Patrosso MC - Search Results

1

Variations in the coding and regulatory sequences of the angiogenin (ANG) gene are not associated to ALS (amyotrophic lateral sclerosis) in the Italian population.

Corrado L, Battistini S, Penco S, Bergamaschi L, Testa L, Ricci C, Giannini F, Greco G, Patrosso MC, Pileggi S, Causarano R, Mazzini L, Momigliano-Richiardi P, D'Alfonso S. Corrado L, et al. Among authors: patrosso mc. J Neurol Sci. 2007 Jul 15;258(1-2):123-7. doi: 10.1016/j.jns.2007.03.009. Epub 2007 Apr 25. J Neurol Sci. 2007. PMID: 17462671

2

SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.

Battistini S, Giannini F, Greco G, Bibbò G, Ferrera L, Marini V, Causarano R, Casula M, Lando G, Patrosso MC, Caponnetto C, Origone P, Marocchi A, Del Corona A, Siciliano G, Carrera P, Mascia V, Giagheddu M, Carcassi C, Orrù S, Garrè C, Penco S. Battistini S, et al. Among authors: patrosso mc. J Neurol. 2005 Jul;252(7):782-8. doi: 10.1007/s00415-005-0742-y. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789135

3

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

4

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.

5

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

6

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

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

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

9

Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.

Lando G, Mosca A, Bonora R, Azzario F, Penco S, Marocchi A, Panteghini M, Patrosso MC. Lando G, et al. Among authors: patrosso mc. Pharmacogenetics. 2003 May;13(5):265-70. doi: 10.1097/00008571-200305000-00005. Pharmacogenetics. 2003. PMID: 12724618

10

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.

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