Serra G - Search Results

1

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.

Serra G, Antona V, Di Pace MR, Giuffrè M, Morgante G, Piro E, Pirrello R, Salerno S, Schierz IAM, Verde V, Corsello G. Serra G, et al. Ital J Pediatr. 2022 Dec 29;48(1):206. doi: 10.1186/s13052-022-01403-6. Ital J Pediatr. 2022. PMID: 36581928 Free PMC article.

2

A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus.

Piccione M, Serra G, Sanfilippo C, Andreucci E, Sani I, Corsello G. Piccione M, et al. Among authors: serra g. Minerva Pediatr. 2012 Feb;64(1):59-64. Minerva Pediatr. 2012. PMID: 22350046

3

Antimicrobial therapy in neonatal intensive care unit.

Tzialla C, Borghesi A, Serra G, Stronati M, Corsello G. Tzialla C, et al. Among authors: serra g. Ital J Pediatr. 2015 Apr 1;41:27. doi: 10.1186/s13052-015-0117-7. Ital J Pediatr. 2015. PMID: 25887621 Free PMC article. Review.

4

Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis.

Giuffrè M, Verso CL, Serra G, Moceri G, Cimador M, Corsello G; Study Group of Neonatal Infectious Diseases Affiliated to the Italian Society of Neonatology. Giuffrè M, et al. Among authors: serra g. Am J Perinatol. 2016 Sep;33(11):1099-103. doi: 10.1055/s-0036-1586102. Epub 2016 Sep 7. Am J Perinatol. 2016. PMID: 27603544

5

Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report.

Serra G, Antona V, Schierz M, Vecchio D, Piro E, Corsello G. Serra G, et al. Clin Case Rep. 2018 Jan 13;6(2):399-401. doi: 10.1002/ccr3.1103. eCollection 2018 Feb. Clin Case Rep. 2018. PMID: 29445485 Free PMC article.

6

Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1.

Corsello G, Antona V, Serra G, Zara F, Giambrone C, Lagalla L, Piccione M, Piro E. Corsello G, et al. Among authors: serra g. Ital J Pediatr. 2018 Apr 4;44(1):45. doi: 10.1186/s13052-018-0483-z. Ital J Pediatr. 2018. PMID: 29618358 Free PMC article.

7

Standard and Specialized Infant Formulas in Europe: Making, Marketing, and Health Outcomes.

Dipasquale V, Serra G, Corsello G, Romano C. Dipasquale V, et al. Among authors: serra g. Nutr Clin Pract. 2020 Apr;35(2):273-281. doi: 10.1002/ncp.10261. Epub 2019 Feb 11. Nutr Clin Pract. 2020. PMID: 30742336 Review.

8

NF1 microdeletion syndrome: case report of two new patients.

Serra G, Antona V, Corsello G, Zara F, Piro E, Falsaperla R. Serra G, et al. Ital J Pediatr. 2019 Nov 8;45(1):138. doi: 10.1186/s13052-019-0718-7. Ital J Pediatr. 2019. PMID: 31703719 Free PMC article.

9

Perinatal and newborn care in a two years retrospective study in a first level peripheral hospital in Sicily (Italy).

Serra G, Miceli V, Albano S, Corsello G. Serra G, et al. Ital J Pediatr. 2019 Nov 29;45(1):152. doi: 10.1186/s13052-019-0751-6. Ital J Pediatr. 2019. PMID: 31783883 Free PMC article.

10

Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion.

Schierz IAM, Serra G, Antona V, Persico I, Corsello G, Piro E. Schierz IAM, et al. Among authors: serra g. Clin Dysmorphol. 2020 Jul;29(3):141-143. doi: 10.1097/MCD.0000000000000325. Clin Dysmorphol. 2020. PMID: 32433043 No abstract available.

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