Keywords: میگرن همی پلژی خانوادگی; Familial hemiplegic migraine; FHM2; ATP1A2; MRI; CT; Perfusion;
مقالات ISI میگرن همی پلژی خانوادگی (ترجمه نشده)
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Keywords: میگرن همی پلژی خانوادگی; CWP; chronic widespread pain; FHM; familial hemiplegic migraine; GWAS; genome-wide association studies; OA; osteoarthritis; SNPs; single nucleotide polymorphisms; TMD; temporomandibular disorder; TMJ; temporomandibular joint; VNTR; variable number of tand
Keywords: میگرن همی پلژی خانوادگی; CSD; cortical spreading depression; FHM type 1; familial hemiplegic migraine type 1; GR; glucocorticoid receptor; MR; mineralocorticoid receptor; CRH; corticotropin-releasing hormone; Migraine; Cortical spreading depression; Familial hemiplegic migraine;
Keywords: میگرن همی پلژی خانوادگی; Na+,K+-ATPase; ATP1A2; Familial hemiplegic migraine; FHM2; Alpha 2 isoform; Baculovirus expression system
In vivo assessment of neurological channelopathies: Application of peripheral nerve excitability studies
Keywords: میگرن همی پلژی خانوادگی; Threshold electrotonus; Threshold tracking; Membrane excitability; Channelopathy; BFNE; Benign Familial Neonatal Epilepsy; CMAP; Compound muscle action potential; CNS; Central nervous system; EA; Episodic Ataxia; FHM; Familial Hemiplegic Migraine; GEFS+;
Clinical ObservationsAn Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2
Keywords: میگرن همی پلژی خانوادگی; ATP1A2; familial hemiplegic migraine; alternating hemiplegia; epilepsy;
Identification of the first in Poland CACNA1A gene mutation in familial hemiplegic migraine. Case report
Keywords: میگرن همی پلژی خانوادگی; Migraine; Familial hemiplegic migraine; Calcium channel; CACNA1A;
Differential trigeminovascular nociceptive responses in the thalamus in the familial hemiplegic migraine 1 knock-in mouse: A Fos protein study
Keywords: میگرن همی پلژی خانوادگی; CGRP; calcitonin gene-related peptide; CSD; cortical spreading depression; CM; centromedian thalamic nucleus; FHM; familial hemiplegic migraine; PF; parafascicular thalamic nucleus; Po; Posterior thalamic nucleus; TCC; trigeminocervical complex; TNC; Trig
Familial hemiplegic migraine mutations affect Na,K-ATPase domain interactions
Keywords: میگرن همی پلژی خانوادگی; Na,K-ATPase; ATP1A2; Familial hemiplegic migraine; FHM2; α2 isoform; Domain interaction;
A Young Man Presenting with Acute Encephalopathy, Hemiparesis, and Headache
Keywords: میگرن همی پلژی خانوادگی; familial hemiplegic migraine; hemiplegic migraine; migraine; encephalopathy; hemiparesis; headache; motor weakness
Effect of systemic kynurenine on cortical spreading depression and its modulation by sex hormones in rat
Keywords: میگرن همی پلژی خانوادگی; CSD; cortical spreading depression; DC; direct current; FHM; familial hemiplegic migraine; HPLC; high performance liquid chromatography; IDO; indoleamine 2,3-dioxygenase; KAT; kynurenine aminotransferases; KYNA; Kynurenic acid; L-KYN; l-kynurenine; nAChR;
CaV2.1 voltage activated calcium channels and synaptic transmission in familial hemiplegic migraine pathogenesis
Keywords: میگرن همی پلژی خانوادگی; CaV2.1 (P/Q-type) Ca2+ channels; Familial hemiplegic migraine; Cortical spreading depression; R192Q and S218L knock in mice; Synaptic transmission;
FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2
Keywords: میگرن همی پلژی خانوادگی; Familial hemiplegic migraine; Mutation;
Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation
Keywords: میگرن همی پلژی خانوادگی; Seizure; Electroencephalography; Familial hemiplegic migraine; Germline mosaicism; CACNA1A gene; S218L; Cortical spreading depression
Mechanically-induced cortical spreading depression associated regional cerebral blood flow changes are blocked by Na+ ion channel blockade
Keywords: میگرن همی پلژی خانوادگی; ANOVA; analysis of variance; AU; arbitrary units; AUC; area under curve; CSD; cortical spreading depression; FHM; familial hemiplegic migraine; HR; hyperemic response; rCBF; regional cerebral blood flow; SP; speed of propagation; TTX; tetrodotoxin; VDCC;
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies
Keywords: میگرن همی پلژی خانوادگی; tottering alleles; Ca(v)2.1 calcium channels; semi-dominant mutation; BHK; baby hamster kidney; B6; B10, BALB, C3H and CAST, five inbred strains of mice; CACNA1A; calcium channel gene encoding the Ca(v)2.1 or P/Q-type subunit; cDNA; complementary DNA; CSD
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures
Keywords: میگرن همی پلژی خانوادگی; Benign familial infantile convulsions; Epilepsy; Familial hemiplegic migraine; Genetics;
Noradrenergic blockade prevents attacks in a model of episodic dysfunction caused by a channelopathy
Keywords: میگرن همی پلژی خانوادگی; Tottering; Calcium channel; Adrenergic; Familial hemiplegic migraine; Episodic ataxia; Paroxysmal dyskinesia; Dystonia; Mutation; Animal model;
Neuron-Astrocyte Interactions: Partnership for Normal Function and Disease in the Central Nervous System
Keywords: میگرن همی پلژی خانوادگی; ADP; adenosine diphosphate; ALS; amyotrophic lateral sclerosis; AQP; aquaporin; ATP; adenosine triphosphate; ATPase; adenosine triphosphatase; AVP; arginine vasopressin; BBB; blood-brain barrier; [Ca2+]i; intracellular Ca2+; CBF; cerebral blood flow; CO2;
Gene dosage-dependent transmitter release changes at neuromuscular synapses of Cacna1a R192Q knockin mice are non-progressive and do not lead to morphological changes or muscle weakness
Keywords: میگرن همی پلژی خانوادگی; CACNA1A; Cav2.1 mutation; migraine; neuromuscular junction; neurotransmitter release; ACh; acetylcholine; ANOVA; analysis of variance; BTx; α-bungarotoxin; CMAP; compound muscle action potential; CSD; cortical spreading depression; EA2; episodic ataxia t