المؤلفون: Maria Elena Onore, Esther Picillo, Paola D’Ambrosio, Salvatore Morra, Vincenzo Nigro, Luisa Politano

المصدر: Biomolecules, Vol 14, Iss 4, p 507 (2024)

مصطلحات موضوعية: KCNJ2 gene, Andersen–Tawil syndrome, channelopathies, Kir2.1 mutations, Arg218Trp, R218W, Microbiology, QR1-502

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2218-273X/14/4/507Test; https://doaj.org/toc/2218-273XTest

الوصول الحر: https://doaj.org/article/4fac10127a764752a311d7b1ad0baf95Test

المؤلفون: Jisook Yim, Kyoung Bo Kim, Minsun Kim, Gun Dong Lee, Myungshin Kim

المصدر: Frontiers in Pediatrics, Vol 9 (2022)

مصطلحات موضوعية: KCNJ2 gene, KIR2.1, periodic paralysis, long QT syndrome, potassium channel, genetic disorder, Pediatrics, RJ1-570

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2021.790075/fullTest; https://doaj.org/toc/2296-2360Test

الوصول الحر: https://doaj.org/article/9d1f245f12b344ff9eba84c67a09cf9aTest

المؤلفون: Celeste Ferraris, Alexandria Turner, Christopher Scarlett, Martin Veysey, Mark Lucock, Tamara Bucher, Emma L. Beckett

المصدر: Nutrients; Volume 13; Issue 3; Pages: 719

مصطلحات موضوعية: sour, taste, genetics, KCNJ2 gene, rs236514, polymorphism, SNP, cognitive impairment, dementia, elderly, diet

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Geriatric Nutrition; https://dx.doi.org/10.3390/nu13030719Test

الإتاحة: https://doi.org/10.3390/nu13030719Test

المؤلفون: Masaki Sekiguchi, Mai Inagaki, Hiroshi Yomogita, Naoyuki Miyasaka, Takayuki Tatsumi, Asuka Hirose, Takuyuki Kubo

المصدر: Journal of Obstetrics and Gynaecology Research. 47:446-451

مصطلحات موضوعية: Painful uterine contractions, medicine.medical_specialty, Pregnancy, 030219 obstetrics & reproductive medicine, Kcnj2 gene, Exacerbation, business.industry, Long QT syndrome, Obstetrics and Gynecology, medicine.disease, 03 medical and health sciences, 0302 clinical medicine, Andersen–Tawil syndrome, 030220 oncology & carcinogenesis, Internal medicine, cardiovascular system, Cardiology, medicine, Missense mutation, cardiovascular diseases, business, Limb paralysis

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::edbb8633ab463799fb18d1738273f484Test
https://doi.org/10.1111/jog.14553Test

المؤلفون: Raimundo Barbosa-Barros, Mauricio Scanavacca, Rodrigo Daminello-Raimundo, Kjell Nikus, Carlos Alberto Pastore, Andrés Ricardo Pérez-Riera, Pedro Brugada, Luiz Carlos de Abreu, Nelson Samesina

المساهمون: Clinical sciences, Heartrhythmmanagement, Cardio-vascular diseases

المصدر: Cardiology in Review. 29:165-177

مصطلحات موضوعية: orphan genetic multisystem channelopathy, medicine.medical_specialty, KCNJ5-GIRK4 gene, heart disease, 030204 cardiovascular system & hematology, Ventricular tachycardia, QT interval, 03 medical and health sciences, 0302 clinical medicine, Andersen–Tawil syndrome, Channelopathy, Internal medicine, medicine, Repolarization, ATS type 1, cardiovascular diseases, 030212 general & internal medicine, ATS type 2, medicine.diagnostic_test, business.industry, Muscle weakness, Periodic paralysis, General Medicine, medicine.disease, KCNJ2 gene, K channel protein Kir2.1, cardiovascular system, Cardiology, medicine.symptom, Cardiology and Cardiovascular Medicine, business, Electrocardiography, Andersen-Tawil Syndrome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb1d2f3853135be50e64579555f837c5Test
https://doi.org/10.1097/crd.0000000000000326Test

المؤلفون: Roberto Keegan, Leonardo Onetto, Franco Gregorietti, Luigi Di Biase, Ricardo Urruti

المصدر: Journal of Interventional Cardiac Electrophysiology.

