectional study
- Primary headache epidemiology in children and adolescents: a systematic review and meta-analysis
- Primary headache types in adult epilepsy patients
- Primary headache with onset in childhood and adolescence: natural history and prognostic factors in a Portuguese population
- Profiling the Spectrum of Headache Disorders on 440 Breast Cancer Patients: Highlights on Clinical and Pathological Mechanisms
- Progressive Ataxia with Hemiplegic Migraines: a Phenotype of CACNA1A Missense Mutations, Not CAG Repeat Expansions
- Relationship between sleep problems and headaches among adolescents: Pelotas 2004 Birth cohort
- Repeated encephalopathy and hemicerebral atrophy in a patient with familial hemiplegic migraine type 1
- RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice
- Simple Partial Seizure
- Spontaneous and optogenetically induced cortical spreading depolarization in familial hemiplegic migraine type 1 mutant mice
- Stroke-prone salt-sensitive spontaneously hypertensive rats show higher susceptibility to spreading depolarization (SD) and altered hemodynamic responses to SD
- Symptoms and patterns of symptom propagation in incipient ischemic stroke and migraine aura
- Synaptic alterations in visual cortex reshape contrast-dependent gamma oscillations and inhibition-excitation ratio in a genetic mouse model of migraine
- The applicability research of the diagnostic criteria for 10.2 Heamodialysis-related headache in the international classification of headache disorders-3<sup>rd</sup> edition
- The association between gastro-oesophageal reflux and migraine in the paediatric population: a multicentre case-control study
- The Association between Migraine and Fetal-Type Posterior Cerebral Artery in Patients with Ischemic Stroke
- The bidirectional temporal relationship between headache and affective disorders: longitudinal data from the HUNT studies
- The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients
- The complexities of CACNA1A in clinical neurogenetics
- The Epidemiology of Primary Headache Disorders
- The familial hemiplegic migraine type 1 mutation K1336E affects direct G protein-mediated regulation of neuronal P/Q-type Ca2+ channels
- The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications
- The mechanism of functional up-regulation of P2X3 receptors of trigeminal sensory neurons in a genetic mouse model of familial hemiplegic migraine type 1 (FHM-1)
- The neuropsychiatric phenotype in CACNA1A mutations: a retrospective single center study and review of the literature
- Time course of downbeat positioning nystagmus in familial hemiplegic migraine type 1 treated with acetazolamide
- Trigeminal ganglion neuron subtype-specific alterations of Ca(V)2.1 calcium current and excitability in a Cacna1a mouse model of migraine
- Trigeminovascular calcitonin gene-related peptide function in Cacna1a R192Q-mutated knock-in mice
- Two Children with Early-Onset Strokes and Intractable Epilepsy, Both with <em>CACNA1A</em> Mutations
- Type and Severity of Migraine Determines Risk of Atrial Fibrillation in Women
- Ultrastructural changes in microvessels in familial hemiplegic migraine with <em>CACNA1A</em> mutation
- Use of combined hormonal contraception and stroke: A case-control study of the impact of migraine type and estrogen dose on ischemic stroke risk
- Verification of a clinical decision support system for the diagnosis of headache disorders based on patient-computer interactions: a multi-center study
- Vestibular migraine
- Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes
- Widespread brain parenchymal HMGB1 and NF-κB neuroinflammatory responses upon cortical spreading depolarization in familial hemiplegic migraine type 1 mice