Search
| Leader | 00000nz a2200037n 45 0 | ||
|---|---|---|---|
| 001 | WKP|Q77157836 (VIAF cluster) (Authority/Source Record) | ||
| 003 | WKP | ||
| 005 | 20241121000116.0 | ||
| 008 | 241121nneanz||abbn n and d | ||
| 035 | ‡a (WKP)Q77157836 | ||
| 024 | ‡a 0000-0003-2826-8562 ‡2 orcid | ||
| 035 | ‡a (OCoLC)Q77157836 | ||
| 100 | 0 | ‡a Andrew M. Davis ‡c paediatric cardiologist ‡9 en | |
| 375 | ‡a 1 ‡2 iso5218 | ||
| 400 | 0 | ‡a A M Davis ‡c wetenschapper ‡9 nl | |
| 670 | ‡a Author's A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia | ||
| 670 | ‡a Author's A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation. | ||
| 670 | ‡a Author's A Prospective Study of Sudden Cardiac Death among Children and Young Adults | ||
| 670 | ‡a Author's Age makes a difference: Symptoms in pediatric supraventricular tachycardia | ||
| 670 | ‡a Author's ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy. | ||
| 670 | ‡a Author's An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia | ||
| 670 | ‡a Author's Brugada syndrome caused by a large deletion in SCN5A only detected by multiplex ligation-dependent probe amplification | ||
| 670 | ‡a Author's Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study | ||
| 670 | ‡a Author's Clinical and genetic features of Australian families with long QT syndrome: A registry-based study. | ||
| 670 | ‡a Author's Clinical, electrocardiographic, and histologic correlations in children with dilated cardiomyopathy | ||
| 670 | ‡a Author's Clinical features and outcomes of childhood dilated cardiomyopathy: results from a national population-based study | ||
| 670 | ‡a Author's Clinical features and outcomes of childhood hypertrophic cardiomyopathy: results from a national population-based study | ||
| 670 | ‡a Author's Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation. | ||
| 670 | ‡a Author's Delay to diagnosis amongst patients with catecholaminergic polymorphic ventricular tachycardia | ||
| 670 | ‡a Author's Establishment of an Australian National Genetic Heart Disease Registry. | ||
| 670 | ‡a Author's Excellent long-term functional outcome after an operation for anomalous left coronary artery from the pulmonary artery | ||
| 670 | ‡a Author's Factors influencing uptake of familial long QT syndrome genetic testing | ||
| 670 | ‡a Author's Long-Term Outcomes of Childhood Left Ventricular Non-Compaction Cardiomyopathy: Results from a National Population-Based Study | ||
| 670 | ‡a Author's Long-term outcomes of dilated cardiomyopathy diagnosed during childhood: results from a national population-based study of childhood cardiomyopathy. | ||
| 670 | ‡a Author's Long-Term Outcomes of Hypertrophic Cardiomyopathy Diagnosed During Childhood: Results From a National Population-Based Study | ||
| 670 | ‡a Author's Long-term results of anatomic correction for congenitally corrected transposition of the great arteries: A 19-year experience. | ||
| 670 | ‡a Author's Long term somatic growth after repair of tetralogy of Fallot: evidence for restoration of genetic growth potential. | ||
| 670 | ‡a Author's Malignant pectus excavatum. | ||
| 670 | ‡a Author's Pediatric & Congenital Electrophysiology Society: building an international paediatric electrophysiology organisation. | ||
| 670 | ‡a Author's Personalized arrhythmia prevention: do the I's have it? | ||
| 670 | ‡a Author's Perspectives in interventional electrophysiology in children and those with congenital heart disease: electrophysiology in children. | ||
| 670 | ‡a Author's Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood | ||
| 670 | ‡a Author's SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups | ||
| 670 | ‡a Author's Successful ablation of refractory neonatal atrial flutter | ||
| 670 | ‡a Author's Successful implantation of a dual-chamber pacemaker in an ELBW infant for long QT syndrome | ||
