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Two-dimensional and pulsed Doppler echocardiography in the postoperative evaluation of total anomalous pulmonary venous connection

Jeffrey F. Smallhorn, Patricia Burroughs, G. Wilson, John Coles, David L. Gilday, Robert M. FreedomHospital for Sick Children.Canada CirculationCirculation 1987; 76: 298-305DOI: 10.1161/01.cir.76.2.298 AbstractThe role of combined two-dimensional and pulsed Doppler echocardiography in the postoperative assessment of patients with total anomalous pulmonary venous connection was evaluated. Twenty-two cases with a median age of 9.5 weeks at […]

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Longitudinal follow-up of mixed connective tissue disease and overlapping autoimmune diseases of childhood onset in the Afro-descendant population of the French West Indies

Arthur Felix, Lindsay Osei, Frederique Delion, Benoit Suzon, Aurore Abel, Moustapha Drame, Yves Hatchuel, Christophe Deligny, Fabienne Louis‑SidneyUniversity of the French West Indies and Martinique University Hospital. CHU de la Martinique La Meynard. Andrée Rosemon Hospital. Guadeloupe University Hospital. France Pediatric Rheumatology Online JournalPediatr Rheumatol Online J 2024; 22:DOI: 10.1186/s12969-023-00951-3 AbstractIntroduction: Overlap autoimmune syndromes (OAS) and mixed

Longitudinal follow-up of mixed connective tissue disease and overlapping autoimmune diseases of childhood onset in the Afro-descendant population of the French West Indies Read More »

Vasopressin in newborns with refractory acute pulmonary hypertension

Simon Ouellet, Christine Drolet, Genevéve Morissette, Annie Pellerin, Audrey HébertCHU de Québec, Université Laval. Canada Pediatric ResearchPediatr Res 2024;DOI: 10.1038/s41390-023-02995-3 AbstractBackground: Acute pulmonary hypertension (aPH) in newborns can be life threatening and challenging to manage. In newborns with refractory aPH, there is currently limited therapeutic agents.Methods: Retrospective single-center cohort study in newborns less than one month old who

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Total anomalous pulmonary venous return. Prenatal damage to pulmonary vascular bed and extrapulmonary veins

Sheila G. HaworthInstitute of Child Health.United Kingdom British Heart JournalBrit Heart J 1982; 48: 513-524DOI: 10.1136/hrt.48.6.513 AbstractTo investigate the possibility that pulmonary vascular disease may be present at birth in children presenting with obstructed total anomalous pulmonary venous return in the neonatal period, pulmonary vascular structure was analysed in the lungs of six babies who died

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Individual pulmonary vein size and survival in infants with totally anomalous pulmonary venous connection

Kathy J. Jenkins, Stephen P. Sanders, E. John Orav, Elizabeth A. Coleman, John E. Mayer Jr., Steven D. ColanChildren’s Hospital, Boston.United States Journal of the American College of CardiologyJ Am Coll Cardiol 1993; 22: 201-206DOI: 10.1016/0735-1097(93)90835-o AbstractObjectives: We investigated whether mortality in totally anomalous pulmonary venous connection could be predicted from preoperative individual pulmonary vein size.Background: Some infants with this anomaly die with or without surgical repair because

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Total anomalous pulmonary venous connection. Long-term results following repair in infancy

Christopher M. Whight, Brian G. Barratt-Boyes, A. Louise Calder, John M. Neutze, Peter W. BrandtGreen Lane Hospital.New Zealand Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 1978; 75: 52-63DOI: Not Available AbstractTwenty-three infants, aged 5 days to 10 months, underwent repair of total anomalous pulmonary venous connection (TAPVC). Coronary sinus drainage was unusually common,

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Total anomalous pulmonary venous drainage

Shunji Sano, William J. Brawn, Roger B. MeeRoyal Children’s Hospital.Australia Journal of Thoracic and Cardiovascular SurgeryJ Thorac Cardiovasc Surg 1989; 97: 886-992DOI: Not Available AbstractForty-four patients with total anomalous pulmonary venous drainage underwent repair between 1979 and 1987. The anomalous drainage was supracardiac in 16, cardiac in 12, and infracardiac in 16. Median age at

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Surgical repair of neonatal total anomalous pulmonary venous connection: A single institutional experience with 241 cases

Jin Shentu, Guocheng Shi, Qian Zhang, Chen Wen, Hao Zhang, Zhongqun Zhu, Huiwen ChenShanghai Children’s Medical Center and Shanghai Jiao Tong University.China Journal of Thoracic and Cardiovascular Surgery OpenJ Thorac Cardiovasc Surg Open 2023; 16: 739-754DOI: 10.1016/j.xjon.2023.07.021 AbstractObjective: Challenges persist in surgery for neonatal total anomalous pulmonary venous connection (neoTAPVC), with the high mortality risk not mitigated

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Fetal MRI-Based Mediastinal Shift Angle (MSA) and Percentage Area of Left Ventricle (pALV) as Prognostic Parameters for Congenital Diaphragmatic Hernia

Greta Thater, Lara Angermann, Silviu-Viorel Virlan, Christel Weiss, Neysan Rafat, Michael Boettcher, Julia Elrod, Tom Bayer, Oliver Nowak, Stefan O. Schönberg, Meike WeisUniversity Medical Center Mannheim. Hospital Stuttgart. Germany Journal of Clinical MedicineJ Clin Med 2024; 13:DOI: 10.3390/jcm13010268 AbstractObjective: Fetal magnetic resonance imaging (MRI) is broadly used as a method for assessing prognosis in congenital diaphragmatic hernia

Fetal MRI-Based Mediastinal Shift Angle (MSA) and Percentage Area of Left Ventricle (pALV) as Prognostic Parameters for Congenital Diaphragmatic Hernia Read More »

Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension

Yi- Yin Tai, Qiujun Yu, Ying Tang, Wei Sun, Neil J. Kelly, Satoshi Okawa, Jingsi Zhao, Tae- Hwi Schwantes-An, Caroline Lacoux, Stephanie Torrino, Yassmin Al Aaraj, Wadih El Khoury, Vinny Negi, Mingjun Liu, Catherine G. Corey, Frances Belmonte, Sara O. Vargas, Brian Schwartz, Bal Bhat, B. Nelson Chau, Jason H. Karnes, Taijyu Satoh, Robert J.

Allele-specific control of rodent and human lncRNA KMT2E-AS1 promotes hypoxic endothelial pathology in pulmonary hypertension Read More »

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