Search Results - "Aricò, Maurizio"

Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry by Cetica, Valentina, PhD, Sieni, Elena, MD, Pende, Daniela, PhD, Danesino, Cesare, MD, De Fusco, Carmen, MD, Locatelli, Franco, MD, Micalizzi, Concetta, MD, Putti, Maria Caterina, MD, Biondi, Andrea, MD, Fagioli, Franca, MD, Moretta, Lorenzo, MD, Griffiths, Gillian M., PhD, Luzzatto, Lucio, MD, Aricò, Maurizio, MD

“…Background Hemophagocytic lymphohistiocytosis (HLH) is a rare life-threatening disease affecting mostly children but also adults and characterized by…”
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Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosis by Gadner, Helmut, Minkov, Milen, Grois, Nicole, Pötschger, Ulrike, Thiem, Elfriede, Aricò, Maurizio, Astigarraga, Itziar, Braier, Jorge, Donadieu, Jean, Henter, Jan-Inge, Janka-Schaub, Gritta, McClain, Kenneth L., Weitzman, Sheila, Windebank, Kevin, Ladisch, Stephan

“…Langerhans cell histiocytosis (LCH)-III tested risk-adjusted, intensified, longer treatment of multisystem LCH (MS-LCH), for which optimal therapy has been…”
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Dexamethasone vs prednisone in induction treatment of pediatric ALL: results of the randomized trial AIEOP-BFM ALL 2000 by Möricke, Anja, Zimmermann, Martin, Valsecchi, Maria Grazia, Stanulla, Martin, Biondi, Andrea, Mann, Georg, Locatelli, Franco, Cazzaniga, Giovanni, Niggli, Felix, Aricò, Maurizio, Bartram, Claus R., Attarbaschi, Andishe, Silvestri, Daniela, Beier, Rita, Basso, Giuseppe, Ratei, Richard, Kulozik, Andreas E., Lo Nigro, Luca, Kremens, Bernhard, Greiner, Jeanette, Parasole, Rosanna, Harbott, Jochen, Caruso, Roberta, von Stackelberg, Arend, Barisone, Elena, Rössig, Claudia, Conter, Valentino, Schrappe, Martin

“…Induction therapy for childhood acute lymphoblastic leukemia (ALL) traditionally includes prednisone; yet, dexamethasone may have higher antileukemic potency,…”
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Imatinib after induction for treatment of children and adolescents with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (EsPhALL): a randomised, open-label, intergroup study by Biondi, Andrea, Prof, Schrappe, Martin, Prof, De Lorenzo, Paola, PhD, Castor, Anders, PhD, Lucchini, Giovanna, MD, Gandemer, Virginie, MD, Pieters, Rob, Prof, Stary, Jan, MD, Escherich, Gabriele, MD, Campbell, Myriam, MD, Li, Chi-Kong, MD, Vora, Ajay, MD, Aricò, Maurizio, MD, Röttgers, Silja, PhD, Saha, Vaskar, Prof, Valsecchi, Maria Grazia, Prof

“…Summary Background Trials of imatinib have provided evidence of activity in adults with Philadelphia-chromosome-positive acute lymphoblastic leukaemia (ALL),…”
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2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative by Ravelli, Angelo, Minoia, Francesca, Davì, Sergio, Horne, AnnaCarin, Bovis, Francesca, Pistorio, Angela, Aricò, Maurizio, Avcin, Tadej, Behrens, Edward M, De Benedetti, Fabrizio, Filipovic, Lisa, Grom, Alexei A, Henter, Jan-Inge, Ilowite, Norman T, Jordan, Michael B, Khubchandani, Raju, Kitoh, Toshiyuki, Lehmberg, Kai, Lovell, Daniel J, Miettunen, Paivi, Nichols, Kim E, Ozen, Seza, Pachlopnik Schmid, Jana, Ramanan, Athimalaipet V, Russo, Ricardo, Schneider, Rayfel, Sterba, Gary, Uziel, Yosef, Wallace, Carol, Wouters, Carine, Wulffraat, Nico, Demirkaya, Erkan, Brunner, Hermine I, Martini, Alberto, Ruperto, Nicolino, Cron, Randy Q

