Epstein–Barr virus-associated gastric carcinoma 33 years after kidney transplantation

por Lunardi, Francesca, Calabrese, Fiorella, Furian, Lucrezia, Rigotti, Paolo, Valente, Marialuisa
Publicado 2011

Cytogenetic findings in lung cancer that illuminate its biological history from adenomatous hyperplasia to bronchioalveolar carcinoma to adenocarcinoma: A case report

por BETTIO, DANIELA, CARIBONI, UMBERTO, VENCI, ANNA, VALENTE, MARIALUISA, SPAGGIARI, PAOLA, ALLOISIO, MARCO
Publicado 2012

A Conservative Approach to a Peripheral Ameloblastoma

por Borrello, Rocco, Bettio, Elia, Bacci, Christian, Valente, Marialuisa, Sivolella, Stefano, Mazzoleni, Sergio, Berengo, Mario
Publicado 2016

Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management

por Zucca, Susanna, Villaraggia, Margherita, Gagliardi, Stella, Grieco, Gaetano Salvatore, Valente, Marialuisa, Cereda, Cristina, Magni, Paolo
Publicado 2016

CXCR3/CXCL10 expression in the synovium of children with juvenile idiopathic arthritis

por Martini, Georgia, Zulian, Francesco, Calabrese, Fiorella, Bortoli, Marta, Facco, Monica, Cabrelle, Anna, Valente, Marialuisa, Zacchello, Franco, Agostini, Carlo
Publicado 2005

De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report

por Gagliardi, Stella, Grieco, Gaetano Salvatore, Gualandi, Francesca, Caniatti, Luisa Maria, Groppo, Elisabetta, Valente, Marialuisa, Nappi, Giuseppe, Neri, Marcella, Cereda, Cristina
Publicado 2017

Marked alveolar apoptosis/proliferation imbalance in end-stage emphysema

por Calabrese, Fiorella, Giacometti, Cinzia, Beghe, Bianca, Rea, Federico, Loy, Monica, Zuin, Renzo, Marulli, Giuseppe, Baraldo, Simonetta, Saetta, Marina, Valente, Marialuisa
Publicado 2005

Erratum to: De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report

por Gagliardi, Stella, Grieco, Gaetano Salvatore, Gualandi, Francesca, Caniatti, Luisa Maria, Groppo, Elisabetta, Valente, Marialuisa, Giuseppe, Nappi, Neri, Marcella, Cereda, Cristina
Publicado 2017

A Novel Mutation in the Stalk Domain of KIF5A Causes a Slowly Progressive Atypical Motor Syndrome

por Filosto, Massimiliano, Piccinelli, Stefano Cotti, Palmieri, Ilaria, Necchini, Nicola, Valente, Marialuisa, Zanella, Isabella, Biasiotto, Giorgio, Lorenzo, Diego Di, Cereda, Cristina, Padovani, Alessandro
Publicado 2018

Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome

por De Giorgis, Valentina, Masnada, Silvia, Varesio, Costanza, Chiappedi, Matteo A., Zanaboni, Martina, Pasca, Ludovica, Filippini, Melissa, Macasaet, Joyce A., Valente, Marialuisa, Ferraris, Cinzia, Tagliabue, Anna, Veggiotti, Pierangelo
Publicado 2019

PSEN1 Compound Heterozygous Mutations Associated with Cerebral Amyloid Angiopathy and Cognitive Decline Phenotype

por Palmieri, Ilaria, Valente, Marialuisa, Farina, Lisa Maria, Gana, Simone, Minafra, Brigida, Zangaglia, Roberta, Pansarasa, Orietta, Sproviero, Daisy, Costa, Alfredo, Pacchetti, Claudio, Pichiecchio, Anna, Gagliardi, Stella, Cereda, Cristina
Publicado 2021

Involvement of the Tubular ClC-Type Exchanger ClC-5 in Glomeruli of Human Proteinuric Nephropathies

por Ceol, Monica, Tiralongo, Emilia, Baelde, Hans J., Vianello, Daniela, Betto, Giovanni, Marangelli, Annunziata, Bonfante, Luciana, Valente, Marialuisa, Della Barbera, Mila, D’Angelo, Angela, Anglani, Franca, Del Prete, Dorella
Publicado 2012

Diagnostic Yield and Cost-Effectiveness of “Dynamic” Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern Italy

por Varesio, Costanza, Gana, Simone, Asaro, Alessia, Ballante, Elena, Cabini, Raffaella Fiamma, Tartara, Elena, Bagnaschi, Michela, Pasca, Ludovica, Valente, Marialuisa, Orcesi, Simona, Cereda, Cristina, Veggiotti, Pierangelo, Borgatti, Renato, Valente, Enza Maria, De Giorgis, Valentina
Publicado 2021

Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy

por Pilichou, Kalliopi, Remme, Carol Ann, Basso, Cristina, Campian, Maria E., Rizzo, Stefania, Barnett, Phil, Scicluna, Brendon P., Bauce, Barbara, van den Hoff, Maurice J.B., de Bakker, Jacques M.T., Tan, Hanno L., Valente, Marialuisa, Nava, Andrea, Wilde, Arthur A.M., Moorman, Antoon F.M., Thiene, Gaetano, Bezzina, Connie R.
Publicado 2009

Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis

por Galli, Jessica, Gavazzi, Francesco, De Simone, Micaela, Giliani, Silvia, Garau, Jessica, Valente, Marialuisa, Vairo, Donatella, Cattalini, Marco, Mortilla, Marzia, Andreoli, (Laura, Badolato, Raffaele, Bianchi, Marika, Carabellese, Nice, Cereda, Cristina, Ferraro, Rosalba, Facchetti, Fabio, Fredi, Micaela, Gualdi, Giulio, Lorenzi, Luisa, Meini, Antonella, Orcesi, Simona, Tincani, Angela, Zanola, Alessandra, Rice, Gillian, Fazzi, Elisa
Publicado 2018

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

por Garau, Jessica, Cavallera, Vanessa, Valente, Marialuisa, Tonduti, Davide, Sproviero, Daisy, Zucca, Susanna, Battaglia, Domenica, Battini, Roberta, Bertini, Enrico, Cappanera, Silvia, Chiapparini, Luisa, Crasà, Camilla, Crichiutti, Giovanni, Giustina, Elvio Dalla, D’Arrigo, Stefano, Giorgis, Valentina De, Simone, Micaela De, Galli, Jessica, Piana, Roberta La, Messana, Tullio, Moroni, Isabella, Nardocci, Nardo, Panteghini, Celeste, Parazzini, Cecilia, Pichiecchio, Anna, Pini, Antonella, Ricci, Federica, Saletti, Veronica, Salvatici, Elisabetta, Santorelli, Filippo M., Sartori, Stefano, Tinelli, Francesca, Uggetti, Carla, Veneselli, Edvige, Zorzi, Giovanna, Garavaglia, Barbara, Fazzi, Elisa, Orcesi, Simona, Cereda, Cristina
Publicado 2019