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	Association Between Atrial Fibrillation Occurrence and Wolff-Parkinson-White Syndrome: Is Prediction Possible? Arq Bras Cardiol Mario ADS, Targueta EP, Darrieux FCDC, Brigido ARD, Ferraz AP, Chokr MO, Pisani CF, Scanavacca MI. PMID: 42484212 [PubMed - indexed for MEDLINE]
	Karyotype-phenotype associations in turner syndrome: a multicenter retrospective cohort study. Front Endocrinol (Lausanne) Watad R, Al Jneibi S, Al Remeithi S, Beck RH, Al Hassani N, Deeb A. PMID: 42483685 [PubMed - indexed for MEDLINE]
	Ovarian function and X chromosome tissue mosaicism in adolescents with Turner syndrome and ongoing spontaneous puberty. Front Endocrinol (Lausanne) Turchinets A, Stupko O, Uvarova E, Tsabai P, Badlaeva A, Asaturova A, Kamaletdinov N, Khashchenko E, Kumykova Z, Trofimov D, Yureneva S, Gavisova A, Sukhikh G. PMID: 42483667 [PubMed - indexed for MEDLINE]
	Clinical and Genetic Study of a Pseudo-Dominant Primary Ciliary Dyskinesia Pedigree: The First DNAAF1-Associated Family Reported in Chinese Population. Mol Genet Genomic Med Guo Z, Li P, Jiang G, Chen W. PMID: 42482351 [PubMed - indexed for MEDLINE]
	Functional Outcomes and Safety of Endovascular Thrombectomy in Pediatric Acute Ischemic Stroke With Cardiac Abnormalities. Neurology Dmytriw AA, Kiani I, Kooshki A, Bhatia KD, Abruzzo T, Pabst L, Fraser S, Chung M, Lo WD, Othmann A, Steinmetz S, Jensen-Kondering U, Schob S, Kaiser D, Marik W, Wendl CF, Kleffner I, Henkes H, Krähling H, Nguyen Kim TDL, Chapot R, Yilmaz U, Wang FS, Hafeez MU, Requejo F, Limbucci N, Kauffmann B, Möhlenbruch M, Nikoubashman O, Schellinger PD, Dugar F, Musolino PL, Alawieh A, Wilson JL, Grieb D, Gersing A, Liebig T, Olivieri M, Schwabova JP, Tomek A, Papanagiotou P, Boulouis G, Naggara O, Fox CK, Orlov K, Kuznetsova A, Parra-Farinas C, Muthusami P, Regenhardt RW, Martinez M, Brechbühl D, Steinlin M, Sun LR, Hassan AE, Kemmling A, Lee S, Fullerton HJ, Fiehler J, Psychogios M, Wildgruber M, Sporns PB. PMID: 42479995 [PubMed - indexed for MEDLINE]
	Classification models for KCNQ1 variants distinguish functional and trafficking effects to enhance pathogenicity interpretation. Proc Natl Acad Sci U S A Chang-Gonzalez AC, Bell EW, Vanoye CG, Guadarrama E, Desai RR, DeKeyser JM, Butcher KR, Scott J, Sanders CR, George AL Jr, Ledwitch KV, Meiler J. PMID: 42479828 [PubMed - indexed for MEDLINE]
	Primary Ciliary Dyskinesia: Insights from a Portuguese tertiary centre cohort. Pulmonology Teixeira-Oliveira S, Pais-Cunha I, Lopes SS, Seixas S, Ferraz C, Amorim A, Azevedo I. PMID: 42478199 [PubMed - indexed for MEDLINE]
	Antenatal tocolytic exposure and postnatal patent ductus arteriosus outcomes in preterm infants born at â‰¤32 weeks: a retrospective cohort study. J Matern Fetal Neonatal Med Tutak E, Ayhan YE, Özdemir SÖ, Öztürk G, C, Do. PMID: 42476923 [PubMed - indexed for MEDLINE]
