Salvatore F - Search Results

1

Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing.

Esposito G, Tremolaterra MR, Savarese M, Spiniello M, Patrizio MP, Lombardo B, Pastore L, Salvatore F, Carsana A. Esposito G, et al. Among authors: salvatore f. Clin Chim Acta. 2018 Jan;476:167-172. doi: 10.1016/j.cca.2017.11.016. Epub 2017 Nov 21. Clin Chim Acta. 2018. PMID: 29170104 Free article.

2

Novel deletion at the M and P promoters of the human dystrophin gene associated with a Duchenne muscular dystrophy.

Frisso G, Sampaolo S, Pastore L, Carlomagno A, Calise RM, Di Iorio G, Salvatore F. Frisso G, et al. Among authors: salvatore f. Neuromuscul Disord. 2002 Jun;12(5):494-7. doi: 10.1016/s0960-8966(01)00323-6. Neuromuscul Disord. 2002. PMID: 12031623

3

Structural and functional analysis of aldolase B mutants related to hereditary fructose intolerance.

Esposito G, Vitagliano L, Santamaria R, Viola A, Zagari A, Salvatore F. Esposito G, et al. Among authors: salvatore f. FEBS Lett. 2002 Nov 6;531(2):152-6. doi: 10.1016/s0014-5793(02)03451-8. FEBS Lett. 2002. PMID: 12417303 Free article.

4

Identification of new polymorphisms in the CACNA1S gene.

Carsana A, Fortunato G, De Sarno C, Brancadoro V, Salvatore F. Carsana A, et al. Among authors: salvatore f. Clin Chem Lab Med. 2003 Jan;41(1):20-2. doi: 10.1515/CCLM.2003.004. Clin Chem Lab Med. 2003. PMID: 12636044

5

Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.

Esposito G, Vitagliano L, Costanzo P, Borrelli L, Barone R, Pavone L, Izzo P, Zagari A, Salvatore F. Esposito G, et al. Among authors: salvatore f. Biochem J. 2004 May 15;380(Pt 1):51-6. doi: 10.1042/BJ20031941. Biochem J. 2004. PMID: 14766013 Free PMC article.

6

AKT participates in endothelial dysfunction in hypertension.

Iaccarino G, Ciccarelli M, Sorriento D, Cipolletta E, Cerullo V, Iovino GL, Paudice A, Elia A, Santulli G, Campanile A, Arcucci O, Pastore L, Salvatore F, Condorelli G, Trimarco B. Iaccarino G, et al. Among authors: salvatore f. Circulation. 2004 Jun 1;109(21):2587-93. doi: 10.1161/01.CIR.0000129768.35536.FA. Epub 2004 May 10. Circulation. 2004. PMID: 15136501

7

Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy.

Frisso G, Carsana A, Tinto N, Calcagno G, Salvatore F, Sacchetti L. Frisso G, et al. Among authors: salvatore f. Clin Chem. 2004 Aug;50(8):1435-8. doi: 10.1373/clinchem.2004.033795. Clin Chem. 2004. PMID: 15277355 Free article. No abstract available.

8

Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene.

Esposito G, Santamaria R, Vitagliano L, Ieno L, Viola A, Fiori L, Parenti G, Zancan L, Zagari A, Salvatore F. Esposito G, et al. Among authors: salvatore f. Hum Mutat. 2004 Dec;24(6):534. doi: 10.1002/humu.9290. Hum Mutat. 2004. PMID: 15532022

9

Ischemic neoangiogenesis enhanced by beta2-adrenergic receptor overexpression: a novel role for the endothelial adrenergic system.

Iaccarino G, Ciccarelli M, Sorriento D, Galasso G, Campanile A, Santulli G, Cipolletta E, Cerullo V, Cimini V, Altobelli GG, Piscione F, Priante O, Pastore L, Chiariello M, Salvatore F, Koch WJ, Trimarco B. Iaccarino G, et al. Among authors: salvatore f. Circ Res. 2005 Nov 25;97(11):1182-9. doi: 10.1161/01.RES.0000191541.06788.bb. Epub 2005 Oct 20. Circ Res. 2005. PMID: 16239589

10

Hereditary fructose intolerance and celiac disease: a novel genetic association.

Ciacci C, Gennarelli D, Esposito G, Tortora R, Salvatore F, Sacchetti L. Ciacci C, et al. Among authors: salvatore f. Clin Gastroenterol Hepatol. 2006 May;4(5):635-8. doi: 10.1016/j.cgh.2005.12.004. Clin Gastroenterol Hepatol. 2006. PMID: 16630753

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