| 670 | ‡a Author's Sudden death in childhood cardiomyopathy: results from a long-term national population-based study. | ||
| 670 | ‡a Author's Sudden Infant Death: QT or Not QT? That Is No Longer the Question | ||
| 670 | ‡a Author's Ten-year experience in atenolol use and exercise evaluation in children with genetically proven long QT syndrome | ||
| 670 | ‡a Author's The Epidemiology of Childhood Cardiomyopathy in Australia | ||
| 670 | ‡a Author's The long QT syndrome and seizures in childhood. | ||
| 670 | ‡a Author's The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy | ||
| 670 | ‡a Author's The QT and corrected QT interval in recovery after exercise in children | ||
| 670 | ‡a Author's The “surreptitious staphylococcus”staphylococcus lugdunensis endocarditis in a child | ||
| 670 | ‡a Author's Torsades de Pointes: 50 Years Later, Can We See It Coming? | ||
| 670 | ‡a Author's Transcatheter closure of perimembranous ventricular septal defect. | ||
| 909 | ‡a (orcid) 0000000328268562 ‡9 1 | ||
| 919 | ‡a factorsinfluencinguptakeoffamiliallongqtsyndromegenetictesting ‡A Factors influencing uptake of familial long QT syndrome genetic testing ‡9 1 | ||
| 919 | ‡a establishmentofanaustraliannationalgeneticheartdiseaseregistry ‡A Establishment of an Australian National Genetic Heart Disease Registry. ‡9 1 | ||
| 919 | ‡a delaytodiagnosisamongstpatientswithcatecholaminergicpolymorphicventriculartachycardia ‡A Delay to diagnosis amongst patients with catecholaminergic polymorphic ventricular tachycardia ‡9 1 | ||
| 919 | ‡a clinicalmanagementofcatecholaminergicpolymorphicventriculartachycardiatheroleofleftcardiacsympatheticdenervation ‡A Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation. ‡9 1 | ||
| 919 | ‡a clinicalfeaturesandoutcomesofchildhoodhypertrophiccardiomyopathyresultsfromanationalpopulationbasedstudy ‡A Clinical features and outcomes of childhood hypertrophic cardiomyopathy: results from a national population-based study ‡9 1 | ||
| 919 | ‡a clinicalfeaturesandoutcomesofchildhooddilatedcardiomyopathyresultsfromanationalpopulationbasedstudy ‡A Clinical features and outcomes of childhood dilated cardiomyopathy: results from a national population-based study ‡9 1 | ||
| 919 | ‡a excellentlongtermfunctionaloutcomeafteranoperationforanomalousleftcoronaryarteryfromthepulmonaryartery ‡A Excellent long-term functional outcome after an operation for anomalous left coronary artery from the pulmonary artery ‡9 1 | ||
| 919 | ‡a novelheterozygousmutationincardiaccalsequestrincausesautosomaldominantcatecholaminergicpolymorphicventriculartachycardia ‡A A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia ‡9 1 | ||
| 919 | ‡a novelmechanismforhumancardiacankyrinbsyndromeduetoreciprocalchromosomaltranslocation ‡A A Novel Mechanism for Human Cardiac Ankyrin-B Syndrome due to Reciprocal Chromosomal Translocation. ‡9 1 | ||
| 919 | ‡a prospectivestudyofsuddencardiacdeathamongchildrenandyoungadults ‡A A Prospective Study of Sudden Cardiac Death among Children and Young Adults ‡9 1 | ||
| 919 | ‡a agemakesadifferencesymptomsinpediatricsupraventriculartachycardia ‡A Age makes a difference: Symptoms in pediatric supraventricular tachycardia ‡9 1 | ||
| 919 | ‡a alpk3deficientcardiomyocytesgeneratedfrompatientderivedinducedpluripotentstemcellsandmutanthumanembryonicstemcellsdisplayabnormalcalciumhandlingandestablishthatalpk3deficiencyunderliesfamilialcardiomyopathy ‡A ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and establish that ALPK3 deficiency underlies familial cardiomyopathy. ‡9 1 | ||
| 919 | ‡a updateonthediagnosisandmanagementofcatecholaminergicpolymorphicventriculartachycardia ‡A An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia ‡9 1 | ||
| 919 | ‡a brugadasyndromecausedbyalargedeletioninscn5aonlydetectedbymultiplexligationdependentprobeamplification ‡A Brugada syndrome caused by a large deletion in SCN5A only detected by multiplex ligation-dependent probe amplification ‡9 1 | ||
