Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sara Silvaroli"'
Autor:
Valentina Trevisan, Eugenio De Corso, Germana Viscogliosi, Roberta Onesimo, Alessandro Cina, Marco Panfili, Lucrezia Perri, Cristiana Agazzi, Valentina Giorgio, Donato Rigante, Giovanni Vento, Patrizia Papacci, Filomena Valentina Paradiso, Sara Silvaroli, Lorenzo Nanni, Nicoletta Resta, Marco Castori, Jacopo Galli, Gaetano Paludetti, Giuseppe Zampino, Chiara Leoni
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-16 (2024)
Abstract Background Lymphatic malformations are vascular developmental anomalies varying from local superficial masses to diffuse infiltrating lesions, resulting in disfigurement. Patients’ outcomes range from spontaneous regression to severe seque
Externí odkaz:
https://doaj.org/article/87792ea812b04cb19a34faf827c6c476
Autor:
Sara Silvaroli, Filomena Valentina Paradiso, Riccardo Rizzo, MariaVittoria Stern, Lorenzo Nanni
Publikováno v:
Pediatrics and Neonatology, Vol 65, Iss 4, Pp 408-409 (2024)
Externí odkaz:
https://doaj.org/article/3e32d09f6928427d98cf78a8de904991
Autor:
Maria Vittoria Stern, Filomena Valentina Paradiso, Riccardo Rizzo, Sara Silvaroli, Francesco Pierconti, Lorenzo Nanni
Publikováno v:
Journal of Neonatal Surgery, Vol 13 (2024)
Background: Double-blind ureteral duplication (DBUD) is a rare condition in which one of the ureters in a duplicated system has no communication with the bladder or the renal pelvis. Case Presentation: We present a neonatal case of DBUD in a newbor
Externí odkaz:
https://doaj.org/article/de26d8b086ed4fbe92c4b2d6ad15c60f
Autor:
Antonio Vitale, Valeria Caggiano, Abdurrahman Tufan, Gaafar Ragab, Ezgi Deniz Batu, Piero Portincasa, Emma Aragona, Jurgen Sota, Giovanni Conti, Amato De Paulis, Donato Rigante, Alma Nunzia Olivieri, Ali Şahin, Francesco La Torre, Giuseppe Lopalco, Marco Cattalini, Maria Cristina Maggio, Antonella Insalaco, Petros P. Sfikakis, Elena Verrecchia, Derya Yildirim, Hamit Kucuk, Riza Can Kardas, Ahmed Hatem Laymouna, Mahmoud Ghanema, Moustafa Ali Saad, Seher Sener, Hulya Ercan Emreol, Seza Ozen, Nour Jaber, Mohamad Khalil, Agostino Di Ciaula, Carla Gaggiano, Giuseppe Malizia, Andrea Affronti, Serena Patroniti, Meri Romeo, Jessica Sbalchiero, Francesca Della Casa, Ilaria Mormile, Sara Silvaroli, Maria Francesca Gicchino, Neşe Çabuk Çelik, Maria Tarsia, Anastasios Karamanakos, José Hernández-Rodríguez, Paola Parronchi, Daniela Opris-Belinski, Patrizia Barone, Andreas Recke, Stefania Costi, Paolo Sfriso, Henrique A. Mayrink Giardini, Stefano Gentileschi, Ewa Wiesik-Szewczyk, Ibrahim Vasi, Roberta Loconte, Karina Jahnz-Różyk, Eduardo Martín-Nares, Jiram Torres-Ruiz, Alberto Cauli, Alessandro Conforti, Giacomo Emmi, Francesca Li Gobbi, Giovanni Rosario Biasi, Riccardo Terribili, Piero Ruscitti, Emanuela Del Giudice, Samar Tharwat, Antonio Luca Brucato, Benson Ogunjimi, Andrea Hinojosa-Azaola, Alberto Balistreri, Claudia Fabiani, Bruno Frediani, Luca Cantarini
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
ObjectiveInflammation has been associated with an increased risk for cancer development, while innate immune system activation could counteract the risk for malignancies. Familial Mediterranean fever (FMF) is a severe systemic inflammatory condition
Externí odkaz:
https://doaj.org/article/da9c0d49f15344b88bb76651719b9863
Publikováno v:
Journal of Neonatal Surgery, Vol 12 (2023)
Background: Esophageal perforation is uncommon and often iatrogenic in the neonatal period, and premature and low birth weight infants (
Externí odkaz:
https://doaj.org/article/a8143e2e44e9416b83a7fe3660ba0325
Autor:
Donato Rigante, Cristina Guerriero, Sara Silvaroli, Filomena Valentina Paradiso, Giorgio Sodero, Francesco Laferrera, Francesco Franceschi, Marcello Candelli
Publikováno v:
Children, Vol 11, Iss 2, p 215 (2024)
Background and objective: IgA vasculitis (IgAV), a predominantly pediatric leukocytoclastic disease, has an unpredictable, though largely benign, evolution. The aim of this study was to retrospectively investigate any potential clinical or laboratory
Externí odkaz:
https://doaj.org/article/fdec768e452046738bbf79dd044c9244
Publikováno v:
Case Reports in Pediatrics, Vol 2023 (2023)
Anorectal malformations (ARM) without a fistula are a rare congenital condition. Although may seem more simple to repair compared with ARM with fistulas, surgery has proved to be challenging. We report the case of a newborn who presented a well-forme
Externí odkaz:
https://doaj.org/article/afc0c6c95a344a7790e51e4ef8f4b999
Publikováno v:
Case Reports in Pediatrics, Vol 2022 (2022)
Percutaneous endoscopic gastrostomy (PEG) is increasingly used in paediatric population. We report a case of a 4-year-old boy who, two weeks after PEG placement, presented persistent diarrhoea interpreted as intolerance to enteral feeding. His CT sca
Externí odkaz:
https://doaj.org/article/ec28f8c15a49456da8a4fa17cc4da881
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 67, Iss , Pp 101816- (2021)
Lymphatic malformations (LM) or lymphangiomas are congenital errors in vascular embryogenesis. Percutaneous sclerosis is considered the best treatment for LM with external localization and yields excellent results. Surgical resection for deep LM is c
Externí odkaz:
https://doaj.org/article/cee5b12a7a6343faab0c925d289c1ba3
Autor:
Filomena Valentina Paradiso, Laura Merli, Sara Silvaroli, Vincenzo Fiorentino, Riccardo Ricci, Lorenzo Nanni
Publikováno v:
Case Reports in Pediatrics, Vol 2020 (2020)
Enteric duplication cysts are rare malformations mostly diagnosed before the age of two, with varied clinical presentations. Ectopic gastrointestinal epithelium can be present, and management involves surgical resection. A three-month-old girl presen
Externí odkaz:
https://doaj.org/article/95fa104d67de49afb4db686f0a2d2f9b