DALPRA', LEDA
DALPRA', LEDA
DIPARTIMENTO DI CHIRURGIA E MEDICINA TRASLAZIONALE (attivo dal 01/11/2013 al 30/09/2015)
Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease
2001 Ferrarese, C; Tremolizzo, L; Rigoldi, M; Sala, G; Begni, B; Brighina, L; Ricci, G; Albizzati, M; Piolti, R; Crosti, F; Dalprà, L; Frattola, L
Genetic study on 231 women affected by premature ovarian failure (POF)
2001 Dalpra', L; Porta, C; Martinoli, E; Patrizi, A; Sala, E; Villa, N; Tibiletti, M; Taborelli, M; Dossena, B; Ginelli, E; Marozzi, A
Mutation analysis of the inhibin alpha gene in an Italian survey of women affected by ovarian failure
2002 Marozzi, A; Porta, C; Vegetti, W; Crosignani, P; Tibiletti, M; Ginelli, E; Dalpra, L
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families
2002 Bonati, M; Combi, R; Asselta, R; Duga, S; Malcovati, M; Oldani, A; Zucconi, M; Ferini Strambi, L; Dalpra', L; Tenchini, M
Mutational analysis of nicotinic acetylcholine receptor β2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy
2002 Duga, S; Asselta, R; Bonati, M; Malcovati, M; Dalpra', L; Oldani, A; Zucconi, M; Ferini Strambi, L; Tenchini, M
A new human cell line, PDSS-26, from poorly differentiated synovial sarcoma, with unique chromosomal anomalies
2003 Berardi, A; Parafioriti, A; Barisani, D; Papp, B; Armiraglio, E; Martinoli, M; Dalpra', L; Santoro, A
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B
2004 Bione, S; Rizzolio, F; Sala, C; Ricotti, R; Goegan, M; Manzini, M; Battaglia, R; Marozzi, A; Vegetti, W; Dalpra', L; Crosignani, P; Ginelli, E; Nappi, R; Bernabini, S; Bruni, V; Torricelli, F; Zuffardi, O; Toniolo, D
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey
2004 Sensi, A; Cavani, S; Villa, N; Pomponi, M; Fogli, A; Gualandi, F; Grasso, M; Sala, E; Pietrobono, R; Baldinotti, F; Savin, E; Ferlini, A; Cecconi, M; Rossi, S; Gallone, S; Bellini, C; Neri, G; Martinoli, E; Simi, P; Dalpra', L; Genuardi, M; Dagna Bricarelli, F; Calzolari, E
Autosomal dominant nocturnal frontal lobe epilepsy - A critical overview
2004 Combi, R; Dalpra', L; Tenchini, M; Ferini Strambi, L
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy
2004 Combi, R; Dalpra', L; Malcovati, M; Oldani, A; Tenchini, M; Ferini Strambi, L
Two new putative loci for ADNFLE identified in an Italian family suggest a digenic inheritance for the disease
2005 Combi, R; Dalpra', L; Ferini Strambi, L; Tenchini, M
Severe intrauterine growth restriction and trisomy 15 confined placental mosaicism: a case report and review of literature.
2005 Redaelli, S; Sala, E; Roncaglia, N; Colombo, C; Crosti, F; Villa, N; Tagliabue, P; Cappellini, A; Dalpra', L
Two new susceptibility loci for ADNFLE
2005 Combi, R; Ferini Strambi, L; Montruccoli, A; Bianchi, V; Malcovati, M; Zucconi, M; Dalpra', L; Tenchini, M
Multi-transgenic pigs expressing three fluorescent proteins produced with high efficiency by sperm mediated gene transfer
2005 Webster, N; Forni, M; Bacci, M; Giovannoni, R; Razzini, R; Fantinati, P; Zannoni, A; Fusetti, L; Dalpra', L; Bianco, M; Papa, M; Seren, E; Sandrin, M; Mc Kenzie, I; Lavitrano, M
Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories
2005 Dalpra', L; Giardino, D; Finelli, P; Corti, C; Valtorta, C; Guerneri, S; Ilardi, P; Fortuna, R; Coviello, D; Nocera, G; Amico, F; Martinoli, E; Sala, E; Villa, N; Crosti, F; Chiodo, F; di Cantogno, L; Savin, E; Croci, G; Franchi, F; Venti, G; Donti, E; Migliori, V; Pettinari, A; Bonifacio, S; Centrone, C; Torricelli, F; Rossi, S; Simi, P; Granata, P; Casalone, R; Lenzini, E; Artifoni, L; Pecile, V; Barlati, S; Bellotti, D; Caufin, D; Police, A; Cavani, S; Piombo, G; Pierluigi, M; Larizza, L
Role of FISH on uncultured amniocytes for the diagnosis of aneuploidies in the presence of fetal anomalies
2005 Locatelli, A; Mariani, S; Ciriello, E; Dalpra', L; Villa, N; Sala, E; Vergani, P
Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene
2005 Combi, R; Dalpra', L; Ferini Strambi, L; Tenchini, M
Maternal polymorphisms for methyltetrahydrofolate reductase (MTHFR) and methioninesynthetasi-reductase (MTRR) and risk of children with down syndrome: A geographic effect?
2006 Pozzi, E; Vergani, P; Dalpra', L; Combi, R; Crosti, F; Dell'Orto, M; Gozzi, M
Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation
2006 Bodega, B; Bione, S; Dalpra', L; Toniolo, D; Ornaghi, F; Vegetti, W; Ginelli, E; Marozzi, A
Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements
2006 Portera, G; Venturin, M; Patrizi, A; Martinoli, E; Riva, P; Dalpra', L