PATROSSO MC[au] - Search Results

Year	Number of Results
1991	1
1992	1
1994	5
1995	3
1996	4
1998	1
2003	3
2004	1
2005	3
2007	4
2008	5
2009	2
2010	3
2011	4
2012	4
2013	3
2014	2
2015	2
2016	2
2026	0

1

Genetic and cellular basis of cerebral cavernous malformations: implications for clinical management.

Bacigaluppi S, Retta SF, Pileggi S, Fontanella M, Goitre L, Tassi L, La Camera A, Citterio A, Patrosso MC, Tredici G, Penco S. Bacigaluppi S, et al. Among authors: patrosso mc. Clin Genet. 2013 Jan;83(1):7-14. doi: 10.1111/j.1399-0004.2012.01892.x. Epub 2012 May 8. Clin Genet. 2013. PMID: 22510019 Review.

2

Genetic variability of the fructosamine 3-kinase gene in diabetic patients.

Mosca L, Penco S, Patrosso MC, Marocchi A, Lapolla A, Sartore G, Chilelli NC, Paleari R, Mosca A. Mosca L, et al. Among authors: patrosso mc. Clin Chem Lab Med. 2011 May;49(5):803-8. doi: 10.1515/CCLM.2011.133. Epub 2011 Feb 3. Clin Chem Lab Med. 2011. PMID: 21288167

3

SOX2, OTX2 and PAX6 analysis in subjects with anophthalmia and microphthalmia.

Mauri L, Franzoni A, Scarcello M, Sala S, Garavelli L, Modugno A, Grammatico P, Patrosso MC, Piozzi E, Del Longo A, Gesu GP, Manfredini E, Primignani P, Damante G, Penco S. Mauri L, et al. Among authors: patrosso mc. Eur J Med Genet. 2015 Feb;58(2):66-70. doi: 10.1016/j.ejmg.2014.12.005. Epub 2014 Dec 23. Eur J Med Genet. 2015. PMID: 25542770

4

SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies.

Mauri L, Barone L, Al Oum M, Del Longo A, Piozzi E, Manfredini E, Stanzial F, Benedicenti F, Penco S, Patrosso MC. Mauri L, et al. Among authors: patrosso mc. Gene. 2014 Jan 1;533(1):398-402. doi: 10.1016/j.gene.2013.09.053. Epub 2013 Oct 3. Gene. 2014. PMID: 24096233

5

Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis.

Cozzi L, Campolo J, Parolini M, De Maria R, Patrosso MC, Marocchi A, Parodi O, Penco S. Cozzi L, et al. Among authors: patrosso mc. Mol Cell Biochem. 2013 Feb;374(1-2):233-8. doi: 10.1007/s11010-012-1525-2. Epub 2012 Dec 6. Mol Cell Biochem. 2013. PMID: 23225229

6

Prevention and modulation of aminoglycoside ototoxicity (Review).

Perletti G, Vral A, Patrosso MC, Marras E, Ceriani I, Willems P, Fasano M, Magri V. Perletti G, et al. Among authors: patrosso mc. Mol Med Rep. 2008 Jan-Feb;1(1):3-13. Mol Med Rep. 2008. PMID: 21479370

7

Electrophoretic separation of biopolymers in a matrix of polyacrylamide covalently linked to agarose.

Chiari M, Campoleoni A, Conti P, Felli C, Patrosso MC, Brogren CH. Chiari M, et al. Among authors: patrosso mc. Electrophoresis. 1996 Mar;17(3):473-8. doi: 10.1002/elps.1150170307. Electrophoresis. 1996. PMID: 8740161

8

The exon-intron organization of the human X-linked gene (FLN1) encoding actin-binding protein 280.

Patrosso MC, Repetto M, Villa A, Milanesi L, Frattini A, Faranda S, Mancini M, Maestrini E, Toniolo D, Vezzoni P. Patrosso MC, et al. Genomics. 1994 May 1;21(1):71-6. doi: 10.1006/geno.1994.1226. Genomics. 1994. PMID: 8088819

9

Detection of the first OCA6 Italian patient in a large cohort of albino subjects.

Veniani E, Mauri L, Manfredini E, Gesu GP, Patrosso MC, Zelante L, D'Agruma L, Del Longo A, Mazza M, Piozzi E, Penco S, Primignani P. Veniani E, et al. Among authors: patrosso mc. J Dermatol Sci. 2016 Mar;81(3):208-9. doi: 10.1016/j.jdermsci.2015.11.012. Epub 2015 Nov 28. J Dermatol Sci. 2016. PMID: 26686029 No abstract available.

10

Lack of association of PON polymorphisms with sporadic ALS in an Italian population.

Ricci C, Battistini S, Cozzi L, Benigni M, Origone P, Verriello L, Lunetta C, Cereda C, Milani P, Greco G, Patrosso MC, Causarano R, Caponnetto C, Giannini F, Corbo M, Penco S. Ricci C, et al. Among authors: patrosso mc. Neurobiol Aging. 2011 Mar;32(3):552.e7-13. doi: 10.1016/j.neurobiolaging.2010.02.010. Epub 2010 Apr 9. Neurobiol Aging. 2011. PMID: 20381198

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