Zobrazeno 1 - 10
of 225
pro vyhledávání: '"Patrizia Accorsi"'
Autor:
Anna Fetta, Francesco Toni, Ilaria Pettenuzzo, Emilia Ricci, Alessandro Rocca, Caterina Gambi, Luca Soliani, Veronica Di Pisa, Silvia Martini, Giacomo Sperti, Valeria Cagnazzo, Patrizia Accorsi, Emanuele Bartolini, Domenica Battaglia, Pia Bernardo, Maria Paola Canevini, Anna Rita Ferrari, Lucio Giordano, Chiara Locatelli, Margherita Mancardi, Alessandro Orsini, Tommaso Pippucci, Dario Pruna, Anna Rosati, Agnese Suppiej, Sara Tagliani, Alessandro Vaisfeld, Aglaia Vignoli, Kosuke Izumi, Ian Krantz, Duccio Maria Cordelli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background Pallister-Killian syndrome (PKS) is a rare genetic disorder caused by mosaic tetrasomy of 12p with wide neurological involvement. Intellectual disability, developmental delay, behavioral problems, epilepsy, sleep disturbances, and
Externí odkaz:
https://doaj.org/article/ba10327d06cc4e8da9702f9d1003ec3b
Autor:
Gianni Cutillo, Silvia Masnada, Gaetan Lesca, Dorothée Ville, Patrizia Accorsi, Lucio Giordano, Anna Pichiecchio, Marialuisa Valente, Paola Borrelli, Ottavia Eleonora Ferraro, Pierangelo Veggiotti
Publikováno v:
Epilepsia Open, Vol 9, Iss 1, Pp 106-121 (2024)
Abstract Objective Adenylosuccinate lyase (ADSL) deficiency is a rare inherited metabolic disorder with a wide phenotypic presentation, classically grouped into three types (neonatal, type I, and type II). We aim to better delineate the pathological
Externí odkaz:
https://doaj.org/article/824525d7bb3b493c91fbe235e276060d
Autor:
Carmine Liberatore, Francesca Fioritoni, Annalisa Natale, Guido Montanaro, Gaetano La Barba, Cecilia Passeri, Ornella Iuliani, Bianca Fabi, Stefano Baldoni, Donatella Fantasia, Giuseppe Calabrese, Patrizia Accorsi, Stella Santarone, Stefano Pulini, Mauro Di Ianni
Publikováno v:
eJHaem, Vol 4, Iss 4, Pp 1152-1156 (2023)
Abstract The coexistence of chronic myeloid leukemia (CML) and multiple myeloma (MM) is a rare clinical condition. By means of FISH and molecular analysis on both sorted CD138 plasma cells and cryopreserved CD34 stem cells, a distinct clonal origin o
Externí odkaz:
https://doaj.org/article/5994fa656fa74960acf90348a876832c
Autor:
Simona Balestrini, Viola Doccini, Sabrina Giometto, Ersilia Lucenteforte, Salvatore De Masi, Elisa Giarola, Isabella Brambilla, Federica Pieroni, Marco Perulli, Domenica Battaglia, Nicola Specchio, Francesca Ragona, Tiziana Granata, Simona Pellacani, Annarita Ferrari, Carla Marini, Sara Matricardi, Elisabetta Cesaroni, Lucio Giordano, Patrizia Accorsi, Vittorio Sciruicchio, Paolo Tinuper, Tullio Messana, Angelo Russo, Dario Pruna, Margherita Nosadini, Valentina De Giorgis, Davide Caputo, Residras Collaboration Group, Serena Pellegrin, Tommaso Lo Barco, Francesca Darra, Bernardo Dalla Bernardina, Renzo Guerrini
Publikováno v:
Epilepsia Open, Vol 8, Iss 2, Pp 517-534 (2023)
Abstract Objectives We describe the Residras registry, dedicated to Dravet syndrome (DS) and to other phenotypes related to SCN1A mutations, as a paradigm of registry for rare and complex epilepsies. Our primary objectives are to present the tools an
Externí odkaz:
https://doaj.org/article/b4967b84c41b483295572c1cca76ccff
Autor:
Serena Bosica, Alexandra Chiaverini, Maria Elisabetta De Angelis, Antonio Petrini, Daniela Averaimo, Michele Martino, Marco Rulli, Maria Antonietta Saletti, Maria Chiara Cantelmi, Franco Ruggeri, Fabrizio Lodi, Paolo Calistri, Francesca Cito, Cesare Cammà, Marco Di Domenico, Antonio Rinaldi, Paolo Fazii, Fabrizio Cedrone, Giuseppe Di Martino, Patrizia Accorsi, Daniela Morelli, Nicola De Luca, Francesco Pomilio, Giustino Parruti, Giovanni Savini