مصطلحات موضوعية: medicine.medical_specialty, Kcnj2 gene, business.industry, medicine.medical_treatment, Autosomal dominant trait, Catheter ablation, medicine.disease, Ablation, Muscular paralysis, Andersen–Tawil syndrome, medicine.anatomical_structure, Ventricle, Physiology (medical), Internal medicine, Cardiology, Medicine, In patient, Cardiology and Cardiovascular Medicine, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d3fa78b5f407f10bc2b9226a13c8a1dTest
https://doi.org/10.1007/s10840-021-01077-wTest

المؤلفون: Rosalie M.E. Meijer van Putten, Isabella eMengarelli, Kaomei eGuan, Jan G. Zegers, Antoni CG van Ginneken, Arie O Verkerk, Ronald eWilders

المصدر: Frontiers in Physiology, Vol 6 (2015)

مصطلحات موضوعية: Action Potentials, patch clamp, Andersen-Tawil syndrome, inward rectifier potassium channel, cardiac ion channelopathies, KCNJ2 gene, Physiology, QP1-981

وصف الملف: electronic resource

العلاقة: http://journal.frontiersin.org/Journal/10.3389/fphys.2015.00007/fullTest; https://doaj.org/toc/1664-042XTest

الوصول الحر: https://doaj.org/article/a2f59ef593a8439a828407c804c0cde8Test

المؤلفون: Mark Lucock, Christopher J. Scarlett, Alexandria Turner, Tamara Bucher, Martin Veysey, Emma L. Beckett, Celeste Ferraris

المصدر: Nutrients, Vol 13, Iss 719, p 719 (2021)
Nutrients
Volume 13
Issue 3

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Taste, sour, SNP, lcsh:TX341-641, Logistic regression, elderly, polymorphism, taste, 03 medical and health sciences, 0302 clinical medicine, stomatognathic system, Polymorphism (computer science), Internal medicine, Genotype, medicine, Dementia, genetics, Allele, cognitive impairment, Nutrition and Dietetics, business.industry, KCNJ2 gene, medicine.disease, 030104 developmental biology, rs236514, Cohort, business, diet, lcsh:Nutrition. Foods and food supply, 030217 neurology & neurosurgery, Food Science, dementia

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932e94714bd3f397e83a53e4102529c2Test
https://www.mdpi.com/2072-6643/13/3/719Test

المؤلفون: Ferraris, Celeste, Turner, Alexandria, Scarlett, Christopher, Veysey, Martin, Lucock, Mark, Bucher, Tamara, Beckett, Emma L.

المساهمون: The University of Newcastle. College of Engineering, Science & Environment, School of Environmental and Life Sciences

مصطلحات موضوعية: sour, taste, diet, genetics, KCNJ2 gene, rs236514, polymorphism, SNP, cognitive impairment, dementia, elderly

العلاقة: Nutrients Vol. 13, Issue 3, p. 719-719; http://hdl.handle.net/1959.13/1446721Test; uon:42951

الإتاحة: http://hdl.handle.net/1959.13/1446721Test

المؤلفون: Maneesh Rai, Syed Waleem Pasha, Gangham Sri Lakshmi Bhavani, Mukund A. Prabhu, Katta M. Girisha, Rohith Pai, Rakshith C. Kedambadi, Padmanabh Kamath, Alfred Joseph Augustine

المصدر: Pacing and Clinical Electrophysiology. 42:201-207

مصطلحات موضوعية: Adult, Male, Phenytoin, Time Factors, Adolescent, Familial periodic paralysis, 030204 cardiovascular system & hematology, Ventricular tachycardia, Phenytoin Sodium, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Andersen–Tawil syndrome, medicine, Humans, 030212 general & internal medicine, Andersen Syndrome, Kcnj2 gene, business.industry, Arrhythmias, Cardiac, Periodic paralysis, General Medicine, medicine.disease, Phenotype, Pedigree, Treatment Outcome, Anesthesia, Female, Cardiology and Cardiovascular Medicine, business, Algorithms, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a34500f221f4c983ad69a4d02d246373Test
https://doi.org/10.1111/pace.13569Test