Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Germana Gizzi"'
Autor:
Vito Maurizio Parato, Sara Belleggia, Andrea Giovanni Parato, Umberto Ianni, Michela Molisana, Germana Gizzi, Simone D'Agostino, Melissa Dottori, Marco Di Eusanio
Publikováno v:
Monaldi Archives for Chest Disease (2023)
We reported a case of non-bacterial thrombotic endocarditis (NBTE) in a 37-year-old woman who presented with signs and symptoms of cardio-embolic cerebral stroke caused by a prothrombotic state due to underlying advanced uterine cancer. Multimodal im
Externí odkaz:
https://doaj.org/article/5f93e534f6384f37a3901b4020c6a1d1
Autor:
Michela Molisana, Adelina Selimi, Germana Gizzi, Simone D’Agostino, Umberto Ianni, Vito Maurizio Parato
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
BackgroundAbnormalities of the mitral valve (MV) apparatus are typical features of hypertrophic cardiomyopathy (HCM). These abnormalities include leaflet elongation, thick leaflets, displacement of papillary muscle, and systolic anterior motion (SAM)
Externí odkaz:
https://doaj.org/article/110aef4bf3634094bd14404083d99a50
Publikováno v:
Monaldi Archives for Chest Disease (2021)
Hypertrophic cardiomyopathy (HCM) is a genetic disorder presenting with a pathological increase of left ventricle (LV) wall thicknesses. The most frequent morphological form is characterized by an abnormal LV basal septal hypertrophy. Tako-Tsubo card
Externí odkaz:
https://doaj.org/article/a4ebb73e598f4e31aa695f94837e312c
Autor:
Vito Maurizio Parato, Camilla Notaristefani, Germana Gizzi, Michele Scarano, Alessandra Baldinelli, Marco Pozzi
Publikováno v:
Cor et Vasa. 63:583-587
Publikováno v:
European Heart Journal Supplements. 23
Aims We know that basal septal hypertrophy is a rare and unique anatomical finding associated with hypertrophic cardiomyopathy (HCM). Tako-Tsubo cardiomyopathy (TTC) is a transient left ventricular systolic dysfunction induced by high physical or emo
Publikováno v:
Cor et Vasa. 60:e508-e511
Arytmogenni dyplazie prave komory (arrhythmogenic right ventricular dysplasia, ARVD) je formou dědicne kardiomyopatie charakterizovane nahrazovanim svaloviny převažně prave komory fibrozni a tukovou tkani. U osob s timto postiženim může dojit
Publikováno v:
Cor et Vasa. 60:e469-e471
Incidence infekcni endokarditidy neni u osob s implantabilnimi elektronickými přistroji pro lecbu srdecnich arytmii nijak výjimecnou komplikaci. Běžnými rizikovými faktory pro rozvoj srdecni endokarditidy u pacientů s těmito přistroji jsou
Publikováno v:
Journal of Cardiovascular Echography
We present a case of a 91-year-old man presenting to the emergency department with a tearing back pain. The patient's history included an endovascular abdominal aortic repair because of an aneurysm. The transthoracic echocardiography (TTE) appeared n
Autor:
Renato Gregorini, Erika Lemme, Maria Penco, Mauro Di Eusanio, Carmine Villani, Silvio Romano, Germana Gizzi, Alessandro Mazzola, Francesco Pellone, Michele Di Mauro, Francesca Faragalli
Publikováno v:
The Annals of Thoracic Surgery. 94:1185-1190
Background The aim of this retrospective study was to compare the early and midterm clinical outcomes of aortic root replacement in elderly patients receiving the Freestyle stentless bioprosthesis (FSB) (Medtronic Inc, Minneapolis, MN) with younger p