Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Italia Loddo"'
Autor:
Roberta Pastorino, Eloisa Arbustini, Andrea Faini, Gianfranco Parati, Grzegorz Bilo, Davide Soranna, Antonella Zambon, Sergio Leonardi, Alessandro Gialluisi, Lorenzo Giovanni Mantovani, Walter Ricciardi, Fabio Blandini, Giovanni Scambia, Catherine Klersy, Marialaura Bonaccio, Augusto Di Castelnuovo, Simona Costanzo, Amalia De Curtis, Mariarosaria Persichillo, Chiara Cerletti, Maria Benedetta Donati, Licia Iacoviello, Giuseppe Remuzzi, Camilla Torlasco, Giuseppe Ambrosio, Gabriele Zoppoli, Maria Chiara Grimaldi, Daniela Pedicino, Giovanna Liuzzo, Serena Pelusi, Daniele Prati, Luca Valenti, Francesca Gorini, Maurizio Sanguinetti, Giuseppe Ferrante, Gianluigi Condorelli, Giulio Pompilio, Stefania Boccia, Luigi Badano, Victor Savevski, Tiziana Bachetti, Gian Franco Gensini, Silvano Bosari, Alice Bonanni, Elena Tremoli, Angelo Santoliquido, Stefano Genovese, Sara Boveri, Gianfranco Gensini, Francesco Gianfagna, Italo Porto, Fabio Tuzzolino, Carolina Lombardi, Egidio Traversi, Fabrizio Veglia, Andrea Urbani, Domenico D’Amario, Gaetano Antonio Lanza, Antonio Uccelli, José Pablo Werba, Livio Luzi, Pietro Ameri, Davide Gentilini, Luisa Gilardini, Cecilia Invitti, Maurizio Volterrani, Maria Teresa La Rovere, Giovanni Gentile, Francesco Clemenza, Mario Urtis, Francesca Ieva, Maria Carla Roncaglioni, Valentina Milani, Paola Baiardi, Debora Rosa, Fabiana Madotto, Emilia Ruggiero, Teresa Panzera, Simona Esposito, Sara Magnacca, Fabrizia Noro, Roberta Parisi, Francesca Bracone, Irene Baroni, Damiano Baldassarre, Roberta Baetta, Luigi Frati, Pier Giulio Conaldi, Massimo Fini, Antonio Di Malta, Mauro Amato, Alice Bonomi, Francesca Colazzo, Martino Pengo, Luciana Auteri, Marta Baviera, Alberico Catapano, Alexis Elias Malavazos, Serenella Castelvecchio, Massimiliano Marco Corsi-Romanelli, Rosanna Cardani, Valentina Agnese, Bianca Pane, Laura Spinardi, Marco Visconti, Anna Di Blasio, Luisa Ojeda-Fernández, Andreana Foresta, Simonetta Scalvini, Antonia Pierobon, Alessandra Gorini, Annarosa Racca, Manuela Bandi, Lorenzo Menicanti, Gualtiero Colombo, Chiara Vavassori, Maria Luisa Biondi, Beatrice Frigerio, Alessio Ravani, Daniela Sansaro, Daniela Coggi, Alessandra Romandini, Monica Giroli, Mattia Giuliani, Maurizio Rondinelli, Catia Trudu, Carmen Cinieri, Massimo Monturano, Elisa Perger, Lucia Zanotti, Lidia Cova, Luca Grappiolo, Laura Papa, Ignazio Romano, Luisa Ojeda, Fiorenza Clerici, Angela Palumbo, Roberto Mattioli, Ermanno Longhi, Anwal Ghulam, Sabatino Orlandi, Sabrina Franciosa, Martina Morelli, Fiorella De Rita, Giovanni de Gaetano, Massimiliano MarcoCorsi Romanelli, Ambra Cerri, Carola Dubini, Manuel Bruno Trevisan, Laura Valentina Renna, Paola Giubbilini, Lucia Ramputi, Giada DeAngeli, Francesca Olmetti, Maurizio Bussotti, Carlo Gaetano, Martina Balbi, Laura Comini, Monica Lorenzoni, Adriana Olivares, Camilla Garrè, Riccardo Sideri, Giuseppe Caruana, Nicola Cuscino, Gabriele Di Gesaro, Alessio Greco, Italia Loddo, Domenico Palombo, Giovanni Spinella, Gaddiel Mozzetta, Alice Finotello, Giovanni Pratesi, Margherita Clerici, Cristiana Bianco, Rossana Carpani, Giulia Periti, Sara Margarita, Anna Severino, Alessia D’Aiello, Ramona Vinci, Mattia Brecciaroli, Simone Filomia, Luca Proto, Dalila Tarquini, Arianna Elia, Alessia Currao, Alessandro Di Toro, Lorenzo Giuliani, Giuseppe Caminiti, Federica Marcolongo, Barbara Sposato, Fiorella Guadagni, Valentina Morsella, Angelica Marziale, Giulia Protti
Publikováno v:
BMJ Open, Vol 13, Iss 7 (2023)
