Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Ilaria Longo"'
Publikováno v:
Discern, Vol 2, Iss 1, Pp 1-15 (2021)
Cities are changing. Wars, climate change and idealised better life opportunities open the doors for massive migration. Unfortunately, however, the new arrivals with their different backgrounds and lifestyles are often perceived as a threat to pre-ex
Externí odkaz:
https://doaj.org/article/bf38d6ace7804a94a28368fb50018fd0
Autor:
Ilaria Catusi, Maria Paola Recalcati, Ilaria Bestetti, Maria Garzo, Chiara Valtorta, Melissa Alfonsi, Alberta Alghisi, Stefania Cappellani, Rosario Casalone, Rossella Caselli, Caterina Ceccarini, Carlo Ceglia, Anna Maria Ciaschini, Domenico Coviello, Francesca Crosti, Annamaria D'Aprile, Antonella Fabretto, Rita Genesio, Marzia Giagnacovo, Paola Granata, Ilaria Longo, Michela Malacarne, Giuseppina Marseglia, Annamaria Montaldi, Anna Maria Nardone, Chiara Palka, Vanna Pecile, Chiara Pessina, Diana Postorivo, Serena Redaelli, Alessandra Renieri, Chiara Rigon, Fabiola Tiberi, Mariella Tonelli, Nicoletta Villa, Anna Zilio, Daniela Zuccarello, Antonio Novelli, Lidia Larizza, Daniela Giardino
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 1, Pp n/a-n/a (2020)
Abstract Background Chromosomal microarray analysis (CMA) is nowadays widely used in the diagnostic path of patients with clinical phenotypes. However, there is no ascertained evidence to date on how to assemble single/combined clinical categories of
Externí odkaz:
https://doaj.org/article/dcd2b41af7c54fef9ac5273be374d880
Autor:
Francesca Romana Grati, Ilaria Bestetti, Daria De Siero, Francesca Malvestiti, Nicoletta Villa, Elena Sala, Francesca Crosti, Valentina Parisi, Anna Maria Nardone, Gianluca Di Giacomo, Antonella Pettinari, Giada Tortora, Annamaria Montaldi, Annapaola Calò, Donatella Saccilotto, Sara Zanchetti, Paola Celli, Silvana Guerneri, Rosamaria Silipigni, Laura Cardarelli, Elisabetta Lippi, Simona Cavani, Michela Malacarne, Rita Genesio, Nicola Beltrami, Maria Carla Pittalis, Laura Desiderio, Mattia Gentile, Romina Ficarella, Maria Paola Recalcati, Ilaria Catusi, Maria Garzo, Lorena Miele, Cecilia Corti, Sara Ghezzo, Veronica Bertini, Francesca Cambi, Angelo Valetto, Barbara Facchinetti, Laura Bernardini, Anna Capalbo, Federica Balducci, Elisabetta Pelo, Barbara Minuti, Chiara Pescucci, Costanza Giuliani, Alessandra Renieri, Ilaria Longo, Rossella Tita, Giuseppe Castello, Rosario Casalone, Rossana Righi, Barbara Raso, Alessandro Civolani, Maria Cristina Muzi, Manuela di Natale, Luigia Varriale, Daniela Gasperini, Maria Cristina Nuzzi, Angelo Cellamare, Paola Casieri, Rosa Busuito, Caterina Ceccarini, Carla Cesarano, Orsola Privitera, Daniela Melani, Cristina Menozzi, Cristina Falcinelli, Olga Calabrese, Paola Battaglia, Antonella Tanzariello, Tamara Stampalija, Carmela Ardisia, Paolo Gasparini, Peter Benn, Antonio Novelli
Objectives: To establish the positive predictive values (PPV) of cfDNA testing based on data from a nationwide survey of independent clinical cytogenetics laboratories. Methods: Prenatal diagnostic test results obtained by Italian laboratories betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deddef97ee50604835da23b5f9aa9edb
https://hdl.handle.net/11368/3035240
https://hdl.handle.net/11368/3035240
Autor:
