Niceta M - Search Results

1

Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness.

Sinibaldi L, Garone G, Mandarino A, Iarossi G, Chioma L, Dentici ML, Merla G, Agolini E, Micalizzi A, Mancini C, Niceta M, Macchiaiolo M, Diodato D, Onesimo R, Blandino R, Delogu AB, De Rosa G, Trevisan V, Iademarco M, Zampino G, Tartaglia M, Novelli A, Bartuli A, Digilio MC, Calcagni G. Sinibaldi L, et al. Among authors: niceta m. Clin Genet. 2023 Nov;104(5):528-541. doi: 10.1111/cge.14404. Epub 2023 Jul 17. Clin Genet. 2023. PMID: 37455656

2

Evaluation of serum CA 125 levels in patients with pelvic pain related to endometriosis.

Maiorana A, Cicerone C, Niceta M, Alio L. Maiorana A, et al. Among authors: niceta m. Int J Biol Markers. 2007 Jul-Sep;22(3):200-2. doi: 10.1177/172460080702200306. Int J Biol Markers. 2007. PMID: 17922463 Free article.

3

Development of S/MAR minicircles for enhanced and persistent transgene expression in the mouse liver.

Argyros O, Wong SP, Fedonidis C, Tolmachov O, Waddington SN, Howe SJ, Niceta M, Coutelle C, Harbottle RP. Argyros O, et al. Among authors: niceta m. J Mol Med (Berl). 2011 May;89(5):515-29. doi: 10.1007/s00109-010-0713-3. Epub 2011 Feb 8. J Mol Med (Berl). 2011. PMID: 21301798

4

MTHFR C677T homozygous as risk factor for complications after OLT for cryptogenic cirrhosis.

Pasta L, Marrone C, D'Amico M, Verdone R, Rizzo A, Sammarco P, Fabiano C, Niceta M, Caltagirone M, D'Amico G, Pagliaro L. Pasta L, et al. Among authors: niceta m. Clin Transplant. 2006 Nov-Dec;20(6):796-8. doi: 10.1111/j.1399-0012.2006.00564.x. Clin Transplant. 2006. PMID: 17100732 No abstract available.

5

Refractory acne and 21-hydroxylase deficiency in a selected group of female patients.

Caputo V, Fiorella S, Curiale S, Caputo A, Niceta M. Caputo V, et al. Among authors: niceta m. Dermatology. 2010;220(2):121-7. doi: 10.1159/000277608. Epub 2010 Jan 29. Dermatology. 2010. PMID: 20110635

6

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: niceta m. 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

7

A novel nonsense mutation in exon 2 of the factor IX gene resulting in severe haemophilia B.

Niceta M, Fabiano C, Sammarco P, Gagliano F, Mancuso G. Niceta M, et al. Intern Emerg Med. 2006;1(4):318-20. doi: 10.1007/BF02934771. Intern Emerg Med. 2006. PMID: 17217158 No abstract available.

8

A large view of CYP21 locus among Sicilians and other populations: identification of a novel CYP21A2 variant in Sicily.

Niceta M, Bono M, Fabiano C, Pojero F, Niceta F, Sammarco P, Corsello G, Garofalo P. Niceta M, et al. Among authors: niceta f. J Endocrinol Invest. 2011 Dec;34(11):847-54. doi: 10.3275/7417. Epub 2010 Dec 15. J Endocrinol Invest. 2011. PMID: 21169732

9

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. 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.

10

Persistent episomal transgene expression in liver following delivery of a scaffold/matrix attachment region containing non-viral vector.

Argyros O, Wong SP, Niceta M, Waddington SN, Howe SJ, Coutelle C, Miller AD, Harbottle RP. Argyros O, et al. Among authors: niceta m. Gene Ther. 2008 Dec;15(24):1593-605. doi: 10.1038/gt.2008.113. Epub 2008 Jul 17. Gene Ther. 2008. PMID: 18633447

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