CONTI, VALERIO
CONTI, VALERIO
Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino (NEUROFARBA)
3D human brain digital istopatology
2018 Costantini I.; Mazzamuto G.; Silvestri L.; Neri M.; Roffilli M.; Conti V.; Guerrini R.; Sacconi L.; Pavone F.S.
3D reconstruction and analysis of four human brain cortex samples with two-photon fluorescence microscopy
2020 I. Constantini; G. Mazzamuto; M. Roffilli; A. Laurino; F. Castelli; M. Neri; G. Lughi; A. Simonetto; E. Lazzeri; L. Pesce; C. Destrieux; L. Silvestri; V. Conti; R. Guerrini; F. Pavone
A versatile clearing agent for multi-modal brain imaging
2015 Costantini, Irene; Ghobril, Jean-Pierre; Di Giovanna, Antonino Paolo; Mascaro, Anna Letizia Allegra; Silvestri, Ludovico; Müllenbroich, Marie Caroline; Onofri, Leonardo; Conti, Valerio; Vanzi, Francesco; Sacconi, Leonardo; Guerrini, Renzo; Markram, Henry; Iannello, Giulio; Pavone, Francesco Saverio
Bi-allelic variants in TM2D3 cause a severe syndromic neurodevelopmental disorder associated with endoplasmic reticulum and mitochondrial abnormalities
2025 Gabillard-Lefort, Claudie; Martinez, Caroline Silveira; Gueguen, Naïg; Desquiret-Dumas, Valérie; Wery, Méline; Legoff, Louis; Guimier, Anne; Rondeau, Sophie; Barcia, Giulia; Barnerias, Christine; Cogne, Benjamin; Besnard, Thomas; Lorino, Elsa; Douglas, Jessica; Bodamer, Olaf; Vetro, Annalisa; Guerrini, Renzo; Balestrini, Simona; Conti, Valerio; Siri, Laura; Chevrollier, Arnaud; Bris, Céline; Colin, Estelle; Procaccio, Vincent; Prunier-Mirebeau, Delphine; Lenaers, Guy; Khiati, Salim; Nizon, Mathilde; Baris, Olivier R
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course
2019 Alessandro Esposito, Antonio Falace, Matias Wagner, Moran Gal, Davide Mei, Valerio Conti, Tiziana Pisano, Davide Aprile, Maria Sabina Cerullo, Antonio De Fusco, Silvia Giovedì, Annette Seibt, Daniella Magen, Tilman Polster, Ayelet Eran, Sarah L Stenton, Chiara Fiorillo, Sarit Ravid, Ertan Mayatepek, Hava Hafner, Saskia Wortmann, Erez Y Levanon, Carla Marini, Hanna Mandel, Fabio Benfenati, Felix Distelmaier, Anna Fassio, Renzo Guerrini
Computer-based automatic identification of neurons in gigavoxel-sized 3D human brain images
2015 Soda, Paolo; Acciai, Ludovica; Cordelli, Ermanno; Costantini, Irene; Sacconi, Leonardo; Pavone, Francesco Saverio; Conti, Valerio; Guerrini, Renzo; Frasconi, Paolo; Iannello, Giulio
Corrigendum to 'Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetase [Seizure: European Journal of Epilepsy 86 (2021) 152-154]
2021 Buccoliero, Anna Maria; Caporalini, Chiara; Scagnet, Mirko; Mussa, Federico; Giordano, Flavio; Sardi, Iacopo; Migliastro, Irene; Moscardi, Selene; Conti, Valerio; Barba, Carmen; Antonelli, Manila; Gianno, Francesca; Rossi, Sabrina; Diomedi-Camassei, Francesca; Gessi, Marco; Donofrio, Vittoria; Bertero, Luca; Giangaspero, Felice; Santi, Mariarita; Aronica, Eleonora; Genitori, Lorenzo; Guerrini, Renzo
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
2023 Guerrini, Renzo; Conti, Valerio; Mantegazza, Massimo; Balestrini, Simona; Galanopoulou, Aristea S; Benfenati, Fabio
Epileptic encephalopathies and progressive neurodegeneration
2024 Guerrini, R; Conti, V
Fiber-probe optical spectroscopy discriminates normal brain from focal cortical dysplasia in pediatric subjects
