FERESE, ROSANGELA
FERESE, ROSANGELA
A Single Nucleotide ADA Genetic Variant Is Associated to Central Inflammation and Clinical Presentation in MS: Implications for Cladribine Treatment
2020 Stampanoni Bassi, Mario; Buttari, Fabio; Simonelli, Ilaria; Gilio, Luana; Furlan, Roberto; Finardi, Annamaria; Marfia, Girolama Alessandra; Visconti, Andrea; Paolillo, Andrea; Storto, Marianna; Gambardella, Stefano; Ferese, Rosangela; Salvetti, Marco; Uccelli, Antonio; Matarese, Giuseppe; Centonze, Diego; De Vito, Francesca
Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants
2021 Ferese, R.; Campopiano, R.; Scala, S.; D'Alessio, C.; Storto, M.; Buttari, F.; Centonze, D.; Logroscino, G.; Zecca, C.; Zampatti, S.; Fornai, F.; Cianci, V.; Manfroi, E.; Giardina, E.; Magnani, M.; Suppa, A.; Novelli, G.; Gambardella, S.
Decipher non-canonical SPAST splicing mutations with the help of functional assays in patients affected by spastic paraplegia 4 (SPG4)
2022 Ferese, Rosangela; Scala, Simona; Suppa, Antonio; Campopiano, Rosa; Asci, Francesco; Chiaravalloti, Maria Antonietta; Zampogna, Alessandro; D'Alessio, Carmelo; Fittipaldi, Filomena; Buttari, Fabio; Di Pardo, Alba; Giardina, Emiliano; Zampatti, Stefania; Fornai, Francesco; Novelli, Giuseppe; Fanelli, Mirco; Zecca, Chiara; Logroscino, Giancarlo; Centonze, Diego; Gambardella, Stefano
Embracing Monogenic Parkinson's Disease. The MJFF Global Genetic PD Cohort
2023 Vollstedt, Eva-Juliane; Schaake, Susen; Lohmann, Katja; Padmanabhan, Shalini; Brice, Alexis; Lesage, Suzanne; Tesson, Christelle; Vidailhet, Marie; Wurster, Isabel; Hentati, Faycel; Mirelman, Anat; Giladi, Nir; Marder, Karen; Waters, Cheryl; Fahn, Stanley; Kasten, Meike; Brüggemann, Norbert; Borsche, Max; Foroud, Tatiana; Tolosa, Eduardo; Garrido, Alicia; Annesi, Grazia; Gagliardi, Monica; Bozi, Maria; Stefanis, Leonidas; Ferreira, Joaquim J; Correia Guedes, Leonor; Avenali, Micol; Petrucci, Simona; Clark, Lorraine; Fedotova, Ekaterina Y; Abramycheva, Natalya Y; Alvarez, Victoria; Menéndez-González, Manuel; Jesús Maestre, Silvia; Gómez-Garre, Pilar; Mir, Pablo; Belin, Andrea Carmine; Ran, Caroline; Lin, Chin-Hsien; Kuo, Ming-Che; Crosiers, David; Wszolek, Zbigniew K; Ross, Owen A; Jankovic, Joseph; Nishioka, Kenya; Funayama, Manabu; Clarimon, Jordi; Williams-Gray, Caroline H; Camacho, Marta; Cornejo-Olivas, Mario; Torres-Ramirez, Luis; Wu, Yih-Ru; Lee-Chen, Guey-Jen; Morgadinho, Ana; Pulkes, Teeratorn; Termsarasab, Pichet; Berg, Daniela; Kuhlenbäumer, Gregor; Kühn, Andrea A; Borngräber, Friederike; de Michele, Giuseppe; De Rosa, Anna; Zimprich, Alexander; Puschmann, Andreas; Mellick, George D; Dorszewska, Jolanta; Carr, Jonathan; Ferese, Rosangela; Gambardella, Stefano; Chase, Bruce; Markopoulou, Katerina; Satake, Wataru; Toda, Tatsushi; Rossi, Malco; Merello, Marcelo; Lynch, Timothy; Olszewska, Diana A; Lim, Shen-Yang; Ahmad-Annuar, Azlina; Tan, Ai