Fresh (PHresh). Less than 1-2 years since publication

Incidental pulmonary arteriovenous malformation

Mallory A. Von Lotten, Eric Howell, J. Andrew WatsonUniversity of Alabama at Birmingham Heersink School of Medicine. United States Journal of Hospital MedicineJ Hosp Med 2026; DOI: 10.1002/jhm.70259 AbstractAbstract Not Available CategoryPulmonary Arteriovenous Malformations Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication Article Access Free PDF […]

Incidental pulmonary arteriovenous malformation Read More »

Hypercapnia as a Key Mechanism in the Development of Pulmonary Hypertension in Malignant Pertussis: A Case Report

Juan Ignacio Muñoz-Bonet, Francisco José Sebastián-Cuevas, Eva María Flor-Macián, María del Carmen Ortega-Sánchez, Andrés Rodríguez-Sacristán, Juan BrinesHospital Clínico Universitario. University of Valencia. Hospital Dr. Peset Valencia. Hospital Universitario Virgen Macarena.Spain Respirology Case ReportsRespirol Case Rep 2026; 14: DOI: 10.1002/rcr2.70528 AbstractMalignant pertussis (MP) is a highly lethal complication of pertussis in young infants, typically associated with hyperleukocytosis, pulmonary

Hypercapnia as a Key Mechanism in the Development of Pulmonary Hypertension in Malignant Pertussis: A Case Report Read More »

A circulating MicroRNA signature for the diagnosis of pulmonary arterial hypertension and functional characterization of candidate miR-3168

Mauro Lago-Docampo, Ainhoa Iglesias-López, Carlos Vilariño, Adolfo Baloira, Joan Albert Barberá, Isabel Blanco, Diana ValverdeUniversidade de Vigo. Galicia Sur Health Research Institute. Hospital Povisa. Complejo Hospitalario Universitario de Pontevedra. University of Barcelona. Stanford University School of Medicine.Spain and United States Scientific ReportsSci Rep 2026; DOI: 10.1038/s41598-026-42550-8 AbstractPulmonary Arterial Hypertension (PAH) is a rare, progressive disorder characterized

A circulating MicroRNA signature for the diagnosis of pulmonary arterial hypertension and functional characterization of candidate miR-3168 Read More »

Mechanical Compression Causes Lung Hypoplasia in Congenital Diaphragmatic Hernia with GATA4 Genetic Variants

Betty Pham, Zhuowei Li, Gidsela Luna, Nicole Talaba, Na Zhang, Giangela M. Stokes, Mark D. Wienjold, Jinhao Xu, Yujuan Su, Rebecca Hernan, Wendy K. Chung, Xin Sun, David J. McCulleyUniversity of California, San Diego and Rady Children’s Hospital. University of Wisconsin-Madison. Boston Children’s Hospital and Harvard Medical School. United States American Journal of Physiology Lung

Mechanical Compression Causes Lung Hypoplasia in Congenital Diaphragmatic Hernia with GATA4 Genetic Variants Read More »

The Pulmonary Hypertension Global Patient Survey: Understanding the Invisible Burden of Paediatric Pulmonary Hypertension

Sadia Quyam, Sarah Drumm, Shiv Mungala, Katherine Bunclark, Gerald Fischer, Eva Otter, Hakim Ghani, Wendy Gin‐Sing, Luke Howard, Marcin Kurzyna, Pisana Ferrari, Lynsay Macdonald, Joseph Newman, Millicent Stone, Mark Toshner, Joanna Pepke Zaba, Maurice Beghetti, Shahin MoledinaGreat Ormond Street Hospital for Children and University College London. Pulmonary Vascular Research Institute. Royal Statistical Society. University of

The Pulmonary Hypertension Global Patient Survey: Understanding the Invisible Burden of Paediatric Pulmonary Hypertension Read More »

Obstructive Sleep Apnea-Hypopnea Syndrome in Children With Down Syndrome Treated at a Tertiary Care Hospital in Northeastern Colombia

Silvia N. Suarez Mantilla, Victor Manuel Mora Bautista, Martha Lucia Africano Leon, Diana C. Vergara Arenas, Yuli E. Rojas, Sergio Serrano-GomezUniversidad Industrial de Santander. Clinica Materno Infantil San Luis. Columbia CureusCureus 2026; 18: DOI: 10.7759/cureus.102624 AbstractObstructive sleep apnea-hypopnea syndrome (OSAHS) is frequent in children with Down Syndrome (DS), associated with anatomical characteristics such as midfacial hypoplasia,

Obstructive Sleep Apnea-Hypopnea Syndrome in Children With Down Syndrome Treated at a Tertiary Care Hospital in Northeastern Colombia Read More »

Reduced gastrointestinal iron uptake in pulmonary arterial hypertension: a prospective cross-sectional study

Luisa Repsold, Satenik Harutyunova, Ekkehard Grünig, Nicola Benjamin, Panagiota Xanthouli, Benjamin Egenlauf, Andreea Florea, Memoona Shaukat, Richard Sparla, Christina Mertens, Martina U. Muckenthaler, Christina A. EichstaedtHeidelberg University Hospital. German Center for Lung Research.Germany Respiratory ResearchRespir Res 2026; DOI: 10.1186/s12931-026-03592-8 AbstractBackground: Iron deficiency (ID) is common in patients with pulmonary arterial hypertension (PAH) and is associated with

Reduced gastrointestinal iron uptake in pulmonary arterial hypertension: a prospective cross-sectional study Read More »

A Combination Of Vein Of Galen Aneurysmal Malformation And Bovine Aortic Arch In Newborn: A Case Report

Krishna Deo Mandal, Kalpana Subedi, Unnati Amatya, Janak PathakParopakar Maternity and Women’s Hospital. Embassy of India.Nepal Journal of the Nepal Medical AssociationJ Nepal Med Assoc 2025; 63: 347-349DOI: 10.31729/jnma.8987 AbstractVein of Galen aneurysmal malformation is a rare intracranial arteriovenous malformation, coexistence with aortic arch anomalies is even more uncommon, carry high risk of morbidity and mortality

A Combination Of Vein Of Galen Aneurysmal Malformation And Bovine Aortic Arch In Newborn: A Case Report Read More »

Pulmonary Hypertension in Infants Who Are Premature

Ana Beatriz Nevarez Gilbert, Adrianne R. BischoffUniversity of Iowa.United States NeoReviewsNeoreviews 2026; 27: e144-e156DOI: 10.1542/neo.27-3-102 AbstractPulmonary hypertension (PH) is a serious and potentially life-threatening condition in neonates, often resulting from impaired transition from fetal to postnatal circulation. Although traditionally associated with elevated pulmonary vascular resistance and hypoxemic respiratory failure, PH in infants who are preterm encompasses

Pulmonary Hypertension in Infants Who Are Premature Read More »

Lamp Oil Poisoning: Pulmonary Hypertension Following Oil Aspiration Successfully Treated with Inhaled Nitric Oxide

Demet Tosun, Ilyas Bingöl Nihal AkçayIstanbul Kanuni Sultan Suleyman Training and Research Hospital.Turkey Klinische PädiatrieKlin Padiatr 2026; DOI: 10.1055/a-2814-3185 AbstractAbstract Not Available CategoryClass I. Drug-induced and Toxin-induced Pulmonary HypertensionMedical Therapy. Efficacy or Lack of Efficacy Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication Article Access Free

Lamp Oil Poisoning: Pulmonary Hypertension Following Oil Aspiration Successfully Treated with Inhaled Nitric Oxide Read More »

Scroll to Top