2017 Anand S.; Cicchi R.; Giordano F.; Conti V.; Buccoliero A.M.; Guerrini R.; Pavone F.S.
International consensus recommendations on the diagnostic work-up for malformations of cortical development
2020 Oegema, Renske; Barakat, Tahsin Stefan; Wilke, Martina; Stouffs, Katrien; Amrom, Dina; Aronica, Eleonora; Bahi-Buisson, Nadia; Conti, Valerio; Fry, Andrew E; Geis, Tobias; Andres, David Gomez; Parrini, Elena; Pogledic, Ivana; Said, Edith; Soler, Doriette; Valor, Luis M; Zaki, Maha S; Mirzaa, Ghayda; Dobyns, William B; Reiner, Orly; Guerrini, Renzo; Pilz, Daniela T; Hehr, Ute; Leventer, Richard J; Jansen, Anna C; Mancini, Grazia M S; Di Donato, Nataliya
Large-scale, cell-resolution volumetric mapping allows layer-specific investigation of human brain cytoarchitecture
2021 Irene Costantini and Giacomo Mazzamuto and Matteo Roffilli and Annunziatina Laurino and Filippo Maria Castelli and Mattia Neri and Giovanni Lughi and Andrea Simonetto and Erica Lazzeri and Luca Pesce and Christophe Destrieux and Ludovico Silvestri and Valerio Conti and Renzo Guerrini and Francesco Saverio Pavone
Leat-associated seizures the possible role of EAAT2, pyruvate carboxylase and glutamine synthetase
2024 Buccoliero, Anna Maria; Caporalini, Chiara; Moscardi, Selene; Cetica, Valentina; Mei, Davide; Conti, Valerio; Nozzoli, Filippo; Bonaudo, Camilla; Battista, Francesca; Giordano, Flavio; Mura, Regina; Spacca, Barbara; Mussa, Federico; D'Onofrio, Vittoria; Guerrini, Renzo; Genitori, Lorenzo; Scagnet, Mirko
Lesional and non-lesional epilepsies: A blurring genetic boundary.
2020 Guerrini R, Parrini E, Esposito A, Fassio A, Conti V
Multimodal fiber-probe spectroscopy allows detecting epileptogenic focal cortical dysplasia in children
2017 Anand, Suresh; Cicchi, Riccardo; Giordano, Flavio; Conti, Valerio; Buccoliero, Anna Maria; Guerrini, Renzo; Pavone, Francesco Saverio
Myxoid glioneuronal tumor: Histopathologic, neuroradiologic, and molecular features in a single center series.
2023 Caporalini C, Scagnet M, Giunti L, Cetica V, Mei D, Conti V, Moscardi S, Macconi L, Giordano F, D'Incerti L, Genitori L, Guerrini R, Buccoliero AM.
Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis
2022 Guerrini, Renzo; Mei, Davide; Kerti-Szigeti, Katalin; Pepe, Sara; Koenig, Mary Kay; Von Allmen, Gretchen; Cho, Megan T; McDonald, Kimberly; Baker, Janice; Bhambhani, Vikas; Powis, Zöe; Rodan, Lance; Nabbout, Rima; Barcia, Giulia; Rosenfeld, Jill A; Bacino, Carlos A; Mignot, Cyril; Power, Lillian H; Harris, Catharine J; Marjanovic, Dragan; Møller, Rikke S; Hammer, Trine B; Keski Filppula, Riikka; Vieira, Päivi; Hildebrandt, Clara; Sacharow, Stephanie; Maragliano, Luca; Benfenati, Fabio; Lachlan, Katherine; Benneche, Andreas; Petit, Florence; de Sainte Agathe, Jean-Madeleine; Hallinan, Barbara; Si, Yue; Wentzensen, Ingrid M; Zou, Fanggeng; Narayanan, Vinodh; Matsumoto, Naomichi; Boncristiano, Alessandra; la Marca, Giancarlo; Kato, Mitsuhiro; Anderson, Kristin; Barba, Carmen; Sturiale, Luisa; Garozzo, Domenico; Bei, Roberto; Masuelli, Laura; Conti, Valerio; Novarino, Gaia; Fassio, Anna
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care
2022 Filomena Pirozzi , Matthew Berkseth , Rylee Shear , Lorenzo Gonzalez , Andrew E Timms , Josef Sulc , Emily Pao , Nora Oyama , Francesca Forzano , Valerio Conti , Renzo Guerrini , Emily S Doherty , Sulagna C Saitta, Christina M Lockwood , Colin C Pritchard , William B Dobyns , Edward Novotny , Jason N N Wright , Russell P Saneto, Seth Friedman , Jason Hauptman , Jeffrey Ojemann , Raj P Kapur , Ghayda M Mirzaa.
