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GREGORIO SERRA

Curriculum e ricerca

Pubblicazioni

Data Titolo Tipologia Scheda
2024 Increased adherence to influenza vaccination among Palermo family pediatricians: a study on safety and compliance of qLAIV vaccination Articolo in rivista Vai
2024 Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome Articolo in rivista Vai
2024 Manifestazioni cutanee anulari e lupus eritematoso neonatale Articolo in rivista Vai
2023 Useless and limits of Postmortem CT (PMCT) in a complex case of preterm infant murder Articolo in rivista Vai
2023 Report and follow-up on two new patients with congenital mesoblastic nephroma Articolo in rivista Vai
2023 Intraoperative ultrasound-assisted endoscopic treatment of primary intermediate and high-grade vesicoureteral reflux in children in a long-term follow-up Articolo in rivista Vai
2023 Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved? Articolo in rivista Vai
2023 Lo spettro dei disordini feto-alcolici: una guida per il pediatra Articolo in rivista Vai
2023 New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception Articolo in rivista Vai
2023 Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved? Articolo in rivista Vai
2023 Follow-Up to Ensure Continuity of Care and Support Preventive Care Capitolo o Saggio Vai
2023 Safety of Rotavirus Vaccination in Preterm Infants Admitted in Neonatal Intensive Care Units in Sicily, Italy: A Multicenter Observational Study Articolo in rivista Vai
2023 La Bioetica sul campo: una sfida per il neonatologo e il pediatra Articolo in rivista Vai
2022 Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report Articolo in rivista Vai
2022 Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles Articolo in rivista Vai
2022 Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2K2 gene Articolo in rivista Vai
2022 Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder Articolo in rivista Vai
2022 Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene Articolo in rivista Vai
2022 Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene Articolo in rivista Vai
2022 Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restriction Articolo in rivista Vai
2022 Quando l’amnios si rompe troppo presto e… da solo Articolo in rivista Vai
2022 Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis Articolo in rivista Vai
2022 Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome Articolo in rivista Vai
2022 Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 gene Articolo in rivista Vai
2022 Quality of life improving after propranolol treatment in patients with Infantile Hemangiomas Articolo in rivista Vai
2021 Lesioni cutanee stellate e simmetriche in un gemello “rimasto solo” Articolo in rivista Vai
2021 THE “SALT-TASTING” NEWBORN Articolo in rivista Vai
2021 Il neonato che “sa di sale” Articolo in rivista Vai
2021 The social role of pediatrics in the past and present times Lettera Vai
2021 Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town Articolo in rivista Vai
2021 Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center Study Articolo in rivista Vai
2021 Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents’ associations Articolo in rivista Vai
2021 Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up Articolo in rivista Vai
2021 Jacobsen syndrome and neonatal bleeding: report on two unrelated patients Articolo in rivista Vai
2021 Smartphone use and addiction during the coronavirus disease 2019 (COVID-19) pandemic: cohort study on 184 Italian children and adolescents Articolo in rivista Vai
2021 2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype Articolo in rivista Vai
2020 Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion Articolo in rivista Vai
2020 LARGE FOR GESTATIONAL AGE, MACROSOMIA, OVERGROWTH: AN UPDATE ON DEFINITIONS AND DETERMINANTS Articolo in rivista Vai
2020 MACROCEPHALY FROM A NORMAL VARIANT TO A THREATENING CONDITION. A SINGLE CENTER RETROSPECTIVE STUDY ON 189 SUBJECTS Articolo in rivista Vai
2020 Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome Articolo in rivista Vai
2020 The child with overgrowth between clinical variability and genetic heterogeneity Articolo in rivista Vai
2020 Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: Case report of an Italian patient Articolo in rivista Vai
2020 Neonatal hyperinsulinemic hypoglycemia: Case report of kabuki syndrome due to a novel KMT2D splicing-site mutation Articolo in rivista Vai
2020 Growth patterns and associated risk factors of congenital malformations in twins Articolo in rivista Vai
2020 Neonatal ten-year retrospective study on neural tube defects in a second level University Hospital Articolo in rivista Vai
2019 Fetal growth restriction: A growth pattern with fetal, neonatal and long-term consequences Review essay (rassegna critica) Vai
2019 Standard and Specialized Infant Formulas in Europe: Making, Marketing, and Health Outcomes Review essay (rassegna critica) Vai
2019 NF1 microdeletion syndrome: Case report of two new patients Articolo in rivista Vai
2019 The vaccinaTion & Hpv Knowledge (THinK) questionnaire: a reliability and validity study on a sample of women living in Sicily (southern-Italy) Articolo in rivista Vai
2019 Perinatal and newborn care in a two years retrospective study in a first level peripheral hospital in Sicily (Italy) Articolo in rivista Vai
2018 Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1 Articolo in rivista Vai
2018 Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report Articolo in rivista Vai
2017 IPOGLICEMIA NEONATALE: RILIEVI EPIDEMIOLOGICI IN UN CAMPIONE DI NEONATI RICOVERATI (2012-2017) Poster non pubblicato Vai
2016 Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis Articolo in rivista Vai
2015 Antimicrobial therapy in neonatal intensive care unit Articolo in rivista Vai
2013 MALFORMATIONS OF CENTRAL NERVOUS SYSTEM: GENERAL ISSUES Articolo in rivista Vai
2013 Neonatal osteomyelitis of the talus due to methicillin-resistant Staphylococcus epidermidis Articolo in rivista Vai
2013 Acute pancreatitis in children and rotavirus infection. Description of a case and minireview Articolo in rivista Vai
2012 14q13.1-21.1 Deletion Encompassing the HPE8 Locus in an Adolescent With Intellectual Disability and Bilateral Microphthalmia, But Without Holoprosencephaly Articolo in rivista Vai
2012 A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus. Articolo in rivista Vai
2009 ADOLESCENTE CON DATTILITE DELLE MANI DA INFEZIONE DA HELICOBACTER PYLORI eedings Vai