Filed (PHiled). Greater than 1-2 years since publication

The Road to Heart Transplant in a Patient With Cardiomyopathy, Shone Complex, and Severe Pulmonary Hypertension

Arif Albulushi, Shabib Al-Asmi, Moosa Al-Abri, Hatem Al-FarhanUniversity of Nebraska Medical Center. Royal Hospital. Heart Hospital, Armed Forces Hospital and Sultan Qaboos University Hospital. Hamad Medical Corporation. United States, Oman and Qatar Journal of the American College of Cardiology Case ReportsJACC Case Rep 2024; 29:DOI: 10.1016/j.jaccas.2024.102323 AbstractOur case report details the journey of a 16-year-old male […]

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Systemic juvenile idiopathic arthritis-associated lung disease: A retrospective cohort study

Konstantin E. Belozerov, Natalia M. Solomatina, Eugenia A. Isupova, Alla A. Kuznetsiva, Mikhail M. KostikSaint-Petersburg State Pediatric Medical University. Children’s City Polyclinic No. 29 of the Kalininsky District of St. Petersburg. Almazov National Medical Research Centre.Russia World Journal of Clinical PediatricsWorld J Clin Pediar 2024; 13:DOI: 10.5409/wjcp.v13.i1.88912 AbstractBackground: Lung damage in systemic juvenile arthritis (sJIA) is one

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Tadalafil in Neonates and Infants With Pulmonary Hypertension Secondary to Bronchopulmonary Dysplasia

Amy Kiskaddon, Tanaka Dang, Daniel MaurielloJohns Hopkins All Children’s Hospital. Johns Hopkins University School of Medicine. Texas Children’s Hospital.United States Journal of Pediatric Pharmacology and TherapeuticsJ Pediatr Pharmacol Ther 2024; 29: 140-143DOI: 10.5863/1551-6776-29.2.140 AbstractObjectives: The primary outcome of this study was to describe the dosing regimen of tadalafil in neonates and infants diagnosed with pulmonary hypertension (PH)

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Non-invasive estimation of pulmonary hypertension and clinical deterioration risk in pediatric congenital heart disease: Development and validation of predictive tools

Ting Wang, Dansha Zhou, Yuqin Chen, Suhua Kuang, Yue Xing, Qijian Yi, Zhengxia Pan, Weibin Xu, Jiao Rao, Yunqi Liu, Guoliang Lu, Ziying Lin, Xiang Li, Yi Xie, Yulong Wu, Peng An, Xiaoxiao Deng, Jiayue He, Jiayi Xie, Chenxi Li, Gang Geng, Daiyin Tian, Enmei Liu, Jingsi Huang, Zhou Fu, Jian WangChildren’s Hospital of Chongqing

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Low global arginine bioavailability: a common phenomenon in pulmonary hypertension

Dunia Hatabah, Teresa De Marco, Dana P. McGlothlin, Mary Malloy, Loretta Z. Reyes, Rawan Korman, Gregory J. Kato, Claudia R. MorrisEmory University School of Medicine. University of California, San Francisco. Kaiser Permanente San Francisco. Children’s Healthcare of Atlanta. Blood Science Consulting.United States American Journal of Physiology Lung Cellular and Molecular PhysiologyAm J Physiol Lung Cell

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The Paradox of Pulmonary Vascular Resistance: Restoration of Pulmonary Capillary Recruitment as a Sine Qua Non for True Therapeutic Success in Pulmonary Arterial Hypertension

David Langleben, Stylianos E. Orfanos, Benjamin D. Fox, Nathan Messas, Michele Giovinazzo, John D. CatravasJewish General Hospital and McGill University. Evangelismos Hospital and National and Kapodistrian University of Athens Medical School. Yitzchak Shamir Hospital and Tel Aviv University. Old Dominion University.Canada, Greece, Israel and United States Journal of Clinical MedicineJ Clin Med 2022; 11:DOI: 10.3390/jcm11154568 AbstractExercise-induced

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Chronic thromboembolic pulmonary disease: Association with exercise-induced pulmonary hypertension and right ventricle adaptation over time: Chronic thromboembolic pulmonary disease and exercise pulmonary hypertension

Rosalinda Madonna, Mattia Alberti, Filippo Biondi, Riccardo Morganti, Roberto Badagliacca, Carmine Dario Vizza, Raffaele De CaterinaPisa University Hospital and University of Pisa. Sapienza University.Italy European Journal of Internal MedicineEur J Intern Med 2023; DOI: 10.1016/j.ejim.2023.11.021 AbstractBackground and aim: Chronic thromboembolic pulmonary disease (CTEPD) is a progressive condition caused by fibrotic thrombi and vascular remodeling in the pulmonary

Chronic thromboembolic pulmonary disease: Association with exercise-induced pulmonary hypertension and right ventricle adaptation over time: Chronic thromboembolic pulmonary disease and exercise pulmonary hypertension Read More »

Congenital diaphragmatic hernia

Elcin Ersöz Köse, Irfan YalcinkayaHealth Sciences University Istanbul Hamidiye Medical Faculty.Turkey Turkish Journal of Thoracic and Cardiovascular SurgeryTurk J Thorac Cardiovasc Surg 2024; 32(Suppl1): S89-S97DOI: 10.5606/tgkdc.dergisi.2024.25705 AbstractCongenital diaphragmatic hernia (CDH) is a rare developmental defect of the diaphragm, characterized by the herniation of abdominal contents into the chest, resulting in varying degrees of pulmonary hypoplasia and

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Viewing Pulmonary Hypertension Through a Pediatric Lens

Stuti Agarwal, Jeffrey Fineman, David N. Cornfield, Cristina M. Alvira, Roham T. Zamanian, Kara Goss, Ke Yuan, Sebastien Bonnet, Olivier Boucherat, Soni Pullamsetti, Miguel A. Alcázar, Elena Goncharova, Tatiana V. Kudryashova, Mark R. Nicolls, Vinicio de Jesús PérezStanford University. University of California, San Francisco. University of Texas Southwestern. Boston Children’s Hospital. University of Laval. Max-Planck-Institute

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Isolated Partial Anomalous Pulmonary Veins: A 10-Year Experience at a Single Center

Can Jin, Yongtao Wu, Zhiyi Wang, Xiaoran Liu, Qiang WangBeijing An Zhen Hospital Affiliated with Capital University of Medical Sciences. China Journal of Surgical ResearchJ Surg Res 2024; 298: 63-70DOI: 10.1016/j.jss.2023.12.022 AbstractIntroduction: Isolated partial anomalous pulmonary venous connection (PAPVC) is difficult to diagnose, and surgical indications remain controversial. We reviewed 10 y of isolated PAPVC cases.Methods: The data

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