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues
2025 Di Meo D.; Sorelli M.; Ramazzotti J.; Cheli F.; Bradley S.; Perego L.; Lorenzon B.; Mazzamuto G.; Emmi A.; Porzionato A.; De Caro R.; Garbelli R.; Biancheri D.; Pelorosso C.; Conti V.; Guerrini R.; Pavone F.S.; Costantini I.
RICTOR variants are associated with neurodevelopmental disorders
2025 Carapito, Raphael; Molitor, Anne; Pavinato, Lisa; Skeyni, Alaa; Lambert, Magalie; Pichot, Angélique; Jiang, Jiuhong; Spinnhirny, Perrine; Zimmermann, Lucie; Boucher, Philippe; Chung, Clara W T; Elserafy, Noha; Blair, Edward M; Li, Dong; Elisabeth, Bhoj; Kotzaeridou, Urania; Karch, Stephanie; Wagner, Matias; Lunsing, Roelineke J; Pfundt, Rolph; Boycott, Kym M; Bruel, Ange-Line; Mau-Them, Frédéric Tran; Moutton, Sébastien; Conti, Valerio; Mei, Davide; Cetica, Valentina; Guerrini, Renzo; Brunet, Theresa; Rump, Patrick; Mussa, Alessandro; Brusco, Alfredo; Lemire, Gabrielle; de Vries, Bert B A; Miao, Zhichao; Isidor, Bertrand; Bahram, Seiamak
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 3D human brain digital istopatology | 2018 | Costantini I.; Mazzamuto G.; Silvestri L.; Neri M.; Roffilli M.; Conti V.; Guerrini R.; Sacconi L.; Pavone F.S. | |
| 3D reconstruction and analysis of four human brain cortex samples with two-photon fluorescence microscopy | 2020 | I. Constantini; G. Mazzamuto; M. Roffilli; A. Laurino; F. Castelli; M. Neri; G. Lughi; A. Simonetto; E. Lazzeri; L. Pesce; C. Destrieux; L. Silvestri; V. Conti; R. Guerrini; F. Pavone | |
| A versatile clearing agent for multi-modal brain imaging | 2015 | Costantini, Irene; Ghobril, Jean-Pierre; Di Giovanna, Antonino Paolo; Mascaro, Anna Letizia Allegra; Silvestri, Ludovico; Müllenbroich, Marie Caroline; Onofri, Leonardo; Conti, Valerio; Vanzi, Francesco; Sacconi, Leonardo; Guerrini, Renzo; Markram, Henry; Iannello, Giulio; Pavone, Francesco Saverio | |
| Bi-allelic variants in TM2D3 cause a severe syndromic neurodevelopmental disorder associated with endoplasmic reticulum and mitochondrial abnormalities | 2025 | Gabillard-Lefort, Claudie; Martinez, Caroline Silveira; Gueguen, Naïg; Desquiret-Dumas, Valérie; Wery, Méline; Legoff, Louis; Guimier, Anne; Rondeau, Sophie; Barcia, Giulia; Barnerias, Christine; Cogne, Benjamin; Besnard, Thomas; Lorino, Elsa; Douglas, Jessica; Bodamer, Olaf; Vetro, Annalisa; Guerrini, Renzo; Balestrini, Simona; Conti, Valerio; Siri, Laura; Chevrollier, Arnaud; Bris, Céline; Colin, Estelle; Procaccio, Vincent; Prunier-Mirebeau, Delphine; Lenaers, Guy; Khiati, Salim; Nizon, Mathilde; Baris, Olivier R | |
| Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course | 2019 | Alessandro Esposito, Antonio Falace, Matias Wagner, Moran Gal, Davide Mei, Valerio Conti, Tiziana Pisano, Davide Aprile, Maria Sabina Cerullo, Antonio De Fusco, Silvia Giovedì, Annette Seibt, Daniella Magen, Tilman Polster, Ayelet Eran, Sarah L Stenton, Chiara Fiorillo, Sarit Ravid, Ertan Mayatepek, Hava Hafner, Saskia Wortmann, Erez Y Levanon, Carla Marini, Hanna Mandel, Fabio Benfenati, Felix Distelmaier, Anna Fassio, Renzo Guerrini | |