Huey; Al-Mubarak, Bashayer; Hanagasi, Hasmet; Koziorowski, Dariusz; Ertan, Sibel; Genç, Gençer; de Carvalho Aguiar, Patricia; Barkhuizen, Melinda; Pimentel, Marcia M G; Saunders-Pullman, Rachel; van de Warrenburg, Bart; Bressman, Susan; Toft, Mathias; Appel-Cresswell, Silke; Lang, Anthony E; Skorvanek, Matej; Boon, Agnita J W; Krüger, Rejko; Sammler, Esther M; Tumas, Vitor; Zhang, Bao-Rong; Garraux, Gaetan; Chung, Sun Ju; Kim, Yun Joong; Winkelmann, Juliane; Sue, Carolyn M; Tan, Eng-King; Damásio, Joana; Klivényi, Péter; Kostic, Vladimir S; Arkadir, David; Martikainen, Mika; Borges, Vanderci; Hertz, Jens Michael; Brighina, Laura; Spitz, Mariana; Suchowersky, Oksana; Riess, Olaf; Das, Parimal; Mollenhauer, Brit; Gatto, Emilia M; Petersen, Maria Skaalum; Hattori, Nobutaka; Wu, Ruey-Meei; Illarioshkin, Sergey N; Valente, Enza Maria; Aasly, Jan O; Aasly, Anna; Alcalay, Roy N; Thaler, Avner; Farrer, Matthew J; Brockmann, Kathrin; Corvol, Jean-Christophe; Klein, Christine
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect
2018 Ferese, R.; Bonetti, M.; Consoli, F.; Guida, V.; Sarkozy, A.; Lepri, F. R.; Versacci, P.; Gambardella, S.; Calcagni, G.; Margiotti, K.; Piceci Sparascio, F.; Hozhabri, H.; Mazza, T.; Digilio, M. C.; Dallapiccola, B.; Tartaglia, M.; Hertog, J. D.; De Luca, A.; Marino, Bruno
Heterozygous pla2g6 mutation leads to iron accumulation within basal ganglia and parkinson's disease
2018 Ferese, Rosangela; Scala, Simona; 1, Francesca Biagioni; Giardina, Emiliano; Zampatti, Stefania; Modugno, Nicola; Colonnese, Claudio; Storto, Marianna; Fornai, Francesco; Novelli, Giuseppe; Ruggieri and Stefano Gambardella, Stefano
Rapamycin ameliorates defects in mitochondrial fission and mitophagy in glioblastoma cells
2021 Lenzi, P.; Ferese, R.; Biagioni, F.; Fulceri, F.; Busceti, C. L.; Falleni, A.; Gambardella, S.; Frati, A.; Fornai, F.
Rapamycin promotes differentiation increasing βIII-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells
2017 Ferrucci, Michela; Biagioni, Francesca; Lenzi, Paola; Gambardella, Stefano; Ferese, Rosangela; Calierno, Maria Teresa; Falleni, Alessandra; Grimaldi, Alfonso; Frati, Alessandro; Esposito, Vincenzo; Limatola, Cristina; Fornai, Francesco
The Autophagy-Related Organelle Autophagoproteasome Is Suppressed within Ischemic Penumbra
2021 Biagioni, Francesca; Mastroiacovo, Federica; Lenzi, Paola; Puglisi-Allegra, Stefano; Busceti, Carla L; Ryskalin, Larisa; Ferese, Rosangela; Bucci, Domenico; Frati, Alessandro; Nicoletti, Ferdinando; Fornai, Francesco
Vacuolar Protein Sorting Genes in Parkinson's Disease: A Re-appraisal of Mutations Detection Rate and Neurobiology of Disease
