Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Luciano De Simone"'
Autor:
Guglielmo Capponi, Gilda Belli, Mattia Giovannini, Giulia Remaschi, Alice Brambilla, Francesca Vannuccini, Silvia Favilli, Giulio Porcedda, Luciano De Simone
Publikováno v:
BMC Cardiovascular Disorders, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Supraventricular tachycardias (SVTs) are common in the first year of life and may be life-threatening. Acute cardioversion is usually effective, with both pharmacological and non-pharmacological procedures. However, as yet no inte
Externí odkaz:
https://doaj.org/article/031e9d0875f34d11869b9596b2d7757c
Autor:
Luciano De Simone, Serena Chiellino, Gaia Spaziani, Giulio Porcedda, Giovan Battista Calabri, Sergio Berti, Silvia Favilli, Laura Stefani, Giuseppe Santoro
Publikováno v:
Children, Vol 10, Iss 3, p 526 (2023)
Hutchinson–Gilford progeria syndrome is an extremely rare genetic disease caused by a de novo mutation in the LMNA gene, leading to an accumulation of a form of Lamin A, called Progerin, which results in a typical phenotype and a marked decrease in
Externí odkaz:
https://doaj.org/article/f41d35970fcc46e99a0c917ec042c627
Autor:
Valentina Spinelli, Francesca Girolami, Chiara Marrone, Veronica Consigli, Maria Iascone, Silvia Passantino, Giulio Porcedda, Giovanni Battista Calabri, Luciano De Simone, Iacopo Olivotto, Giuseppe Santoro, Silvia Favilli
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3368-3372 (2020)
Abstract Genetic investigation of early‐onset Dilatative cardiomyopathy phenotype, including molecular autopsy, is the key to appropriate recognition and management of rare etiologies and atypical presentations and to offer genetic counseling to th
Externí odkaz:
https://doaj.org/article/a1839f6f9f5b438fa2629f0563cfa98f
Autor:
Guglielmo Capponi, Mattia Giovannini, Ioanna Koniari, Francesca Mori, Chiara Rubino, Gaia Spaziani, Giovanni Battista Calabri, Silvia Favilli, Elio Novembre, Giuseppe Indolfi, Luciano De Simone, Sandra Trapani
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
A 12-year-old male patient suffering from congenital glaucoma developed bradycardia, left ventricular failure, and hypotension after induction of anesthesia. Electrocardiography and echocardiography revealed a complete normalization of ECG and a comp
Externí odkaz:
https://doaj.org/article/cace6e7d1ba3441ead5a9675866f6bad
Publikováno v:
Journal of Functional Morphology and Kinesiology, Vol 7, Iss 2, p 37 (2022)
COVID 19 pandemic has induced a large sedentarism in several kinds of sports. Some peculiar categories of athletes could particularly suffer from a prolonged inactivity as those affected by minimal cardiopathies as bicuspid aortic valve (BAV) athlete
Externí odkaz:
https://doaj.org/article/9acbc70beb21448586d052c396d1f434
Autor:
Luciano De Simone, Laura Capirchio, Rosa Maria Roperto, Paola Romagnani, Michele Sacchini, Maria Alice Donati, Maurizio de Martino
Publikováno v:
Italian Journal of Pediatrics, Vol 44, Iss 1, Pp 1-5 (2018)
Abstract Background Cobalamin C (cblC) defect is the most common inborn error of Vitamin B12 metabolism often causing severe neurological, renal, gastrointestinal and hematological symptoms. Onset with pulmonary hypertension (PAH) and atypical hemoly
Externí odkaz:
https://doaj.org/article/b4f2e65be6a44c46b5d909ed3089e440
Autor:
Mariangela Manfredi, Silvia Gentile, Nicholas G. Kounis, Giulio Porcedda, Luciano De Simone, Mattia Giovannini, Francesca Mori, Chiara Di Filippo, Silvia Favilli, Giovanni Battista Calabri
Publikováno v:
JACC Case Reports
We describe the case of a 15-year-old female patient with Peutz-Jeghers syndrome who presented with vomiting and abdominal pain secondary to ileoileal invagination. Initial analgesic treatment was not effective, and subsequent tramadol infusion resul
Autor:
Silvia Favilli, Francesca Girolami, Giuseppe Santoro, Maria Iascone, Giulio Porcedda, Veronica Consigli, Silvia Passantino, Valentina Spinelli, Luciano De Simone, Chiara Marrone, Giovanni Battista Calabri, Iacopo Olivotto
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3368-3372 (2020)
Clinical Case Reports
Clinical Case Reports
Genetic investigation of early‐onset Dilatative cardiomyopathy phenotype, including molecular autopsy, is the key to appropriate recognition and management of rare etiologies and atypical presentations and to offer genetic counseling to the family.
Autor:
Mattia Giovannini, Silvia Favilli, Giulio Porcedda, Marco Moroni, Guglielmo Capponi, Gilda Belli, Giancarlo la Marca, Luciano De Simone
Publikováno v:
Pediatric Reports
Supraventricular tachyarrhythmia (SVT) is the most common type of arrhythmia in childhood. Management can be challenging with an associated risk of mortality. A female neonate was diagnosed with episodes of SVT, controlled antenatally with digoxin. F
Autor:
Giovanni Battista Calabri, Luciano De Simone, Ioanna Koniari, Elio Novembre, Mattia Giovannini, Giuseppe Indolfi, Gaia Spaziani, Sandra Trapani, Guglielmo Capponi, Silvia Favilli, Chiara Rubino, Francesca Mori
Publikováno v:
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
A 12-year-old male patient suffering from congenital glaucoma developed bradycardia, left ventricular failure, and hypotension after induction of anesthesia. Electrocardiography and echocardiography revealed a complete normalization of ECG and a comp