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- Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
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- Alterations in DNA methylation associate with reduced migraine and headache days after medication withdrawal treatment in chronic migraine patients
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- Cluster headache genomewide association study and meta-analysis identifies eight loci and implicates smoking as causal risk factor
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- Optogenetic cortical spreading depolarization induces headache-related behaviour and neuroinflammatory responses some prolonged in familial hemiplegic migraine type 1 mice
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- Spinocerebellar ataxia type 1 characteristics in patient-derived fibroblast and iPSC-derived neuronal cultures
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- Potent dual MAGL/FAAH inhibitor AKU-005 engages endocannabinoids to diminish meningeal nociception implicated in migraine pain
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- Whole exome sequencing of hemiplegic migraine patients shows an increased burden of missense variants in CACNA1H and CACNA1I genes
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- Spontaneous epileptic recordings from hiPSC-derived cortical neurons cultured with a human epileptic brain biopsy on a multi electrode array
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- Correction to: Migraine-relevant sex-dependent activation of mouse meningeal afferents by TRPM3 agonists
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- Activation of Meningeal Afferents Relevant to Trigeminal Headache Pain after Photothrombotic Stroke Lesion
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- Quantification of endocannabinoids in human cerebrospinal fluid using a novel micro-flow liquid chromatography-mass spectrometry method
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- Quantification of endocannabinoids in human cerebrospinal fluid using a novel micro-flow liquid chromatography-mass spectrometry method
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- Ca(V)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
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- Changes in plasma lipid levels following cortical spreading depolarization in a transgenic mouse model of familial hemiplegic migraine