2016 Gambardella, Stefano; Biagioni, Francesca; Ferese, Rosangela; Busceti, Carla L; Frati, Alessandro; Novelli, Giuseppe; Ruggieri, Stefano; Fornai, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A Single Nucleotide ADA Genetic Variant Is Associated to Central Inflammation and Clinical Presentation in MS: Implications for Cladribine Treatment | 2020 | Stampanoni Bassi, Mario; Buttari, Fabio; Simonelli, Ilaria; Gilio, Luana; Furlan, Roberto; Finardi, Annamaria; Marfia, Girolama Alessandra; Visconti, Andrea; Paolillo, Andrea; Storto, Marianna; Gambardella, Stefano; Ferese, Rosangela; Salvetti, Marco; Uccelli, Antonio; Matarese, Giuseppe; Centonze, Diego; De Vito, Francesca | |
| Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants | 2021 | Ferese, R.; Campopiano, R.; Scala, S.; D'Alessio, C.; Storto, M.; Buttari, F.; Centonze, D.; Logroscino, G.; Zecca, C.; Zampatti, S.; Fornai, F.; Cianci, V.; Manfroi, E.; Giardina, E.; Magnani, M.; Suppa, A.; Novelli, G.; Gambardella, S. | |
| Decipher non-canonical SPAST splicing mutations with the help of functional assays in patients affected by spastic paraplegia 4 (SPG4) | 2022 | Ferese, Rosangela; Scala, Simona; Suppa, Antonio; Campopiano, Rosa; Asci, Francesco; Chiaravalloti, Maria Antonietta; Zampogna, Alessandro; D'Alessio, Carmelo; Fittipaldi, Filomena; Buttari, Fabio; Di Pardo, Alba; Giardina, Emiliano; Zampatti, Stefania; Fornai, Francesco; Novelli, Giuseppe; Fanelli, Mirco; Zecca, Chiara; Logroscino, Giancarlo; Centonze, Diego; Gambardella, Stefano | |
| Embracing Monogenic Parkinson's Disease. The MJFF Global Genetic PD Cohort | 2023 | Vollstedt, Eva-Juliane; Schaake, Susen; Lohmann, Katja; Padmanabhan, Shalini; Brice, Alexis; Lesage, Suzanne; Tesson, Christelle; Vidailhet, Marie; Wurster, Isabel; Hentati, Faycel; Mirelman, Anat; Giladi, Nir; Marder, Karen; Waters, Cheryl; Fahn, Stanley; Kasten, Meike; Brüggemann, Norbert; Borsche, Max; Foroud, Tatiana; Tolosa, Eduardo; Garrido, Alicia; Annesi, Grazia; Gagliardi, Monica; Bozi, Maria; Stefanis, Leonidas; Ferreira, Joaquim J; Correia Guedes, Leonor; Avenali, Micol; Petrucci, Simona; Clark, Lorraine; Fedotova, Ekaterina Y; Abramycheva, Natalya Y; Alvarez, Victoria; Menéndez-González, Manuel; Jesús Maestre, Silvia; Gómez-Garre, Pilar; Mir, Pablo; Belin, Andrea Carmine; Ran, Caroline; Lin, Chin-Hsien; Kuo, Ming-Che; Crosiers, David; Wszolek, Zbigniew K; Ross, Owen A; Jankovic, Joseph; Nishioka, Kenya; Funayama, Manabu; Clarimon, Jordi; Williams-Gray, Caroline H; Camacho, Marta; Cornejo-Olivas, Mario; Torres-Ramirez, Luis; Wu, Yih-Ru; Lee-Chen, Guey-Jen; Morgadinho, Ana; Pulkes, Teeratorn; Termsarasab, Pichet; Berg, Daniela; Kuhlenbäumer, Gregor; Kühn, Andrea A; Borngräber, Friederike; de Michele, Giuseppe; De Rosa, Anna; Zimprich, Alexander; Puschmann, Andreas; Mellick, George D; Dorszewska, Jolanta; Carr, Jonathan; Ferese, Rosangela; Gambardella, Stefano; Chase, Bruce; Markopoulou, Katerina; Satake, Wataru; Toda, Tatsushi; Rossi, Malco; Merello, Marcelo; Lynch, Timothy; Olszewska, Diana A; Lim, Shen-Yang; Ahmad-Annuar, Azlina; Tan, Ai