Results 41 to 50 of about 10,298 (208)

Pulmonary Arteriovenous Malformations in a 18-months-old Child: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2022
Pulmonary Arteriovenous Malformation (PAVM) is a cardiovascular anomaly in which an anatomic communication between the pulmonary artery and pulmonary vein is formed, resulting in an additional cardiac shunt from right to left side.
Hesham Mohamad Fayad, Fatema Chowdhury, Godfred Antony Menezes, Shria Sadhu, Samiha Anjum Hossain   +4 more
doaj   +1 more source

Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia [PDF]

, 2015
Hereditary hemorrhagic telangiectasia (HHT) is mechanistically and therapeutically challenging, not only because of the molecular and cellular perturbations that generate vascular abnormalities, but also the modifications to circulatory physiology that ...
Shovlin, CL
core   +2 more sources

Pulmonary arteriovenous malformation in chronic thromboembolic pulmonary hypertension

Indian Journal of Radiology and Imaging, 2016
Chronic thromboembolic pulmonary hypertension is a morbid condition associated with complications such as hemoptysis, right heart failure, paradoxical embolism, and even death.
Arun Sharma, Gurpreet S Gulati, Neeraj Parakh, Abhinav Aggarwal   +3 more
doaj   +1 more source

A Rare Cause of Pulmonary Hypertension in a 4-Year-Old Toddler: Association of Cor Triatriatum Sinister and Pulmonary Arteriovenous Malformation

Case Reports in Pediatrics, 2020
Cor triatriatum sinister is a rare congenital cardiac anomaly. The anomaly is caused by a fibromuscular membrane that divides the left atrium into two cavities.
Can Yilmaz Yozgat, Erkan Cakir, Hakan Yazan, Hafize Otcu Temur, Kahraman Yakut, Yilmaz Yozgat   +5 more
doaj   +1 more source

Pulmonary arteriovenous malformation revealing Osler‐Weber‐Rendu disease: A case report

Clinical Case Reports, 2022
Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The present case was a 34‐year‐
Herveat Ramanandafy, Finaritra Princy Parfait Andriamahenina, Michel Harison Tiaray, Anjara Mihaja Nandimbiniaina, Angela Zamelina Razafindrasoa, Sonia Razafimpihanina, Diamondra Andriarimanga, Jean Noêl Solohery Ratsimbazafy, Jocelyn Robert Rakotomizao, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana   +10 more
doaj   +1 more source

Pediatric lung transplantation: The years 1985 to 1992 and the clinical trial of FK 506 [PDF]

, 1993
The application of lung transplantation to the pediatric population was a natural extension of the success realized in our adult transplantation program, which began in 1982. Twenty pediatric patients (age range 3 to 18 years) have had heart-lung (n = 11)
Armitage, Armitage, Baldwin, Bartley P. Griffith, Billingham, Bisson, Cooper, Frederick J. Fricker, Geoffrey Kurland, Griffith, Hardesty, John M. Armitage, Keenan, Krien, Kusne, Marian Michaels, Patterson, Robert L. Hardesty, Ronald Jaffe, Rosendale, Samuel A. Yousem, Shigeki Morita, Tamaura, Thomas E. Starzl, Yousem, Zeevi, Zenati, Zenati   +27 more
core   +1 more source

Pulmonary arteriovenous malformations: Haemodynamics and shunt closure [PDF]

, 2014
Introduction The Abernethy malformation is a rare anomaly with a widely variable clinical presentation. Many diagnostic dilemmas have been reported. Nowadays, with the evolution of medical imaging, diagnosis can be made more easily, but management of ...
CL Shovlin, ER Chilvers, MK Whyte, MK Whyte, P Andrivet, P Gupta, R Cartin-Ceba, T Churton, VMM Vorselaars, W Li   +9 more
core   +10 more sources

Die hereditäre hemorrhagische Telangiektasie: Untersuchungen zur Multiorganbeteiligung bei Patienten mit Epistaxis als Leitsymptom [PDF]

, 2004
Die hereditäre hämorrhagische Telangiektasie (Morbus Rendu-Osler-Weber) ist ein autosomal-dominant vererbtes vaskuläres Fehlbildungssyndrom. Hierbei werden multiple arteriovenöse Malformationen (AVM) im Bereich der Schleimhaut der oberen ...
Cerra Wollstein, Ana, Prof. Dr. J. A. Werner   +1 more
core   +1 more source

Impact of pulmonary arteriovenous malformations on respiratory-related quality of life in patients with hereditary haemorrhagic telangiectasia.

PLoS ONE, 2014
Fifteen to fifty percent of patients with hereditary haemorrhagic telangiectasia have pulmonary arteriovenous malformations. The objective of this study was to measure the effect of the presence of pulmonary arteriovenous malformations and of their ...
Sandra Blivet, Daniel Cobarzan, Alain Beauchet, Mostafa El Hajjam, Pascal Lacombe, Thierry Chinet   +5 more
doaj   +1 more source

Arterial oxygen content is precisely maintained by graded erythrocytotic responses in settings of high/normal serum iron levels, and predicts exercise capacity: an observational study of hypoxaemic patients with pulmonary arteriovenous malformations. [PDF]

, 2014
Oxygen, haemoglobin and cardiac output are integrated components of oxygen transport: each gram of haemoglobin transports 1.34 mls of oxygen in the blood.
AD Kjeldsen, AM Evans, AN Friedman, BE Phillips, BM Silva, BR O'Driscoll, CG Mason, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, CL Shovlin, Claire L. Shovlin, CM Fletcher, D Pennington, DZ Levett, E McLean, ER Chilvers, H Finnamore, Hannah C. Tighe, IS Anand, JA Dutton, JA Livesey, James E. Jackson, JE Van de Pette, JJ Mager, JL Hart, L Boyer, LC Ou, Louisa C. Williams, LS Valberg, M Hu, M Moussouttas, ME Faughnan, MF McMullin, MK Whyte, MK Whyte, MP Grocott, MW van Gent, P Gupta, P Shovlin CL Wilmshurst, PB Terry, PC Hébert, PM Sondel, RC Hewes, RD Thompson, S Honda, T Ueki, Tracey Rouault, V Cottin, Vatshalan Santhirapala, WB Porter, WS Smellie   +53 more
core   +4 more sources