Introduction Prevention of cardiovascular disease (CVD) is of key importance in reducing morbidity, disability and mortality worldwide. Observational studies suggest that digital health interventions can be an effective strategy to reduce cardiovascu
Externí odkaz:
https://doaj.org/article/0b48f5d650b049b28dd773c39b063361
Autor:
Antonella Mosca, Sabrina Cardile, Valerio Nobili, Italia Loddo, Tommaso Alterio, Claire Trayers, Roxana Mardare, Simona Valenti
Publikováno v:
Scandinavian Journal of Gastroenterology. 54:822-829
Eosinophilic Esophagitis (EoE) is a chronic immune/antigen-mediated condition which is also driven by genetic and environmental factors. It has been deeply investigated over the last years and its incidence is widely increasing in childhood. Although
Autor:
Tommaso, Alterio, Sabrina, Cardile, Claire, Trayers, Simona, Valenti, Italia, Loddo, Roxana, Mardare, Antonella, Mosca, Valerio, Nobili
Publikováno v:
Scandinavian journal of gastroenterology. 54(7)
Eosinophilic Esophagitis (EoE) is a chronic immune/antigen-mediated condition which is also driven by genetic and environmental factors. It has been deeply investigated over the last years and its incidence is widely increasing in childhood. Although
Autor:
Chiara Perria, Italia Loddo, Marco Seri, Milena Crippa, Stefano Sotgiu, Maria Piccione, Marina Frontali, Lidia Larizza, Elisa Biamino, Palma Finelli, Pamela Magini, Maria Chiara Gandini, Elisa Colombo, Gloria Negri, Antonella Boni, Donatella Milani, Tommaso Pippucci, Michael J. Bamshad, Deborah A. Nickerson, Joshua D. Smith, Elisabetta Di Fede, Cristina Gervasini, Giuseppina Vitiello
Publikováno v:
Human genetics (Berl., Internet) 138 (2019). doi:10.1007/s00439-019-01985-y
info:cnr-pdr/source/autori:Negri G.; Magini P.; Milani D.; Crippa M.; Biamino E.; Piccione M.; Sotgiu S.; Perria C.; Vitiello G.; Frontali M.; Boni A.; Di Fede E.; Gandini M.C.; Colombo E.A.; Bamshad M.J.; Nickerson D.A.; Smith J.D.; Loddo I.; Finelli P.; Seri M.; Pippucci T.; Larizza L.; Gervasini C./titolo:Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders/doi:10.1007%2Fs00439-019-01985-y/rivista:Human genetics (Berl., Internet)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume:138
info:cnr-pdr/source/autori:Negri G.; Magini P.; Milani D.; Crippa M.; Biamino E.; Piccione M.; Sotgiu S.; Perria C.; Vitiello G.; Frontali M.; Boni A.; Di Fede E.; Gandini M.C.; Colombo E.A.; Bamshad M.J.; Nickerson D.A.; Smith J.D.; Loddo I.; Finelli P.; Seri M.; Pippucci T.; Larizza L.; Gervasini C./titolo:Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders/doi:10.1007%2Fs00439-019-01985-y/rivista:Human genetics (Berl., Internet)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume:138
Rubinstein–Taybi syndrome (RSTS) is an autosomal-dominant neurodevelopmental disease affecting 1:125,000 newborns characterized by intellectual disability, growth retardation, facial dysmorphisms and skeletal abnormalities. RSTS is caused by mutati
Autor:
A. Salpietro, Claudio Romano, Marco Sciveres, Silvana Briuglia, Maria Concetta Cutrupi, Romina Gallizzi, Italia Loddo, Valeria Ferraù, Silvia Riva
Publikováno v:
European Journal of Medical Genetics. 58:188-190
Noonan Syndrome (NS) is characterized by short stature, typical facial dysmorphology and congenital heart defects. The incidence of NS is estimated to be between 1:1000 and 1:2500 live births. The syndrome is transmitted as an autosomal dominant trai
Autor:
Claudio Romano, Italia Loddo
Publikováno v:
Frontiers in Immunology, Vol 6 (2015)
Frontiers in Immunology
Frontiers in Immunology
