Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Amanda Papa"'
Autor:
Sara Isoldi, Giovanni Di Nardo, Saverio Mallardo, Pasquale Parisi, Umberto Raucci, Renato Tambucci, Paolo Quitadamo, Silvia Salvatore, Enrico Felici, Fabio Cisarò, Licia Pensabene, Claudia Banzato, Caterina Strisciuglio, Claudio Romano, Patrizia Fusco, Francesca Rigotti, Naire Sansotta, Silvia Caimmi, Salvatore Savasta, Giovanna Zuin, Marina Di Stefano, Silvia Provera, Angelo Campanozzi, Paolo Rossi, Simona Gatti, Mara Corpino, Patrizia Alvisi, Stefano Martelossi, Agnese Suppiej, Paolo Gandullia, Alberto Verrotti, Gianluca Terrin, Caterina Pacenza, Fabiola Fornaroli, Donatella Comito, Stefano D’Arrigo, Pasquale Striano, Federico Raviglione, Marco Carotenuto, Alessandro Orsini, Vincenzo Belcastro, Giovanna Di Corcia, Vincenzo Raieli, Michela Ada Noris Ferilli, Claudia Ruscitto, Elisabetta Spadoni, Salvatore Grosso, Renato D’Alonzo, Amanda Papa, Piero Pavone, Mariaclaudia Meli, Mario Velardita, Martina Mainetti, Nicola Vanacore, Osvaldo Borrelli
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-9 (2022)
Abstract Background Cyclic Vomiting Syndrome (CVS) is a rare functional gastrointestinal disorder, which has a considerable burden on quality of life of both children and their family. Aim of the study was to evaluate the diagnostic modalities and th
Externí odkaz:
https://doaj.org/article/2aea540e6a29406da26f892dd9d53b66
Autor:
Simona Mellone, Chiara Puricelli, Denise Vurchio, Sara Ronzani, Simone Favini, Arianna Maruzzi, Cinzia Peruzzi, Amanda Papa, Alice Spano, Fabio Sirchia, Giorgia Mandrile, Alessandra Pelle, Paolo Rasmini, Fabiana Vercellino, Andrea Zonta, Ivana Rabbone, Umberto Dianzani, Maurizio Viri, Mara Giordano
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Neurodevelopmental disorders comprise a clinically and genetically heterogeneous group of conditions that affect 2%–5% of children and represents a public health challenge due to complexity of the etiology. Only few patients with unexpl
Externí odkaz:
https://doaj.org/article/edf91342563a4c4b8c9586727480c023
Autor:
Elisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, Maria Stella Vari, Francesca Marchese, Veronica Di Pisa, Maria Margherita Mancardi, Thea Giacomini, Laura Siri, Fabiana Vercellino, Domenico Serino, Alessandro Orsini, Alice Bonuccelli, Irene Bagnasco, Amanda Papa, Carlo Minetti, Duccio Maria Cordelli, Pasquale Striano
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-9 (2020)
Abstract Background Childhood epilepsies are a heterogeneous group of conditions differing in diagnostic criteria, management, and outcome. Late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) is a neurodegenerative condition caused by biallel
Externí odkaz:
https://doaj.org/article/37130414555649a190c5a80fa2b786f8
Autor:
