CETICA, VALENTINA
CETICA, VALENTINA
Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino (NEUROFARBA)
Clinical and molecular characterization of patients with YWHAG-related epilepsy
2024 Cetica, Valentina; Pisano, Tiziana; Lesca, Gaetan; Marafi, Dana; Licchetta, Laura; Riccardi, Florence; Mei, Davide; Chung, Hon-Yin B; Bayat, Allan; Balasubramanian, Meena; Lowenstein, Daniel H; Endzinienė, Milda; Alotaibi, Maha; Villeneuve, Nathalie; Jacobs, Julia; Isidor, Bertrand; Solazzi, Roberta; den Hollander, Nicolette S; Marjanovic, Dragan; Rougeot-Jung, Christelle; Jung, Julien; Lesieur-Sebellin, Marion; Accogli, Andrea; Salpietro, Vincenzo; Saadi, Nebal W; Panagiotakaki, Eleni; Foiadelli, Thomas; Redon, Sylvia; Tsai, Meng-Han; Bisulli, Francesca; Hammer, Trine B; Lupski, James R; Parrini, Elena; Guerrini, Renzo
Clinico-pathological and molecular characteristics of pediatric-juvenile pituitary neuroendocrine tumors (PitNETs): A mono-institutional series
2025 Buccoliero, Anna Maria; Giunti, Laura; Ponticelli, Abramo; Innocenti, Lorenzo; Ricci, Franco; Cetica, Valentina; Tirinnanzi, Bianca; Moscardi, Selene; Stagi, Stefano; Sardi, Iacopo; Mussa, Federico; Genitori, Lorenzo; Scagnet, Mirko
Double gonosomal mosaicism as an unusual hereditary mechanism in familial GRIN2A-related disorder
2024 Cetica, Valentina; Cavallin, Mara; Ricci, Maria Luisa; Mandorlini, Claudia; Bartolini, Emanuele; Parrini, Elena; Guerrini, Renzo
Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies
2019 Mei D, Cetica V, Marini C, Guerrini R,
Familial Hemophagocytic Lymphohistiocytosis May Present during Adulthood: Clinical and Genetic Features of a Small Series
2012 Sieni, Elena; Cetica, Valentina; Piccin, Andrea; Gherlinzoni, Filippo; Sasso, Ferdinando Carlo; Rabusin, Marco; Attard, Luciano; Bosi, Alberto; Pende, Daniela; Moretta, Lorenzo; Aricò, Maurizio
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
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.
Opioid response in paediatric cancer patients and the Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene: an Italian study on 87 cancer children and a systematic review
2019 Lucenteforte E.; Vannacci A.; Crescioli G.; Lombardi N.; Vagnoli L.; Giunti L.; Cetica V.; Coniglio M.L.; Pugi A.; Bonaiuti R.; Arico M.; Giglio S.; Messeri A.; Barale R.; Giovannelli L.; Mugelli A.; Maggini V.
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
STOP Pain Project—Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways
2022 Crescioli G.; Lombardi N.; Vagnoli L.; Bettiol A.; Giunti L.; Cetica V.; Coniglio M.L.; Provenzano A.; Giglio S.; Bonaiuti R.; Mugelli A.; Arico M.; Messeri A.; Vannacci A.; Maggini V.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Clinical and molecular characterization of patients with YWHAG-related epilepsy | 2024 | Cetica, Valentina; Pisano, Tiziana; Lesca, Gaetan; Marafi, Dana; Licchetta, Laura; Riccardi, Florence; Mei, Davide; Chung, Hon-Yin B; Bayat, Allan; Balasubramanian, Meena; Lowenstein, Daniel H; Endzinienė, Milda; Alotaibi, Maha; Villeneuve, Nathalie; Jacobs, Julia; Isidor, Bertrand; Solazzi, Roberta; den Hollander, Nicolette S; Marjanovic, Dragan; Rougeot-Jung, Christelle; Jung, Julien; Lesieur-Sebellin, Marion; Accogli, Andrea; Salpietro, Vincenzo; Saadi, Nebal W; Panagiotakaki, Eleni; Foiadelli, Thomas; Redon, Sylvia; Tsai, Meng-Han; Bisulli, Francesca; Hammer, Trine B; Lupski, James R; Parrini, Elena; Guerrini, Renzo | |
| Clinico-pathological and molecular characteristics of pediatric-juvenile pituitary neuroendocrine tumors (PitNETs): A mono-institutional series | 2025 | Buccoliero, Anna Maria; Giunti, Laura; Ponticelli, Abramo; Innocenti, Lorenzo; Ricci, Franco; Cetica, Valentina; Tirinnanzi, Bianca; Moscardi, Selene; Stagi, Stefano; Sardi, Iacopo; Mussa, Federico; Genitori, Lorenzo; Scagnet, Mirko | |
| Double gonosomal mosaicism as an unusual hereditary mechanism in familial GRIN2A-related disorder | 2024 | Cetica, Valentina; Cavallin, Mara; Ricci, Maria Luisa; Mandorlini, Claudia; Bartolini, Emanuele; Parrini, Elena; Guerrini, Renzo | |
| Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies | 2019 | Mei D, Cetica V, Marini C, Guerrini R, | |
| Familial Hemophagocytic Lymphohistiocytosis May Present during Adulthood: Clinical and Genetic Features of a Small Series | 2012 | Sieni, Elena; Cetica, Valentina; Piccin, Andrea; Gherlinzoni, Filippo; Sasso, Ferdinando Carlo; Rabusin, Marco; Attard, Luciano; Bosi, Alberto; Pende, Daniela; Moretta, Lorenzo; Aricò, Maurizio | |
| 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 | |
| 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. | |
| Opioid response in paediatric cancer patients and the Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene: an Italian study on 87 cancer children and a systematic review | 2019 | Lucenteforte E.; Vannacci A.; Crescioli G.; Lombardi N.; Vagnoli L.; Giunti L.; Cetica V.; Coniglio M.L.; Pugi A.; Bonaiuti R.; Arico M.; Giglio S.; Messeri A.; Barale R.; Giovannelli L.; Mugelli A.; Maggini V. | |
| 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 | |
| STOP Pain Project—Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways | 2022 | Crescioli G.; Lombardi N.; Vagnoli L.; Bettiol A.; Giunti L.; Cetica V.; Coniglio M.L.; Provenzano A.; Giglio S.; Bonaiuti R.; Mugelli A.; Arico M.; Messeri A.; Vannacci A.; Maggini V. |