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18 results for Cetica,+Valentina

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Familial Hemophagocytic Lymphohistiocytosis May Present during Adulthood: Clinical and Genetic Features of a Small Series
Author / Creator:Sieni, Elena ; Cetica, Valentina ; Piccin, Andrea ; Gherlinzoni, Filippo ; Sasso, Ferdinando Carlo ; Rabusin, Marco ; Attard, Luciano ; Bosi, Alberto ; Pende, Daniela ; Moretta, Lorenzo ; Aricò, Maurizio
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-09, Vol.7 (9), p.e44649-e44649
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STOP Pain Project—Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways
Author / Creator:Crescioli, Giada ; Lombardi, Niccolò ; Vagnoli, Laura ; Bettiol, Alessandra ; Giunti, Laura ; Cetica, Valentina ; Coniglio, Maria Luisa ; Provenzano, Aldesia ; Giglio, Sabrina ; Bonaiuti, Roberto ; Mugelli, Alessandro ; Aricò, Maurizio ; Messeri, Andrea ; Vannacci, Alfredo ; Maggini, Valentina
Publisher:Switzerland: MDPI AG
Journal title:Pharmaceutics, 2022-03, Vol.14 (3), p.619
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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
Author / Creator:Lucenteforte, Ersilia ; Vannacci, Alfredo ; Crescioli, Giada ; Lombardi, Niccolò ; Vagnoli, Laura ; Giunti, Laura ; Cetica, Valentina ; Coniglio, Maria Luisa ; Pugi, Alessandra ; Bonaiuti, Roberto ; Aricò, Maurizio ; Giglio, Sabrina ; Messeri, Andrea ; Barale, Roberto ; Giovannelli, Lisa ; Mugelli, Alessandro ; Maggini, Valentina
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2019-01, Vol.19 (1), p.113-113, Article 113
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Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants
Author / Creator:Panza, Norman ; Bianchini, Claudia ; Cetica, Valentina ; Balestrini, Simona ; Barba, Carmen ; Ferrari, Anna Rita ; Mei, Davide ; Parmeggiani, Lucio ; Parrini, Elena ; Guerrini, Renzo
Publisher:United States: John Wiley & Sons, Inc
Journal title:Epilepsia open, 2024-02, Vol.9 (1), p.417-423
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Familial hemophagocytic lymphohistiocytosis: a model for understanding the human machinery of cellular cytotoxicity
Author / Creator:Sieni, Elena ; Cetica, Valentina ; Mastrodicasa, Elena ; Pende, Daniela ; Moretta, Lorenzo ; Griffiths, Gillian ; Aricò, Maurizio
Publisher:Basel: SP Birkhäuser Verlag Basel
Journal title:Cellular and molecular life sciences : CMLS, 2012-01, Vol.69 (1), p.29-40
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Variations of the UNC13D Gene in Patients with Autoimmune Lymphoproliferative Syndrome
Author / Creator:Aricò, Maurizio ; Boggio, Elena ; Cetica, Valentina ; Melensi, Matteo ; Orilieri, Elisabetta ; Clemente, Nausicaa ; Cappellano, Giuseppe ; Buttini, Sara ; Soluri, Maria Felicia ; Comi, Cristoforo ; Dufour, Carlo ; Pende, Daniela ; Dianzani, Irma ; Ellis, Steven R. ; Pagliano, Sara ; Marcenaro, Stefania ; Ramenghi, Ugo ; Chiocchetti, Annalisa ; Dianzani, Umberto
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-07, Vol.8 (7), p.e68045-e68045
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Double gonosomal mosaicism as an unusual hereditary mechanism in familial GRIN2A-related disorder
Author / Creator:Cetica, Valentina ; Cavallin, Mara ; Ricci, Maria Luisa ; Mandorlini, Claudia ; Bartolini, Emanuele ; Parrini, Elena ; Guerrini, Renzo
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2024-10, Vol.61 (10), p.999-1002
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Clinico-pathological and molecular characteristics of pediatric-juvenile pituitary neuroendocrine tumors (PitNETs): A mono-institutional series
Author / Creator: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
Publisher:Germany
Journal title:Clinical neuropathology, 2025-06
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National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy
Author / Creator:Mei, Davide ; Balestrini, Simona ; Parrini, Elena ; Gambardella, Antonio ; Annesi, Grazia ; De Giorgis, Valentina ; Gana, Simone ; Bassi, Maria Teresa ; Zucca, Claudio ; Elia, Maurizio ; Vetri, Luigi ; Castellotti, Barbara ; Ragona, Francesca ; Mastrangelo, Mario ; Pisani, Francesco ; d'Orsi, Giuseppe ; Carella, Massimo ; Pruna, Dario ; Giglio, Sabrina ; Marini, Carla ; Cesaroni, Elisabetta ; Riva, Antonella ; Scala, Marcello ; Licchetta, Laura ; Minardi, Raffaella ; Contaldo, Ilaria ; Gambardella, Maria Luigia ; Cossu, Alberto ; Proietti, Jacopo ; Cantalupo, Gaetano ; Trivisano, Marina ; De Dominicis, Angela ; Specchio, Nicola ; Tassi, Laura ; Guerrini, Renzo ; Cellini, Elena ; Cetica, Valentina ; De Vita, Dalila ; Mandorlini, Claudia ; Pucatti, Daniela ; Rutigliano, Domenico ; Virdò, Simona ; Fortunato, Francesco ; Gagliardi, Monica ; Talarico, Mariagrazia ; Valente, Enza Maria ; Tartara, Elena ; Galimberti, Carlo Andrea ; Pasca, Ludovica ; Mambretti, Fabiana ; Bonanni, Paolo ; De Rinaldis, Marta ; Calì, Francesco ; Vinci, Mirella ; Musumeci, Antonino ; Messina, Giuliana ; Gellera, Cinzia ; Granata, Tiziana ; Freri, Elena ; Solazzi, Roberta ; Canafoglia, Laura ; Ricciardi, Giacomina ; Bove, Rossella ; Palumbo, Orazio ; Palumbo, Pietro ; Benvenuto, Mario ; Adragna, Carola ; Cossu, Silvia ; Siliquini, Sabrina ; Cappanera, Silvia ; Iacomino, Michele ; Madia, Francesca ; Striano, Pasquale ; Zara, Federico ; Bisulli, Francesca ; Muccioli, Lorenzo ; Pippucci, Tommaso ; Battaglia, Domenica Immacolata ; Quintiliani, Michela ; Perulli, Marco ; Veredice, Chiara ; Darra, Francesca ; Ghobert, Anna Ludovica ; Fiorini, Elena ; Fontana, Elena ; Terracciano, Alessandra
