Esposito T - Search Results

1

Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts.

Liquori CL, Penco S, Gault J, Leedom TP, Tassi L, Esposito T, Awad IA, Frati L, Johnson EW, Squitieri F, Marchuk DA, Gianfrancesco F. Liquori CL, et al. Among authors: esposito t. Neurogenetics. 2008 Feb;9(1):25-31. doi: 10.1007/s10048-007-0109-x. Epub 2007 Dec 1. Neurogenetics. 2008. PMID: 18060436

2

Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.

Gianfrancesco F, Cannella M, Martino T, Maglione V, Esposito T, Innocenzi G, Vitale E, Liquori CL, Marchuk DA, Squitieri F. Gianfrancesco F, et al. Among authors: esposito t. Am J Med Genet B Neuropsychiatr Genet. 2007 Jul 5;144B(5):691-5. doi: 10.1002/ajmg.b.30381. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17440989

3

ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations.

Gianfrancesco F, Esposito T, Penco S, Maglione V, Liquori CL, Patrosso MC, Zuffardi O, Ciccodicola A, Marchuk DA, Squitieri F. Gianfrancesco F, et al. Among authors: esposito t. Neuroscience. 2008 Aug 13;155(2):345-9. doi: 10.1016/j.neuroscience.2008.05.030. Epub 2008 Jul 16. Neuroscience. 2008. PMID: 18632209

4

Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort.

Maher BH, Kerr M, Cox HC, MacMillan JC, Brimage PJ, Esposito T, Gianfrancesco F, Haupt LM, Nyholt DR, Lea RA, Griffiths LR. Maher BH, et al. Among authors: esposito t. Neurogenetics. 2012 Feb;13(1):97-101. doi: 10.1007/s10048-011-0312-7. Neurogenetics. 2012. PMID: 22294494

5

piR_015520 belongs to Piwi-associated RNAs regulates expression of the human melatonin receptor 1A gene.

Esposito T, Magliocca S, Formicola D, Gianfrancesco F. Esposito T, et al. PLoS One. 2011;6(7):e22727. doi: 10.1371/journal.pone.0022727. Epub 2011 Jul 26. PLoS One. 2011. PMID: 21818375 Free PMC article.

6

ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.

Scotto di Carlo F, Pazzaglia L, Mumm S, Benassi MS, De Chiara A, Franchi A, Parafioriti A, Righi A, Esposito T, Whyte MP, Gianfrancesco F. Scotto di Carlo F, et al. Among authors: esposito t. J Bone Miner Res. 2020 Oct;35(10):1974-1980. doi: 10.1002/jbmr.3993. Epub 2020 Mar 11. J Bone Miner Res. 2020. PMID: 32106343 Free article.

7

[Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis].

Gianfrancesco F, Esposito T. Gianfrancesco F, et al. Among authors: esposito t. Minerva Med. 2005 Dec;96(6):409-16. Minerva Med. 2005. PMID: 16518303 Review. Italian.

8

Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage.

Gianfrancesco F, Esposito T, Casu G, Maninchedda G, Roberto R, Pirastu M. Gianfrancesco F, et al. Among authors: esposito t. Gene. 2004 Sep 15;339:131-8. doi: 10.1016/j.gene.2004.06.030. Gene. 2004. PMID: 15363853

9

ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of bone.

Divisato G, Scotto di Carlo F, Petrillo N, Esposito T, Gianfrancesco F. Divisato G, et al. Among authors: esposito t. Clin Genet. 2018 Jun;93(6):1240-1244. doi: 10.1111/cge.13247. Epub 2018 Apr 11. Clin Genet. 2018. PMID: 29493781

10

The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone.

Scotto di Carlo F, Pazzaglia L, Esposito T, Gianfrancesco F. Scotto di Carlo F, et al. Among authors: esposito t. J Bone Miner Res. 2020 Aug;35(8):1387-1398. doi: 10.1002/jbmr.3964. Epub 2020 Feb 19. J Bone Miner Res. 2020. PMID: 31991009 Free article.

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