Lista de obras -

5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian Cohort

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Catheter and Laryngeal Mask Endotracheal Surfactant Therapy: the CALMEST approach as a novel MIST technique

artículo científico publicado en 2016

Correlation between placental histopathology and fetal/neonatal outcome: chorioamnionitis and funisitis are associated to intraventricular haemorrage and retinopathy of prematurity in preterm newborns

artículo científico publicado en 2010

Erythema multiforme as first sign of incomplete Kawasaki disease

artículo científico publicado en 2013

ExtraUterine Growth Restriction (EUGR) in Preterm Infants: Growth Patterns, Nutrition, and Epigenetic Markers. A Pilot Study

Hypothyroxinemia in extremely low birth weight infants.

artículo científico publicado en 2015

Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome ⬇️

artículo científico publicado el 12 de octubre de 2010

Lutein and Neurodevelopment in Preterm Infants.

artículo científico publicado en 2016

Maternal anthropometric variables and clinical factors shape neonatal microbiome

artículo científico publicado en 2022

Measuring Cot-Side the Effects of Parenteral Nutrition on Preterm Cortical Function

scientific article published on 17 March 2020

Mineral homeostasis in late preterm infants

Nutrition, epigenetic markers and growth in preterm infants

scientific article published on 16 December 2019

Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction ⬇️

artículo científico publicado en 2020

Simulation on neonatal stabilization and transport.

artículo científico publicado en 2015

Technical realization of a sensorized neonatal intubation skill trainer for operators' retraining and a pilot study for its validation.

artículo científico publicado en 2018

Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia.

artículo científico publicado en 2017

Lista de obras de

5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian Cohort

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

Catheter and Laryngeal Mask Endotracheal Surfactant Therapy: the CALMEST approach as a novel MIST technique

Correlation between placental histopathology and fetal/neonatal outcome: chorioamnionitis and funisitis are associated to intraventricular haemorrage and retinopathy of prematurity in preterm newborns

Erythema multiforme as first sign of incomplete Kawasaki disease

ExtraUterine Growth Restriction (EUGR) in Preterm Infants: Growth Patterns, Nutrition, and Epigenetic Markers. A Pilot Study

Hypothyroxinemia in extremely low birth weight infants.

Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome ⬇️

Lutein and Neurodevelopment in Preterm Infants.

Maternal anthropometric variables and clinical factors shape neonatal microbiome

Measuring Cot-Side the Effects of Parenteral Nutrition on Preterm Cortical Function

Mineral homeostasis in late preterm infants

Nutrition, epigenetic markers and growth in preterm infants

Role of OPRM1, clinical and anthropometric variants in neonatal pain reduction ⬇️

Simulation on neonatal stabilization and transport.

Technical realization of a sensorized neonatal intubation skill trainer for operators' retraining and a pilot study for its validation.

Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia.