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Caterina Caputi

sapienza university rome

10H-index
22Paper Count
275Citation Count
Published Papers 8
Publication Date
Pathogenic cryptic variants detectable through exome data reanalysis significantly increase the diagnostic yield in Joubert syndrome
err2024-10-11
err1
errOAAI
errD'Abrusco, Fulvio; Serpieri, Valentina; Taccagni, Cecilia Maria; Garau, Jessica; Cattaneo, Luca; Boggioni, Monica; Gana, Simone; Battini, Roberta; Bertini, Enrico; Zanni, Ginevra; Boltshauser, Eugen; Borgatti, Renato; Romaniello, Romina; Signorini, Sabrina; Leuzzi, Vincenzo; Caputi, Caterina; Manti, Filippo; D'Arrigo, Stefano; De Laurentiis, Arianna; Graziano, Claudio; Lemke, Johannes R.; Morelli, Federica; Ramadza, Danijela Petkovic; Sirchia, Fabio; Giorgio, Elisa; Valente, Enza Maria
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Clinical variability at the mild end of BRAT1-related spectrum: Evidence from two families with genotype-phenotype discordance
err2021-11-15
err12
errOAAI
errNuovo, Sara; Baglioni, Valentina; De Mori, Roberta; Tardivo, Silvia; Caputi, Caterina; Ginevrino, Monia; Micalizzi, Alessia; Masuelli, Laura; Federici, Giulia; Casella, Antonella; Lorefice, Elisa; Anello, Danila; Tolve, Manuela; Farini, Donatella; Bertini, Enrico; Zanni, Ginevra; Travaglini, Lorena; Vasco, Gessica; Sette, Claudio; Carducci, Carla; Valente, Enza M.; Leuzzi, Vincenzo
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De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus
errBRAIN
IF11.7
err2021-08-11
err16
errOAAI
errGalosi, Serena; Edani, Ban H.; Martinelli, Simone; Hansikova, Hana; Eklund, Erik A.; Caputi, Caterina; Masuelli, Laura; Corsten-Janssen, Nicole; Srour, Myriam; Oegema, Renske; Bosch, Danielle G. M.; Ellis, Colin A.; Amlie-Wolf, Louise; Accogli, Andrea; Atallah, Isis; Averdunk, Luisa; Baranano, Kristin W.; Bei, Roberto; Bagnasco, Irene; Brusco, Alfredo; Demarest, Scott; Alaix, Anne-Sophie; Di Bonaventura, Carlo; Distelmaier, Felix; Elmslie, Frances; Gan-Or, Ziv; Good, Jean-Marc; Gripp, Karen; Kamsteeg, Erik-Jan; Macnamara, Ellen; Marcelis, Carlo; Mercier, Noelle; Peeden, Joseph; Pizzi, Simone; Pannone, Luca; Shinawi, Marwan; Toro, Camilo; Verbeek, Nienke E.; Venkateswaran, Sunita; Wheeler, Patricia G.; Zdrazilova, Lucie; Zhang, Rong; Zorzi, Giovanna; Guerrini, Renzo; Sessa, William C.; Lefeber, Dirk; Tartaglia, Marco; Hamdan, Fadi F.; Grabinska, Kariona A.; Leuzzi, Vincenzo
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PNKP deficiency mimicking a benign hereditary chorea: The misleading presentation of a neurodegenerative disorder
err2019-07-01
err5
PREAI
errCaputi, C.; Tolve, M.; Galosi, S.; Inghilleri, M.; Carducci, C.; Angeloni, A.; Leuzzi, V.
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Ataxia-telangiectasia A new remitting form with a peculiar transcriptome signature
err2018-04-01
err9
errOAAI
errLeuzzi, Vincenzo; D'Agnano, Daniela; Menotta, Michele; Caputi, Caterina; Chessa, Luciana; Magnani, Mauro
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The outcome of white matter abnormalities in early treated phenylketonuric patients: A retrospective longitudinal long-term study
err2015-11-01
err29
PREAI
errMastrangelo, Mario; Chiarotti, Flavia; Berillo, Luana; Caputi, Caterina; Carducci, Claudia; Di Biasi, Claudio; Manti, Filippo; Nardecchia, Francesca; Leuzzi, Vincenzo
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Teaching Video NeuroImages: Clinical course of infantile ascending hereditary spastic paralysis
err2014-02-18
err0
errOAAI
errMastrangelo, Mario; Bernasconi, Pia; De Liso, Paola; Caputi, Caterina; Bertino, Sara; Leuzzi, Vincenzo
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Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency
err2013-02-06
err14
PREAI
errMastrangelo, Mario; Caputi, Caterina; Galosi, Serena; Giannini, Maria Teresa; Leuzzi, Vincenzo
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