Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ivan Pietro Aloi"'
Case Report: Double Pectus Up in severe pectus excavatum, the new frontier of modified taulinoplasty
Autor:
Simone Frediani, Letizia Corbi, Valerio Pardi, Ivan Pietro Aloi, Arianna Bertocchini, Antonella Accinni, Simone Reali, Paolo Maria Salvatore Schingo, Alessandro Inserra
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionPectus excavatum, also known as “sunken chest” or “funnel chest,” is a congenital condition where the sternum caves inward, creating a noticeable depression in the chest. This deformity can range from mild to severe cases, and can
Externí odkaz:
https://doaj.org/article/2c5d6ddb66484f4489fd4f03f81f202d
Autor:
Giorgia Romano, Simone Frediani, Ivan Pietro Aloi, Arianna Bertocchini, Valerio Pardi, Antonella Accinni, Alessandro Inserra
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionMidgut volvulus and intussusception are prevalent paediatric abdominal emergencies. To the best of our knowledge, this is the first reported case of a connection between intestinal volvulus and a massive intussusception.Case reportAn 8-mo
Externí odkaz:
https://doaj.org/article/a031312469de4c579a38a3aa2f8e7c95
Autor:
Letizia Corbi, Simone Frediani, Ivan Pietro Aloi, Arianna Bertocchini, Antonella Accinni, Valerio Pardi, Alessandro Inserra
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
IntroductionOne of the most prevalent congenital wall abnormalities in children, umbilical hernias are often linked to premature or small-for-gestational-age babies. In cases of intestinal malrotation or if the cecum is very movable, generalized peri
Externí odkaz:
https://doaj.org/article/6600f17ae2214f9aaa3adb37e4939308
Autor:
Simone Frediani, Federico Beati, Valerio Pardi, Ivan Pietro Aloi, Arianna Bertocchini, Antonella Accinni, Simone Reali, Paolo Maria Salvatore Schingo, Alessandro Inserra
Publikováno v:
Frontiers in Surgery, Vol 10 (2024)
IntroductionAbout 95% of congenital chest wall deformities are pectus abnormalities, with pectus excavatum (PE) being the most common. The purpose of this work is to offer a modified Taulinoplasty Technique based on 35 consecutive PE patients' 1-year
Externí odkaz:
https://doaj.org/article/76a870f1e425402fbc50dafe21154225
Autor:
Angelo Zarfati, Simone Frediani, Valerio Pardi, Ivan Pietro Aloi, Silvia Madafferi, Antonella Accinni, Arianna Bertocchini, Alessandro Inserra
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Background and objectivesMarfan syndrome (MS) is a systemic disease of connective tissues consisting of a variable combination of anomalies. These patients have an increased risk of spontaneous pneumothorax (SP). However, there is a scarcity of pedia
Externí odkaz:
https://doaj.org/article/72cb0fffef334d9cb5324e274b628b83
Autor:
Simone Frediani, Giorgia Romano, Valerio Pardi, Ivan Pietro Aloi, Arianna Bertocchini, Antonella Accinni, Angelo Zarfati, Alessandro Inserra
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionThe digital chest drainage monitoring system (Medela Thopaz+), unlike analogical systems, reliably regulates the pressure applied to the patient's chest and digitally and silently monitors critical therapeutic indicators (volume of fluid
Externí odkaz:
https://doaj.org/article/dcbf115491eb4b18bc6554259fcf5ac1
Autor:
Alessandro Inserra, Angelo Zarfati, Valerio Pardi, Arianna Bertocchini, Antonella Accinni, Ivan Pietro Aloi, Cristina Martucci, Simone Frediani
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundDescribed for the first time in 1954, Jeune syndrome (JS), often called asphyxiating thoracic dystrophy, is a congenital musculoskeletal disease characterized by short ribs, a narrow thorax, and small limbs. In this study, we analyzed and p
Externí odkaz:
https://doaj.org/article/347c006bb0db428fafa33d5915cd79e9
Autor:
Alessandro Crocoli, Cristina Martucci, Giorgio Persano, Maria Debora De Pasquale, Annalisa Serra, Antonella Accinni, Ivan Pietro Aloi, Arianna Bertocchini, Simone Frediani, Silvia Madafferi, Valerio Pardi, Alessandro Inserra
Publikováno v:
Children, Vol 9, Iss 1, p 70 (2022)
Management and successful use of vascular access are critical issues in pediatric patients affected by malignancies. Prolonged course of disease, complex and various treatment protocols require long-lasting vascular access providing adequate tools to
Externí odkaz:
https://doaj.org/article/8b7866a905884a1cbcc58d2dcd2ec152
Autor:
Aurelio Mazzei, Antonella Centonze, Ivan Pietro Aloi, Arianna Bertocchini, Emanuele Baldassarre
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 26, Iss 1, Pp 66-67 (2021)
Externí odkaz:
https://doaj.org/article/9ffcf061c13a47af9fcda09691f759d5
Autor:
Katia Paciaroni, Gioia De Angelis, Cristiano Gallucci, Cecilia Alfieri, Michela Ribersani, Andrea Roveda, Antonella Isgrò, Marco Marziali, Ivan Pietro Aloi, Alessandro Inserra, Javid Gaziev, Pietro Sodani, Guido Lucarelli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 7, Iss 1, Pp e2015006-e2015006 (2015)
Sickle Cell Anaemia (SCA) is the most common inherited blood disorder and is associated with severe morbidity and decreased survival. Allogeneic Haematopoietic Stem Cell Transplantation (HSCT) is the only curative approach. Nevertheless the decision
Externí odkaz:
https://doaj.org/article/0a726cdebb4d4721b7ae2ce4b32b0f63