Tinto N - Search Results

1

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: tinto n. Clin Chem. 2004 Aug;50(8):1435-8. doi: 10.1373/clinchem.2004.033795. Clin Chem. 2004. PMID: 15277355 Free article. No abstract available.

2

Efficiency of two different nine-loci short tandem repeat systems for DNA typing purposes.

Sacchetti L, Calcagno G, Coto I, Tinto N, Vuttariello E, Salvatore F. Sacchetti L, et al. Among authors: tinto n. Clin Chem. 1999 Feb;45(2):178-83. Clin Chem. 1999. PMID: 9931038

3

A case of discordance between genotype and phenotype in a malignant hyperthermia family.

Fortunato G, Carsana A, Tinto N, Brancadoro V, Canfora G, Salvatore F. Fortunato G, et al. Among authors: tinto n. Eur J Hum Genet. 1999 May-Jun;7(4):415-20. doi: 10.1038/sj.ejhg.5200314. Eur J Hum Genet. 1999. PMID: 10352931

4

Multiplex PCR typing of the three most frequent HLA alleles in celiac disease.

Sacchetti L, Tinto N, Calcagno G, Improta P, Salvatore F. Sacchetti L, et al. Among authors: tinto n. Clin Chim Acta. 2001 Aug 20;310(2):205-7. doi: 10.1016/s0009-8981(01)00575-7. Clin Chim Acta. 2001. PMID: 11498087 No abstract available.

5

The first large population based twin study of coeliac disease.

Greco L, Romino R, Coto I, Di Cosmo N, Percopo S, Maglio M, Paparo F, Gasperi V, Limongelli MG, Cotichini R, D'Agate C, Tinto N, Sacchetti L, Tosi R, Stazi MA. Greco L, et al. Among authors: tinto n. Gut. 2002 May;50(5):624-8. doi: 10.1136/gut.50.5.624. Gut. 2002. PMID: 11950806 Free PMC article.

6

A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women.

Fortunato G, Rubba P, Panico S, Trono D, Tinto N, Mazzaccara C, De Michele M, Iannuzzi A, Vitale DF, Salvatore F, Sacchetti L. Fortunato G, et al. Among authors: tinto n. Atherosclerosis. 2003 Mar;167(1):141-8. doi: 10.1016/s0021-9150(02)00423-9. Atherosclerosis. 2003. PMID: 12618279

7

HLA related genetic risk for coeliac disease.

Bourgey M, Calcagno G, Tinto N, Gennarelli D, Margaritte-Jeannin P, Greco L, Limongelli MG, Esposito O, Marano C, Troncone R, Spampanato A, Clerget-Darpoux F, Sacchetti L. Bourgey M, et al. Among authors: tinto n. Gut. 2007 Aug;56(8):1054-9. doi: 10.1136/gut.2006.108530. Epub 2007 Mar 7. Gut. 2007. PMID: 17344279 Free PMC article.

8

Increased prevalence of celiac disease without gastrointestinal symptoms in adults MICA 5.1 homozygous subjects from the Campania area.

Tinto N, Ciacci C, Calcagno G, Gennarelli D, Spampanato A, Farinaro E, Tortora R, Sacchetti L. Tinto N, et al. Dig Liver Dis. 2008 Apr;40(4):248-52. doi: 10.1016/j.dld.2007.11.028. Epub 2008 Feb 20. Dig Liver Dis. 2008. PMID: 18282752

9

Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy.

Tinto N, Zagari A, Capuano M, De Simone A, Capobianco V, Daniele G, Giugliano M, Spadaro R, Franzese A, Sacchetti L. Tinto N, et al. PLoS One. 2008 Apr 2;3(4):e1870. doi: 10.1371/journal.pone.0001870. PLoS One. 2008. PMID: 18382660 Free PMC article.

10

Comprehensive mutation analysis (20 families) of the choroideremia gene reveals a missense variant that prevents the binding of REP1 with Rab geranylgeranyl transferase.

Esposito G, De Falco F, Tinto N, Testa F, Vitagliano L, Tandurella IC, Iannone L, Rossi S, Rinaldi E, Simonelli F, Zagari A, Salvatore F. Esposito G, et al. Among authors: tinto n. Hum Mutat. 2011 Dec;32(12):1460-9. doi: 10.1002/humu.21591. Epub 2011 Oct 11. Hum Mutat. 2011. PMID: 21905166

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

39 results

Search Page

Filters