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Brain Research, ISSN 0006-8993, 10/2019, Volume 1720, pp. 146289 - 146289
The prevalence of delivery through cesarean-section (C-section) has been increasing worldwide. Although different modes of delivery, such as vaginal birth and... 
Cesarean delivery | Vaginal delivery | Atp1a2 | Na pump | Respiratory neural activity | Neural development | Index Medicus
Journal Article
Cephalalgia, ISSN 0333-1024, 8/2018, Volume 38, Issue 9, pp. 1515 - 1524
Background Patients with familial hemiplegic migraine type 2 (FHM2) have a mutated ATP1A2 gene (encoding Na+,K+-ATPase α2 subunit) and show prolonged migraine... 
ATPase α2 subunit | cortical spreading depression | Atp1a2 | familial hemiplegic migraine 2
Journal Article
Brain, ISSN 0006-8950, 2007, Volume 130, Issue 3, pp. 828 - 835
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset of dystonia and parkinsonism and is caused by mutations in... 
parkinsonism | Na+/K+-ATPase | dystonia | ATP1A2 | LINKAGE | FAMILIAL HEMIPLEGIC MIGRAINE | NEUROSCIENCES | ATPIA3 | rapid-onset dystonia-parkinsonism | CLINICAL NEUROLOGY | RDP
Journal Article
Journal of Clinical Neurophysiology, ISSN 0736-0258, 01/2018, Volume 35, Issue 1, pp. e3 - e7
INTRODUCTION:Familial hemiplegic migraine (FHM) is a genetic disease with a variable clinical phenotype. The imaging and electroencephalogram (EEG) correlates... 
Familial hemiplegic migraine | ATP1A2 | EEG | Encephalopathy | NEUROSCIENCES | SPREADING DEPRESSION | CLINICAL NEUROLOGY | Index Medicus
Journal Article
Neurology, ISSN 0028-3878, 11/2012, Volume 79, Issue 21, pp. 2122 - 2124
Objective: Hemiplegic migraine (HM) is a rare subtype of migraine with aura that occurs as a familial or sporadic condition. The 3 culprit genes identified so... 
ATP1A2 | CLINICAL NEUROLOGY | EPILEPSY | Membrane Proteins - genetics | Humans | Adolescent | Female | Male | Migraine with Aura - genetics | Mutation - genetics | Child | Migraine with Aura - diagnosis | Nerve Tissue Proteins - genetics | Index Medicus | Abridged Index Medicus
Journal Article
European journal of medical genetics, ISSN 1769-7212, 01/2019
The Na /K - ATPase acts as an ion pump maintaining the essential plasma membrane potential in all mammalian cell types, and is essential for many cellular... 
Journal Article
Journal Article
Voprosy Sovremennoj Pediatrii, ISSN 1682-5527, 01/2016, Volume 14, Issue 6, pp. 732 - 734
The article describes the individual peculiarities of a rare disease — hemiplegic migraine — in 3 patients (two girls aged 2 and 14 years old and a boy of 16... 
CACNA1A | hemiplegic migraine | ATP1A2 | children | MRI
Journal Article
CEPHALALGIA, ISSN 0333-1024, 08/2018, Volume 38, Issue 9, pp. 1515 - 1524
Background Patients with familial hemiplegic migraine type 2 (FHM2) have a mutated ATP1A2 gene (encoding Na+,K+-ATPase 2 subunit) and show prolonged migraine... 
Atp1a2 | TRANSPORTERS | ATPASE ALPHA-2 SUBUNIT | NEUROSCIENCES | CLINICAL NEUROLOGY | BLOOD-CELL VELOCITY | MUTANT MICE | DEPOLARIZATION | K+-ATPase 2 subunit | CORTEX | familial hemiplegic migraine 2 | INTRAPARENCHYMAL CAPILLARIES | Na+ | cortical spreading depression | AURA | BRAIN | PROPAGATION
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 09/2018, Volume 392, pp. 22 - 27
Familial hemiplegic migraine (FHM) is a rare monogenic form of migraine with aura with three distinct genetic subtypes (FHM1-3). Imaging studies during acute... 
Familial hemiplegic migraine | ATP1A2 | MRI | Perfusion | FHM2 | CT | HYPERPERFUSION | MECHANISMS | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOPHYSIOLOGY | ENCEPHALOPATHY | EDEMA | MUTATION | BIPHASIC NEUROVASCULAR CHANGES | AURA | COMA | CT imaging | Genetic aspects | Diagnostic imaging | Migraine | Index Medicus
Journal Article
Cephalalgia, ISSN 0333-1024, 11/2014, Volume 34, Issue 13, pp. 1035 - 1037
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2013, Volume 288, Issue 2, pp. 1226 - 1237
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 16959 - 12
Migraine is a highly prevalent, debilitating, episodic headache disorder affecting roughly 15% of the population. Familial hemiplegic migraine type 2 (FHM2) is... 
GLUTAMATE TRANSPORTERS | MULTIDISCIPLINARY SCIENCES | DISEASE | CAT | ALPHA-2 SUBUNIT | MECHANISMS | HEMIPLEGIC MIGRAINE TYPE-2 | EPILEPSY | CEREBRAL-CORTEX | BRAIN | PATHOPHYSIOLOGY | Headache | Mental disorders | Astrocytes | Migraine | Epilepsy | Cortical spreading depression | Cortex | Na+/K+-exchanging ATPase | Potassium chloride | Patients | Sex hormones | ATP1A2 gene | Rodents | Mutation | Age
Journal Article