Valeria Pizzuti, Provvidenza Maria Abruzzo, Alexandros Chatgilialoglu, Pasquale Marrazzo, Giovannamaria Petrocelli, Ilaria Longo, Paola Poggi, Federica Facchin, Silvia Canaider, Laura Bonsi, Francesco Alviano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::a64ca5d455b6a56ec43f011603fc4c76
http://hdl.handle.net/11585/853123
http://hdl.handle.net/11585/853123
Autor:
Anna Maria Pinto, Arianna Calonaci, Daniela Galimberti, Alessandra Renieri, Flavia Privitera, Francesca Ariani, Francesca Mari, Gabriella Doddato, Margherita Baldassarri, Ilaria Longo, Sonia De Francesco, Filomena Tiziana Papa, Mauro Caini, Theodora Hadjistilianou
Publikováno v:
Genes
Volume 12
Issue 9
Genes, Vol 12, Iss 1318, p 1318 (2021)
Volume 12
Issue 9
Genes, Vol 12, Iss 1318, p 1318 (2021)
Retinoblastoma (RB) is an ocular tumor of the pediatric age caused by biallelic inactivation of the RB1 gene (13q14). About 10% of cases are due to gross-sized molecular deletions. The deletions can involve the surrounding genes delineating a contigu
Autor:
Serena Redaelli, Annamaria Montaldi, Francesca Crosti, Marzia Giagnacovo, Maria Paola Recalcati, Chiara Palka, Carlo Ceglia, Lidia Larizza, Caterina Ceccarini, Chiara Rigon, Anna Maria Nardone, Antonio Novelli, Domenico Coviello, Stefania Cappellani, Alessandra Renieri, Anna Maria Ciaschini, Alberta Alghisi, Ilaria Catusi, Daniela Zuccarello, Vanna Pecile, Mariella Tonelli, Paola Granata, Ilaria Bestetti, Ilaria Longo, Giuseppina Marseglia, Nicoletta Villa, Chiara Pessina, Michela Malacarne, Fabiola Tiberi, Chiara Valtorta, Melissa Alfonsi, Anna Zilio, Maria Garzo, Rossella Caselli, Annamaria D'Aprile, Daniela Giardino, Rosario Casalone, Diana Postorivo, Rita Genesio, Antonella Fabretto
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 1, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 1, Pp n/a-n/a (2020)
Background Chromosomal microarray analysis (CMA) is nowadays widely used in the diagnostic path of patients with clinical phenotypes. However, there is no ascertained evidence to date on how to assemble single/combined clinical categories of developm
Autor:
Anna Maria Pinto, Francesca Mari, Margherita Baldassarri, Laura Massella, Guido Garosi, Sergio Daga, Ilaria Longo, Valentina Imperatore, Elisa Frullanti, Alessandra Renieri, Chiara Fallerini, Maria Antonietta Mencarelli, Caterina Lo Rizzo, Carmine Pecoraro, Elisa Landucci, Francesca Ariani
Publikováno v:
Human Mutation. 39:302-314
Alport Syndrome (ATS) is a rare genetic disorder caused by collagen IV genes mutations, leading to glomerular basement membrane damage up to end-stage renal disease. Podocytes, the main component of the glomerular structure, are the only cells able t
Autor:
Maria Antonietta Mencarelli, Silvia Ferranti, Alessandra Renieri, Salvatore Grosso, Chiara Romano, Ilaria Longo
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 41(8)
The short arm of chromosome 17 is characterized by a high density of low copy repeats, creating the opportunity for non-allelic homologous recombination to occur. Microdeletions of the 17p13.3 region are responsible for neuronal migration disorders i
Autor:
Ilaria Longo1, Luisa Russo2, Ilaria Meloni1, Iolanda Ricci2, Francesca Ariani1, Chiara Pescucci1, Carmela Tiziana Giordano2, Roberto Canitano3, Giuseppe Hayek3, Michele Zappella3, Giovanni Neri2, Alessandra Renieri1, Fiorella Gurrieri2 fgurrieri@rm.unicatt.it
Publikováno v:
European Journal of Human Genetics. Aug2004, Vol. 12 Issue 8, p682-685. 4p.