	Effects of curcumin and nicorandil on nilotinib-induced QT interval prolongation in rats: A telemetry-based study. Pak J Pharm Sci Harmanci N, Kaltus Z, Eroglu E, Cengelli Unel C, Yigitaslan S, Sirmagul B. PMID: 42474156 [PubMed - indexed for MEDLINE]
	mHealth Technologies for the Care of Children With Congenital Heart Disease: Scoping Review. JMIR Mhealth Uhealth Wang M, Pan Q, Tan S, Kong Y, Dai Z, Cai J, Bi D, Zhou J. PMID: 42467841 [PubMed - indexed for MEDLINE]
	Incidence and risk factors of postoperative delirium in children with congenital heart disease. PLoS One An RG, Tang JQ, Xu J, Xie H, Dong BF, Wang Y, Tan ZQ, Zhou MQ. PMID: 42467607 [PubMed - indexed for MEDLINE]
	BRIGHT pathways: recommendations to improve the developmental follow-up of children with CHD in Canada - protocol for a nominal group study. BMJ Open Bolduc ME, Saini BS, Patey AM, Sadiku E, Miller SP, Simard MN, Brossard-Racine M, Majnemer A, Ly LG, Sananes R, Seed M. PMID: 42463189 [PubMed - indexed for MEDLINE]
	Cleft lip repair in trisomy 18: ethical considerations for aesthetic surgery in a life-limiting paediatric disease. BMJ Case Rep Landeen KC, Patel KG, Tanious MK. PMID: 42463173 [PubMed - indexed for MEDLINE]
	Factors associated with procedural difficulty and major adverse events during transcatheter closure of the patent ductus arteriosus. PLoS One Tipsungnoen A, Jarutach J, Roymanee S, Wongwaitaweewong K, Buntharikpornpun R, Puttarak S, Chumchuen K. PMID: 42461944 [PubMed - indexed for MEDLINE]
	Latent Vasculopathy of a Peripheral Pulmonary Artery in FBN1-Related Marfan Syndrome. Pathol Int Aragaki M, Otsuka N, Furuya M, Yamazawa H, Morisaki H, Morisaki T, Kato T, Nakatani Y. PMID: 42458917 [PubMed - indexed for MEDLINE]
	Synonymous variants in IRX4 and their association with congenital heart disease: an in-silico functional assessment. Mol Biol Rep Maddhesiya J, Jain D, Kumar A, Mohapatra B. PMID: 42455270 [PubMed - indexed for MEDLINE]
	[Diagnosis of congenital heart disease using Deep Learning in pediatric chest X-rays: A proof of concept]. Rev Med Inst Mex Seguro Soc Ramírez-Terán ÓA, Tomás-Alvarado E, Ruiz-Correa S, Segura-Quintanilla H, López-Revilla R, Ovando-Vázquez CM, Trujillo-Acatitla R. PMID: 42447261 [PubMed - indexed for MEDLINE]
	Exploring Social Determinants of Health in Primary Ciliary Dyskinesia. Pediatr Pulmonol Akgül Erdal M, Kantemir T, , Do, Yalç, Emiralio, Özçelik U. PMID: 42444258 [PubMed - indexed for MEDLINE]
	Heart Transplant for Noncompaction Cardiomyopathy in NONO-Related Syndromic Intellectual Disability. Mol Genet Genomic Med Singer JS, Garczarczyk-Asim D, Michel M, Müller T, Hackl L, Janecke AR. PMID: 42444102 [PubMed - indexed for MEDLINE]
	Anaesthetic management of a child with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) and supravalvular aortic stenosis (SVAS) associated with Williams-Beuren syndrome undergoing combined coronary reimplantation and supravalvular aortoplasty. BMJ Case Rep Sharafat MA, Yousuf MS, Zahid MA, Samad K. PMID: 42442851 [PubMed - indexed for MEDLINE]

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