Serra G - Search Results

1

Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town.

Serra G, Antona V, D'Alessandro MM, Maggio MC, Verde V, Corsello G. Serra G, et al. Ital J Pediatr. 2021 Jun 16;47(1):138. doi: 10.1186/s13052-021-01080-x. Ital J Pediatr. 2021. PMID: 34134742 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

14q13.1-21.1 deletion encompassing the HPE8 locus in an adolescent with intellectual disability and bilateral microphthalmia, but without holoprosencephaly.

Piccione M, Serra G, Consiglio V, Di Fiore A, Cavani S, Grasso M, Malacarne M, Pierluigi M, Viaggi C, Corsello G. Piccione M, et al. Among authors: serra g. Am J Med Genet A. 2012 Jun;158A(6):1427-33. doi: 10.1002/ajmg.a.35334. Epub 2012 May 11. Am J Med Genet A. 2012. PMID: 22581785

4

[Neonatal osteomyelitis of the talus due to methicillin-resistant Staphylococcus epidermidis].

Pampinella D, Serra G, Giordano S, Dones P, Di Gangi M, Failla MC, Corsello G. Pampinella D, et al. Among authors: serra g. Infez Med. 2013 Jun;21(2):142-5. Infez Med. 2013. PMID: 23774980 Free article. Italian.

5

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.

6

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

7

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.

8

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.

9

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.

10

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.

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