Cardillo G - Search Results

1

Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management.

Berni Canani R, Terrin G, Cardillo G, Tomaiuolo R, Castaldo G. Berni Canani R, et al. Among authors: cardillo g. J Pediatr Gastroenterol Nutr. 2010 Apr;50(4):360-6. doi: 10.1097/MPG.0b013e3181d135ef. J Pediatr Gastroenterol Nutr. 2010. PMID: 20216094 Review.

2

Butyrate as an effective treatment of congenital chloride diarrhea.

Canani RB, Terrin G, Cirillo P, Castaldo G, Salvatore F, Cardillo G, Coruzzo A, Troncone R. Canani RB, et al. Among authors: cardillo g. Gastroenterology. 2004 Aug;127(2):630-4. doi: 10.1053/j.gastro.2004.03.071. Gastroenterology. 2004. PMID: 15300594

3

Molecular epidemiology of phenylalanine hydroxylase deficiency in Southern Italy: a 96% detection rate with ten novel mutations.

Daniele A, Cardillo G, Pennino C, Carbone MT, Scognamiglio D, Correra A, Pignero A, Castaldo G, Salvatore F. Daniele A, et al. Among authors: cardillo g. Ann Hum Genet. 2007 Mar;71(Pt 2):185-93. doi: 10.1111/j.1469-1809.2006.00328.x. Epub 2006 Nov 10. Ann Hum Genet. 2007. PMID: 17096675

4

Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: a multicentric Italian study.

Tomaiuolo R, Sangiuolo F, Bombieri C, Bonizzato A, Cardillo G, Raia V, D'Apice MR, Bettin MD, Pignatti PF, Castaldo G, Novelli G. Tomaiuolo R, et al. Among authors: cardillo g. J Cyst Fibros. 2008 Sep;7(5):347-51. doi: 10.1016/j.jcf.2007.12.004. Epub 2008 Feb 14. J Cyst Fibros. 2008. PMID: 18280224 Free article.

5

Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants.

Daniele A, Cardillo G, Pennino C, Carbone MT, Scognamiglio D, Esposito L, Correra A, Castaldo G, Zagari A, Salvatore F. Daniele A, et al. Among authors: cardillo g. Biochim Biophys Acta. 2008 Jun;1782(6):378-84. doi: 10.1016/j.bbadis.2008.01.012. Epub 2008 Feb 20. Biochim Biophys Acta. 2008. PMID: 18346471 Free article.

6

Different outcome of six homozygotes for prothrombin A20210A gene variant.

Di Micco P, Di Fiore R, Niglio A, Quaranta S, Angiolillo A, Cardillo G, Castaldo G. Di Micco P, et al. Among authors: cardillo g. J Transl Med. 2008 Jul 15;6:36. doi: 10.1186/1479-5876-6-36. J Transl Med. 2008. PMID: 18627609 Free PMC article.

7

Three novel CFTR polymorphic repeats improve segregation analysis for cystic fibrosis.

Elce A, Boccia A, Cardillo G, Giordano S, Tomaiuolo R, Paolella G, Castaldo G. Elce A, et al. Among authors: cardillo g. Clin Chem. 2009 Jul;55(7):1372-9. doi: 10.1373/clinchem.2008.119545. Epub 2009 May 14. Clin Chem. 2009. PMID: 19443567 Free article.

8

Extensive molecular analysis of patients bearing CFTR-related disorders.

Amato F, Bellia C, Cardillo G, Castaldo G, Ciaccio M, Elce A, Lembo F, Tomaiuolo R. Amato F, et al. Among authors: cardillo g. J Mol Diagn. 2012 Jan;14(1):81-9. doi: 10.1016/j.jmoldx.2011.09.001. Epub 2011 Oct 20. J Mol Diagn. 2012. PMID: 22020151 Free article.

9

Twelve Novel Mutations in the SLC26A3 Gene in 17 Sporadic Cases of Congenital Chloride Diarrhea.

Amato F, Cardillo G, Liguori R, Scorza M, Comegna M, Elce A, Giordano S, Lucaccioni L, Lugli L, Cardile S, Romano C, Pezzella V, Castaldo G, Berni Canani R. Amato F, et al. Among authors: cardillo g. J Pediatr Gastroenterol Nutr. 2017 Jul;65(1):26-30. doi: 10.1097/MPG.0000000000001418. J Pediatr Gastroenterol Nutr. 2017. PMID: 28644346

10

Functional and structural characterization of novel mutations and genotype-phenotype correlation in 51 phenylalanine hydroxylase deficient families from Southern Italy.

Daniele A, Scala I, Cardillo G, Pennino C, Ungaro C, Sibilio M, Parenti G, Esposito L, Zagari A, Andria G, Salvatore F. Daniele A, et al. Among authors: cardillo g. FEBS J. 2009 Apr;276(7):2048-59. doi: 10.1111/j.1742-4658.2009.06940.x. FEBS J. 2009. PMID: 19292873 Free article.

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