| 919 | ‡a cardiacphenotypeinatp1a3relatedsyndromesamulticentrecohortstudy ‡A Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study ‡9 1 | ||
| 919 | ‡a clinicalandgeneticfeaturesofaustralianfamilieswithlongqtsyndromearegistrybasedstudy ‡A Clinical and genetic features of Australian families with long QT syndrome: A registry-based study. ‡9 1 | ||
| 919 | ‡a clinicalelectrocardiographicandhistologiccorrelationsinchildrenwithdilatedcardiomyopathy ‡A Clinical, electrocardiographic, and histologic correlations in children with dilated cardiomyopathy ‡9 1 | ||
| 919 | ‡a transcatheterclosureofperimembranousventricularseptaldefect ‡A Transcatheter closure of perimembranous ventricular septal defect. ‡9 1 | ||
| 919 | ‡a torsadesdepointes50yearslatercanweseeitcoming ‡A Torsades de Pointes: 50 Years Later, Can We See It Coming? ‡9 1 | ||
| 919 | ‡a surreptitiousstaphylococcusstaphylococcuslugdunensisendocarditisinachild ‡A The “surreptitious staphylococcus”staphylococcus lugdunensis endocarditis in a child ‡9 1 | ||
| 919 | ‡a qtandcorrectedqtintervalinrecoveryafterexerciseinchildren ‡A The QT and corrected QT interval in recovery after exercise in children ‡9 1 | ||
| 919 | ‡a mitochondrialdnac3303tmutationcancausecardiomyopathyandorskeletalmyopathy ‡A The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy ‡9 1 | ||
| 919 | ‡a longqtsyndromeandseizuresinchildhood ‡A The long QT syndrome and seizures in childhood. ‡9 1 | ||
| 919 | ‡a epidemiologyofchildhoodcardiomyopathyinaustralia ‡A The Epidemiology of Childhood Cardiomyopathy in Australia ‡9 1 | ||
| 919 | ‡a 10yearexperienceinatenololuseandexerciseevaluationinchildrenwithgeneticallyprovenlongqtsyndrome ‡A Ten-year experience in atenolol use and exercise evaluation in children with genetically proven long QT syndrome ‡9 1 | ||
| 919 | ‡a suddeninfantdeathqtornotqtthatisnolongerthequestion ‡A Sudden Infant Death: QT or Not QT? That Is No Longer the Question ‡9 1 | ||
| 919 | ‡a suddendeathinchildhoodcardiomyopathyresultsfromalongtermnationalpopulationbasedstudy ‡A Sudden death in childhood cardiomyopathy: results from a long-term national population-based study. ‡9 1 | ||
| 919 | ‡a successfulimplantationofadualchamberpacemakerinanelbwinfantforlongqtsyndrome ‡A Successful implantation of a dual-chamber pacemaker in an ELBW infant for long QT syndrome ‡9 1 | ||
| 919 | ‡a successfulablationofrefractoryneonatalatrialflutter ‡A Successful ablation of refractory neonatal atrial flutter ‡9 1 | ||
| 919 | ‡a scn5amutationsin442neonatesandchildrengenotypephenotypecorrelationandidentificationofhigherrisksubgroups ‡A SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups ‡9 1 | ||
| 919 | ‡a psychosocialimplicationsoflivingwithcatecholaminergicpolymorphicventriculartachycardiainadulthood ‡A Psychosocial Implications of Living with Catecholaminergic Polymorphic Ventricular Tachycardia in Adulthood ‡9 1 | ||
| 919 | ‡a perspectivesininterventionalelectrophysiologyinchildrenandthosewithcongenitalheartdiseaseelectrophysiologyinchildren ‡A Perspectives in interventional electrophysiology in children and those with congenital heart disease: electrophysiology in children. ‡9 1 | ||
| 919 | ‡a personalizedarrhythmiapreventiondotheishaveit ‡A Personalized arrhythmia prevention: do the I's have it? ‡9 1 | ||
| 919 | ‡a pediatricandcongenitalelectrophysiologysocietybuildinganinternationalpaediatricelectrophysiologyorganisation ‡A Pediatric & Congenital Electrophysiology Society: building an international paediatric electrophysiology organisation. ‡9 1 | ||
| 919 | ‡a malignantpectusexcavatum ‡A Malignant pectus excavatum. ‡9 1 | ||
| 919 | ‡a longtermsomaticgrowthafterrepairoftetralogyoffallotevidenceforrestorationofgeneticgrowthpotential ‡A Long term somatic growth after repair of tetralogy of Fallot: evidence for restoration of genetic growth potential. ‡9 1 | ||
