Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura Valfré"'
Autor:
Flaminia Pugnaloni, Domenico Umberto De Rose, Maria Cristina Digilio, Monia Magliozzi, Annabella Braguglia, Laura Valfrè, Alessandra Toscano, Andrea Dotta, Alessandra Di Pede
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-8 (2024)
Abstract Background Neonatal Marfan syndrome (nMFS) is a rare condition characterized by severe phenotype and poor prognosis. nMFS is caused by mutations in a specific region of the fibrillin 1 gene (FBN1). Prompt recognition of typical signs of neon
Externí odkaz:
https://doaj.org/article/4674a37b1dbd413094568f5841ec4ec4
Autor:
Laura Valfré, Andrea Conforti, Francesco Morini, Neil Patel, Francesca Bevilacqua, Maria Chiara Cianci, Pietro Bagolan, Annabella Braguglia
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
In patients affected by CDH, survival beyond the neonatal period continues to increase thanks to technological and pharmacological improvements. Conversely, patients, families and caregivers are more and more frequently facing “new” complex late
Externí odkaz:
https://doaj.org/article/11c6ff49121245f18328bd8ae8771702
Autor:
Renato Tambucci, Francesca Rea, Giulia Angelino, Monica Malamisura, Maurizio Mennini, Carla Riccardi, Giovanni Farello, Laura Valfré, Luigi Dall’Oglio, Jonathan E. Markowitz, Alessandro G. Fiocchi, Paola De Angelis
Publikováno v:
World Allergy Organization Journal, Vol 13, Iss 4, Pp - (2020)
Background: A high prevalence (9.5–30%) of eosinophilic esophagitis (EoE) in patients with esophageal atresia (EA) has been reported. The application of the EoE criteria to EA patients might be problematic. To date, only studies using a “routine
Externí odkaz:
https://doaj.org/article/e57735664bae46de8641c884a559571f
Autor:
Federica Porcaro, Laura Valfré, Lelia Rotondi Aufiero, Luigi Dall’Oglio, Paola De Angelis, Alberto Villani, Pietro Bagolan, Sergio Bottero, Renato Cutrera
Publikováno v:
Italian Journal of Pediatrics, Vol 43, Iss 1, Pp 1-9 (2017)
Abstract Background Children with congenital esophageal atresia (EA) and tracheoesophageal fistula (TEF) have chronic respiratory symptoms including recurrent pneumonia, wheezing and persistent cough. The aim of this study is to describe the clinical
Externí odkaz:
https://doaj.org/article/fca59969656740c4aaa9f4a93b73ab7c
Autor:
Andrea Conforti, Chiara Pellegrino, Laura Valfré, Chiara Iacusso, Paolo Maria Salvatore Schingo, Irma Capolupo, Stefania Sgro’, Lars Rasmussen, Pietro Bagolan
Publikováno v:
Journal of pediatric surgery.
Aim of study is to report our preliminary experience with magnetic anastomosis (magnamosis) treating long-gap esophageal atresia (LGEA), the most challenging condition of esophageal atresia continuum. Magnamosis has been reported in 20 patients world
Autor:
Marianna Scuglia, Andrea Conforti, Laura Valfrè, Giorgia Totonelli, Chiara Iacusso, Barbara D. Iacobelli, Duino Meucci, Milena Viggiano, Fabio Fusaro, Andrea Diociaiuti, Francesco Morini, May El Hachem, Pietro Bagolan
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Aim of the study: Lymphatic malformations (LMs) are rare entities, sometimes difficult to treat, that may be life-threatening when intricately connected to airway structures. Invasive treatments are occasionally required, with sclerotherapy considere
Externí odkaz:
https://doaj.org/article/adb7a03665e541a09330d6c9d6e7d7dc
Autor:
Andrea Conforti, Laura Valfrè, Marianna Scuglia, Marilena Trozzi, Duino Meucci, Stefania Sgrò, Sergio Bottero, Pietro Bagolan
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Importance: Presence of laryngotracheal abnormalities is associated with increased morbidity and higher mortality rate in esophageal atresia patients.Objective: Determine the prevalence of laryngotracheal abnormalities (LTA) in a prospectively collec
Externí odkaz:
https://doaj.org/article/643cfbc0e0b6423bbdae71acdb3b146d