Publikováno v:
Emerging Infectious Diseases, Vol 29, Iss 5, Pp 1020-1024 (2023)
During November 2021–May 2022, we identified 37 clinical cases of Streptococcus equi subspecies zooepidemicus infections in central Italy. Epidemiologic investigations and whole-genome sequencing showed unpasteurized fresh dairy products were the o
Externí odkaz:
https://doaj.org/article/182ca6cd5ffe4f81aee0fe61d1a38e49
Autor:
Luciana Teofili, Patrizia Papacci, Nicoletta Orlando, Maria Bianchi, Tina Pasciuto, Iolanda Mozzetta, Fernando Palluzzi, Luciano Giacò, Carmen Giannantonio, Giulia Remaschi, Michela Santosuosso, Enrico Beccastrini, Marco Fabbri, Caterina Giovanna Valentini, Tiziana Bonfini, Eleonora Cloclite, Patrizia Accorsi, Antonella Dragonetti, Francesco Cresi, Giulia Ansaldi, Genny Raffaeli, Stefania Villa, Giulia Pucci, Isabella Mondello, Michele Santodirocco, Stefano Ghirardello, Giovanni Vento
Publikováno v:
Trials, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Extremely low gestational age neonates (ELGANs, i.e., neonates born before 28 weeks of gestation) are at high risk of developing retinopathy of prematurity (ROP), with potential long-life visual impairment. Due to concomitant anem
Externí odkaz:
https://doaj.org/article/2bb1737d0fba4c1e869a6e99709012df
Autor:
Tommaso Perini, Carmine Liberatore, Girlando Virginia, Cecilia Passeri, Valeria Ferla, Ornella Iuliani, Alessia Orsini, Guido Montanaro, Francesca Farina, Alessandro DI Nicola, Sarah Marktel, Stefano Pulini, Stella Santarone, Patrizia Accorsi, Fabio Ciceri, Mauro DI Ianni, Magda Marcatti
Publikováno v:
HemaSphere, Vol 7, p e05968ba (2023)
Externí odkaz:
https://doaj.org/article/b4443acf4f1f4ab3b765b2a3c4996506
Autor:
Carmine Liberatore, Tommaso Perini, Cecilia Passeri, Valeria Ferla, Francesca Fioritoni, Virginia Girlando, Ornella Iuliani, Alessia Orsini, Guido Montanaro, Francesca Farina, Alessandro Di Nicola, Rosamaria Nitti, Stefano Pulini, Sara Mastaglio, Stella Santarone, Milena Coppola, Sarah Marktel, Patrizia Accorsi, Fabio Ciceri, Magda Marcatti, Mauro Di Ianni
Publikováno v:
Haematologica, Vol 108, Iss 12 (2023)
Externí odkaz:
https://doaj.org/article/2faeca43bdfe458789e26abcbaabee20
Autor:
Mauro Di Ianni, Carmine Liberatore, Nicole Santoro, Paola Ranalli, Francesco Guardalupi, Giulia Corradi, Ida Villanova, Barbara Di Francesco, Stefano Lattanzio, Cecilia Passeri, Paola Lanuti, Patrizia Accorsi
Publikováno v:
Cells, Vol 13, Iss 2, p 134 (2024)
GvHD still remains, despite the continuous improvement of transplantation platforms, a fearful complication of transplantation from allogeneic donors. Being able to separate GvHD from GvL represents the greatest challenge in the allogeneic transplant
Externí odkaz:
https://doaj.org/article/6748348bb1944195ab354513c33db7ff
Autor:
Maria Chiara G. Monaco, Dragan Maric, Ombretta Salvucci, Cristina Antonetti Lamorgese Passeri, Patrizia Accorsi, Eugene O. Major, Anna Concetta Berardi
Publikováno v:
Stem Cell Research & Therapy, Vol 12, Iss 1, Pp 1-5 (2021)
Abstract Erythro-myeloid progenitors (EMP) are found in a population of cells expressing CD31 and CD45 markers (CD31+CD45+). A recent study indicated that EMPs persist until adulthood and can be a source of endothelial cells. We identified two sub-po
Externí odkaz:
https://doaj.org/article/db2238b5b920428d8a0286920995aa04