Arduino C - Search Results

1

Arduino C, Gaia E. Arduino C, et al. Biomed Pharmacother. 2000 Aug;54(7):394-9. doi: 10.1016/S0753-3322(01)80007-X. Biomed Pharmacother. 2000. PMID: 10989979 Review.

2

Polyvariant mutant CFTR genes in patients with chronic pancreatitis.

Arduino C, Gallo M, Brusco A, Garnerone S, Piana MR, Di Maggio S, Gerbino Promis G, Ferrone M, Angeli A, Gaia E. Arduino C, et al. Clin Genet. 1999 Nov;56(5):400-4. doi: 10.1034/j.1399-0004.1999.560509.x. Clin Genet. 1999. PMID: 10668931

3

Association of a new cationic trypsinogen gene mutation (V39A) with chronic pancreatitis in an Italian family.

Arduino C, Salacone P, Pasini B, Brusco A, Salmin P, Bacillo E, Robecchi A, Cestino L, Cirillo S, Regge D, Cappello N, Gaia E. Arduino C, et al. Gut. 2005 Nov;54(11):1663-4. doi: 10.1136/gut.2004.062992. Gut. 2005. PMID: 16227369 Free PMC article. No abstract available.

4

Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene.

Arduino C, Ferrone M, Brusco A, Garnerone S, Fontana D, Rolle L, Carbonara AO. Arduino C, et al. Clin Genet. 1998 Mar;53(3):202-4. doi: 10.1111/j.1399-0004.1998.tb02677.x. Clin Genet. 1998. PMID: 9630075

5

Brand new SPINK1 and CFTR mutations in a child with acute recurrent pancreatitis: a case report.

Terlizzi V, De Gregorio F, Sepe A, Amato N, Arduino C, Casale A, Majo F, Tomaiuolo R, Castaldo G, Raia V. Terlizzi V, et al. Among authors: arduino c. Minerva Pediatr. 2013 Dec;65(6):669-72. Minerva Pediatr. 2013. PMID: 24217635

6

Hereditary pancreatitis in Paediatrics: the causative role of p.Leu104Pro mutation of cationic trypsinogen gene also in young subjects.

Enea A, Pizzol A, Pinon M, Cisarò F, Tandoi F, Arduino C, Calvo PL. Enea A, et al. Among authors: arduino c. Gut. 2019 Apr;68(4):767-768. doi: 10.1136/gutjnl-2018-316443. Epub 2018 Apr 17. Gut. 2019. PMID: 29666173 No abstract available.

7

Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis.

De Rose V, Arduino C, Cappello N, Piana R, Salmin P, Bardessono M, Goia M, Padoan R, Bignamini E, Costantini D, Pizzamiglio G, Bennato V, Colombo C, Giunta A, Piazza A. De Rose V, et al. Among authors: arduino c. Eur J Hum Genet. 2005 Jan;13(1):96-101. doi: 10.1038/sj.ejhg.5201285. Eur J Hum Genet. 2005. PMID: 15367919

8

Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.

Di Gregorio E, Riberi E, Belligni EF, Biamino E, Spielmann M, Ala U, Calcia A, Bagnasco I, Carli D, Gai G, Giordano M, Guala A, Keller R, Mandrile G, Arduino C, Maffè A, Naretto VG, Sirchia F, Sorasio L, Ungari S, Zonta A, Zacchetti G, Talarico F, Pappi P, Cavalieri S, Giorgio E, Mancini C, Ferrero M, Brussino A, Savin E, Gandione M, Pelle A, Giachino DF, De Marchi M, Restagno G, Provero P, Cirillo Silengo M, Grosso E, Buxbaum JD, Pasini B, De Rubeis S, Brusco A, Ferrero GB. Di Gregorio E, et al. Among authors: arduino c. Clin Genet. 2017 Oct;92(4):415-422. doi: 10.1111/cge.13009. Epub 2017 Jul 25. Clin Genet. 2017. PMID: 28295210

9

Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia.

Brussino A, Graziano C, Giobbe D, Ferrone M, Dragone E, Arduino C, Lodi R, Tonon C, Gabellini A, Rinaldi R, Miccoli S, Grosso E, Bellati MC, Orsi L, Migone N, Brusco A. Brussino A, et al. Among authors: arduino c. Mov Disord. 2010 Jul 15;25(9):1269-73. doi: 10.1002/mds.22835. Mov Disord. 2010. PMID: 20629122

10

An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene.

Saluto A, Brussino A, Tassone F, Arduino C, Cagnoli C, Pappi P, Hagerman P, Migone N, Brusco A. Saluto A, et al. Among authors: arduino c. J Mol Diagn. 2005 Nov;7(5):605-12. doi: 10.1016/S1525-1578(10)60594-6. J Mol Diagn. 2005. PMID: 16258159 Free PMC article.

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