Inflammatory Bowel Diseases (IBDs) are complex, multifactorial disorders characterized by chronic relapsing intestinal inflammation. Although aetiology remains largely unknown, recent research has suggested that genetic factors, environment, microbio
Publikováno v:
Current Clinical Pharmacology. 6:41-47
Gastroesophageal reflux (GER) is defined as the passage of gastric contents into the esophagus. It occurs in healthy infants and can be considered physiological process. Uncomplicated GER can present with recurrent vomiting or regurgitation without a
Autor:
Giulia Severi, Emilio Franzoni, Pamela Magini, Silvana Briuglia, Barbara Buldrini, Maria Lisa Dentici, Teresa Arrigo, Italia Loddo, Antonio Novelli, Claudio Graziano, Laura Bernardini, Duccio Maria Cordelli, Stefania Bigoni, Sergio Fini, Eleonora Italyankina
Publikováno v:
American journal of medical genetics. Part A. (1)
Temple syndrome (TS) is caused by abnormal expression of genes at the imprinted locus 14q32. A subset of TS patients carry 14q32 deletions of paternal origin. We aimed to define possible genotype-phenotype correlations and to highlight the prevalence
Autor:
Martino Ruggieri, Laura Bernardini, Teresa Arrigo, Italia Loddo, Vincenzo Salpietro, Antonio Novelli, Emanuela Moschella, Kshitij Mankad, Francesca Granata, Anna Capalbo, Maria Pia Calabrò, Agata Polizzi, Silvana Briuglia, Gabriella Di Rosa, Daniela G. Seidler
Publikováno v:
American journal of medical genetics. Part A 167 (2015): 2042–2051. doi:10.1002/ajmg.a.37118
info:cnr-pdr/source/autori:Salpietro, Vincenzo; Ruggieri, Martino; Mankad, Kshitij; Di Rosa, Gabriella; Granata, Francesca; Loddo, Italia; Moschella, Emanuela; Calabro, Maria Pia; Capalbo, Anna; Bernardini, Laura; Novelli, Antonio; Polizzi, Agata; Seidler, Daniela G.; Arrigo, Teresa; Briuglia, Silvana/titolo:A De Novo 0.63 Mb 6q25.1 Deletion Associated with Growth Failure, Congenital Heart Defect, Underdeveloped Cerebellar Vermis, Abnormal Cutaneous Elasticity and Joint Laxity/doi:10.1002%2Fajmg.a.37118/rivista:American journal of medical genetics. Part A/anno:2015/pagina_da:2042/pagina_a:2051/intervallo_pagine:2042–2051/volume:167
info:cnr-pdr/source/autori:Salpietro, Vincenzo; Ruggieri, Martino; Mankad, Kshitij; Di Rosa, Gabriella; Granata, Francesca; Loddo, Italia; Moschella, Emanuela; Calabro, Maria Pia; Capalbo, Anna; Bernardini, Laura; Novelli, Antonio; Polizzi, Agata; Seidler, Daniela G.; Arrigo, Teresa; Briuglia, Silvana/titolo:A De Novo 0.63 Mb 6q25.1 Deletion Associated with Growth Failure, Congenital Heart Defect, Underdeveloped Cerebellar Vermis, Abnormal Cutaneous Elasticity and Joint Laxity/doi:10.1002%2Fajmg.a.37118/rivista:American journal of medical genetics. Part A/anno:2015/pagina_da:2042/pagina_a:2051/intervallo_pagine:2042–2051/volume:167
Deletions of the long arm of chromosome 6 are rare and are characterized by great clinical variability according to the deletion breakpoint. We report a on 6-year-old girl with a de novo 0.63Mb deletion on chromosome 6q25.1 who demonstrated multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83746c93211c4bb76d0e6bf78db40279
Wiley Online Library
Wiley Online Library
Autor:
Italia Loddo, Valeria Ferraù, Carmelo Salpietro, Vincenzo Salpietro, Antonio Lacquaniti, Valeria Chirico, T. Arrigo, Silvana Briuglia, Maria Amorini
Aim This report highlights the metabolic, endocrine and cardiovascular comorbidities in a case of familial partial lipodystrophy (FPLD), and also evaluates the efficacy and safety of metformin therapy. Methods Mutational analysis was carried out of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eac32416b47f6fe2006fe54e0ef4613
http://hdl.handle.net/11567/981690
http://hdl.handle.net/11567/981690