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

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

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

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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Cardiac phenotypic spectrum of KCNT1 mutations

Utkarsh Kohli, Chitra Ravishankar, Douglas NordliComer Children’s Hospital and Pritzker School of Medicine of the University of Chicago. he Children’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania. United States Cardiology in the YoungCardiol Young 2020; 30: 1935-1939DOI: 10.1017/S1047951120002735 AbstractWe report a 10-month-old girl with KCNT1 (c1420C > T; p. Arg474Cys,

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Invasive haemodynamics predict outcomes in paediatric pulmonary artery hypertension

Rupesh Kumar Natarajan, Nathan Rodgers, Shanti Narasimhan, Matthew Ambrose, Abraham Rothman, Michael Shyne, Michael Evans, Varun AggarwalUniversity of Minnesota. University of Nevada, Las Vegas School of Medicine.United States Cardiology in the YoungCardiol Young 2024;DOI: 10.1017/S1047951124000647 AbstractBackground: Invasive haemodynamics are often performed for initiating and guiding pulmonary artery hypertension therapy. Little is known about the predictive value of

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Patent Ductus Arteriosus and Lung MRI Phenotype in Moderate and Severe Bronchopulmonary Dysplasia-Pulmonary Hypertension

Kurt R. Bjorkman, Kimberley G. Miles, Laura E. Bellew, Kristin A. Schneider, S. Melissa Magness, Nara S. Higano, Nicholas J. Ollberding, X. Hoyos Cordon, Russel M. Hirsch, Erik B. Hysinger, Jason C. Woods, Paul J. CritserCincinnati Children’s Hospital Medical Center and University of Cincinnati.United States American Journal of Respiratory and Critical Care MedicineAm J Respir

Patent Ductus Arteriosus and Lung MRI Phenotype in Moderate and Severe Bronchopulmonary Dysplasia-Pulmonary Hypertension Read More »

Digital Spatial Profiling Identifies Distinct Molecular Signatures of Vascular Lesions in Pulmonary Arterial Hypertension

Rubin M. Tuder, Aneta Gandjeva, Sarah Williams, Sushil Kumar, Vitaly O. Kheyfets, Kyle Matthew Hatton-Jones, Jacqueline R. Starr, Jeong Yun, Jason Hong, Nicholas R. West, Kurt R. StenmarkUniversity of Colorado Anschutz Medical Campus School of Medicine. University of Colorado. Griffith University. Brigham and Women’s Hospital and Harvard Medical School. University of California, Los Angeles.United States

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