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

Restoration of Foxp3+ Regulatory T Cells by HDAC-dependent Epigenetic Modulation Plays a Pivotal Role in Resolving Pulmonary Arterial Hypertension Pathology

Chien-Nien Chen, Nabil Hajji, Fu-Chiang Yeh, Sunniyat Rahman, Souad Ali, John Wharton, Nicoleta Baxan, Lin Zhao, Chong-Yang Xie, Yi-Guan Chen, Maria G. Frid, Prakash Chelladurai, Soni Savai Pullamsetti, Kurt R. Stenmark, Martin R. Wilkins, Lan ZhaoImperial College London. Tri-Service General Hospital. University of Colorado. University Giessen Lung Centre. Max Planck Institute for Heart and Lung […]

Restoration of Foxp3+ Regulatory T Cells by HDAC-dependent Epigenetic Modulation Plays a Pivotal Role in Resolving Pulmonary Arterial Hypertension Pathology Read More »

MRI pulmonary artery flow detects lung vascular pathology in preterms with lung disease

Friederike Häfner, Alida Kindt, Kathrin Strobl, Kai Förster, Motaharehsadat Heydarian, Erika Gonzalez, Benjamin Schubert, Yvonne Kraus, Robert Dalla Pozza, Andreas W. Flemmer, Birgit Ertl-Wagner, Olaf Dietrich, Sophia Stoecklein, Khodr Tello, Anne HilgendorffHelmholtz Center Munich, Haunersches Children’s Hospital. Leiden University. University Children’s Hospital, University Hospital and Ludwig-Maximilian University. Hospital for Sick Children. Justus-Liebig-University Giessen. Germany, Netherlands

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2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

Marc Humbert, Gabor Kovacs, Marius M. Hoeper, Roberto Badagliacca, Rolf M. F. Berger, Margarita Brida, Jorn Carlsen, Andrew J. S. Coats, Pilar Escribano-Subias, Pisana Ferrari, Diogenes S. Ferreira, Hossein Ardeschir Ghofrani, George Giannakoulas, David G. Kiely, Eckhard Mayer, Gergely Meszaros, Blin Nagavci, Karen M. Olsson, Joanna Pepke-Zaba, Göran Radegran, Gerald Simonneau, Oliver Sitbon, Thomy Tonia,

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Management of congenital and acquired pulmonary vein stenosis

Eric J. Devaney, Andrew C. Chang, Richard G. Ohye, Edward L. BoveUniversity of Michigan School of Medicine.United States Annals of Thoracic SurgeryAnn Thorac Surg 2006; 81: 992-995DOI: 10.1016/j.athoracsur.2005.08.020 AbstractBackground: Pulmonary vein (PV) stenosis, whether congenital or after repair of total anomalous pulmonary venous connection (TAPVC), continues to carry a poor prognosis.Methods: A retrospective review identified 36 patients who

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Stenting of the vertical vein in obstructed total anomalous pulmonary venous return as rescue procedure in a neonate

Shirley M. Lo-A-Njoe, Nico A. Blom, Regina Bökenkamp, Jaap OttenkampLeiden University Medical Center.Netherlands Catheterization and Cardiovascular InterventionsCatheter Cardiovasc Interv 2006; 67: 668-670DOI: 10.1002/ccd.20715 AbstractA newborn girl with progressive respiratory distress and cyanosis was found to have severely obstructed supracardiac total pulmonary venous return (TAPVR). Stenting of the stenosis provided immediate and effective relief of the obstruction

Stenting of the vertical vein in obstructed total anomalous pulmonary venous return as rescue procedure in a neonate Read More »

Pulmonary vein stenosis following repair of total anomalous pulmonary venous connection

Eric J. Devaney, Richard G. Ohye, Edward L. BoveUniversity of Michigan. United States Seminars in Thoracic and Cardiovascular Surgery Pediatric Cardiac Surgery AnnualSemin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2006; 51-55.DOI: 10.1053/j.pcsu.2006.02.023 AbstractPulmonary vein stenosis may occur following the repair of total anomalous pulmonary venous connection and carries a poor prognosis. Conventional surgical therapies have

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Low-affinity insulin-like growth factor binding protein 7 and its association with pulmonary arterial hypertension severity and survival

Guillermo Torres, Andrew C. Lancaster, Jun Yang, Megan Griffiths, Stephanie Brandal, Rachel Damico, Dhananjay Vaidya, Catherine E. Simpson, Lisa J. Martin, Michael W. Pauciulo, William C. Nichols, D. Dunbar Ivy, Eric D. Austin, Paul M. Hassoun, Allen D. EverettJohns Hopkins University. University of Texas Southwestern Medical Center. Cincinnati Children’s Hospital Medical Center and University of

Low-affinity insulin-like growth factor binding protein 7 and its association with pulmonary arterial hypertension severity and survival Read More »

Corrigendum: Case report: Selexipag in pediatric pulmonary hypertension: initiation, transition, and titration

Jenna M. Faircloth, Neelam D. Bhatt, Corey A. Chartan, Ryan D. Coleman, Natalie Villafranco, Fadel E. Ruiz, Raysa Morales-Demori, Elise Whalen, Erin Ely, Rozmeen Fombin, Nidhy P. VargheseTexas Children’s Hospital and Baylor College of Medicine.United States Frontiers in PediatricsFront Pediatr 2023; 11DOI: 10.3389/fped.2023.1275389 AbstractThis corrects the article DOI: 10.3389/fped.2023.1050508. CategoryClass I. Idiopathic Pulmonary HypertensionClass I. Heritable

Corrigendum: Case report: Selexipag in pediatric pulmonary hypertension: initiation, transition, and titration Read More »

Mid-Systolic Notching of the Pulmonary Valve Doppler Signal is Highly Associated with Pulmonary Hypertension

Robert W. Loar, Christopher Tsao, Fadeke Ogunyankin, J. Kevin Wilkes, Dennis VanLoozen, Deborah Shutte, Adrian DyerCook Children’s Medical Center. TCU Burnett School of Medicine. United States Pediatric CardiologyPediatr Cardiol 2023; DOI: 10.1007/s00246-023-03285-9 AbstractMid-systolic notching (MSN) of the pulmonary valve Doppler signal represents a reflected systolic pressure wave from the pulmonary vasculature and is often seen in

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Usefulness of cutting balloon angioplasty for pulmonary vein in-stent stenosis

Amanda L. Cook, Lourdes R. Prieto, Jeffrey W. Delaney, John F. RhodesDuke University Medical Center.United States American Journal of CardiologyAm J Cardiol 2006; 98: 407-410DOI: 10.1016/j.amjcard.2006.02.049 AbstractAfter radiofrequency ablation for atrial fibrillation, patients may develop pulmonary vein stenoses requiring stent angioplasty. The treatment options for when such patients develop in-stent stenoses are poorly defined. The investigators

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