F. Matina

发表

First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant?

G. Corsello, M. Tumminello, A. Gangemi, 2021, Italian Journal of Pediatrics.

First report of X-linked hypohidrotic ectodermal dysplasia with a hemizygous c.1142G > C in the EDA gene: variant of uncertain significance or new pathogenic variant?

G. Corsello, M. Tumminello, A. Gangemi, 2021, Italian Journal of Pediatrics.

Type IV Laryngotracheoesophageal Cleft Associated with Type III Esophageal Atresia in 1p36 Deletions Containing the RERE Gene: Is There a Causal Role for the Genetic Alteration?

V. Calcaterra, M. Piccione, G. Pelizzo, 2018, Case reports in pediatrics.

A novel L1CAM mutation in a fetus detected by prenatal diagnosis

M. Fichera, M. Lo Giudice, M. Piccione, 2010, European Journal of Pediatrics.

Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?

M. Piccione, V. Antona, G. Corsello, 2013, Italian Journal of Pediatrics.

A premature infant with Costello syndrome due to a rare G13C HRAS mutation

G. Neri, M. Piccione, G. Corsello, 2009, American journal of medical genetics. Part A.

Etiological heterogeneity and clinical variability in newborns with esophageal atresia

M. Cimador, V. Antona, G. Corsello, 2018, Italian Journal of Pediatrics.

Acute hemorrhagic edema of infancy (AHEI): Alarming cutaneous presentation of a benign and self‐limited disease

D. Termini, G. Corsello, M. Tumminello, 2022, Clinical case reports.

CONGENITAL DIAPHRAGMATIC HERNIA AND ESOPHAGEAL ATRESIA : THE IMPORTANCE OF RESPIRATORY FOLLOW-UP IN CONGENITAL THORACIC MALFORMATIONS

E. Piro, F. Matina, M. Giuffré, 2013 .

Inhaled Surfactant in the treatment of accidental Talc Powder inhalation: a new case report

G. Corsello, F. Matina, P. Vitulo, 2011, Italian journal of pediatrics.

Fluid restriction in management of patent ductus arteriosus in Italy: a nationwide survey

R. Cerbo, M. Savoia, I. Corsini, 2022, European Journal of Pediatrics.

Reply to the comment on “Fluid restriction in management of patent ductus arteriosus in Italy: a nationwide survey”

R. Cerbo, M. Savoia, I. Corsini, 2023, European Journal of Pediatrics.

A premature infant with Costello syndrome due to a rare G13C HRAS mutation

G. Neri, M. Piccione, G. Corsello, 2009, American journal of medical genetics. Part A.

Comparison among three lung ultrasound scores used to predict the need for surfactant replacement therapy: a retrospective diagnostic accuracy study in a cohort of preterm infants.

I. Corsini, F. Raimondi, L. Capasso, 2023, European journal of pediatrics.