| 919 | ‡a longtermresultsofanatomiccorrectionforcongenitallycorrectedtranspositionofthegreatarteriesa19yearexperience ‡A Long-term results of anatomic correction for congenitally corrected transposition of the great arteries: A 19-year experience. ‡9 1 | ||
| 919 | ‡a longtermoutcomesofhypertrophiccardiomyopathydiagnosedduringchildhoodresultsfromanationalpopulationbasedstudy ‡A Long-Term Outcomes of Hypertrophic Cardiomyopathy Diagnosed During Childhood: Results From a National Population-Based Study ‡9 1 | ||
| 919 | ‡a longtermoutcomesofdilatedcardiomyopathydiagnosedduringchildhoodresultsfromanationalpopulationbasedstudyofchildhoodcardiomyopathy ‡A Long-term outcomes of dilated cardiomyopathy diagnosed during childhood: results from a national population-based study of childhood cardiomyopathy. ‡9 1 | ||
| 919 | ‡a longtermoutcomesofchildhoodleftventricularnoncompactioncardiomyopathyresultsfromanationalpopulationbasedstudy ‡A Long-Term Outcomes of Childhood Left Ventricular Non-Compaction Cardiomyopathy: Results from a National Population-Based Study ‡9 1 | ||
| 946 | ‡a b ‡9 1 | ||
| 996 | ‡2 SUDOC|072311215 | ||
| 996 | ‡2 BNF|16233461 | ||
| 996 | ‡2 LC|n 2005064810 | ||
| 996 | ‡2 NYNYRILM|170216 | ||
| 996 | ‡2 LC|no2012117817 | ||
| 996 | ‡2 NUKAT|n 2015009694 | ||
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| 996 | ‡2 LC|no2022050477 | ||
| 996 | ‡2 ISNI|0000000076663290 | ||
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| 996 | ‡2 NTA|338219994 | ||
| 996 | ‡2 DNB|1043193138 | ||
| 996 | ‡2 LNB|LNC10-000335200 | ||
| 996 | ‡2 N6I|vtls000026436 | ||
| 996 | ‡2 LC|n 2009019008 | ||
| 996 | ‡2 CAOONL|ncf11047749 | ||
| 996 | ‡2 RERO|A025524028 | ||
| 996 | ‡2 NUKAT|n 2016177920 | ||
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| 996 | ‡2 ISNI|0000000070363174 | ||
| 996 | ‡2 ISNI|0000000027169560 | ||
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| 996 | ‡2 J9U|987007431174905171 | ||
| 996 | ‡2 LC|no2020106514 | ||
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| 996 | ‡2 PLWABN|9810635724505606 | ||
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| 996 | ‡2 ISNI|0000000355744157 | ||
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| 996 | ‡2 ISNI|0000000107711268 | ||
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| 996 | ‡2 SUDOC|184089883 | ||
| 996 | ‡2 CAOONL|ncf10002693 | ||
| 996 | ‡2 BLBNB|001136481 | ||
| 996 | ‡2 CAOONL|ncf10072461 | ||
| 996 | ‡2 ISNI|0000000084360644 | ||
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| 996 | ‡2 LC|n 2014022744 | ||
| 996 | ‡2 NII|DA02448119 | ||
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| 996 | ‡2 NII|DA05858933 | ||
| 996 | ‡2 LC|n 84087150 | ||
| 996 | ‡2 ISNI|0000000499062534 | ||
| 996 | ‡2 LNB|LNC10-000068906 | ||
| 996 | ‡2 DNB|1236605179 | ||
| 996 | ‡2 NTA|243895232 | ||
| 996 | ‡2 LC|no2006018527 | ||
| 996 | ‡2 ISNI|0000000078173703 | ||
| 996 | ‡2 LC|no2019166281 | ||
| 996 | ‡2 PTBNP|1717217 | ||
| 996 | ‡2 SUDOC|227088093 | ||
| 996 | ‡2 LC|no2014038051 | ||
| 996 | ‡2 SIMACOB|296246627 | ||
| 996 | ‡2 ISNI|0000000129179903 | ||
| 996 | ‡2 SIMACOB|116428643 | ||
| 996 | ‡2 DNB|134498461 | ||
| 996 | ‡2 LC|no2009117445 | ||
| 996 | ‡2 LC|no2018057584 | ||
| 996 | ‡2 JPG|500083389 | ||
| 996 | ‡2 BIBSYS|13012406 | ||
| 996 | ‡2 LC|n 2018037928 | ||
| 996 | ‡2 ISNI|0000000123984311 | ||
| 996 | ‡2 DNB|137936818 | ||
| 996 | ‡2 LC|n 2010183447 | ||
| 996 | ‡2 LIH|LNB:B_g_Y,;=B_j_ | ||
| 996 | ‡2 PLWABN|9810702419705606 | ||
| 996 | ‡2 ISNI|0000000077321372 | ||
| 996 | ‡2 ISNI|0000000083274285 | ||
| 996 | ‡2 RERO|A003157961 | ||
| 996 | ‡2 RERO|A003157962 | ||
| 996 | ‡2 ISNI|000000004300968X | ||
| 996 | ‡2 BIBSYS|12027556 | ||
| 996 | ‡2 BIBSYS|2059636 | ||
| 996 | ‡2 CAOONL|ncf10362927 | ||
| 997 | ‡a 0 0 lived 0 0 ‡9 1 |
