Corsello G - Search Results

1

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?

Tumminello M, Gangemi A, Matina F, Guardino M, Giuffrè BL, Corsello G. Tumminello M, et al. Among authors: corsello g. Ital J Pediatr. 2021 Jun 2;47(1):128. doi: 10.1186/s13052-021-01078-5. Ital J Pediatr. 2021. PMID: 34078430 Free PMC article.

2

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

Piccione M, Piro E, Pomponi MG, Matina F, Pietrobono R, Candela E, Gabriele B, Neri G, Corsello G. Piccione M, et al. Among authors: corsello g. Am J Med Genet A. 2009 Mar;149A(3):487-9. doi: 10.1002/ajmg.a.32674. Am J Med Genet A. 2009. PMID: 19213030

3

A novel L1CAM mutation in a fetus detected by prenatal diagnosis.

Piccione M, Matina F, Fichera M, Lo Giudice M, Damiani G, Jakil MC, Corsello G. Piccione M, et al. Among authors: corsello g. Eur J Pediatr. 2010 Apr;169(4):415-9. doi: 10.1007/s00431-009-1037-6. Epub 2009 Aug 16. Eur J Pediatr. 2010. PMID: 19685344

4

Inhaled surfactant in the treatment of accidental talc powder inhalation: a new case report.

Matina F, Collura M, Maggio MC, Vitulo P, Lo Piparo C, Corsello G. Matina F, et al. Among authors: corsello g. Ital J Pediatr. 2011 Sep 27;37:47. doi: 10.1186/1824-7288-37-47. Ital J Pediatr. 2011. PMID: 21951993 Free PMC article.

5

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: corsello g. Minerva Pediatr. 2012 Feb;64(1):59-64. Minerva Pediatr. 2012. PMID: 22350046

6

Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery.

Piro E, Piccione M, Marrone G, Giuffrè M, Corsello G. Piro E, et al. Among authors: corsello g. Ital J Pediatr. 2013 May 14;39:32. doi: 10.1186/1824-7288-39-32. Ital J Pediatr. 2013. PMID: 23672850 Free PMC article.

7

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

La Placa S, Giuffrè M, Gangemi A, Di Noto S, Matina F, Nociforo F, Antona V, Di Pace MR, Piccione M, Corsello G. La Placa S, et al. Among authors: corsello g. Ital J Pediatr. 2013 Jul 10;39:45. doi: 10.1186/1824-7288-39-45. Ital J Pediatr. 2013. PMID: 23842449 Free PMC article.

8

Congenital cytomegalovirus related intestinal malrotation: a case report.

Colomba C, Giuffrè M, La Placa S, Cascio A, Trizzino M, De Grazia S, Corsello G. Colomba C, et al. Among authors: corsello g. Ital J Pediatr. 2016 Dec 7;42(1):105. doi: 10.1186/s13052-016-0318-8. Ital J Pediatr. 2016. PMID: 27923378 Free PMC article.

9

Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant.

Borghesi A, Mencarelli MA, Memo L, Ferrero GB, Bartuli A, Genuardi M, Stronati M, Villani A, Renieri A, Corsello G; their respective Scientific Societies. Borghesi A, et al. Among authors: corsello g. Ital J Pediatr. 2017 Nov 3;43(1):100. doi: 10.1186/s13052-017-0418-0. Ital J Pediatr. 2017. PMID: 29100554 Free PMC article. Review.

10

Etiological heterogeneity and clinical variability in newborns with esophageal atresia.

Piro E, Schierz IAM, Giuffrè M, Cuffaro G, La Placa S, Antona V, Matina F, Puccio G, Cimador M, Corsello G. Piro E, et al. Among authors: corsello g. Ital J Pediatr. 2018 Jan 26;44(1):19. doi: 10.1186/s13052-018-0445-5. Ital J Pediatr. 2018. PMID: 29373986 Free PMC article.

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