Persistent pulmonary hypertension of the newborn.
Mandell E, Kinsella JP, Abman SH.
Pediatr Pulmonol. 2021 Mar;56(3):661-669. doi: 10.1002/ppul.25073.
Diagnosis of fetal non-chromosomal abnormalities on routine ultrasound examination at 11-13 weeks' gestation.
Syngelaki A, Hammami A, Bower S, Zidere V, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol. 2019 Oct;54(4):468-476. doi: 10.1002/uog.20844.
Sudden cardiac death.
Kuriachan VP, Sumner GL, Mitchell LB.
Curr Probl Cardiol. 2015 Apr;40(4):133-200. doi: 10.1016/j.cpcardiol.2015.01.002. Epub 2015 Feb 7.
Cardiac Imaging In Athletes.
Khan AA, Safi L, Wood M.
Methodist Debakey Cardiovasc J. 2016 Apr-Jun;12(2):86-92. doi: 10.14797/mdcj-12-2-86.
Cardiomyopathies in children: An overview.
Tsatsopoulou A, Protonotarios I, Xylouri Z, Papagiannis I, Anastasakis A, Germanakis I, Patrianakos A, Nyktari E, Gavras C, Papadopoulos G, Meditskou S, Lazarou E, Miliou A, Lazaros G.
Hellenic J Cardiol. 2023 Jul-Aug;72:43-56. doi: 10.1016/j.hjc.2023.02.007. Epub 2023 Mar 3.
Arrhythmogenic right ventricular dysplasia: cardiomyopathy current opinions on diagnostic and therapeutic aspects.
Naccarella F, Naccarelli G, Fattori R, Nava A, Martini B, Corrado D, Masotti A, Gatti M.
Curr Opin Cardiol. 2001 Jan;16(1):8-16. doi: 10.1097/00001573-200101000-00002.
Neonatal neoplasms.
Halperin EC.
Int J Radiat Oncol Biol Phys. 2000 Apr 1;47(1):171-8. doi: 10.1016/s0360-3016(00)00424-7.
[Recognizing rare cardiac diseases by electrocardiogram].
Grimm W, Grimm A, Grimm K, Efimova E.
Internist (Berl). 2018 Jun;59(6):618-629. doi: 10.1007/s00108-018-0400-y.
Videoscopic left cardiac sympathetic denervation for patients with recurrent ventricular fibrillation/malignant ventricular arrhythmia syndromes besides congenital long-QT syndrome.
Coleman MA, Bos JM, Johnson JN, Owen HJ, Deschamps C, Moir C, Ackerman MJ.
Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):782-8. doi: 10.1161/CIRCEP.112.971754. Epub 2012 Jul 11.
Left Ventricular Systolic Dysfunction Related to Adrenal Insufficiency in a Case due to Autoimmune Polyendocrine Syndrome Type 1 with a Novel Variant.
Özer Y, Turan H, Dağdeviren Çakır A, Gökalp S, Ocak Z, Ercan O, Evliyaoğlu O.
Mol Syndromol. 2023 Feb;14(1):65-70. doi: 10.1159/000526221. Epub 2022 Oct 6.
