Paraboschi, Elvezia Maria
Paraboschi, Elvezia Maria
A Frequent Oligogenic Involvement in Congenital Hypothyroidism
2017-01-01 de Filippis, T; Gelmini, G; Paraboschi, E; Vigone, Mc; Di Frenna, M; Marelli, F; Bonomi, M; Cassio, A; Larizza, D; Moro, M; Radetti, G; Salerno, M; Ardissino, D; Weber, G; Gentilini, D; Guizzardi, F; Duga, S; Persani, L.
Abiotic ligation of DNA oligomers templated by their liquid crystal ordering
2015-01-01 Fraccia, Tp; Smith, Gp; Zanchetta, G; Paraboschi, E; Yi, Y; Walba, Dm; Dieci, G; Clark, Na; Bellini, T
ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy
2020-01-01 Asselta, Rosanna; Paraboschi, Elvezia Maria; Mantovani, Alberto; Duga, Stefano
Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis
2011-01-01 Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients
2009-01-01 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease
2021-01-01 Vecellio, Matteo; Paraboschi, Elvezia Maria; Ceribelli, Angela; Isailovic, Natasa; Motta, Francesca; Cardamone, Giulia; Robusto, Michela; Asselta, Rosanna; Brescianini, Sonia; Sacrini, Francesco; Costanzo, Antonio; De Santis, Maria; Stazi, Maria Antonietta; Duga, Stefano; Selmi, Carlo
DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease
2021-01-01 Vecellio, Matteo; Paraboschi, Elvezia Maria; Ceribelli, Angela; Isailovic, Natasa; Motta, Francesca; Cardamone, Giulia; Robusto, Michela; Asselta, Rosanna; Brescianini, Sonia; Sacrini, Francesco; Costanzo, Antonio; De Santis, Maria; Stazi, Maria Antonietta; Duga, Stefano; Selmi, Carlo
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
2017-01-01 Asselta, R; Paraboschi, E; Rimoldi, V; Menegatti, M; Peyvandi, F; Salomon, O; Duga, S
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains
2017-01-01 Paraboschi, E; Duga, S; Asselta, R
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction
2008-01-01 Guella, I; Rimoldi, V; Merlini, Pa; Asselta, R; Paraboschi, Em; Francolini, M; Peyvandi, F; Ardissimo, D; Mannucci, Pm; Duga, S
Functional and clinical implications of genetic structure in 1686 Italian exomes
2021-01-01 Birolo, Giovanni; Aneli, Serena; Di Gaetano, Cornelia; Cugliari, Giovanni; Russo, Alessia; Allione, Alessandra; Casalone, Elisabetta; Giorgio, Elisa; Paraboschi, Elvezia M; Ardissino, Diego; Duga, Stefano; Asselta, Rosanna; Matullo, Giuseppe
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
2012-01-01 Paraboschi, E; Kayıran, Sm; Özbek, N; Gürakan, B; Guella, I; Duga, S; Asselta, R
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.
2014-01-01 Paraboschi, E; Rimoldi, V; Soldà, G; Tabaglio, T; Dall'Osso, C; Saba, E; Vigliano, M; Salviati, A; Leone, M; Benedetti, Md; Fornasari, D; Saarela, J; De Jager, Pl; Patsopoulos, Na; D'Alfonso, S; Gemmati, D; Duga, S; Asselta, R.
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases
2018-01-01 Tisato, V; Zuliani, G; Vigliano, M; Longo, G; Franchini, E; Secchiero, P; Zauli, G; Paraboschi, Em; Vikram Singh, A; Serino, Ml; Ortolani, B; Zurlo, A; Bosi, C; Greco, A; Seripa, D; Asselta, R; Gemmati, D
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients
2018-01-01 Cardamone, G; Paraboschi, E; Solda', G; Duga, S; Saarela, J; Asselta, R.
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
2011-01-01 Paraboschi, E.; Solda', G.; Gemmati, D.; Orioli, E.; Zeri, G.; Benedetti, D.; Salviati, A.; Barizzone, N.; Leone, M.; Duga, S.; Asselta, R.
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.
2014-01-01 Biguzzi, E; Franchi, F; Acaia, B; Ossola, W; Nava, U; Paraboschi, Em; Asselta, R; Peyvandi, F.
