Podolec
Journal of Rare Cardiovascular Diseases: Another exciting quarter in the ‘usual’ life of the Journal Piotr Podolec Full Text: PDF Abstract Dear Friends and Colleagues, Our Dear Readers and Supporters of the Journal, It is an extreme pleasure to deliver at your hand the 7th issue of the Journal of Rare Cardiovascular Diseases. Our two‑year anniversary […]
Czajkowski
Long QT syndrome type 2 – can alarm clock really kill? (RCD code: V-1A.2) Marek Czajkowski Full Text: PDF Abstract This paper’s aim was to critically analyze existing research supporting statement found in many review articles that auditory stimuli may specifically and exclusively trigger cardiac events in patients with type 2 of congenital long QT syndrome […]
Rubis
Different biochemical profile of stable and decompensated systolic heart failure patients due to ischemic or dilated cardiomyopathy hospitalized in the tertiary cardiology center (RCD code: III-1) Pawel Rubis, Jakub Stępniewski, Mariusz Staszek, Łukasz Sikora, Patrycja Faltyn, Ewa Zawadzka, Lusine Khachatryan, Piotr Podolec Full Text: PDF Abstract Aim: This study aims to compare the extended biochemical profile of unselected […]
Oryshchyn
A rare cause of the left ventricular outflow tract obstruction: accessory mitral valve tissue (RCD code: IV-1D.2o) Nelia Oryshchyn, Ulyana Cherniaga, Yurij Palamarchuk Full Text: PDF Abstract Accessory mitral valve tissue is a rare congenital malformation, which often causes left ventricular outflow tract (LVOT) obstruction. Patients with accessory MVT and LVOT obstruction have poor exercise tolerance, fatigue, palpitations. […]
Dziedzic-Oleksy
The association between aortic stenosis and intestinal angiodysplasia – the Heyde’s Syndrome (RCD code: VIII-1) Hanna Dziedzic-Oleksy, Jakub Podolec, Agnieszka Sarnecka, Jakub Stępniewski, Monika Komar, Grzegorz Kopeć, Piotr Podolec Full Text: PDF Abstract Heyde’s syndrome is defined as a combination of gastrointestinal bleeding from a gastrointestinal angiodysplasia in patients with aortic stenosis. An acquired von Willebrand factor deficiency secondary to […]
Karch
Isolated left ventricular noncompaction in an asymptomatic althlete (RCD code: III-5A.1.0) Izabela Karch, Lidia Tomkiewicz‑Pająk, Monika Komar, Maria Olszowska, Paweł Rubiś, Piotr Podolec Full Text: PDF Abstract Left ventricular noncompaction (LVNC) is a rare form of cardiomyopathy due to abnormal morphogenesis of the endocardium and myocardium that occurs in early stages of foetal life. Given the increased […]
Drabik
Female patient after correction of tetralogy of Fallot with severe pulmonary regurgitation and significant left-to-right shunt at the ventricular septal level (RCD code: IV-5A2) Leszek Drabik, Lidia Tomkiewicz‑Pająk, Tomasz Miszalski-Jamka, Jacek Pająk, Bogusław Kapelak, Piotr Podolec Full Text: PDF Abstract Tetralogy of Fallot (ToF) is the most common cyanotic congenital heart disease after 1 year of age. Less […]
Tomkiewicz-Pająk
The 4th Conference of Working Group in Congenital Heart Diseases of Polish Society of Cardiology Lidia Tomkiewicz-Pająk Full Text: PDF Abstract Congenital heart disease (CHD) is the most common developmental anomaly and represents about 1% of all live-born children. Recent progress in cardiac surgery and pediatric cardiology has resulted in large numbers of adult patients who have […]