“…To develop criteria for the classification of macrophage activation syndrome (MAS) in patients with systemic juvenile idiopathic arthritis (JIA). A multistep…”
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Predictive value of minimal residual disease in Philadelphia-chromosome-positive acute lymphoblastic leukemia treated with imatinib in the European intergroup study of post-induction treatment of Philadelphia-chromosome-positive acute lymphoblastic leukemia, based on immunoglobulin/T-cell receptor and BCR/ABL1 methodologies by Cazzaniga, Giovanni, De Lorenzo, Paola, Alten, Julia, Röttgers, Silja, Hancock, Jeremy, Saha, Vaskar, Castor, Anders, Madsen, Hans O, Gandemer, Virginie, Cavé, Hélène, Leoni, Veronica, Köhler, Rolf, Ferrari, Giulia M, Bleckmann, Kirsten, Pieters, Rob, van der Velden, Vincent, Stary, Jan, Zuna, Jan, Escherich, Gabriele, Stadt, Udo Zur, Aricò, Maurizio, Conter, Valentino, Schrappe, Martin, Valsecchi, Maria Grazia, Biondi, Andrea

“…The prognostic value of minimal residual disease (MRD) in Philadelphia-chromosome-positive (Ph+) childhood acute lymphoblastic leukemia (ALL) treated with…”
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Childhood high-risk acute lymphoblastic leukemia in first remission: results after chemotherapy or transplant from the AIEOP ALL 2000 study by Conter, Valentino, Valsecchi, Maria Grazia, Parasole, Rosanna, Putti, Maria Caterina, Locatelli, Franco, Barisone, Elena, Lo Nigro, Luca, Santoro, Nicola, Aricò, Maurizio, Ziino, Ottavio, Pession, Andrea, Testi, Anna Maria, Micalizzi, Concetta, Casale, Fiorina, Zecca, Marco, Casazza, Gabriella, Tamaro, Paolo, La Barba, Gaetano, Notarangelo, Lucia Dora, Silvestri, Daniela, Colombini, Antonella, Rizzari, Carmelo, Biondi, Andrea, Masera, Giuseppe, Basso, Giuseppe

“…The outcome of high-risk (HR) acute lymphoblastic leukemia patients enrolled in the AIEOP-BFM ALL 2000 study in Italy is described. HR criteria were minimal…”
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Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding by Cetica, Valentina, PhD, Hackmann, Yvonne, PhD, Grieve, Samantha, Sieni, Elena, MD, Ciambotti, Benedetta, PhD, Coniglio, Maria Luisa, PhD, Pende, Daniela, PhD, Gilmour, Kimberly, MD, Romagnoli, Paolo, MD, Griffiths, Gillian M., PhD, Aricò, Maurizio, MD

“…Background Familial hemophagocytic lymphohistiocytosis (FHL) is a rare and often fatal disorder characterized by defective cellular cytotoxicity and…”
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The use of quantitative ultrasound in a tertiary-level children hospital: role in the follow-up of chronically ill patients by Tummolo, Albina, Brunetti, Giacomina, Giordano, Mario, Carbone, Vincenza, Faienza, Maria Felicia, Aricò, Maurizio, Pesce, Sabino

“…Purpose To evaluate the use of QUS for the bone status assessment in children cared because of a chronic disease such as: inherited metabolic disorder, kidney…”
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Outcome of primary hemophagocytic lymphohistiocytosis: a report on 143 patients from the Italian Registry by Pegoraro, Francesco, Chinnici, Aurora, Beneforti, Linda, Tanturli, Michele, Trambusti, Irene, De Fusco, Carmela, Micalizzi, Concetta, Barat, Veronica, Cesaro, Simone, Gaspari, Stefania, Dell'Acqua, Fabiola, Todesco, Alessandra, Timeus, Fabio, Aricò, Maurizio, Favre, Claudio, Tondo, Annalisa, Coniglio, Maria Luisa, Sieni, Elena

“…Primary hemophagocytic lymphohistiocytosis (pHLH) is a severe, life-threatening hyperinflammatory syndrome caused by defects in genes of the granule-dependent…”
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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 by 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

“…Genetic polymorphisms in genes involved in pain modulation have been reported to be associated to opioid efficacy and safety in different clinical settings…”
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Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3 by 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

“…Mutations of UNC13D are causative for familial haemophagocytic lymphohistiocytosis type 3 (FHL3; OMIM 608898). To carry out a genotype-phenotype study of…”
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Single-Day Trimethoprim/Sulfamethoxazole Prophylaxis for Pneumocystis Pneumonia in Children with Cancer by Caselli, Désirée, MD, Petris, Maria Grazia, MD, Rondelli, Roberto, MD, Carraro, Francesca, MD, Colombini, Antonella, MD, Muggeo, Paola, MD, Ziino, Ottavio, MD, Melchionda, Fraia, MD, Russo, Giovanna, MD, Pierani, Paolo, MD, Soncini, Elena, MD, DeSantis, Raffaella, MD, Zanazzo, Giulio, MD, Barone, Angelica, MD, Cesaro, Simone, MD, Cellini, Monica, MD, Mura, Rossella, MD, Milano, Giuseppe M., MD, Meazza, Cristina, MD, Cicalese, Maria P., MD, Tropia, Serena, MD, De Masi, Salvatore, MD, Castagnola, Elio, MD, Aricò, Maurizio, MD