Huey; Al-Mubarak, Bashayer; Hanagasi, Hasmet; Koziorowski, Dariusz; Ertan, Sibel; Genç, Gençer; de Carvalho Aguiar, Patricia; Barkhuizen, Melinda; Pimentel, Marcia M G; Saunders-Pullman, Rachel; van de Warrenburg, Bart; Bressman, Susan; Toft, Mathias; Appel-Cresswell, Silke; Lang, Anthony E; Skorvanek, Matej; Boon, Agnita J W; Krüger, Rejko; Sammler, Esther M; Tumas, Vitor; Zhang, Bao-Rong; Garraux, Gaetan; Chung, Sun Ju; Kim, Yun Joong; Winkelmann, Juliane; Sue, Carolyn M; Tan, Eng-King; Damásio, Joana; Klivényi, Péter; Kostic, Vladimir S; Arkadir, David; Martikainen, Mika; Borges, Vanderci; Hertz, Jens Michael; Brighina, Laura; Spitz, Mariana; Suchowersky, Oksana; Riess, Olaf; Das, Parimal; Mollenhauer, Brit; Gatto, Emilia M; Petersen, Maria Skaalum; Hattori, Nobutaka; Wu, Ruey-Meei; Illarioshkin, Sergey N; Valente, Enza Maria; Aasly, Jan O; Aasly, Anna; Alcalay, Roy N; Thaler, Avner; Farrer, Matthew J; Brockmann, Kathrin; Corvol, Jean-Christophe; Klein, Christine | |
| Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect | 2018 | Ferese, R.; Bonetti, M.; Consoli, F.; Guida, V.; Sarkozy, A.; Lepri, F. R.; Versacci, P.; Gambardella, S.; Calcagni, G.; Margiotti, K.; Piceci Sparascio, F.; Hozhabri, H.; Mazza, T.; Digilio, M. C.; Dallapiccola, B.; Tartaglia, M.; Hertog, J. D.; De Luca, A.; Marino, Bruno | |
| Heterozygous pla2g6 mutation leads to iron accumulation within basal ganglia and parkinson's disease | 2018 | Ferese, Rosangela; Scala, Simona; 1, Francesca Biagioni; Giardina, Emiliano; Zampatti, Stefania; Modugno, Nicola; Colonnese, Claudio; Storto, Marianna; Fornai, Francesco; Novelli, Giuseppe; Ruggieri and Stefano Gambardella, Stefano | |
| Rapamycin ameliorates defects in mitochondrial fission and mitophagy in glioblastoma cells | 2021 | Lenzi, P.; Ferese, R.; Biagioni, F.; Fulceri, F.; Busceti, C. L.; Falleni, A.; Gambardella, S.; Frati, A.; Fornai, F. | |
| Rapamycin promotes differentiation increasing βIII-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells | 2017 | Ferrucci, Michela; Biagioni, Francesca; Lenzi, Paola; Gambardella, Stefano; Ferese, Rosangela; Calierno, Maria Teresa; Falleni, Alessandra; Grimaldi, Alfonso; Frati, Alessandro; Esposito, Vincenzo; Limatola, Cristina; Fornai, Francesco | |
| The Autophagy-Related Organelle Autophagoproteasome Is Suppressed within Ischemic Penumbra | 2021 | Biagioni, Francesca; Mastroiacovo, Federica; Lenzi, Paola; Puglisi-Allegra, Stefano; Busceti, Carla L; Ryskalin, Larisa; Ferese, Rosangela; Bucci, Domenico; Frati, Alessandro; Nicoletti, Ferdinando; Fornai, Francesco | |
| Vacuolar Protein Sorting Genes in Parkinson's Disease: A Re-appraisal of Mutations Detection Rate and Neurobiology of Disease | 2016 | Gambardella, Stefano; Biagioni, Francesca; Ferese, Rosangela; Busceti, Carla L; Frati, Alessandro; Novelli, Giuseppe; Ruggieri, Stefano; Fornai, Francesco |