Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Razvan Capsa"'
Autor:
Sebastian Onciul, Oana Popa, Radu Nicolaescu, Vlad Bataila, Lucian Calmac, Cosmin Mihai, Mugur Marinescu, Radu Dan Andrei, Alexandru Deaconu, Stefan Bogdan, Raluca Ciomag, Nicoleta Popa-Fotea, Sorin Popescu, Stefan Radu, Claudia Nica, Bogdan Baciu, Oana Gheorghe Fronea, Maria Florescu, Radu Sascau, Cristian Statescu, Alexandru Scafa, Maria Dorobantu, Razvan Capsa
Publikováno v:
Romanian Journal of Cardiology, Vol 31, Iss 1, Pp 52-62 (2021)
Objectives – To provide preliminary data on practice of stress perfusion cardiovascular magnetic resonance (CMR) in a single center in Romania. Methods – We retrospectively reviewed the clinical files and CMR reports of patients who underwent str
Externí odkaz:
https://doaj.org/article/8254417609ed4fd4aa5044b8bb5e487a
Publikováno v:
Romanian Journal of Cardiology. 31:903-910
Neurofibromatosis 1-Noonan syndrome is considered a distinct clinical entity, combining characteristics of both autosomal dominant disorders: neurofibromatosis 1 and Noonan syndrome. We present the case of a 20-year-old patient clinically diagnosed w
Autor:
Ioana, Lupescu, Narcis, Masala, Razvan, Capsa, Nicoara, Câmpeanu, Serban Alexandru, Georgescu
Publikováno v:
Journal of gastrointestinal and liver diseases : JGLD. 15(4)
In this educational presentation, we offer an overview of acquired anomalies of the portal venous system explored by biphasic helical CT and MRI. Portosystemic collateral vessels, cavernous transformation of the portal vein, intrahepatic vascular shu
Publikováno v:
Journal of gastrointestinal and liver diseases : JGLD. 15(3)
The liver has a unique dual blood supply from the hepatic artery (25%) and the portal vein (75%). Helical computer tomography (CT) and also magnetic resonance imaging (MRI) are suitable techniques for hepatic imaging. Helical CT and MR angiography al
Autor:
Adrian Giucă, Cristina Mitu, Bogdan Ovidiu Popescu, Alexandra Eugenia Bastian, Răzvan Capşa, Adriana Mursă, Viorica Rădoi, Bogdan Alexandru Popescu, Ruxandra Jurcuţ
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Hypertrophic cardiomyopathy (HCM) is a genetic disorder mostly caused by sarcomeric gene mutations, but almost 10% of cases are attributed to inherited metabolic and neuromuscular disorders. First described in 2008 in an American-
Externí odkaz:
https://doaj.org/article/9cac997c41704de2aec48cded7b400e9