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	Arrhythmogenic left ventricular cardiomyopathy managed with CRT-D: A case report. Medicine (Baltimore) Cheng X, Wang X, Liu Y. PMID: 41790641 [PubMed - indexed for MEDLINE]
	Intravenous Haloperidol, Agitation, and the QTc: Misconceptions and Heuristics. Harv Rev Psychiatry Levinsohn E, Radhakrishnan V, Singh S, Celano CM, Beach SR. PMID: 41790521 [PubMed - indexed for MEDLINE]
	[Exertional syncope: A diagnosis of long QT syndrome. A practice-oriented case report on risk stratification and management]. Praxis (Bern 1994) Brecka M, Brecka M, Patricio F, Haegeli LM, Berg J. PMID: 41784516 [PubMed - indexed for MEDLINE]
	Development of 3D-Printed Congenital Heart Disease Models Using Feasible Low-Cost Workflow - A Potential Tool to Improve Pediatric Cardiology Education. Arq Bras Cardiol Cajueiro FCM, Croti UA, Amorim Júnior RF, Cardoso MRR, Costa CH, Marchi CH, Borim BC, Godoy MF, Freitas MB, Moscardini AC. PMID: 41779486 [PubMed - indexed for MEDLINE]
	Model informed assessment of QT prolongation during drug development: a five-year retrospective analysis of EMA scientific advices. J Pharmacokinet Pharmacodyn Djokoto HP, Dogné JM, Musuamba FT. PMID: 41772263 [PubMed - indexed for MEDLINE]
	Delayed Diagnosis of Tricuspid Atresia: A Case Report. JNMA J Nepal Med Assoc Yogi RN, Awasthi SR, Mandal AK, Shahi K, Thani KP, Pradhan S. PMID: 41766834 [PubMed - indexed for MEDLINE]
	Maternal and Perinatal Outcome in Women with Congenital Heart Disease: An Observational Study. JNMA J Nepal Med Assoc Paudyal P, Ghimire A, Parajuli BD, Khakural P. PMID: 41766829 [PubMed - indexed for MEDLINE]
	Enhanced patient outcomes and improved budget impact from increased PFO diagnostic testing in cryptogenic stroke workup: a US hospital perspective. J Med Econ Volpi JJ, Tiozzo G, Neervoort J, Louwsma T, Marti AK, Landaas EJ, Nakum M, Imhoff RJ. PMID: 41764033 [PubMed - indexed for MEDLINE]
	Newborn With Abnormal ECG and Family History of Sudden Cardiac Arrest. Neoreviews Devaris A, Cole Y, Hojnicki M. PMID: 41763575 [PubMed - indexed for MEDLINE]
	Silencing the Mutant KCNH2 Allele to Reduce the Effects of Long QT Syndrome Type 2. Front Biosci (Landmark Ed) Wilders R. PMID: 41761963 [PubMed - indexed for MEDLINE]
	Nomograms Based on Myocardial Strain and Myocardial Work to Predict Low Cardiac Output Syndrome in Children Undergoing Surgery for Congenital Heart Disease. J Cardiothorac Vasc Anesth Qin X, Dan Y, Zhang K, Tong C, Wang H, Sun L, Mamtili I, Huang Y, Zheng J. PMID: 41761731 [PubMed - indexed for MEDLINE]
	A Comparison of Treatment Options for Right Ventricular Outflow Tract Obstruction. Thorac Cardiovasc Surg Rahlfs SS, Sachweh JS, Kozlik-Feldmann RG, Biermann D, Hübler M, Carstens H. PMID: 41760349 [PubMed - indexed for MEDLINE]
	Exploring the influence of risk factors on outcomes following surgical closure of ventricular septal defects. Cardiovasc J Afr Ozcifci G, Altug U, Durak F, Anil AB, Kulluoglu P, Isik O, Akyuz M, Demircan T, Narin N. PMID: 41758206 [PubMed - indexed for MEDLINE]
	A Double-Chambered Left Ventricle Mimicking a Left Ventricular Aneurysm. Echocardiography Yavuz ST, Inan D, Pamuk FO, Sisman A, K. PMID: 41758065 [PubMed - indexed for MEDLINE]
	One-stage repair of Taussig-Bing anomaly in a neonate with aortic arch hypoplasia and single coronary artery. Multimed Man Cardiothorac Surg Said SM, Dawary M, Wahba A. PMID: 41757411 [PubMed - indexed for MEDLINE]
	The Combined Double-Orifice and Single-Patch Technique for Partial Atrioventricular Septal Defect in Adults: A Novel Strategy. Cardiovasc Ther Zheng HJ, Xiao RH, Ye MT, Li J, Guo M, Yu SJ, Cheng YB, Cheng W. PMID: 41756014 [PubMed - indexed for MEDLINE]
	Hospital Surgical Volume and Regional Disparities in Congenital Heart Surgery Outcomes: Analysis of Korean National Health Insurance Claims Data, 2002-2021. Medicina (Kaunas) Kim JS, Woo HT, Kim JY, Nam HM, Lee HJ. PMID: 41752754 [PubMed - indexed for MEDLINE]
	Application of Prenatal Whole Exome Sequencing for Congenital Heart Anomalies. Int J Mol Sci Kamlungkuea T, Tongprasert F, Wattanasirichaigoon D, Kumfu S, Chattipakorn SC, Chattipakorn N, Tongsong T. PMID: 41751857 [PubMed - indexed for MEDLINE]
	Genetic Mapping of the 22q11.2 Deletion Syndrome (DiGeorge Syndrome) Microdeletion Types Revealed Novel Candidate Breakpoints. Genes (Basel) Papageorgiou L, Nikolopoulou E, Koniari E, Hatziagapiou K, Chaniotis D, Beloukas A, Chrousos GP, Eliopoulos E, Thireou T. PMID: 41751632 [PubMed - indexed for MEDLINE]
	Tetralogy of Fallot: Genetic, Epigenetic and Clinical Insights into a Multifactorial Congenital Heart Disease. Genes (Basel) Gagliardi MF, Micaglio E, Micheletti A, Benedetti S, Negura DG, Bevilacqua F, Guglielmi G, Pasqualin G, Giamberti A, Chessa M. PMID: 41751564 [PubMed - indexed for MEDLINE]

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