| Computer-based automatic identification of neurons in gigavoxel-sized 3D human brain images | 2015 | Soda, Paolo; Acciai, Ludovica; Cordelli, Ermanno; Costantini, Irene; Sacconi, Leonardo; Pavone, Francesco Saverio; Conti, Valerio; Guerrini, Renzo; Frasconi, Paolo; Iannello, Giulio | |
| Corrigendum to 'Angiocentric glioma-associated seizures: The possible role of EATT2, pyruvate carboxylase and glutamine synthetase [Seizure: European Journal of Epilepsy 86 (2021) 152-154] | 2021 | Buccoliero, Anna Maria; Caporalini, Chiara; Scagnet, Mirko; Mussa, Federico; Giordano, Flavio; Sardi, Iacopo; Migliastro, Irene; Moscardi, Selene; Conti, Valerio; Barba, Carmen; Antonelli, Manila; Gianno, Francesca; Rossi, Sabrina; Diomedi-Camassei, Francesca; Gessi, Marco; Donofrio, Vittoria; Bertero, Luca; Giangaspero, Felice; Santi, Mariarita; Aronica, Eleonora; Genitori, Lorenzo; Guerrini, Renzo | |
| Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum | 2023 | Guerrini, Renzo; Conti, Valerio; Mantegazza, Massimo; Balestrini, Simona; Galanopoulou, Aristea S; Benfenati, Fabio | |
| Epileptic encephalopathies and progressive neurodegeneration | 2024 | Guerrini, R; Conti, V | |
| Fiber-probe optical spectroscopy discriminates normal brain from focal cortical dysplasia in pediatric subjects | 2017 | Anand S.; Cicchi R.; Giordano F.; Conti V.; Buccoliero A.M.; Guerrini R.; Pavone F.S. | |
| International consensus recommendations on the diagnostic work-up for malformations of cortical development | 2020 | Oegema, Renske; Barakat, Tahsin Stefan; Wilke, Martina; Stouffs, Katrien; Amrom, Dina; Aronica, Eleonora; Bahi-Buisson, Nadia; Conti, Valerio; Fry, Andrew E; Geis, Tobias; Andres, David Gomez; Parrini, Elena; Pogledic, Ivana; Said, Edith; Soler, Doriette; Valor, Luis M; Zaki, Maha S; Mirzaa, Ghayda; Dobyns, William B; Reiner, Orly; Guerrini, Renzo; Pilz, Daniela T; Hehr, Ute; Leventer, Richard J; Jansen, Anna C; Mancini, Grazia M S; Di Donato, Nataliya | |
| Large-scale, cell-resolution volumetric mapping allows layer-specific investigation of human brain cytoarchitecture | 2021 | Irene Costantini and Giacomo Mazzamuto and Matteo Roffilli and Annunziatina Laurino and Filippo Maria Castelli and Mattia Neri and Giovanni Lughi and Andrea Simonetto and Erica Lazzeri and Luca Pesce and Christophe Destrieux and Ludovico Silvestri and Valerio Conti and Renzo Guerrini and Francesco Saverio Pavone | |
| Leat-associated seizures the possible role of EAAT2, pyruvate carboxylase and glutamine synthetase | 2024 | Buccoliero, Anna Maria; Caporalini, Chiara; Moscardi, Selene; Cetica, Valentina; Mei, Davide; Conti, Valerio; Nozzoli, Filippo; Bonaudo, Camilla; Battista, Francesca; Giordano, Flavio; Mura, Regina; Spacca, Barbara; Mussa, Federico; D'Onofrio, Vittoria; Guerrini, Renzo; Genitori, Lorenzo; Scagnet, Mirko | |
| Lesional and non-lesional epilepsies: A blurring genetic boundary. | 2020 | Guerrini R, Parrini E, Esposito A, Fassio A, Conti V | |
