Results 181 to 190 of about 37,848 (274)

KCNH2-L693P Causes Long QT Syndrome Type 2 Through hERG Channel Dysfunction: Functional Validation of a Variant of Uncertain Significance. [PDF]

Mol Genet Genomic Med
Zheng XF, Chen Q, Lu XT, Dai HL, Guang XF.   +4 more
europepmc   +1 more source

Dengue Myocarditis with Gitelman Syndrome Presenting as Arrhythmic Syncope: A Case Report of Acute Fulminant Dengue Myocarditis Resulting to Acquired Long QT Syndrome [PDF]

Billy Joseph David, Maderazo Donna Aurea, Gaspar-Cabrera Dianne Camille, Castro Rod   +3 more
openalex   +1 more source

Mutation-specific roles of sustained sodium current (I_Na) in guiding precision medicine for long QT syndrome type 3. [PDF]

PNAS Nexus
Auvichayapat V, Lekchuensakul S, Wandee P, Mauleekoonphairoj J, Vongseenin S, Ingrungruanglert P, Israsena N, Suthivanich P, Jinarat D, Khongphatthanayothin A, Bongsebandhu-Phubhakdi S.   +10 more
europepmc   +1 more source

Syntrophin mutation associated with long QT syndrome through activation of the nNOS–SCN5A macromolecular complex

, 2008
Kazuo Ueda, Carmen R. Valdivia, Argelia Medeiros‐Domingo, David J. Tester, Matteo Vatta, Gianrico Farrugia, Michael J. Ackerman, Jonathan C. Makielski   +7 more
openalex   +1 more source

TP-fusion at peak exercise: a novel marker for the recognition of unsuspected long QT syndrome patients. [PDF]

Europace
Boeri C, Sarto P, Cerea P, Crotti L, Dagradi F, Giovenzana FLF, Alberio C, Meneguzzo G, Lucini D, Musu G, Spazzolini C, Schwartz PJ.   +11 more
europepmc   +1 more source

Calibrated Functional Data Decrease Clinical Uncertainty for <i>KCNH2</i>-Related Long-QT Syndrome. [PDF]

Circ Genom Precis Med
Ng CA, O'Neill MJ, Padigepati SR, Ting YL, Facio FM, Vatta M, Poll SR, Reuter JA, Vandenberg JI, Kroncke BM.   +9 more
europepmc   +1 more source

Software-based analysis of T-wave morphology: identifying the electrocardiogram signature of high-risk long QT syndrome. [PDF]

Europace
Porretta AP, Morgat C, Surget E, Fressart V, Bloch A, Neyroud N, Badilini F, Vaglio M, Denjoy I, Extramiana F.   +9 more
europepmc   +1 more source

Beyond the Beat, Next-Generation Sequencing Discovery of Novel <i>RYR2</i> Gene Variant in Long QT Syndrome. [PDF]

Cardiol Res Pract
Kalayinia S, Jolfayi AG, Soheili A, Maleki M, Dalili M, Soveizi M, Komijani S.   +6 more
europepmc   +1 more source

Case report: A 56-year-old woman presenting with torsades de pointes and cardiac arrest associated with levosimendan administration and underlying congenital long QT syndrome type 1

Feng-yan Zha, Xing Li, Hui Yin, Di Huang, Yu Du, Chuzhi Zhou   +5 more
openalex   +1 more source