19 results for author:"Patrosso M.C." in Literature citations
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| Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study. Cantarini L., Lucherini O.M., Brucato A., Barone L., Cumetti D., Iacoponi F., Rigante D., Brambilla G., Penco S., Brizi M.G. et al. Clin Res Cardiol 101:525-531(2012) · Mapped (4) |
| p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients. Concolino P., Mello E., Patrosso M.C., Penco S., Zuppi C., Capoluongo E. Metab. Clin. Exp. 61:519-524(2012) · Mapped (33) |
| Genetic variability of the fructosamine 3-kinase gene in diabetic patients. Mosca L., Penco S., Patrosso M.C., Marocchi A., Lapolla A., Sartore G., Chilelli N.C., Paleari R., Mosca A. Clin. Chem. Lab. Med. 49:803-808(2011) · Mapped (3) |
| 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 M.C., Marocchi A., Corbo M. J. Mol. Neurosci. 44:25-30(2011) · Mapped (2) |
| 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 M.C., Marocchi A., Brunori P., Battistini S., Penco S. J. Mol. Neurosci. 42:235-242(2010) · Mapped (11) |
| 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. et al. Neurobiol. Aging 32:552.e7-13(2011) · Mapped (11) |
| 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 M.C., Marocchi A., Tassi L., La Camera A., Collice M. J. Neurosurg. 110:929-934(2009) · Mapped (11) |
| Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation. Trojani A., Ripamonti C.B., Penco S., Beghini A., Nadali G., Di Bona E., Viola A., Castagnola C., Colapietro P., Grillo G. et al. Anticancer Res. 28:2745-2751(2008) · Mapped (5) |
| New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background. Penco S., Buscema M., Patrosso M.C., Marocchi A., Grossi E. BMC Bioinformatics 9:254-254(2008) · Mapped (201) |
| 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 M.C., Cighetti G., Marocchi A. et al. Am. Heart J. 154:1123-1129(2007) · Mapped (4) |
| A novel type of familial transthyretin amyloidosis, ATTR Asn124Ser, with co-localization of kappa light chains. Bergstroem J., Patrosso M.C., Colussi G., Salvadore M., Penco S., Lando G., Marocchi A., Ueda A., Nakamura M., Ando Y. Amyloid 14:141-145(2007) · UniProtKB (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 M.C., Pileggi S. et al. J. Neurol. Sci. 258:123-127(2007) · Mapped (3) |
| 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 M.C., Marocchi A., Buscema M. Ann. Hum. Genet. 69:693-706(2005) · Mapped (28) |
| SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study. Battistini S., Giannini F., Greco G., Bibbo G., Ferrera L., Marini V., Causarano R., Casula M., Lando G., Patrosso M.C. et al. J. Neurol. 252:782-788(2005) · Mapped (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 M.C. Pharmacogenetics 13:265-270(2003) · Mapped (3) |
| Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis. Patrosso M.C., Salvi F., De Grandis D., Vezzoni P., Jacobson D.R., Ferlini A. Am. J. Med. Genet. 77:135-138(1998) · UniProtKB (1) |
| The exon-intron organization of the human X-linked gene (FLN1) encoding actin-binding protein 280. Patrosso M.C., Repetto M., Villa A., Milanesi L., Frattini A., Faranda S., Mancini M., Maestrini E., Toniolo D., Vezzoni P. Genomics 21:71-76(1994) · UniProtKB (1) |
| Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28. Frattini A., Faranda S., Redolfi E., Zucchi I., Villa A., Patrosso M.C., Strina D., Susani L., Vezzoni P. |
| X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene. Villa A., Notarangelo L., Macchi P., Mantuano E., Cavagni G., Brugnoni D., Strina D., Patrosso M.C., Ramenghi U., Sacco M.G. et al. Nat. Genet. 9:414-417(1995) · UniProtKB (1) |