STUPPIA, Liborio
STUPPIA, Liborio
DIPARTIMENTO DI NEUROSCIENZE, IMAGING E SCIENZE CLINICHE
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer.
2012-01-01 Palka Bayard de Volo, C; Alfonsi, M; Gatta, Valentina; Novelli, A; Bernardini, L; Fantasia, D; Antonucci, Ivana; Angelucci, D; Zori, R; Stuppia, Liborio; Chiarelli, Francesco; Calabrese, Giuseppe
5-HT2AR and BDNF gene variants in eating disorders susceptibility
2020-01-01 Ceccarini, M. R.; Tasegian, A.; Franzago, M.; Patria, F. F.; Albi, E.; Codini, M.; Conte, C.; Bertelli, M.; Dalla Ragione, L.; Stuppia, L.; Beccari, T.
5HTR2A and COMT genes in attention-deficit/hyperactivity disorder: a preliminary study
2007-01-01 Grilli, Alfredo; Antonucci, Ivana; Gatta, Valentina; Buono, R.; Marmorato, S.; Saggino, Aristide; Felaco, Mario; Bonetta, Gaetano; Stuppia, Liborio
[Cytogenetic study of 140 patients with changes in sexual features].
1987-01-01 Palka, Giandomenico; Parruti, G; Calabrese, Giuseppe; Stuppia, Liborio; GUANCIALI FRANCHI, Paolo Emilio; Marino, M.
[Cytogenetic study of 201 subjects with altered reproductive fitness].
1990-01-01 Palka, Giandomenico; Bianchi, Pg; Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Stuppia, Liborio; Marino, M; Parruti, G; Di Virgilio, C; Di Sante, O; Grilli, Alfredo
A Case of Suspected Hyperphenylalaninemia at Newborn Screening by Tandem Mass Spectrometry during Total Parenteral Nutrition
2020-01-01 Pieragostino, Damiana; Cicalini, Ilaria; Di Michele, Silvia; Fusilli, Paola; Cotugno, Giovanna; Ferrante, Rossella; Bucci, Ines; Dionisi-Vici, Carlo; Stuppia, Liborio; De Laurenzi, Vincenzo; Rossi, Claudia
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL).
1987-01-01 Palka, Giandomenico; Fioritoni, G; Lombardo, M; Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Di Marzio, A; Stuppia, Liborio; Parruti, G; Geraci, L.
A morpho-functional analysis of embryoid body-like structures from human amniotic fluid-derived stem cells (AFSCs) unselected for c-kit
2012-01-01 Centurione, Lucia; Antonucci, Ivana; Sancilio, Silvia; Centurione, Ma; Stuppia, Liborio; DI PIETRO, Roberta
A Neural "Tuning Curve" for Multisensory Experience and Cognitive-Perceptual Schizotypy
2017-01-01 Ferri, Francesca; Nikolova, Yuliya S; Perrucci, Mauro Gianni; Costantini, Marcello; Ferretti, Antonio; Gatta, Valentina; Huang, Zirui; Edden, Richard A. E; Yue, Qiang; D'Aurora, Marco; Sibille, Etienne; Stuppia, Liborio; Romani, Gian Luca; Northoff, Georg
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer
2017-01-01 Antonucci, Ivana; Provenzano, Martina; Sorino, Luca; Rodrigues, Melissa; Palka, Giandomenico; Stuppia, Liborio
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature.
1988-01-01 Palka, Giandomenico; Geraci, L; Calabrese, Giuseppe; Stuppia, Liborio; GUANCIALI FRANCHI, Paolo Emilio; Parruti, G; D'Antonio, D; Fioritoni, G.
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.
2008-01-01 GUANCIALI FRANCHI, Paolo Emilio; Calabrese, Giuseppe; Morizio, Elisena; Gatta, Valentina; Palka, Chiara; Stuppia, Liborio; Zuffardi, O.
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22.
1989-01-01 Parruti, G; DI ILIO, Carmine; Calabrese, Giuseppe; Stuppia, Liborio; GUANCIALI FRANCHI, Paolo Emilio; Aceto, Antonio; Palka, Giandomenico
A new case of Yq microdeletion transmitted from a normal father to two infertile sons.