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2025-01, Vol.62 (1), p.25-31
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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3
Author / Creator:Sieni, Elena ; Cetica, Valentina ; Santoro, Alessandra ; Beutel, Karin ; Mastrodicasa, Elena ; Meeths, Marie ; Ciambotti, Benedetta ; Brugnolo, Francesca ; zur Stadt, Udo ; Pende, Daniela ; Moretta, Lorenzo ; Griffiths, Gillian M ; Henter, Jan-Inge ; Janka, Gritta ; Aricò, Maurizio
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2011-05, Vol.48 (5), p.343-352
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Pediatric brain tumors: mutations of two dioxygenases (hABH2 and hABH3) that directly repair alkylation damage
Author / Creator:Cetica, Valentina ; Genitori, Lorenzo ; Giunti, Laura ; Sanzo, Massimiliano ; Bernini, Gabriella ; Massimino, Maura ; Sardi, Iacopo
Publisher:Boston: Springer US
Journal title:Journal of neuro-oncology, 2009-09, Vol.94 (2), p.195-201
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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5
Author / Creator:Cetica, Valentina ; Santoro, Alessandra ; Gilmour, Kimberly C ; Sieni, Elena ; Beutel, Karin ; Pende, Daniela ; Marcenaro, Stefania ; Koch, Florian ; Grieve, Samantha ; Wheeler, Rachel ; Zhao, Fang ; zur Stadt, Udo ; Griffiths, Gillian M ; Aricò, Maurizio
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2010-09, Vol.47 (9), p.595-600
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Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome
Author / Creator:Giunti, Laura ; Cetica, Valentina ; Ricci, Ugo ; Giglio, Sabrina ; Sardi, Iacopo ; Paglierani, Milena ; Andreucci, Elena ; Sanzo, Massimiliano ; Forni, Marco ; Buccoliero, Anna Maria ; Genitori, Lorenzo ; Genuardi, Maurizio
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2009-07, Vol.17 (7), p.919-927
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Cytophagic histiocytic panniculitis, hemophagocytic lymphohistiocytosis and undetermined autoimmune disorder: reconciling the puzzle
Author / Creator:Pasqualini, Claudia ; Jorini, Mauro ; Carloni, Ines ; Giangiacomi, Mirella ; Cetica, Valentina ; Aricò, Maurizio ; de Benedictis, Fernando Maria
Publisher:England: BioMed Central
Journal title:Italian journal of pediatrics, 2014-02, Vol.40 (1), p.17-17, Article 17
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STXBP2 mutations in children with Familial Hemophagocytic Lymphohistiocytosis type 5
Author / Creator:Cetica, Valentina ; Santoro, Alessandra ; Gilmour, Kimberly ; Sieni, Elena ; Pende, Daniela ; Marcenaro, Stefania ; Koch, Florian ; Grieve, Samantha ; Wheeler, Rachel ; Zhao, Roseanne ; Zur Stadt, Udo ; Griffiths, Gillian M ; Arico', Maurizio
Publisher:BMJ Publishing Group
Journal title:Journal of medical genetics, 2010-08, Vol.47 (9)
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Mutations of familial hemophagocytic lymphohistiocytosis (FHL) related genes and abnormalities of cytotoxicity function tests in patients with macrophage activation syndrome (MAS) occurring in systemi...
Author / Creator:Bracaglia, Claudia ; Sieni, Elena ; Da Ros, Martina ; De Fusco, Carmela ; Micalizzi, Concetta ; Cetica, Valentina ; Ciambotti, Benedetta ; Coniglio, Maria Luisa ; Insalaco, Antonella ; De Benedetti, Fabrizio ; Aricò, Maurizio
Publisher:BioMed Central Ltd
Journal title:Pediatric rheumatology online journal, 2014-09, Vol.12 (S1), p.P53-P53, Article P53
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GENOTYPE-PHENOTYPE STUDY OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS TYPE 3
Author / Creator:Sieni, Elena ; Cetica, Valentina ; Santoro, Alessandra ; Beutel, Karin ; Mastrodicasa, Elena ; Meeths, Marie ; Ciambotti, Benedetta ; Brugnolo, Francesca ; Zur Stadt, Udo ; Pende, Daniela ; Moretta, Lorenzo ; Griffiths, Gillian M. ; Henter, Jan-Inge ; Janka, Gritta ; Arico, Maurizio
Publisher:BMJ Publishing Group
Journal title:Journal of medical genetics, 2011-01, Vol.48 (5)
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Variations of the UNC13D Gene in Patients with Autoimmune Lymphoproliferative Syndrome. e68045
Author / Creator:Arico, Maurizio ; Boggio, Elena ; Cetica, Valentina ; Melensi, Matteo ; Orilieri, Elisabetta ; Clemente, Nausicaa ; Cappellano, Giuseppe ; Buttini, Sara ; Soluri, Maria Felicia ; Comi, Cristoforo
Journal title:PloS one, 2013-07, Vol.8 (7)
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Familial Hemophagocytic Lymphohistiocytosis May Present during Adulthood: Clinical and Genetic Features of a Small Series

