Zarrilli F - Search Results

1

Haemophilia A: the consequences of de novo mutations. Two case reports.

Zarrilli F, Coppola A, Schiavulli M, Cimino E, Elce A, Rescigno G, Castaldo G, Amato F. Zarrilli F, et al. Blood Transfus. 2018 Jul;16(4):392-393. doi: 10.2450/2017.0292-16. Epub 2017 Apr 5. Blood Transfus. 2018. PMID: 28488976 Free PMC article. No abstract available.

2

Haemophilia A: molecular insights.

Castaldo G, D'Argenio V, Nardiello P, Zarrilli F, Sanna V, Rocino A, Coppola A, Di Minno G, Salvatore F. Castaldo G, et al. Among authors: zarrilli f. Clin Chem Lab Med. 2007;45(4):450-61. doi: 10.1515/CCLM.2007.093. Clin Chem Lab Med. 2007. PMID: 17439320 Review.

3

Mutational spectrum of F8 gene and prothrombotic gene variants in haemophilia A patients from Southern Italy.

Sanna V, Zarrilli F, Nardiello P, D'Argenio V, Rocino A, Coppola A, DI Minno G, Castaldo G. Sanna V, et al. Among authors: zarrilli f. Haemophilia. 2008 Jul;14(4):796-803. doi: 10.1111/j.1365-2516.2008.01705.x. Epub 2008 Apr 30. Haemophilia. 2008. PMID: 18459951

4

TrkB gene expression and DNA methylation state in Wernicke area does not associate with suicidal behavior.

Keller S, Sarchiapone M, Zarrilli F, Tomaiuolo R, Carli V, Angrisano T, Videtic A, Amato F, Pero R, di Giannantonio M, Iosue M, Lembo F, Castaldo G, Chiariotti L. Keller S, et al. Among authors: zarrilli f. J Affect Disord. 2011 Dec;135(1-3):400-4. doi: 10.1016/j.jad.2011.07.003. Epub 2011 Jul 29. J Affect Disord. 2011. PMID: 21802740

5

Aberrant F8 gene intron 1 inversion with concomitant duplication and deletion in a severe hemophilia A patient from Southern Italy.

Sanna V, Ceglia C, Tarsitano M, Lombardo B, Coppola A, Zarrilli F, Castaldo G, Di Minno G. Sanna V, et al. Among authors: zarrilli f. J Thromb Haemost. 2013 Jan;11(1):195-7. doi: 10.1111/jth.12061. J Thromb Haemost. 2013. PMID: 23140572 Free article. No abstract available.

6

Prothrombotic gene variants as risk factors of acute myocardial infarction in young women.

Tomaiuolo R, Bellia C, Caruso A, Di Fiore R, Quaranta S, Noto D, Cefalù AB, Di Micco P, Zarrilli F, Castaldo G, Averna MR, Ciaccio M. Tomaiuolo R, et al. Among authors: zarrilli f. J Transl Med. 2012 Nov 21;10:235. doi: 10.1186/1479-5876-10-235. J Transl Med. 2012. PMID: 23171482 Free PMC article.

7

Molecular and functional analysis of the large 5' promoter region of CFTR gene revealed pathogenic mutations in CF and CFTR-related disorders.

Giordano S, Amato F, Elce A, Monti M, Iannone C, Pucci P, Seia M, Angioni A, Zarrilli F, Castaldo G, Tomaiuolo R. Giordano S, et al. Among authors: zarrilli f. J Mol Diagn. 2013 May;15(3):331-40. doi: 10.1016/j.jmoldx.2013.01.001. Epub 2013 Mar 5. J Mol Diagn. 2013. PMID: 23470247 Free article.

8

Gene mutation in microRNA target sites of CFTR gene: a novel pathogenetic mechanism in cystic fibrosis?

Amato F, Seia M, Giordano S, Elce A, Zarrilli F, Castaldo G, Tomaiuolo R. Amato F, et al. Among authors: zarrilli f. PLoS One. 2013;8(3):e60448. doi: 10.1371/journal.pone.0060448. Epub 2013 Mar 26. PLoS One. 2013. PMID: 23555973 Free PMC article.

9

Prenatal diagnosis of haemophilia: our experience of 44 cases.

Zarrilli F, Sanna V, Ingino R, Santamaria R, Rocino A, Coppola A, Di Minno G, Castaldo G. Zarrilli F, et al. Clin Chem Lab Med. 2013 Dec;51(12):2233-8. doi: 10.1515/cclm-2013-0205. Clin Chem Lab Med. 2013. PMID: 23857941

10

An update on laboratory diagnosis of liver inherited diseases.

Zarrilli F, Elce A, Scorza M, Giordano S, Amato F, Castaldo G. Zarrilli F, et al. Biomed Res Int. 2013;2013:697940. doi: 10.1155/2013/697940. Epub 2013 Oct 8. Biomed Res Int. 2013. PMID: 24222913 Free PMC article. Review.

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