2002-01-01 Gatta, Valentina; Stuppia, Liborio; Calabrese, Giuseppe; Morizio, Elisena; GUANCIALI FRANCHI, Paolo Emilio; Palka, Giandomenico
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia.
1994-01-01 Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Stuppia, Liborio; Mingarelli, R; Ramenghi, L; Marino, Mario; Morizio, Elisena; Peila, R; Antonucci, Adriano; Palka, Giandomenico
A Novel Heterozygous Mutation of the CYP17A1 Gene in a Child with a Micropenis and Isolated 17,20-Lyase Deficiency
2022-01-01 Saltarelli, MARIA ALESSANDRA; Ferrante, Rossella; DI MARCELLO, Francesca; David, Daniela; Valentinuzzi, Silvia; Pilenzi, Lucrezia; Federici, Luca; Rossi, Claudia; Stuppia, Liborio; Stefano Tumini, And
A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome
2004-01-01 Gatta, V.; Scarciolla, O.; Cupaioli, M.; Palka, C.; Chiesa, P. L.; Stuppia, L.
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient
2002-01-01 Pizzuti, A; Calabrese, Giuseppe; Bozzali, M; Telvi, L; Morizio, Elisena; Guida, V; Gatta, Valentina; Stuppia, Liborio; Ion, A; Palka, Giandomenico; Dallapiccola, B.
A protective genetic variant for adverse environments? The role of childhood traumas and serotonin transporter gene on resilience and depressive severity in a high-risk population
2011-01-01 Carli, V; Mandelli, L; Zaninotto, L; Roy, A; Recchia, L; Stuppia, Liborio; Gatta, Valentina; Sarchiapone, M; Serretti, A.
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11
1998-01-01 Stuppia, Liborio; Gatta, Valentina; Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Morizio, Elisena; Bombieri, C; Mingarelli, R; Sforza, V; Frajese, G; Tenaglia, Raffaele; Palka, Giandomenico
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. | 2012 | Palka Bayard de Volo, C; Alfonsi, M; Gatta, Valentina; Novelli, A; Bernardini, L; Fantasia, D; Antonucci, Ivana; Angelucci, D; Zori, R; Stuppia, Liborio; Chiarelli, Francesco; Calabrese, Giuseppe | |
5-HT2AR and BDNF gene variants in eating disorders susceptibility | 2020 | Ceccarini, M. R.; Tasegian, A.; Franzago, M.; Patria, F. F.; Albi, E.; Codini, M.; Conte, C.; Bertelli, M.; Dalla Ragione, L.; Stuppia, L.; Beccari, T. | |
5HTR2A and COMT genes in attention-deficit/hyperactivity disorder: a preliminary study | 2007 | Grilli, Alfredo; Antonucci, Ivana; Gatta, Valentina; Buono, R.; Marmorato, S.; Saggino, Aristide; Felaco, Mario; Bonetta, Gaetano; Stuppia, Liborio | |
[Cytogenetic study of 140 patients with changes in sexual features]. | 1987 | Palka, Giandomenico; Parruti, G; Calabrese, Giuseppe; Stuppia, Liborio; GUANCIALI FRANCHI, Paolo Emilio; Marino, M. | |
[Cytogenetic study of 201 subjects with altered reproductive fitness]. | 1990 | Palka, Giandomenico; Bianchi, Pg; Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Stuppia, Liborio; Marino, M; Parruti, G; Di Virgilio, C; Di Sante, O; Grilli, Alfredo | |
A Case of Suspected Hyperphenylalaninemia at Newborn Screening by Tandem Mass Spectrometry during Total Parenteral Nutrition | 2020 | Pieragostino, Damiana; Cicalini, Ilaria; Di Michele, Silvia; Fusilli, Paola; Cotugno, Giovanna; Ferrante, Rossella; Bucci, Ines; Dionisi-Vici, Carlo; Stuppia, Liborio; De Laurenzi, Vincenzo; Rossi, Claudia | |
