Penco S - Search Results

1

Combined evaluation of genotype and phenotype of thiopurine S-methyltransferase (TPMT) in the clinical management of patients in chronic therapy with azathioprine.

Rucci F, Cigoli MS, Marini V, Fucile C, Mattioli F, Robbiano L, Cavallari U, Scaglione F, Perno CF, Penco S, Marocchi A. Rucci F, et al. Among authors: penco s. Drug Metab Pers Ther. 2019 Mar 6;34(1). doi: 10.1515/dmpt-2018-0037. Drug Metab Pers Ther. 2019. PMID: 30840585

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

An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation.

Ferrera L, Caponnetto C, Marini V, Rizzi D, Bordo D, Penco S, Amoroso A, Origone P, Garrè C. Ferrera L, et al. Among authors: penco s. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):167-70. doi: 10.1080/aml.4.3.167.170. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129804

4

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. 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.

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

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

8

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: penco s. 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

9

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. 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

10

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: penco s. 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

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