Corsello G - Search Results

1

Epidemic spread of ST1-MRSA-IVa in a neonatal intensive care unit, Italy.

Giuffrè M, Cipolla D, Bonura C, Geraci DM, Aleo A, Di Noto S, Nociforo F, Corsello G, Mammina C. Giuffrè M, et al. Among authors: corsello g. BMC Pediatr. 2012 Jun 8;12:64. doi: 10.1186/1471-2431-12-64. BMC Pediatr. 2012. PMID: 22682025 Free PMC article.

2

New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.

Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A. Giuffrè L, et al. Among authors: corsello g. Am J Med Genet. 1994 Jul 1;51(3):266-9. doi: 10.1002/ajmg.1320510319. Am J Med Genet. 1994. PMID: 8074157

3

Lymphoproliferative disorders in Sotos syndrome: observation of two cases.

Corsello G, Giuffrè M, Carcione A, Cuzto ML, Piccione M, Ziino O. Corsello G, et al. Am J Med Genet. 1996 Sep 6;64(4):588-93. doi: 10.1002/(SICI)1096-8628(19960906)64:4<588::AID-AJMG12>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870927

4

Autosomal recessive severe dwarfism in a Sicilian girl: a new form of osteodysplastic primordial dwarfism?

Corsello G, Albanese A, Piccione M, Giuffrè M, Opitz JM. Corsello G, et al. Am J Med Genet. 1996 Dec 18;66(3):265-8. doi: 10.1002/(SICI)1096-8628(19961218)66:3<265::AID-AJMG5>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8985484

5

Osteodysplastic primordial dwarfism (ODPD): notes on brain imaging.

Corsello G, Giuffrè M. Corsello G, et al. Am J Med Genet. 1998 Oct 30;80(1):90-1. Am J Med Genet. 1998. PMID: 9800914 No abstract available.

6

Aminoacid profile and oxidative status in children affected by Down syndrome before and after supplementary nutritional treatment.

Ciaccio M, Piccione M, Giuffrè M, Macaione V, Vocca L, Bono A, Corsello G. Ciaccio M, et al. Among authors: corsello g. Ital J Biochem. 2003 Jun;52(2):72-9. Ital J Biochem. 2003. PMID: 14677423

7

Hypercalciuria and kidney calcifications in terminal 4q deletion syndrome: further evidence for a putative gene on 4q.

Giuffrè M, La Placa S, Carta M, Cataliotti A, Marino M, Piccione M, Pusateri F, Meli F, Corsello G. Giuffrè M, et al. Among authors: corsello g. Am J Med Genet A. 2004 Apr 15;126A(2):186-90. doi: 10.1002/ajmg.a.20561. Am J Med Genet A. 2004. PMID: 15057984

8

Identification of a new nonsense mutation (Tyr129Stop) of the SRY gene in a newborn infant with XY sex-reversal.

Giuffrè M, Sammarco P, Fabiano C, Giardina F, Lunetta F, Corsello G. Giuffrè M, et al. Among authors: corsello g. Am J Med Genet A. 2004 Jul 1;128A(1):46-7. doi: 10.1002/ajmg.a.30075. Am J Med Genet A. 2004. PMID: 15211655

9

Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report.

Carta M, Maresi E, Giuffrè M, Catalano G, Piro E, Siracusa F, Corsello G. Carta M, et al. Among authors: corsello g. J Pediatr Surg. 2005 May;40(5):e37-9. doi: 10.1016/j.jpedsurg.2005.02.018. J Pediatr Surg. 2005. PMID: 15937805

10

Evaluation of cytokine polymorphisms (TNFalpha, IFNgamma and IL-10) in Down patients with coeliac disease.

Cataldo F, Scola L, Piccione M, Giuffrè M, Crivello A, Forte GI, Lio D, Corsello G. Cataldo F, et al. Among authors: corsello g. Dig Liver Dis. 2005 Dec;37(12):923-7. doi: 10.1016/j.dld.2005.08.001. Epub 2005 Sep 22. Dig Liver Dis. 2005. PMID: 16182624

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