Penco S - 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: penco s. 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

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: penco s. Pharmacogenetics. 2003 May;13(5):265-70. doi: 10.1097/00008571-200305000-00005. Pharmacogenetics. 2003. PMID: 12724618

3

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: penco s. J Neurol. 2005 Jul;252(7):782-8. doi: 10.1007/s00415-005-0742-y. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789135

4

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: penco s. Arch Neurol. 2007 Jun;64(6):843-8. doi: 10.1001/archneur.64.6.843. Arch Neurol. 2007. PMID: 17562932

5

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: penco s. 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

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. BMC Bioinformatics. 2008 May 30;9:254. doi: 10.1186/1471-2105-9-254. BMC Bioinformatics. 2008. PMID: 18513389 Free PMC article.

7

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

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

8

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: penco s. Neurol Sci. 2009 Apr;30(2):143-7. doi: 10.1007/s10072-009-0020-3. Epub 2009 Jan 30. Neurol Sci. 2009. PMID: 19184323

9

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. J Neurosurg. 2009 May;110(5):929-34. doi: 10.3171/2008.8.17640. J Neurosurg. 2009. PMID: 19199464

10

No association of DPP6 with amyotrophic lateral sclerosis in an Italian population.

Fogh I, D'Alfonso S, Gellera C, Ratti A, Cereda C, Penco S, Corrado L, Sorarù G, Castellotti B, Tiloca C, Gagliardi S, Cozzi L, Lupton MK, Ticozzi N, Mazzini L, Shaw CE, Al-Chalabi A, Powell J, Silani V. Fogh I, et al. Among authors: penco s. Neurobiol Aging. 2011 May;32(5):966-7. doi: 10.1016/j.neurobiolaging.2009.05.014. Epub 2009 Jun 13. Neurobiol Aging. 2011. PMID: 19525032

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