Luigi Francesco Iannone, Gabriele Arena, Domenica Battaglia, Francesca Bisulli, Paolo Bonanni, Antonella Boni, Maria Paola Canevini, Gaetano Cantalupo, Elisabetta Cesaroni, Manuela Contin, Antonietta Coppola, Duccio Maria Cordelli, Giovanni Cricchiuti, Valentina De Giorgis, Maria Fulvia De Leva, Marta De Rinaldis, Giuseppe d'Orsi, Maurizio Elia, Carlo Andrea Galimberti, Alessandra Morano, Tiziana Granata, Renzo Guerrini, Monica A. M. Lodi, Angela La Neve, Francesca Marchese, Silvia Masnada, Roberto Michelucci, Margherita Nosadini, Nicola Pilolli, Dario Pruna, Francesca Ragona, Anna Rosati, Margherita Santucci, Alberto Spalice, Nicola Pietrafusa, Pasquale Striano, Elena Tartara, Laura Tassi, Amanda Papa, Claudio Zucca, Emilio Russo, Oriano Mecarelli, The CBD LICE Italy Study Group
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Purified cannabidiol (CBD) was administered to highly refractory patients with Dravet (DS) or Lennox–Gastaut (LGS) syndromes in an ongoing expanded access program (EAP). Herein, we report interim results on CBD safety and seizure outcom
Externí odkaz:
https://doaj.org/article/49784ef07e554ec88badc2927a8fcd4e
Autor:
Irene Toldo, Francesco Brunello, Paola Cavasin, Margherita Nosadini, Stefano Sartori, Anna Chiara Frigo, Roberto Mai, Veronica Pelliccia, Maria Margherita Mancardi, Pasquale Striano, Marisavina Severino, Federico Zara, Romana Rizzi, Susanna Casellato, Gabriella Di Rosa, Mario Mastrangelo, Alberto Spalice, Mauro Budetta, Luca De Palma, Renzo Guerrini, Dario Pruna, Duccio Maria Cordelli, Vito Sofia, Amanda Papa, Valentina Chiesa, Francesca Ragona, Pasquale Parisi, Alfredo D'Aniello, Pierangelo Veggiotti, Filippo Dainese, Lucio Giordano, Laura Licchetta, Paolo Tinuper, Giuseppe D'Orsi, Matteo Cassina, Renzo Manara
Publikováno v:
Pediatric Neurology. 141:58-64
Autor:
Ganna Balagura, Julie Xian, Antonella Riva, Francesca Marchese, Bruria Ben Zeev, Loreto Rios, Deepa Sirsi, Patrizia Accorsi, Elisabetta Amadori, Guja Astrea, Simona Baldassari, Francesca Beccaria, Antonella Boni, Mauro Budetta, Gaetano Cantalupo, Giuseppe Capovilla, Elisabetta Cesaroni, Valentina Chiesa, Antonietta Coppola, Robertino Dilena, Raffaella Faggioli, Annarita Ferrari, Elena Fiorini, Francesca Madia, Elena Gennaro, Thea Giacomini, Lucio Giordano, Michele Iacomino, Simona Lattanzi, Carla Marini, Maria Margherita Mancardi, Massimo Mastrangelo, Tullio Messana, Carlo Minetti, Lino Nobili, Amanda Papa, Antonia Parmeggiani, Tiziana Pisano, Angelo Russo, Vincenzo Salpietro, Salvatore Savasta, Marcello Scala, Andrea Accogli, Barbara Scelsa, Paolo Scudieri, Alberto Spalice, Nicola Specchio, Marina Trivisano, Michal Tzadok, Massimiliano Valeriani, Maria Stella Vari, Alberto Verrotti, Federico Vigevano, Aglaia Vignoli, Ruud Toonen, Federico Zara, Ingo Helbig, Pasquale Striano
Publikováno v:
Balagura, G, Xian, J, Riva, A, Marchese, F, Zeev, B B, Rios, L, Sirsi, D, Accorsi, P, Amadori, E, Astrea, G, Baldassari, S, Beccaria, F, Boni, A, Budetta, M, Cantalupo, G, Capovilla, G, Cesaroni, E, Chiesa, V, Coppola, A, Dilena, R, Faggioli, R, Ferrari, A, Fiorini, E, Madia, F, Gennaro, E, Giacomini, T, Giordano, L, Iacomino, M, Lattanzi, S, Marini, C, Mancardi, M M, Mastrangelo, M, Messana, T, Minetti, C, Nobili, L, Papa, A, Parmeggiani, A, Pisano, T, Russo, A, Salpietro, V, Savasta, S, Scala, M, Accogli, A, Scelsa, B, Scudieri, P, Spalice, A, Specchio, N, Trivisano, M, Tzadok, M, Valeriani, M, Vari, M S, Verrotti, A, Vigevano, F, Vignoli, A, Toonen, R, Zara, F, Helbig, I & Striano, P 2022, ' Epilepsy Course and Developmental Trajectories in STXBP1-DEE ', Neurology: Genetics, vol. 8, no. 3, e676, pp. 1-15 . https://doi.org/10.1212/NXG.0000000000000676
