medline.ch Kardiovaskuläre Erkrankungen Kardiologie Kongenitale Herzerkrankungen

	Magnitude and Risk Factors for Paediatric Congenital Heart Surgery Complication and its association with Patient Outcomes in the Cardiac Center of Ethiopia. Ethiop J Health Sci Beshir MN, Ahmed M, Tsega T, Getahun T. PMID: 39981013 [PubMed - indexed for MEDLINE]
	Throwing thrombi: noncompaction cardiomyopathy causing renal infarct and catastrophic stroke - a case report. BMC Cardiovasc Disord Javed M, Desai S, DeRon N Jr, Villamil M. PMID: 39979848 [PubMed - indexed for MEDLINE]
	Long-Term Longitudinal Computational Study of a Marfan Syndrome Patient After Hybrid Repair of Aortic Arch Dissection With Parallel Stent-Grafts. Int J Numer Method Biomed Eng Liu Y, Li W, Ding Z, Tang Z, Luo Y, Hu J. PMID: 39979238 [PubMed - indexed for MEDLINE]
	Integrative analysis of KCNQ1 variants reveals molecular mechanisms of type 1 long QT syndrome pathogenesis. Proc Natl Acad Sci U S A Brewer KR, Vanoye CG, Huang H, Clowes Moster KR, Desai RR, Hayes JB, Burnette DT, George AL, Sanders CR. PMID: 39969993 [PubMed - indexed for MEDLINE]
	Fluoroscopy-free Transcatheter Atrial Septal Defect Closure: A Simplified Approach. Curr Cardiol Rep Lwin N, Suursalmi P, Yong S, Kabir S, Jones MI, Savis A, Qureshi SA, Rosenthal E. PMID: 39969687 [PubMed - indexed for MEDLINE]
	The value of red blood cell distribution width in perioperative cardiac function assessment in children with congenital heart disease: A retrospective cohort study. Medicine (Baltimore) Wang Q, Yin J, Wang X, Luo T, Wei M, Zhang X, Ou H, Wan W, Li F, Zhang Y, Guo C. PMID: 39969308 [PubMed - indexed for MEDLINE]
	Novel mutation in KCNJ2 gene causes long QT interval syndrome type 7 and learning disability: A case report. Medicine (Baltimore) Zhang HY, Zhang Y. PMID: 39969299 [PubMed - indexed for MEDLINE]
	CBP/CREB Regulates the Proliferation and Apoptosis of Cardiomyocytes by Interacting With SERCA. J Cell Mol Med Zhouguo Y, Yuan Z, Abdul M, Xi S, Wei T, Yan W, Wang Y, Guo R, Xing Q, Zhou Q. PMID: 39969158 [PubMed - indexed for MEDLINE]
	Impact of 3D Printing on Cardiac Surgery in Congenital Heart Diseases: A Systematic Review and Meta-Analysis. Arq Bras Cardiol Yahiro DS, Cruz MP, Ribeiro BFC, Teixeira LM, Oliveira MFRM, Souza ALAAG, Torbey AFM, Silveira JSD, Mesquita CT. PMID: 39968976 [PubMed - indexed for MEDLINE]
	Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study. Orphanet J Rare Dis Santoro M, Barisic I, Coi A, Tan J, Garne E, Loane M, Odak L, Abate MV, Ballardini E, Cavero-Carbonell C, Gatt M, Gissler M, Klungsøyr K, Lelong N, Tucker D, Wellesley D, Morris JK. PMID: 39962527 [PubMed - indexed for MEDLINE]
	Peripandemic outcomes of infants treated for sentinel congenital heart diseases in England and Wales. Open Heart Huang Q, Lawlor DA, Nolan J, Espuny-Pujol F, Caputo M, Pagel C, Crowe S, Franklin RC, Brown KL, CVD-COVID-UK/COVID-IMPACT Consortium. PMID: 39961700 [PubMed - indexed for MEDLINE]
	Identification of key autophagy-related genes in arrhythmogenic right ventricular cardiomyopathy through gene expression profiling. Medicine (Baltimore) Yin J, Zhu Q, Yu C, Wang L, Ge R, Wang L, Wang J. PMID: 39960965 [PubMed - indexed for MEDLINE]
	Heart Disease in Children: Cardiac Dysrhythmias. FP Essent Barstow C, Flanagan R. PMID: 39960777 [PubMed - indexed for MEDLINE]
	Heart Disease in Children: Heart Murmurs. FP Essent Barstow C, Flanagan R. PMID: 39960775 [PubMed - indexed for MEDLINE]
	Thymus transplantation for DiGeorge Syndrome: a systematic review. Pediatr Surg Int Ahmed HS, Dias AF, Pulkurthi SR. PMID: 39960552 [PubMed - indexed for MEDLINE]
	SUCCESSFUL ABLATION OF CONCEALED ACCESSORY PATHWAY MEDIATED SUPRAVENTRICULAR TACHYCARDIA IN A 5-YEAR-OLD CHILD WITH EBSTEIN ANOMALY. Acta Clin Croat Krmek N, Jegdi, Rode M. PMID: 39959329 [PubMed - indexed for MEDLINE]
	THE SUCCESS RATE OF INTRAUTERINE CONGENITAL HEART DISEASE DETECTION AT DEPARTMENT OF GYNECOLOGY AND OBSTETRICS, SVETI DUH UNIVERSITY HOSPITAL FROM ZAGREB, 2016-2020. Acta Clin Croat Stojanovi, Sirac R, S, , Pavlovi, Blagai. PMID: 39959326 [PubMed - indexed for MEDLINE]
	The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development. Commun Biol Suntharalingham JP, Del Valle I, Buonocore F, McGlacken-Byrne SM, Brooks T, Ogunbiyi OK, Liptrot D, Dunton N, Madhan GK, Metcalfe K, Nel L, Marshall AR, Ishida M, Sebire NJ, Moore GE, Crespo B, Solanky N, Conway GS, Achermann JC. PMID: 39956831 [PubMed - indexed for MEDLINE]
	Congenital unilateral pericardial agenesis presenting as an isolated chest pain in an adolescent: a case report and comprehensive review. J Cardiothorac Surg Jafari F, Taheri M, Ebrahimi P, Soflaee M, Rafie RA, Anafje M. PMID: 39955569 [PubMed - indexed for MEDLINE]
	Neuromonitoring and follow-up in patients with congenital heart disease in Spain. An Pediatr (Engl Ed) Belfi A, Vega L, Aguar M, Carmen Bravo M, Cañizo D, Díaz Rueda L, Camprubí-Camprubí M, en representación del Grupo de Neuromonitorización del paciente con cardiopatía congénita. PMID: 39952855 [PubMed - indexed for MEDLINE]

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