Genomewide Association Study of Severe Covid-19 with Respiratory Failure
2020-01-01 Ellinghaus, David; Degenhardt, Frauke; Bujanda, Luis; Buti, Maria; Albillos, Agustín; Invernizzi, Pietro; Fernández, Javier; Prati, Daniele; Baselli, Guido; Asselta, Rosanna; Grimsrud, Marit M; Milani, Chiara; Aziz, Fátima; Kässens, Jan; May, Sandra; Wendorff, Mareike; Wienbrandt, Lars; Uellendahl-Werth, Florian; Zheng, Tenghao; Yi, Xiaoli; de Pablo, Raúl; Chercoles, Adolfo G; Palom, Adriana; Garcia-Fernandez, Alba-Estela; Rodriguez-Frias, Francisco; Zanella, Alberto; Bandera, Alessandra; Protti, Alessandro; Aghemo, Alessio; Lleo, Ana; Biondi, Andrea; Caballero-Garralda, Andrea; Gori, Andrea; Tanck, Anja; Carreras Nolla, Anna; Latiano, Anna; Fracanzani, Anna Ludovica; Peschuck, Anna; Julià, Antonio; Pesenti, Antonio; Voza, Antonio; Jiménez, David; Mateos, Beatriz; Nafria Jimenez, Beatriz; Quereda, Carmen; Paccapelo, Cinzia; Gassner, Christoph; Angelini, Claudio; Cea, Cristina; Solier, Aurora; Pestaña, David; Muñiz-Diaz, Eduardo; Sandoval, Elena; Paraboschi, Elvezia M; Navas, Enrique; García Sánchez, Félix; Ceriotti, Ferruccio; Martinelli-Boneschi, Filippo; Peyvandi, Flora; Blasi, Francesco; Téllez, Luis; Blanco-Grau, Albert; Hemmrich-Stanisak, Georg; Grasselli, Giacomo; Costantino, Giorgio; Cardamone, Giulia; Foti, Giuseppe; Aneli, Serena; Kurihara, Hayato; Elabd, Hesham; My, Ilaria; Galván-Femenia, Iván; Martín, Javier; Erdmann, Jeanette; Ferrusquía-Acosta, Jose; Garcia-Etxebarria, Koldo; Izquierdo-Sanchez, Laura; Bettini, Laura R; Sumoy, Lauro; Terranova, Leonardo; Moreira, Leticia; Santoro, Luigi; Scudeller, Luigia; Mesonero, Francisco; Roade, Luisa; Rühlemann, Malte C; Schaefer, Marco; Carrabba, Maria; Riveiro-Barciela, Mar; Figuera Basso, Maria E; Valsecchi, Maria G; Hernandez-Tejero, María; Acosta-Herrera, Marialbert; D'Angiò, Mariella; Baldini, Marina; Cazzaniga, Marina; Schulzky, Martin; Cecconi, Maurizio; Wittig, Michael; Ciccarelli, Michele; Rodríguez-Gandía, Miguel; Bocciolone, Monica; Miozzo, Monica; Montano, Nicola; Braun, Nicole; Sacchi, Nicoletta; Martínez, Nilda; Özer, Onur; Palmieri, Orazio; Faverio, Paola; Preatoni, Paoletta; Bonfanti, Paolo; Omodei, Paolo; Tentorio, Paolo; Castro, Pedro; Rodrigues, Pedro M; Blandino Ortiz, Aaron; de Cid, Rafael; Ferrer, Ricard; Gualtierotti, Roberta; Nieto, Rosa; Goerg, Siegfried; Badalamenti, Salvatore; Marsal, Sara; Matullo, Giuseppe; Pelusi, Serena; Juzenas, Simonas; Aliberti, Stefano; Monzani, Valter; Moreno, Victor; Wesse, Tanja; Lenz, Tobias L; Pumarola, Tomas; Rimoldi, Valeria; Bosari, Silvano; Albrecht, Wolfgang; Peter, Wolfgang; Romero-Gómez, Manuel; D'Amato, Mauro; Duga, Stefano; Banales, Jesus M; Hov, Johannes R; Folseraas, Trine; Valenti, Luca; Franke, Andre; Karlsen, Tom H
Hereditary Hypofibrinogenemia with Hepatic Storage
2020-01-01 Asselta, Rosanna; Paraboschi, Elvezia Maria; Duga, Stefano
Identification and characterization of 6 novel genetic defects leading to factor V deficiency
2008-01-01 Guella, I; Paraboschi, Em; Duga, S; Asselta, R
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A Frequent Oligogenic Involvement in Congenital Hypothyroidism | 1-gen-2017 | de Filippis, T; Gelmini, G; Paraboschi, E; Vigone, Mc; Di Frenna, M; Marelli, F; Bonomi, M; Cassio, A; Larizza, D; Moro, M; Radetti, G; Salerno, M; Ardissino, D; Weber, G; Gentilini, D; Guizzardi, F; Duga, S; Persani, L. | |
