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

Burden of pulmonary arterial hypertension in Asia from 1990 to 2021: Findings from Global Burden of Disease Study 2021

Shenshen Huang, Jiayong Qiu, Anyi Wang, Yuejiao Ma, Peiwen Wang, Dong Ding, Luhong Qiu, Shuangping Li, Mengyi Liu, Jiexin Zhang, Yimin Mao, Yi Yan, Xiqi Xu, Zhicheng JingFirst Affiliated Hospital and College of Clinical Medicine of Henan University of Science and Technology. Second Hospital of Hebei Medical University. Peking Union Medical College Hospital, Chinese Academy

Burden of pulmonary arterial hypertension in Asia from 1990 to 2021: Findings from Global Burden of Disease Study 2021 Read More »

[Cyanosis for more than 4 years in a girl aged 4 years and 3 months]

Mao-Lan Wu, Xiang-Rong Zheng, Yan-Tong Zhu, Guo-Yuan Zhang, Chen-Tao Liu, Xia Wang, Yong-Jun TangXiangya Hospital and Central South University.China Chinese Journal of Contemporary PediatricsZhongguo Dang Dai Er Ke Za Zhi 2020; 22: 387-390DOI: 10.7499/j.issn.1008-8830.1910147 AbstractA girl, aged 4 years and 3 months, presented with cyanosis of the lips shortly after birth. She then experienced shortness of

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Pulmonary Arteriovenous Malformations in Non-hereditary Hemorrhagic Telangiectasia Patients: An 18-Year Retrospective Study

Hasan Ahmad Hasan Albitar, Justin M. Segraves, Yahya Almodallal, Catarina Aragon Pinto, Alice Gallo De Moraes, Vivek N. IyerMayo Clinic. Baylor College of Medicine. United States LungLung 2020; 98: 679-686DOI: 10.1007/s00408-020-00367-w AbstractPurpose: Pulmonary arteriovenous malformations (PAVMs) are most commonly associated with hereditary hemorrhagic telangiectasia (HHT). Patients with PAVMs can present with serious complications including stroke, transient ischemic

Pulmonary Arteriovenous Malformations in Non-hereditary Hemorrhagic Telangiectasia Patients: An 18-Year Retrospective Study Read More »

Hepatic Vein Blood Increases Lung Microvascular Angiogenesis and Endothelial Cell Survival-Toward an Understanding of Univentricular Circulation

Andrew D. Spearman, Ankan Gupta, Amy Y. Pan, Emily I. Gronseth, Karthikeyan Thirugnanam, Todd M. Gudausky, Susan R. Foerster, Ramani RamchandranMedical College of Wisconsin and Children’s Hospital of Wisconsin.United States Seminars in Thoracic and Cardiovascular SurgerySemin Thorac Cardiovasc Surg 2020; 32: 980-987DOI: 10.1053/j.semtcvs.2020.03.004 AbstractTo improve our understanding of pulmonary arteriovenous malformations in univentricular congenital heart disease,

Hepatic Vein Blood Increases Lung Microvascular Angiogenesis and Endothelial Cell Survival-Toward an Understanding of Univentricular Circulation Read More »

Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

Saniye Girit, Ebru Senol, Özge Karatas, Ayse Inci YıldırımIstanbul Medeniyet University. Göztepe Training and Research Hospital. University of Health Sciences Medical School Dr. Lutfi Kırdar Kartal Educational and Research Hospital. University of Health Sciences Medical School Kartal Kosuyolu High Speciality Educational and Research Hospital.Turkey Respiratory Medicine Case ReportsRespir Med Case Rep 2020; 30: DOI: 10.1016/j.rmcr.2020.101137 AbstractPulmonary

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Homozygous GDF2-Related Hereditary Hemorrhagic Telangiectasia in a Chinese Family

Jinrong Liu, Jigang Yang, Xiaolei Tang, Huimin Li, Yuelin Shen, Weiyue Gu, Shunying ZhaoBeijing Children’s Hospital, National Center for Children’s Health and Capital Medical University. Beijing Friendship Hospital. Beijing Chigene Translational Medicine Research Center.China PediatricsPediatrics 2020; DOI: 10.1542/peds.2019-1970 AbstractHereditary hemorrhagic telangiectasia (HHT) can be clinically diagnosed, but children often lack characteristic features. We report a family

Homozygous GDF2-Related Hereditary Hemorrhagic Telangiectasia in a Chinese Family Read More »

Incidental diagnosis of four pulmonary arteriovenous fistulas during patent foramen ovale closure: a case report

Alessandro Andreis, Gabriella Agnoletti, Paolo ScacciatellaCittà della Salute e della Scienza di Torino Hospital and University of Turin.Italy Cardiology in the YoungCardiol Young 2020; 30: 1363-1365DOI: 10.1017/S1047951120002152 Abstractryptogenic cerebral ischemia in young patients is commonly ascribed to paradoxical embolism. We report the clinical case of a young patient with cryptogenic stroke and a patent foramen ovale,

Incidental diagnosis of four pulmonary arteriovenous fistulas during patent foramen ovale closure: a case report Read More »

Pulmonary artery-targeted low-dose metformin-loaded nanocapsules safely improve pulmonary arterial hypertension in rats

Ayako Chida-Nagai, Naoki Masaki, Hiroki Sato, Tatsuya Kato, Emi Takakuwa, Yoshihiro Matsuno, Atsushi Manabe, Atsuhito TakedaHokkaido University Hospital. Tokyo Women’s Medical University. Tohoku University Graduate School of Medicine. Oita University and Oita University Hospital.Japan Frontiers in PediatricsFront Pediatr 2025; 16: DOI: 10.3389/fphar.2025.1577570 AbstractIntroduction: Pulmonary arterial hypertension (PAH) remains a challenge to tackle despite various available medications. Metformin,

Pulmonary artery-targeted low-dose metformin-loaded nanocapsules safely improve pulmonary arterial hypertension in rats Read More »

Risk factors for severe pertussis in children and the application of exchange transfusion

Qihong Chen, Lihua Lin, Shuping Xiong, DandanGe, Yungang YangFirst Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University. Pediatric Key Laboratory of Xiamen. Pediatric Quality Control Center of Xiamen. China Pediatric ResearchPediatr Res 2025; DOI: 10.1038/s41390-025-04118-6 AbstractObjective: To identify risk factors for severe pertussis and assess the efficacy of exchange transfusion in children.Methods: We analyzed pediatric pertussis

Risk factors for severe pertussis in children and the application of exchange transfusion Read More »

Pulmonary Hypertension and Lung Transplantation

Sophie Kruszona, Khalil Aburahma, Nunzio Davide de Manna, Dmitry Bobylev, Arjang Ruhparwar, Christian Kuehn, Jawad Salman, Fabio IusHannover Medical School.Germany Zentralblatt für ChirurgieZentralbl Chir 2025; DOI: 10.1055/a-2590-2620 AbstractPulmonary artery hypertension (PAH), a subtype of pulmonary hypertension, is a rare end-stage lung disease. Bilateral lung and combined heart and lung transplantation have long been considered as a gold standard therapy for PAH. This manuscript

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