Corsello 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. Among authors: corsello g. 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

Kabuki make-up (Niikawa-Kuroki) syndrome: clinical and radiological observations in two Sicilian children.

Carcione A, Piro E, Albano S, Corsello G, Benenati A, Piccione M, Verde V, Giuffrè L, Albancse A. Carcione A, et al. Among authors: corsello g. Pediatr Radiol. 1991;21(6):428-31. doi: 10.1007/BF02026678. Pediatr Radiol. 1991. PMID: 1749676

3

Gluten-free diet impact on leptin levels in asymptomatic coeliac adolescents: one year of follow-up.

Maggio MC, Corsello G, Iacono G, Teresi S, Guicciardino E, Terrana S, Liotta A. Maggio MC, et al. Among authors: corsello g. Horm Res. 2007;67(2):100-4. doi: 10.1159/000096422. Epub 2006 Oct 19. Horm Res. 2007. PMID: 17057405

4

Epidemiological study of nonsyndromic hearing loss in Sicilian newborns.

Niceta M, Fabiano C, Sammarco P, Piccione M, Antona V, Giuffrè M, Corsello G. Niceta M, et al. Among authors: corsello g. Am J Med Genet A. 2007 Jul 15;143A(14):1666-70. doi: 10.1002/ajmg.a.31836. Am J Med Genet A. 2007. PMID: 17568408 No abstract available.

5

A case of Kawasaki disease mimicking acute appendicitis.

Maggio MC, Liotta A, Vitaliti SM, Corsello G. Maggio MC, et al. Among authors: corsello g. Med J Aust. 2007 Sep 3;187(5):316-7. doi: 10.5694/j.1326-5377.2007.tb01258.x. Med J Aust. 2007. PMID: 17767443 No abstract available.

6

Polycystic ovary and gonadoblastoma in Turner's syndrome.

Maggio MC, Liotta A, De Grazia E, Cimador M, Di Pace R, Corsello G. Maggio MC, et al. Among authors: corsello g. Minerva Pediatr. 2007 Aug;59(4):397-401. Minerva Pediatr. 2007. PMID: 17947845

7

10qter deletion: a new case.

Piccione M, Antona V, Piro E, Cavani S, Malacarne M, Pierluigi M, Corsello G. Piccione M, et al. Among authors: corsello g. Am J Med Genet A. 2008 Sep 15;146A(18):2435-8. doi: 10.1002/ajmg.a.32467. Am J Med Genet A. 2008. PMID: 18698621 No abstract available.

8

Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.

Piccione M, Antona V, Niceta M, Fabiano C, Martines M, Bianchi A, Corsello G. Piccione M, et al. Among authors: corsello g. Eur J Pediatr. 2009 Sep;168(9):1135-9. doi: 10.1007/s00431-008-0884-x. Epub 2008 Dec 6. Eur J Pediatr. 2009. PMID: 19066959

9

Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III.

Piccione M, Niceta M, Antona V, Di Fiore A, Cariola F, Gentile M, Corsello G. Piccione M, et al. Among authors: corsello g. Am J Med Genet A. 2009 Aug;149A(8):1837-41. doi: 10.1002/ajmg.a.32952. Am J Med Genet A. 2009. PMID: 19610100 No abstract available.

10

Array CGH defined interstitial deletion on chromosome 14: a new case.

Piccione M, Antona V, Scavone V, Malacarne M, Pierluigi M, Grasso M, Corsello G. Piccione M, et al. Among authors: corsello g. Eur J Pediatr. 2010 Jul;169(7):845-51. doi: 10.1007/s00431-009-1128-4. Epub 2010 Jan 21. Eur J Pediatr. 2010. PMID: 20087602

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