| Multimodal fiber-probe spectroscopy allows detecting epileptogenic focal cortical dysplasia in children | 2017 | Anand, Suresh; Cicchi, Riccardo; Giordano, Flavio; Conti, Valerio; Buccoliero, Anna Maria; Guerrini, Renzo; Pavone, Francesco Saverio | |
| Myxoid glioneuronal tumor: Histopathologic, neuroradiologic, and molecular features in a single center series. | 2023 | Caporalini C, Scagnet M, Giunti L, Cetica V, Mei D, Conti V, Moscardi S, Macconi L, Giordano F, D'Incerti L, Genitori L, Guerrini R, Buccoliero AM. | |
| Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis | 2022 | Guerrini, Renzo; Mei, Davide; Kerti-Szigeti, Katalin; Pepe, Sara; Koenig, Mary Kay; Von Allmen, Gretchen; Cho, Megan T; McDonald, Kimberly; Baker, Janice; Bhambhani, Vikas; Powis, Zöe; Rodan, Lance; Nabbout, Rima; Barcia, Giulia; Rosenfeld, Jill A; Bacino, Carlos A; Mignot, Cyril; Power, Lillian H; Harris, Catharine J; Marjanovic, Dragan; Møller, Rikke S; Hammer, Trine B; Keski Filppula, Riikka; Vieira, Päivi; Hildebrandt, Clara; Sacharow, Stephanie; Maragliano, Luca; Benfenati, Fabio; Lachlan, Katherine; Benneche, Andreas; Petit, Florence; de Sainte Agathe, Jean-Madeleine; Hallinan, Barbara; Si, Yue; Wentzensen, Ingrid M; Zou, Fanggeng; Narayanan, Vinodh; Matsumoto, Naomichi; Boncristiano, Alessandra; la Marca, Giancarlo; Kato, Mitsuhiro; Anderson, Kristin; Barba, Carmen; Sturiale, Luisa; Garozzo, Domenico; Bei, Roberto; Masuelli, Laura; Conti, Valerio; Novarino, Gaia; Fassio, Anna | |
| Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care | 2022 | Filomena Pirozzi , Matthew Berkseth , Rylee Shear , Lorenzo Gonzalez , Andrew E Timms , Josef Sulc , Emily Pao , Nora Oyama , Francesca Forzano , Valerio Conti , Renzo Guerrini , Emily S Doherty , Sulagna C Saitta, Christina M Lockwood , Colin C Pritchard , William B Dobyns , Edward Novotny , Jason N N Wright , Russell P Saneto, Seth Friedman , Jason Hauptman , Jeffrey Ojemann , Raj P Kapur , Ghayda M Mirzaa. | |
| Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues | 2025 | Di Meo D.; Sorelli M.; Ramazzotti J.; Cheli F.; Bradley S.; Perego L.; Lorenzon B.; Mazzamuto G.; Emmi A.; Porzionato A.; De Caro R.; Garbelli R.; Biancheri D.; Pelorosso C.; Conti V.; Guerrini R.; Pavone F.S.; Costantini I. | |
| RICTOR variants are associated with neurodevelopmental disorders | 2025 | Carapito, Raphael; Molitor, Anne; Pavinato, Lisa; Skeyni, Alaa; Lambert, Magalie; Pichot, Angélique; Jiang, Jiuhong; Spinnhirny, Perrine; Zimmermann, Lucie; Boucher, Philippe; Chung, Clara W T; Elserafy, Noha; Blair, Edward M; Li, Dong; Elisabeth, Bhoj; Kotzaeridou, Urania; Karch, Stephanie; Wagner, Matias; Lunsing, Roelineke J; Pfundt, Rolph; Boycott, Kym M; Bruel, Ange-Line; Mau-Them, Frédéric Tran; Moutton, Sébastien; Conti, Valerio; Mei, Davide; Cetica, Valentina; Guerrini, Renzo; Brunet, Theresa; Rump, Patrick; Mussa, Alessandro; Brusco, Alfredo; Lemire, Gabrielle; de Vries, Bert B A; Miao, Zhichao; Isidor, Bertrand; Bahram, Seiamak |