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STOP Pain Project—Opioid Response in Pediatric Cancer Patients and Gene Polymorphisms of Cytokine Pathways

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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

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Bilateral temporal lobe dysplasia and seizure onset associated with biallelic CNTNAP2 variants

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Familial hemophagocytic lymphohistiocytosis: a model for understanding the human machinery of cellular cytotoxicity

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Variations of the UNC13D Gene in Patients with Autoimmune Lymphoproliferative Syndrome

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Double gonosomal mosaicism as an unusual hereditary mechanism in familial GRIN2A-related disorder

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Clinico-pathological and molecular characteristics of pediatric-juvenile pituitary neuroendocrine tumors (PitNETs): A mono-institutional series

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National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy

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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3

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Pediatric brain tumors: mutations of two dioxygenases (hABH2 and hABH3) that directly repair alkylation damage

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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5

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Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome

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Cytophagic histiocytic panniculitis, hemophagocytic lymphohistiocytosis and undetermined autoimmune disorder: reconciling the puzzle

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STXBP2 mutations in children with Familial Hemophagocytic Lymphohistiocytosis type 5

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Mutations of familial hemophagocytic lymphohistiocytosis (FHL) related genes and abnormalities of cytotoxicity function tests in patients with macrophage activation syndrome (MAS) occurring in systemi...

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GENOTYPE-PHENOTYPE STUDY OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS TYPE 3

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Variations of the UNC13D Gene in Patients with Autoimmune Lymphoproliferative Syndrome. e68045

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