Neurology: Genetics, 8(3):e676, 1-15. Lippincott Williams and Wilkins
Neurology: Genetics, 8(3):e676, 1-15. Lippincott Williams and Wilkins
Background and ObjectivesClinical manifestations in STXBP1 developmental and epileptic encephalopathy (DEE) vary in severity and outcome, and the genotypic spectrum is diverse. We aim to trace the neurodevelopmental trajectories in individuals with S
Autor:
Sara Matricardi, Elisabetta Cesaroni, Paolo Bonanni, Nicoletta Foschi, Alfredo D′Aniello, Giancarlo Di Gennaro, Pasquale Striano, Silvia Cappanera, Sabrina Siliquini, Elena Freri, Francesca Ragona, Tiziana Granata, Francesco Deleo, Flavio Villani, Angelo Russo, Tullio Messana, Laura Siri, Irene Bagnasco, Aglaia Vignoli, Francesca Felicia Operto, Alessandro Orsini, Alice Bonuccelli, Amanda Papa, Cinzia Peruzzi, Claudio Liguori, Alberto Verrotti, Francesco Chiarelli, Carla Marini, Simona Lattanzi
Publikováno v:
Epilepsia.
Autor:
Piero Pavone, Patrizia Dassi, Chiara Marra, Clara Malattia, Anna Fetta, Irene Bagnasco, Alberto Verrotti, Alessandro Orsini, Filippo Greco, Alice Bonuccelli, Salvatore Savasta, Stefano Sartori, Patrizia Bergonzini, Mariasole Magistrali, Bernadette Marrè Brunenghi, Daniele Marcotulli, Rita Consolini, Carlotta Canavese, Diego Peroni, Elisa De Grandis, Margherita Nosadini, Niccolò Carli, Gian Luigi Marseglia, Maurizio Viri, Thomas Foiadelli, Duccio Maria Cordelli, Francesco Nicita, Francesco Bassanese, Gabriele Simonini, Sabrina Siquilini, Francesca Marchese, Amanda Papa, Pasquale Striano, Alessandro Capuano, Sara Matricardi
Publikováno v:
European Journal of Paediatric Neurology. 36:1-6
Sydenham's Chorea (SC) is a neuropsychiatric disorder and a major manifestation of acute rheumatic fever. The erroneous assumption that SC is a benign and self-limiting disease, has led to a lack of high-quality scientific evidence of the therapeutic
Autor:
Duccio Maria Cordelli, Domenico Serino, Elisabetta Amadori, Laura Siri, Maria Margherita Mancardi, Pasquale Striano, Carlo Minetti, Francesca Marchese, Veronica Di Pisa, Maria Stella Vari, Alice Bonuccelli, Amanda Papa, Fabiana Vercellino, Giulia Sofia Cereda, Irene Bagnasco, Alessandro Orsini, Marcello Scala, Thea Giacomini
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-9 (2020)
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-9 (2020)
Background Childhood epilepsies are a heterogeneous group of conditions differing in diagnostic criteria, management, and outcome. Late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) is a neurodegenerative condition caused by biallelic TPP1 v
Autor:
Francesca Zottarelli, Cinzia Peruzzi, Valentina Chierici, Amanda Papa, Laura Cristina Gironi, Agostina Marolda, Enrico Colombo, Gianni Bona, Paola Savoia
Publikováno v:
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 16:360-364