Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Togănel RO"'
Autor:
Gábor-Miklósi Dorottya, Cerghit-Paler Andreea, Sus Ioana, Ghiragosian-Rusu Simina, Făgărășan Amalia, Togănel Rodica, Gozar Liliana
Publikováno v:
Journal of Interdisciplinary Medicine, Vol 7, Iss 3, Pp 69-73 (2022)
We present the case of a neonatal patient with atrial tachycardia with unusual characteristics – abrupt onset and cessation, non-responsiveness to overdrive, termination by direct cardio-version – in association with an ostium secundum-type atria
Externí odkaz:
https://doaj.org/article/a9eeed5b7df148c98abf632b6ec5b26a
Autor:
Stănescu Alexandra, Manuca Rareș, Togănel Rodica, Cernica Daniel, Benedek Theodora, Benedek Imre
Publikováno v:
Journal of Interdisciplinary Medicine, Vol 6, Iss 2, Pp 92-99 (2021)
Background: Multimodality imaging improves the accuracy of cardiac assessment in patients with prior myocardial infarction. The aim of this study was to investigate the association between coronary plaque vulnerability (PV) and myocardial viability i
Externí odkaz:
https://doaj.org/article/55f3940e07cb4df2865fedfdb0412d94
Autor:
Șuteu Carmen Corina, Blesneac Cristina, Pop Marian, Făgărășan Amalia, Gozar Liliana, Togănel Rodica
Publikováno v:
Journal of Cardiovascular Emergencies, Vol 7, Iss 1, Pp 17-21 (2021)
Scimitar syndrome is a rare congenital cardiovascular malformation that includes a partially anomalous drainage of the pulmonary veins in the inferior vena cava, right pulmonary hypoplasia, and systemic-pulmonary collaterals originating from various
Externí odkaz:
https://doaj.org/article/8a6edea8563d44f384a9ea0983997000
Publikováno v:
Journal of Cardiovascular Emergencies, Vol 6, Iss 4, Pp 104-108 (2020)
Pulmonary arterial hypertension (PAH) is a rare but severe complication that should be investigated in patients diagnosed with transposition of the great arteries who have undergone neonatal arterial switch operation. Early diagnosis and aggressive c
Externí odkaz:
https://doaj.org/article/6fcfb70267414feb825ae034927488c6
Autor:
Cerghit Andreea Paler, Făgărășan Amalia, Muntean Iolanda, Pasc Sorina, Miklósi Dorottya, Gozar Liliana, Togănel Rodica
Publikováno v:
Journal of Cardiovascular Emergencies, Vol 6, Iss 3, Pp 67-71 (2020)
Introduction: The incidence of cardiac arrhythmia is approximately 1% in the neonatal period and 1–3% in late pregnancy. Atrial flutter (AF), a rhythm disorder based on the mechanism of reentry, represents approximately 32% of all neonatal cardiac
Externí odkaz:
https://doaj.org/article/f07e3dc42aae4fbc9b0c949b5f3f948e
Publikováno v:
Journal of Cardiovascular Emergencies, Vol 6, Iss 2, Pp 43-47 (2020)
Dilated cardiomyopathy (DCM) is the most common type of cardiomyopathy in children. Heart transplantation is considered standard therapy in dilated cardiomyopathy with end-stage heart failure. We present a case of a 15-year-old patient diagnosed with
Externí odkaz:
https://doaj.org/article/784627ea9257442c88cbe2411849c5c0
Publikováno v:
Journal of Cardiovascular Emergencies, Vol 6, Iss 1, Pp 20-23 (2020)
Congenital aortic stenosis (AS) occurs in around 0.2–0.5% of newborns, and its clinical severity is quite variable. Some of the newborns with AS require urgent medical care: prostaglandin infusion, balloon aortic valvuloplasty, or surgical interven
Externí odkaz:
https://doaj.org/article/85ac9bb171514301b33945ebfe7c8b4d
Publikováno v:
Journal of Cardiovascular Emergencies, Vol 5, Iss 4, Pp 140-147 (2019)
Background: Acute myocarditis, a primary inflammatory cardiac disease commonly caused by viral infection, is an important cause of morbidity and mortality in children. Data obtained from forensic studies found an incidence of 15–33% for acute myoca
Externí odkaz:
https://doaj.org/article/85eb1530ca984d28830f9e85ee495bd1
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 26, Iss 3, Pp 305-312 (2018)
Pulmonary arterial hypertension (PAH) is a progressive disease with a complex pathogenesis. The polymorphism of the gene of multidrug resistance-1 (MDR1) has been associated with many diseases including PAH.
Externí odkaz:
https://doaj.org/article/3b75e7cffd82462189c2c0069d79ac82
Publikováno v:
Journal of Interdisciplinary Medicine, Vol 3, Iss 2, Pp 110-113 (2018)
Truncus arteriosus communis (TA) is a rare cyanotic congenital heart defect, in which the aorta and the pulmonary artery have not been separated during the normal development of the fetal heart, so a single truncal artery is arising from the base of
Externí odkaz:
https://doaj.org/article/3512bea49f564840a0dd7df14c3e9fa5