“…Objective To determine whether a simplified, 1-day/week regimen of trimethoprim/sulfamethoxazole is sufficient to prevent Pneumocystis ( jirovecii [ carinii ])…”
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Long-Term Results of a Randomized Trial on Extended Use of High Dose l-Asparaginase for Standard Risk Childhood Acute Lymphoblastic Leukemia by PESSION, Andrea, VALSECCHI, Maria Grazia, BASSO, Gmseppe, ARICO, Maurizio, MASERA, Giuseppe, KAMPS, Willem A, MAGYAROSY, Edina, RIZZARI, Carmelo, VAN WERING, Elisabeth R, LO NIGRO, Luca, VAN DER DOES, Anna, LOCATELLI, Franco

“…Between September 1991 and May 1997, within the International Berlin-Frankfurt-Muenster Study Group (I-BFM-SG), a randomized study was performed aimed at…”
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Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation by Henter, Jan-Inge, Samuelsson-Horne, AnnaCarin, Aricò, Maurizio, Egeler, R. Maarten, Elinder, Göran, Filipovich, Alexandra H., Gadner, Helmut, Imashuku, Shinsaku, Komp, Diane, Ladisch, Stephan, Webb, David, Janka, Gritta

“…Hemophagocytic lymphohistiocytosis (HLH) comprises familial (primary) hemophagocytic lymphohistiocytosis (FHL) and secondary HLH (SHLH), both clinically…”
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Marriage and parenthood among childhood cancer survivors: a report from the Italian AIEOP Off-Therapy Registry by PIVETTA, Emanuele, MAULE, Milena M, KIREN, Valentina, LOCATELLI, Franco, PALUMBO, Giovanna, PESSION, Andrea, PILLON, Marta, SANTORO, Nicola, TERENZIANI, Monica, GRAZIA VALSECCHI, Maria, DAMA, Elisa, MAGNANI, Corrado, PISANI, Paola, MERLETTI, Franco, PASTORE, Guido, ZUGNA, Daniela, HAUPT, Riccardo, JANKOVIC, Momcilo, ARICO, Maurizio, CASALE, Fiorina, CLERICO, Anna, CORDERO DI MONTEZEMOLO, Luca

“…The aim of this study was to describe the patterns of marriage and parenthood in a cohort of childhood cancer survivors included in the Off-Therapy Registry…”
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Timely follow-up of a GATA2 deficiency patient allows successful treatment by Ciullini Mannurita, Sara, MSc, Vignoli, Marina, PhD, Colarusso, Gloria, MD, PhD, Tucci, Fabio, MD, Veltroni, Marinella, MD, Frenos, Stefano, MD, Tintori, Veronica, MD, Aricò, Maurizio, MD, Bigley, Venetia, MD, PhD, Collin, Matthew, MD, PhD, Favre, Claudio, MD, Gambineri, Eleonora, MD

“…[...]because of the onset of MDS, at age 9 years, he underwent hematopoietic stem cell transplant from his HLA-matched (GATA2 wild-type) brother. Cytogenetic…”
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Correction to: The use of quantitative ultrasound in a tertiary-level children hospital: role in the follow-up of chronically ill patients by Tummolo, Albina, Brunetti, Giacomina, Giordano, Mario, Carbone, Vincenza, Faienza, Maria Felicia, Aricò, Maurizio, Pesce, Sabino

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Langerhans cell histiocytosis in children: from the bench to bedside for an updated therapy by Arico, Maurizio

“…Summary Langerhans cell histiocytosis (LCH) is a rare disease, affecting subjects of any age, with extremely variable clinical manifestations. Although most…”
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Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis by Meazza, Raffaella, PhD, Tuberosa, Claudia, PhD, Cetica, Valentina, PhD, Falco, Michela, PhD, Parolini, Silvia, PhD, Grieve, Sam, PhD, Griffiths, Gillian M., PhD, Sieni, Elena, MD, Marcenaro, Stefania, PhD, Micalizzi, Concetta, MD, Montin, Davide, MD, Fagioli, Franca, MD, Moretta, Alessandro, MD, Mingari, Maria C., PhD, Moretta, Lorenzo, MD, Notarangelo, Luigi D., MD, Bottino, Cristina, MD, Aricò, Maurizio, MD, Pende, Daniela, PhD

“…Background Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening, heterogeneous, hyperinflammmatory disorder. Prompt identification of inherited forms…”
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