Patrosso MC - Search Results

1

Molecular screening test in familial forms of cerebral cavernous malformation: the impact of the Multiplex Ligation-dependent Probe Amplification approach.

Penco S, Ratti R, Bianchi E, Citterio A, Patrosso MC, Marocchi A, Tassi L, La Camera A, Collice M. Penco S, et al. Among authors: patrosso mc. J Neurosurg. 2009 May;110(5):929-34. doi: 10.3171/2008.8.17640. J Neurosurg. 2009. PMID: 19199464

2

Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.

Battistini S, Rocchi R, Cerase A, Citterio A, Tassi L, Lando G, Patrosso MC, Galli R, Brunori P, Sgrò DL, Pitillo G, Lo Russo G, Marocchi A, Penco S. Battistini S, et al. Among authors: patrosso mc. Arch Neurol. 2007 Jun;64(6):843-8. doi: 10.1001/archneur.64.6.843. Arch Neurol. 2007. PMID: 17562932

3

Genetic variations within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a large Italian family harbouring a Krit1/CCM1 mutation.

Pileggi S, Buscone S, Ricci C, Patrosso MC, Marocchi A, Brunori P, Battistini S, Penco S. Pileggi S, et al. Among authors: patrosso mc. J Mol Neurosci. 2010 Oct;42(2):235-42. doi: 10.1007/s12031-010-9360-y. Epub 2010 Apr 24. J Mol Neurosci. 2010. PMID: 20419355

4

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.

5

Familial cerebral cavernous malformation: report of a further Italian family.

Nannucci S, Pescini F, Poggesi A, Ciolli L, Patrosso MC, Marocchi A, Inzitari D, Penco S, Pantoni L. Nannucci S, et al. Among authors: patrosso mc. Neurol Sci. 2009 Apr;30(2):143-7. doi: 10.1007/s10072-009-0020-3. Epub 2009 Jan 30. Neurol Sci. 2009. PMID: 19184323

6

New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

Penco S, Buscema M, Patrosso MC, Marocchi A, Grossi E. Penco S, et al. Among authors: patrosso mc. BMC Bioinformatics. 2008 May 30;9:254. doi: 10.1186/1471-2105-9-254. BMC Bioinformatics. 2008. PMID: 18513389 Free PMC article.

7

Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex disease.

Penco S, Lunetta C, Mosca L, Maestri E, Avemaria F, Tarlarini C, Patrosso MC, Marocchi A, Corbo M. Penco S, et al. Among authors: patrosso mc. J Mol Neurosci. 2011 May;44(1):25-30. doi: 10.1007/s12031-010-9480-4. Epub 2010 Dec 1. J Mol Neurosci. 2011. PMID: 21120636

8

Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.

Patrosso MC, Lando G, Penco S. Patrosso MC, et al. Hum Genet. 2008 Oct;124(3):294. Hum Genet. 2008. PMID: 18846608 No abstract available.

9

Glutamate-cysteine ligase polymorphism, hypertension, and male sex are associated with cardiovascular events. Biochemical and genetic characterization of Italian subpopulation.

Campolo J, Penco S, Bianchi E, Colombo L, Parolini M, Caruso R, Sedda V, Patrosso MC, Cighetti G, Marocchi A, Parodi O. Campolo J, et al. Among authors: patrosso mc. Am Heart J. 2007 Dec;154(6):1123-9. doi: 10.1016/j.ahj.2007.07.029. Epub 2007 Sep 6. Am Heart J. 2007. PMID: 18035085

10

Assessment of the role of genetic polymorphism in venous thrombosis through artificial neural networks.

Penco S, Grossi E, Cheng S, Intraligi M, Maurelli G, Patrosso MC, Marocchi A, Buscema M. Penco S, et al. Among authors: patrosso mc. Ann Hum Genet. 2005 Nov;69(Pt 6):693-706. doi: 10.1111/j.1529-8817.2005.00206.x. Ann Hum Genet. 2005. PMID: 16266408 Clinical Trial.

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