| Abiotic ligation of DNA oligomers templated by their liquid crystal ordering | 1-gen-2015 | Fraccia, Tp; Smith, Gp; Zanchetta, G; Paraboschi, E; Yi, Y; Walba, Dm; Dieci, G; Clark, Na; Bellini, T | |
| ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy | 1-gen-2020 | Asselta, Rosanna; Paraboschi, Elvezia Maria; Mantovani, Alberto; Duga, Stefano | |
| Characterization of miR-634, a microRNA potentially relevant for multiple sclerosis | 1-gen-2011 | Paraboschi, Em; Rimoldi, V; Tabaglio, T; Solda', Giulia; Duga, Stefano; Asselta, Rosanna | |
| Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients | 1-gen-2009 | Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R | |
| DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease | 1-gen-2021 | Vecellio, Matteo; Paraboschi, Elvezia Maria; Ceribelli, Angela; Isailovic, Natasa; Motta, Francesca; Cardamone, Giulia; Robusto, Michela; Asselta, Rosanna; Brescianini, Sonia; Sacrini, Francesco; Costanzo, Antonio; De Santis, Maria; Stazi, Maria Antonietta; Duga, Stefano; Selmi, Carlo | |
| DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease | 1-gen-2021 | Vecellio, Matteo; Paraboschi, Elvezia Maria; Ceribelli, Angela; Isailovic, Natasa; Motta, Francesca; Cardamone, Giulia; Robusto, Michela; Asselta, Rosanna; Brescianini, Sonia; Sacrini, Francesco; Costanzo, Antonio; De Santis, Maria; Stazi, Maria Antonietta; Duga, Stefano; Selmi, Carlo | |
| Exploring the global landscape of genetic variation in coagulation factor XI deficiency | 1-gen-2017 | Asselta, R; Paraboschi, E; Rimoldi, V; Menegatti, M; Peyvandi, F; Salomon, O; Duga, S | |
| Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains | 1-gen-2017 | Paraboschi, E; Duga, S; Asselta, R | |
| Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction | 1-gen-2008 | Guella, I; Rimoldi, V; Merlini, Pa; Asselta, R; Paraboschi, Em; Francolini, M; Peyvandi, F; Ardissimo, D; Mannucci, Pm; Duga, S | |
| Functional and clinical implications of genetic structure in 1686 Italian exomes | 1-gen-2021 | Birolo, Giovanni; Aneli, Serena; Di Gaetano, Cornelia; Cugliari, Giovanni; Russo, Alessia; Allione, Alessandra; Casalone, Elisabetta; Giorgio, Elisa; Paraboschi, Elvezia M; Ardissino, Diego; Duga, Stefano; Asselta, Rosanna; Matullo, Giuseppe | |
| Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency | 1-gen-2012 | Paraboschi, E; Kayıran, Sm; Özbek, N; Gürakan, B; Guella, I; Duga, S; Asselta, R | |
| Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. | 1-gen-2014 | Paraboschi, E; Rimoldi, V; Soldà, G; Tabaglio, T; Dall'Osso, C; Saba, E; Vigliano, M; Salviati, A; Leone, M; Benedetti, Md; Fornasari, D; Saarela, J; De Jager, Pl; Patsopoulos, Na; D'Alfonso, S; Gemmati, D; Duga, S; Asselta, R. | |
| Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases | 1-gen-2018 | Tisato, V; Zuliani, G; Vigliano, M; Longo, G; Franchini, E; Secchiero, P; Zauli, G; Paraboschi, Em; Vikram Singh, A; Serino, Ml; Ortolani, B; Zurlo, A; Bosi, C; Greco, A; Seripa, D; Asselta, R; Gemmati, D | |
| Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients | 1-gen-2018 | Cardamone, G; Paraboschi, E; Solda', G; Duga, S; Saarela, J; Asselta, R. | |
| Genetic association and altered gene expression of mir-155 in multiple sclerosis patients | 1-gen-2011 | Paraboschi, E.; Solda', G.; Gemmati, D.; Orioli, E.; Zeri, G.; Benedetti, D.; Salviati, A.; Barizzone, N.; Leone, M.; Duga, S.; Asselta, R. | |
| Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. | 1-gen-2014 | Biguzzi, E; Franchi, F; Acaia, B; Ossola, W; Nava, U; Paraboschi, Em; Asselta, R; Peyvandi, F. | |
| Genomewide Association Study of Severe Covid-19 with Respiratory Failure | 1-gen-2020 | Ellinghaus, David; Degenhardt, Frauke; Bujanda, Luis; Buti, Maria; Albillos, Agustín; Invernizzi, Pietro; Fernández, Javier; Prati, Daniele; Baselli, Guido; Asselta, Rosanna; Grimsrud, Marit M; Milani, Chiara; Aziz, Fátima; Kässens, Jan; May, Sandra; Wendorff, Mareike; Wienbrandt, Lars; Uellendahl-Werth, Florian; Zheng, Tenghao; Yi, Xiaoli; de Pablo, Raúl; Chercoles, Adolfo G; Palom, Adriana; Garcia-Fernandez, Alba-Estela; Rodriguez-Frias, Francisco; Zanella, Alberto; Bandera, Alessandra; Protti, Alessandro; Aghemo, Alessio; Lleo, Ana; Biondi, Andrea; Caballero-Garralda, Andrea; Gori, Andrea; Tanck, Anja; Carreras Nolla, Anna; Latiano, Anna; Fracanzani, Anna Ludovica; Peschuck, Anna; Julià, Antonio; Pesenti, Antonio; Voza, Antonio; Jiménez, David; Mateos, Beatriz; Nafria Jimenez, Beatriz; Quereda, Carmen; Paccapelo, Cinzia; Gassner, Christoph; Angelini, Claudio; Cea, Cristina; Solier, Aurora; Pestaña, David; Muñiz-Diaz, Eduardo; Sandoval, Elena; Paraboschi, Elvezia M; Navas, Enrique; García Sánchez, Félix; Ceriotti, Ferruccio; Martinelli-Boneschi, Filippo; Peyvandi, Flora; Blasi, Francesco; Téllez, Luis; Blanco-Grau, Albert; Hemmrich-Stanisak, Georg; Grasselli, Giacomo; Costantino, Giorgio; Cardamone, Giulia; Foti, Giuseppe; Aneli, Serena; Kurihara, Hayato; Elabd, Hesham; My, Ilaria; Galván-Femenia, Iván; Martín, Javier; Erdmann, Jeanette; Ferrusquía-Acosta, Jose; Garcia-Etxebarria, Koldo; Izquierdo-Sanchez, Laura; Bettini, Laura R; Sumoy, Lauro; Terranova, Leonardo; Moreira, Leticia; Santoro, Luigi; Scudeller, Luigia; Mesonero, Francisco; Roade, Luisa; Rühlemann, Malte C; Schaefer, Marco; Carrabba, Maria; Riveiro-Barciela, Mar; Figuera Basso, Maria E; Valsecchi, Maria G; Hernandez-Tejero, María; Acosta-Herrera, Marialbert; D'Angiò, Mariella; Baldini, Marina; Cazzaniga, Marina; Schulzky, Martin; Cecconi, Maurizio; Wittig, Michael; Ciccarelli, Michele; Rodríguez-Gandía, Miguel; Bocciolone, Monica; Miozzo, Monica; Montano, Nicola; Braun, Nicole; Sacchi, Nicoletta; Martínez, Nilda; Özer, Onur; Palmieri, Orazio; Faverio, Paola; Preatoni, Paoletta; Bonfanti, Paolo; Omodei, Paolo; Tentorio, Paolo; Castro, Pedro; Rodrigues, Pedro M; Blandino Ortiz, Aaron; de Cid, Rafael; Ferrer, Ricard; Gualtierotti, Roberta; Nieto, Rosa; Goerg, Siegfried; Badalamenti, Salvatore; Marsal, Sara; Matullo, Giuseppe; Pelusi, Serena; Juzenas, Simonas; Aliberti, Stefano; Monzani, Valter; Moreno, Victor; Wesse, Tanja; Lenz, Tobias L; Pumarola, Tomas; Rimoldi, Valeria; Bosari, Silvano; Albrecht, Wolfgang; Peter, Wolfgang; Romero-Gómez, Manuel; D'Amato, Mauro; Duga, Stefano; Banales, Jesus M; Hov, Johannes R; Folseraas, Trine; Valenti, Luca; Franke, Andre; Karlsen, Tom H | |
| Hereditary Hypofibrinogenemia with Hepatic Storage | 1-gen-2020 | Asselta, Rosanna; Paraboschi, Elvezia Maria; Duga, Stefano | |
| Identification and characterization of 6 novel genetic defects leading to factor V deficiency | 1-gen-2008 | Guella, I; Paraboschi, Em; Duga, S; Asselta, R |