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). | 1987 | Palka, Giandomenico; Fioritoni, G; Lombardo, M; Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Di Marzio, A; Stuppia, Liborio; Parruti, G; Geraci, L. | |
A morpho-functional analysis of embryoid body-like structures from human amniotic fluid-derived stem cells (AFSCs) unselected for c-kit | 2012 | Centurione, Lucia; Antonucci, Ivana; Sancilio, Silvia; Centurione, Ma; Stuppia, Liborio; DI PIETRO, Roberta | |
A Neural "Tuning Curve" for Multisensory Experience and Cognitive-Perceptual Schizotypy | 2017 | Ferri, Francesca; Nikolova, Yuliya S; Perrucci, Mauro Gianni; Costantini, Marcello; Ferretti, Antonio; Gatta, Valentina; Huang, Zirui; Edden, Richard A. E; Yue, Qiang; D'Aurora, Marco; Sibille, Etienne; Stuppia, Liborio; Romani, Gian Luca; Northoff, Georg | |
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer | 2017 | Antonucci, Ivana; Provenzano, Martina; Sorino, Luca; Rodrigues, Melissa; Palka, Giandomenico; Stuppia, Liborio | |
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. | 1988 | Palka, Giandomenico; Geraci, L; Calabrese, Giuseppe; Stuppia, Liborio; GUANCIALI FRANCHI, Paolo Emilio; Parruti, G; D'Antonio, D; Fioritoni, G. | |
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. | 2008 | GUANCIALI FRANCHI, Paolo Emilio; Calabrese, Giuseppe; Morizio, Elisena; Gatta, Valentina; Palka, Chiara; Stuppia, Liborio; Zuffardi, O. | |
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. | 1989 | Parruti, G; DI ILIO, Carmine; Calabrese, Giuseppe; Stuppia, Liborio; GUANCIALI FRANCHI, Paolo Emilio; Aceto, Antonio; Palka, Giandomenico | |
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. | 2002 | Gatta, Valentina; Stuppia, Liborio; Calabrese, Giuseppe; Morizio, Elisena; GUANCIALI FRANCHI, Paolo Emilio; Palka, Giandomenico | |
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. | 1994 | Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Stuppia, Liborio; Mingarelli, R; Ramenghi, L; Marino, Mario; Morizio, Elisena; Peila, R; Antonucci, Adriano; Palka, Giandomenico | |
A Novel Heterozygous Mutation of the CYP17A1 Gene in a Child with a Micropenis and Isolated 17,20-Lyase Deficiency | 2022 | Saltarelli, MARIA ALESSANDRA; Ferrante, Rossella; DI MARCELLO, Francesca; David, Daniela; Valentinuzzi, Silvia; Pilenzi, Lucrezia; Federici, Luca; Rossi, Claudia; Stuppia, Liborio; Stefano Tumini, And | |
A novel mutation of the IRF6 gene in an Italian family with Van der Woude syndrome | 2004 | Gatta, V.; Scarciolla, O.; Cupaioli, M.; Palka, C.; Chiesa, P. L.; Stuppia, L. | |
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient | 2002 | Pizzuti, A; Calabrese, Giuseppe; Bozzali, M; Telvi, L; Morizio, Elisena; Guida, V; Gatta, Valentina; Stuppia, Liborio; Ion, A; Palka, Giandomenico; Dallapiccola, B. | |
A protective genetic variant for adverse environments? The role of childhood traumas and serotonin transporter gene on resilience and depressive severity in a high-risk population | 2011 | Carli, V; Mandelli, L; Zaninotto, L; Roy, A; Recchia, L; Stuppia, Liborio; Gatta, Valentina; Sarchiapone, M; Serretti, A. | |
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 | 1998 | Stuppia, Liborio; Gatta, Valentina; Calabrese, Giuseppe; GUANCIALI FRANCHI, Paolo Emilio; Morizio, Elisena; Bombieri, C; Mingarelli, R; Sforza, V; Frajese, G; Tenaglia, Raffaele; Palka, Giandomenico |