Niceta M - Search Results

1

Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome.

Galosi S, Mancini C, Commone A, Calligari P, Caputo V, Nardecchia F, Carducci C, van den Heuvel LP, Pizzi S, Bruselles A, Niceta M, Martinelli S, Rodenburg RJ, Tartaglia M, Leuzzi V. Galosi S, et al. Among authors: niceta m. Mov Disord. 2024 Jul;39(7):1225-1231. doi: 10.1002/mds.29795. Epub 2024 Apr 30. Mov Disord. 2024. PMID: 38685873

2

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

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

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.

5

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

6

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.

7

Novel human pathological mutations. Gene symbol: F8. Disease: Haemophilia A.

Niceta M, Fabiano C, Sammarco P. Niceta M, et al. Hum Genet. 2010 Jan;127(1):115. Hum Genet. 2010. PMID: 20108391 No abstract available.

8

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.

9

Novel human pathological mutations. Gene symbol: F8. Disease: Haemophilia A.

Fabiano C, Niceta M, Sammarco P. Fabiano C, et al. Among authors: niceta m. Hum Genet. 2010 Jan;127(1):113. Hum Genet. 2010. PMID: 20108389 No abstract available.

10

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: niceta m. 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.

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