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

Exploring new heights with pulmonary functional imaging: insights into high-altitude pulmonary edema

Sean B. Fain, Marlowe W. EldridgeUniversity of Wisconsin-Madison Medical School.United States Journal of Applied PhysiologyJ Appl Physiol 2017; 122: 853-854DOI: 10.1152/japplphysiol.00168.2017 AbstractAbstract Not Available CategoryHigh Altitude Pulmonary Edema Age Focus: Pediatric Pulmonary Vascular Disease or Adult Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article Access Free PDF File […]

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An Approach to Children with Pulmonary Edema at High Altitude

Deborah R. Liptzin, Steven H. Abman, Ann Giesenhagen, D. Dunbar IvyUniversity of Colorado School of Medicine and Children’s Hospital ColoradoUnited States High Altitude Medicine and BiologyHigh Altit Med Biol 2018;DOI: 10.1089/ham.2017.0096 AbstractIntroduction: Diagnosis of high-altitude illness can be more challenging in children, especially those who are preverbal. Families often travel to high elevations for family vacations, either

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Clinical Care for Cardiovascular Disease in Patients With Williams-Beuren Syndrome

R. Thomas Collins II, Verena Gravenhorst, Gilles Faury, Joanna Kwiatkowska, Christian E. H. Schmelzer, Heike Schneider, Anna Waldoch, Rainer PankauUniversity of Kentucky College of Medicine. University Medical Center and Georg-August-University Göttingen. Université Grenoble. Medical University of Gdańsk. Fraunhofer Institute for Microstructure of Materials and Systems. University Medical Center Schleswig-Holstein and Christian-Albrechts-University.United States, Germany, France and

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Congenital unilateral pulmonary venous atresia with pulmonary veno-occlusive disease in contralateral lung: an unusual association

Savitri Shrivastava, James H . Moller, Jesse E . EdwardsUniversity of Minnesota.United States Pediatric CardiologyPediatr Cardiol 1986; 7: 213-219DOI: 10.1007/BF02093183 AbstractA patient presenting with the rare association of congenital unilateral pulmonary venous atresia in one lung and pulmonary veno-occlusive disease in the other is described. The patient first presented at the age of 3 1/2 years

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Down syndrome and congenital heart disease: perioperative planning and management

Dennis R. Delany, Stephanie S. Gaydos, Deborah A. Romeo, Heather T. Henderson, Kristi L. Fogg, Angela S. McKeta, Minoo N. Kavarana, John M. CostelloMedical University of South Carolina. United States Journal of Congenital CardiologyJ Congenit Cardiol 2021; 5: DOI: 10.1186/s40949-021-00061-3 AbstractApproximately 50% of newborns with Down syndrome have congenital heart disease. Non-cardiac comorbidities may also be

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Efficacy of bubble contrast echocardiography in detecting pulmonary arteriovenous fistulas in children with univentricular heart after total cavopulmonary connection

Dai Asada, Yuma Morishita, Yoko Kawai, Yo Kajiyama, Kazuyuki IkedaKyoto Prefectural University of Medicine.Japan Cardiology in the YoungCardiol Young 2020; 30: 227-230DOI: 10.1017/S104795111900324X AbstractBackground: Development of pulmonary arteriovenous fistulas in patients with cavopulmonary anastomosis may result in a significant morbidity. Although the use of bubble contrast echocardiography with selective injection into both the branch pulmonary arteries in

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[Pulmonary arteriovenous fistulas in a pediatric patient: a case report]

Yuli T. Samboni, Liliana P. Tordecilla, Gilberto Acuña, Ana L. MuñozUniversidad Antonio Nariño.Columbia Archivos Argentinos de PediatriaArch Argent Pediatr 2020; 118: e170-e173DOI: 10.5546/aap.2020.e170 AbstractPulmonary arteriovenous fistulas are congenital malformations due to anomalous direct communication between arteries and veins; the incidence is 2-3:100,000 inhabitants. This condition is usually asymptomatic and incidentally appearing in adult imaging findings. Transcutaneous

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CT Angiography Findings of Pulmonary Arteriovenous Malformations in Children and Young Adults With Hereditary Hemorrhagic Telangiectasia

Su-Mi Shin, Hee Kyung Kim, Eric J. Crotty, Adrienne M. Hammill, Katherine Wusik, Dong-Hoon KimSMG-SNU Boramae Medical Center. Cincinnati Children’s Hospital Medical Center and University of Cincinnati College of Medicine. Korea University College of Medicine.Republic of Korea and United States American Journal of RoengenologyAJR Am J Roentgenol 2020; 214: 1369-1376DOI: 10.2214/AJR.19.22012 AbstractObjective. The purpose of this study

CT Angiography Findings of Pulmonary Arteriovenous Malformations in Children and Young Adults With Hereditary Hemorrhagic Telangiectasia 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

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