Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.
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Genotype-phenotype correlation in long QT syndromeGenetics of inherited primary arrhythmia disordersLong-QT syndrome: from genetics to managementCongenital long QT syndromes: clinical features, molecular genetics and genetic testing.Identification of a possible pathogenic link between congenital long QT syndrome and epilepsyQT Interval in Pregnant and Non-pregnant Women.Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome.Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of StellenboschGenetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice.Progesterone modulates SERCA2a expression and function in rabbit cardiomyocytes.Specific therapy based on the genotype and cellular mechanism in inherited cardiac arrhythmias. Long QT syndrome and Brugada syndromeEstradiol promotes sudden cardiac death in transgenic long QT type 2 rabbits while progesterone is protectiveStrategies for the prevention and treatment of sudden cardiac death.Potential depot medroxyprogesterone acetate-triggered torsades de pointes in a case of congenital type 2 long QT syndromeManagement of long QT syndrome.Atrial Fibrillation and Long QT Syndrome Presenting in a 12-Year-Old Girl.Pharmacogenetic issues in thorough QT trials.Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane traffickingPharmacological approach to the treatment of long and short QT syndromesGenotype-specific QT correction for heart rate and the risk of life-threatening cardiac events in adolescents with congenital long-QT syndromeSudden cardiac death: prevalence, pathogenesis, and prevention.Maternal cardiac arrhythmias during pregnancy and lactation.Tbx20 controls the expression of the KCNH2 gene and of hERG channels.Genotype- and phenotype-guided management of congenital long QT syndrome.Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy.Long QT syndrome: beyond the causal mutation.Congenital Long QT syndrome and torsade de pointes.Exploiting ion channel structure to assess rare variant pathogenicity.Congenital long QT syndrome
P2860
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P2860
Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Identification of a common gen ...... n congenital long QT syndrome.
@ast
Identification of a common gen ...... n congenital long QT syndrome.
@en
type
label
Identification of a common gen ...... n congenital long QT syndrome.
@ast
Identification of a common gen ...... n congenital long QT syndrome.
@en
prefLabel
Identification of a common gen ...... n congenital long QT syndrome.
@ast
Identification of a common gen ...... n congenital long QT syndrome.
@en
P2093
P1433
P1476
Identification of a common gen ...... n congenital long QT syndrome.
@en
P2093
Anant Khositseth
Carla M Bell
David J Tester
Melissa L Will
Michael J Ackerman
P356
10.1016/J.HRTHM.2004.01.006
P577
2004-05-01T00:00:00Z