Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Margarita Bartsota"'
Autor:
Margarita Bartsota, Guido Michielon, Alain Fraisse, Julene S. Carvalho, Pierce Daubeney, Sylvia Krupickova, Carles Bautista, Margarita Burmester, Ajay Desai, Giovanni DiSalvo, Zdenek Slavik, Duncan Macrae
Publikováno v:
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery. 57(6)
OBJECTIVES The interstage mortality rate after a Norwood stage 1 operation remains 12–20% in current series. In-hospital interstage facilitates escalation of care, possibly improving outcome. METHODS A retrospective study was designed for hypoplast
Publikováno v:
Fetal and Maternal Medicine Review. 25:79-94
Autor:
Bejal Pandya, Merlin R. McMillan, Sheila G. Haworth, Kristian H. Mortensen, Vivek Muthurangu, Margarita Bartsota, Shahin Moledina, Andrew M. Taylor, Sadia Quyam, Ingram Schulze-Neick
Publikováno v:
Circulation: Cardiovascular Imaging. 6:407-414
Background— There are very few validated prognostic markers in pediatric pulmonary hypertension. Cardiac MRI is a useful, noninvasive method for determining prognosis in adults. The present study is the first to assess its prognostic value in child
Autor:
Vassos Neocleous, Nicos Skordis, Constandina Eleni Costi, Yiannis S. Ioannou, Margarita Bartsota, Leonidas A. Phylactou
Publikováno v:
Clinical Biochemistry. 42:1363-1367
Objectives The purpose of this study was to identify and determine the frequencies of rare CYP21A2 gene mutations in patients with 21-hydroxylase deficiency (21-OHD) in the Cypriot population. Design and methods Direct sequencing and MLPA analysis of
Autor:
Dominic Abrams, Sarah Mead-Regan, Juan Pablo Kaski, Margarita Bartsota, Martin Lowe, Jasveer Mangat, Thomas G. Day, Merlin R. McMillan, Rory Bryant
Publikováno v:
Open Heart
Objectives Brugada syndrome (BrS) is an inherited arrhythmia syndrome that causes sudden cardiac death in the young. The class Ia antiarrhythmic ajmaline can be used to provoke the diagnostic ECG pattern. Its use has been established in adults, but l
Autor:
Sarah Mead-Reagan, Dominic Abrams, Rory Bryant, Martin Lowe, Margarita Bartsota, Jasveer Mangat, Juan Pablo Kaski, Thomas G. Day
Publikováno v:
Heart. 99:A48.3-A49
Background Brugada syndrome (BS) is a genetic disorder characterised by J point elevation in the right ventricular leads, ventricular arrhythmia and sudden cardiac death (SCD). The diagnostic ECG changes can be provoked by sodium channel blocking age
Autor:
Rory Bryant, Martin Lowe, Thomas G. Day, Jasveer Mangat, Juan Pablo Kaski, Margarita Bartsota, Dominic Abrams, Sarah Mead-Reagan
Publikováno v:
Journal of the American College of Cardiology. (10):E293
Brugada syndrome (BS) is a genetic disorder characterised by J point elevation in the right ventricular leads, ventricular arrhythmia and sudden cardiac death (SCD). The diagnostic ECG changes can be provoked by sodium channel blocking agents includi