Accès ouvert
2026
article
OpenAlex
Wentao Wang, Shenghua He, Lihong Ou, Federico Canavese et autres
BACKGROUND: The Delbet-Colonna (DC) classification guides treatment of pediatric femoral neck fractures (PFNFs) but relies on clinical experience. No deep learning (DL) model has been developed and validated to differentiate between PFNFs and proximal femoral growth plates (PFGPs) and classify PFNFs via …
cn, it
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Accès ouvert
2025
review
OpenAlex
Marta Molteni, Gianluca Trocchio, Antonio Verrico, Maria Derchi et autres
BACKGROUND: Gorlin syndrome (GS) is a rare autosomal dominant disorder, associated with pathogenic PTCH1 or SUFU variants, predisposing to tumors such as basal cell carcinoma, medulloblastoma (MB), odontogenic keratocyst, and, rarely, cardiac fibroma (CF). MB occurs in ~5% of GS cases, typically …
it
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2025
article
OpenAlex
Martina Monti, Vittorio Guerriero, Roberto D’Agostino, Oliviero Sacco et autres
BACKGROUND: Pediatric tracheal surgery includes several complex and rare procedures. We report the surgical experience at our center. METHODS: Our center has multidisciplinary team manages laryngotracheal malformations. We retrospectively analyzed all tracheal surgeries from January 2009 to September 2023, excluding endoscopic cases …
it, jp
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Accès ouvert
2025
article
OpenAlex
Liliana Piro, Arianna Roggero, Nicola Stagnaro, Valerio Gaetano Vellone et autres
Introduction: Esophageal duplication cysts (EDCs) associated with pulmonary sequestration (PS) are rare congenital anomalies originating from the embryonic foregut. They often present diagnostic challenges due to their complex nature and non-communicating features. Case Report: We report the case of a one-year-old girl …
it
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2024
article
OpenAlex
Pierluigi Festa, Luigi Lovato, Francesco Bianco, Annalisa Alaimo et autres
Cardiovascular magnetic resonance (CMR) and computed tomography (CCT) are advanced imaging modalities that recently revolutionized the conventional diagnostic approach to congenital heart diseases (CHD), supporting echocardiography and often replacing cardiac catheterization. This is the second of two complementary documents, endorsed by experts …
it, il
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2024
article
OpenAlex
Liliana Piro, Federica Lena, Arianna Roggero, Nicola Stagnaro et autres
it
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Accès ouvert
2024
article
OpenAlex
Lamia Ait-Alì, Nicola Martini, Elisa Listo, Elisa Valenti et autres
Abstract We sought to evaluate the potential clinical role of 4D-flow cardiac magnetic resonance (CMR)-derived energetics and flow parameters in a cohort of patients’ post-Fontan palliation. In patients with Fontan circulation who underwent 4D-Flow CMR, streamlines distribution was evaluated, as well a …
it, cl
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Accès ouvert
2023
article
OpenAlex
Lamia Ait-Alì, Benedetta Leonardi, Annalisa Alaimo, Giovanna Baccano et autres
Background: Managing repaired tetralogy of Fallot (TOF) patients is still challenging despite the fact that published studies identified prognostic clinical or imaging data with rather good negative predictive accuracy but weak positive predictive accuracy. Heterogeneity of the initial anatomy, the surgical approach, …
it
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Accès ouvert
2023
article
OpenAlex
Elisa Listo, Nicola Martini, Stefano Salvadori, Elisa Valenti et autres
Background: The assessment of Fontan circuit’s flow is traditionally evaluated by multiple through-plane phase-contrast MRI acquisitions (2D flow), while recently, a single volumetric 4D-flow MRI acquisition is emerging as a comprehensive tool for the hemodynamic evaluation in congenital heart diseases. Purpose: To …
it
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2022
article
OpenAlex
Federica Lena, Liliana Piro, Valentina Forlini, Vittorio Guerriero et autres
INTRODUCTION: Jeune's syndrome, or asphyxiating thoracic dystrophy (ATD), is a rare autosomal recessive disorder characterized by skeletal dysplasia. Ribs are typically short and horizontal resulting-in lethal variant-in severe lung hypoplasia, progressive respiratory failure, and death. Lateral thoracic expansion (LTE) consists in staggered …
it
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Accès ouvert
2022
article
OpenAlex
Chiara Panicucci, Maria Cristina Schiaffino, Claudia Nesti, Maria Derchi et autres
BACKGROUND: Sengers syndrome is characterized by congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy, and lactic acidosis associated with mutations in AGK gene. Clinical course ranges from a severe fatal neonatal form, to a more benign form allowing survival into adulthood, to an isolated …
it
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Accès ouvert
2022
article
OpenAlex
Nicoletta Cantarutti, Virginia Battista, Nicola Stagnaro, Marianna Eleonora Labate et autres
MIS-C is a multisystem inflammatory syndrome that is characterized by multi-organ failure and cardiac involvement. The aim of this study was to describe the long-term cardiovascular outcome in a cohort of MIS-C pediatric patients, who were admitted to two Italian Pediatric Referral …
it
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