Publications by authors named "Francesca Moscuzza"

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Maternal anthropometric variables and clinical factors shape neonatal microbiome.
Riccardo Farinella, Cosmeri Rizzato, Daria Bottai, Alice Bedini, Federica Gemignani, Francesca Moscuzza

Sci Rep· February 2022

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Nutrition, epigenetic markers and growth in preterm infants.
Maria Giulia Tozzi, Francesca Moscuzza, Angela Michelucci, Rosa T Scaramuzzo, Cinzia Cosini

J Matern Fetal Neonatal Med· December 2021

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Polymorphic variants in Sweet and Umami taste receptor genes and birthweight.
Riccardo Farinella, Ilaria Erbi, Alice Bedini, Sara Donato, Manuel Gentiluomo, Francesca Moscuzza

Sci Rep· March 2021

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Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction.
Ilaria Erbi, Massimiliano Ciantelli, Riccardo Farinella, Cristina Tuoni, Manuel Gentiluomo, Francesca Moscuzza

Sci Rep· April 2020

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Measuring Cot-Side the Effects of Parenteral Nutrition on Preterm Cortical Function.
Viviana Marchi, Nathan Stevenson, Ninah Koolen, Raffaele Mazziotti, Francesca Moscuzza

Front Hum Neurosci· March 2020

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ExtraUterine Growth Restriction (EUGR) in Preterm Infants: Growth Patterns, Nutrition, and Epigenetic Markers. A Pilot Study.
Maria Giulia Tozzi, Francesca Moscuzza, Angela Michelucci, Francesca Lorenzoni, Cinzia Cosini

Front Pediatr· December 2018

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Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia.
Rosa T Scaramuzzo, Soara Menabò, Lilia Baldazzi, Francesca Moscuzza, Alessandro Saba

Sex Dev· March 2018

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Technical realization of a sensorized neonatal intubation skill trainer for operators' retraining and a pilot study for its validation.
Davide Panizza, Rosa T Scaramuzzo, Francesca Moscuzza, Ilaria Vannozzi, Massimiliano Ciantelli

Ital J Pediatr· January 2018

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5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian Cohort.
Silvano Bertelloni, Fulvia Baldinotti, Gianni Russo, Paolo Ghirri, Eleonora Dati, Francesca Moscuzza

Sex Dev· November 2017

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A Novel Missense Mutation of the NSD1 Gene Associated with Overgrowth in Three Generations of an Italian Family: Case Report, Differential Diagnosis, and Review of Mutations of NSD1 Gene in Familial Sotos Syndrome.
Gianluigi Laccetta, Francesca Moscuzza, Angela Michelucci, Andrea Guzzetta, Sara Lunardi

Front Pediatr· November 2017

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Catheter and Laryngeal Mask Endotracheal Surfactant Therapy: the CALMEST approach as a novel MIST technique.
Ilaria Vannozzi, Massimiliano Ciantelli, Francesca Moscuzza, Rosa T Scaramuzzo, Davide Panizza

J Matern Fetal Neonatal Med· October 2017

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Lutein and Neurodevelopment in Preterm Infants.
Matteo Giampietri, Francesca Lorenzoni, Francesca Moscuzza, Antonio Boldrini, Paolo Ghirri

Front Neurosci· September 2016

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Erythema multiforme as first sign of incomplete Kawasaki disease.
Francesco Vierucci, Cristina Tuoni, Francesca Moscuzza, Giuseppe Saggese, Rita Consolini

Ital J Pediatr· February 2013

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Correlation between placental histopathology and fetal/neonatal outcome: chorioamnionitis and funisitis are associated to intraventricular haemorrage and retinopathy of prematurity in preterm newborns.
Francesca Moscuzza, Francesca Belcari, Vincenzo Nardini, Ambra Bartoli, Chiara Domenici

Gynecol Endocrinol· May 2011

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Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome.
Angela Michelucci, Paolo Ghirri, Paola Iacopetti, Maria Elena Conidi, Antonella Fogli, Francesca Moscuzza

Int J Pediatr Otorhinolaryngol· December 2010

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