Sfoglia per Autore NAPOLIONI, Valerio
Genetic polymorphisms and idiopathic generalized epilepsies
2007-01-01 Lucarini, Nazzareno; Verrotti, A; Napolioni, Valerio; Bosco, G; Curatolo, P.
Genetics and molecular biology of Tuberous Sclerosis Complex
2008-01-01 Napolioni, V.; Curatolo, P.
Unfaithful association of FCGR2B genetic polymorphisms with susceptibility to SLE.
2009-01-01 Napolioni, V; Barucca, A; Bolli, E; Concetti, Antonio; Venanzi, Franco
Recent advances in neurobiology of Tuberous Sclerosis Complex
2009-01-01 Napolioni, V.; Moavero, R.; Curatolo, P.
Recent patents on epilepsy genetics
2009-01-01 Napolioni, V.
PCR-based methods for CDA K27Q and A70T genotyping: genotypes and alleles distribution in a Central Italy population
2010-01-01 Carpi, FRANCESCO MARTINO; Vincenzetti, Silvia; Micozzi, D; Vita, Alberto; Napolioni, Valerio
Gender-specific association of ADA genetic polymorphism with human longevity.
2010-01-01 Napolioni, Valerio; Lucarini, Nazzareno
Age- and gender-specific association between ADA (22G>A) and TNF-α (-308G>A) genetic polymorphisms
2010-01-01 Napolioni, V.; Predazzi, I. M.
Autism spectrum disorders in tuberous sclerosis: Pathogenetic pathways and implications for treatment
2010-01-01 Curatolo, P.; Napolioni, V.; Moavero, R.
ADA (22G>A) polymorphism: A possible genetic marker for predictive medicine of human reproduction?
2010-01-01 Napolioni, V.
Insights into the role of fc gamma receptors (FcγRs) genetic variations in monoclonal antibody-based anti-cancer therapy
2010-01-01 Concetti, F.; Napolioni, V.
Human DNA extraction methods: patents and applications.
2011-01-01 Carpi, Fm; DI PIETRO, Fabio; Vincenzetti, Silvia; Mignini, Fiorenzo; Napolioni, Valerio
APOE haplotypes are associated with human longevity in a Central Italy population: Evidence for epistasis with HP 1/2 polymorphism
2011-01-01 Napolioni, V.; Gianni, P.; Carpi, F. M.; Predazzi, I. M.; Lucarini, N.
PTPN22 1858C>T (R620W) functional polymorphism and human longevity
2011-01-01 Napolioni, V.; Natali, A.; Saccucci, P.; Lucarini, N.
Rapid allele-specific PCR method for CDA 79A>C (K27Q) genotyping: a useful pharmacogenetic tool and world-wide polymorphism distribution.
2011-01-01 Carpi, FRANCESCO MARTINO; Xu, J.; Vincenzetti, Silvia; Vita, Alberto; Cai, W. M.; Napolioni, Valerio
Family-based association study of ITGB3 in autism spectrum disorder and its endophenotypes
2011-01-01 Napolioni, V.; Lombardi, F.; Sacco, R.; Curatolo, P.; Manzi, B.; Alessandrelli, R.; Militerni, R.; Bravaccio, C.; Lenti, C.; Saccani, M.; Schneider, C.; Melmed, R.; Pascucci, T.; Puglisi-Allegra, S.; Reichelt, K. -L.; Rousseau, F.; Lewin, P.; Persico, A. M.
PTPN22 1858C>T polymorphism distribution in europe and association with rheumatoid arthritis: Case-control study and meta-analysis
2011-01-01 Totaro, M. C.; Tolusso, B.; Napolioni, V.; Faustini, F.; Canestri, S.; Mannocci, A.; Gremese, E.; Bosello, S. L.; Alivernini, S.; Ferraccioli, G.
Regarding "haptoglobin 2-1 phenotype predicts rapid growth of abdominal aortic aneurysms"
2011-01-01 Napolioni, V.
The mitochondrial aspartate/glutamate carrier AGC1 and calcium homeostasis: Physiological links and abnormalities in autism
2011-01-01 Napolioni, V.; Persico, A. M.; Porcelli, V.; Palmieri, L.
Single dose bioavailability and pharmacokinetic study of a innovative formulation of α-lipoic acid (ALA600) in healthy volunteers.
2011-01-01 Mignini, Fiorenzo; Capacchietti, Mariolina; Napolioni, Valerio; Reggiardo, G; Fasani, R; Ferrari, P.
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