Hasil Pencarian - Marina Lanciotti

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  1. 1
    Digenic mutations in severe congenital neutropenia

    Digenic mutations in severe congenital neutropenia oleh Manuela Germeshausen, Cornelia Zeidler, Manfred Stuhrmann, Marina Lanciotti, Matthias Ballmaier, Karl Welte

    Diterbitkan 2010-07-01
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  2. 2
    The molecular pathogenesis of craniopharyngiomas

    The molecular pathogenesis of craniopharyngiomas oleh Marina Lanciotti Campanini, João Paulo Almeida, Clarissa Silva Martins, Margaret de Castro

    Diterbitkan 2023-02-01
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  3. 3
    Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins

    Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins oleh Cristina Olivieri, Anna Mondino, Matteo Chinello, Alessandra Risso, Enrico Finale, Marina Lanciotti, Andrea Guala

    Diterbitkan 2017-10-01
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  4. 4
    Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia

    Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia oleh Marina Lanciotti, Stefania Indaco, Sonia Bonanomi, Tiziana Coliva, Elena Mastrodicasa, Gianluca Caridi, Michaela Calvillo, Carlo Dufour

    Diterbitkan 2010-01-01
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  5. 5
    Autoimmune Neutropenia and Immune-Dysregulation in a Patient Carrying a <i>TINF2</i> Variant

    Autoimmune Neutropenia and Immune-Dysregulation in a Patient Carrying a <i>TINF2</i> Variant oleh Benedetta Chianucci, Alice Grossi, Gianluca Dell'Orso, Elena Palmisani, Marina Lanciotti, Paola Terranova, Filomena Pierri, Michela Lupia, Luca Arcuri, Marica Laurino, Isabella Ceccherini, Fabian Beier, Carlo Dufour, Francesca Fioredda, Maurizio Miano

    Diterbitkan 2022-11-01
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  6. 6
    Underlying Inborn Errors of Immunity in Patients With Evans Syndrome and Multilineage Cytopenias: A Single-Centre Analysis

    Underlying Inborn Errors of Immunity in Patients With Evans Syndrome and Multilineage Cytopenias: A Single-Centre Analysis oleh Maurizio Miano, Daniela Guardo, Alice Grossi, Elena Palmisani, Francesca Fioredda, Paola Terranova, Enrico Cappelli, Michela Lupia, Monica Traverso, Gianluca Dell’Orso, Fabio Corsolini, Andrea Beccaria, Marina Lanciotti, Isabella Ceccherini, Carlo Dufour

    Diterbitkan 2022-05-01
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  7. 7
    PB2052: THE HEMATOLOGICAL SIDE OF TNFRSF13B/TACI: A MONOCENTRIC EXPERIENCE

    PB2052: THE HEMATOLOGICAL SIDE OF TNFRSF13B/TACI: A MONOCENTRIC EXPERIENCE oleh Andrea Beccaria, Marina Lanciotti, Maria Carla Giarratana, Elena Palmisani, Isabella Ceccherini, Alice Grossi, Roberta Caorsi, Marco Gattorno, Paola Terranova, Michela Lupia, Domenico Coviello, Massimo Maffei, Sabrina Zanardi, Maurizio Miano, Carlo Dufour, Francesca Fioredda

    Diterbitkan 2023-08-01
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  8. 8
    Infection risk in patients with autoimmune cytopenias and immune dysregulation treated with mycophenolate mofetil and sirolimus

    Infection risk in patients with autoimmune cytopenias and immune dysregulation treated with mycophenolate mofetil and sirolimus oleh Mattia Comella, Mattia Comella, Elena Palmisani, Marcello Mariani, Gianluca Dell’Orso, Maria Licciardello, Maria Carla Giarratana, Luca Arcuri, Sara Pestarino, Alice Grossi, Marina Lanciotti, Giorgia Brucci, Daniela Guardo, Giovanna Russo, Carlo Dufour, Francesca Fioredda, Elio Castagnola, Maurizio Miano

    Diterbitkan 2024-05-01
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  9. 9
    Changes in cytokine profile pre- and post-immunosuppression in acquired aplastic anemia

    Changes in cytokine profile pre- and post-immunosuppression in acquired aplastic anemia oleh Carlo Dufour, Elisa Ferretti, Francesca Bagnasco, Oriana Burlando, Marina Lanciotti, Ugo Ramenghi, Paola Saracco, Maria Teresa Van Lint, Daniela Longoni, Giovanni Fernando Torelli, Marta Pillon, Anna Locasciulli, Aldo Misuraca, Milena La Spina, Andrea Bacigalupo, Vito Pistoia, Anna Corcione, Johanna Svahn

    Diterbitkan 2009-12-01
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  10. 10
    P756: IMPAIRED MITOCHONDRIAL FUNCTION AND MARROW FAILURE IN PATIENTS CARRYING A MUTATION ON SRSF4 GENE

    P756: IMPAIRED MITOCHONDRIAL FUNCTION AND MARROW FAILURE IN PATIENTS CARRYING A MUTATION ON SRSF4 GENE oleh Maurizio Miano, Nadia Bertola, Alice Grossi, Gianluca Dell’orso, Stefano Regis, Francesca Fioredda, Michela Lupia, Marina Lanciotti, Elena Palmisani, Maria Carla Giarratana, Luca Arcuri, Fabio Corsolini, Marta Rusmini, Paolo Uva, Diego Vozzi, Isabella Ceccherini, Silvia Ravera, Enrico Cappelli, Carlo Dufour

    Diterbitkan 2023-08-01
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  11. 11
    Mutational analysis of ribosomal proteins in a cohort of pediatric patients with T-cell acute lymphoblastic leukemia reveals Q123R, a novel mutation in RPL10

    Mutational analysis of ribosomal proteins in a cohort of pediatric patients with T-cell acute lymphoblastic leukemia reveals Q123R, a novel mutation in RPL10 oleh Lorenza Bacci, Lorenza Bacci, Valentina Indio, Guglielmo Rambaldelli, Cristina Bugarin, Franco Magliocchetti, Franco Magliocchetti, Alberto Del Rio, Alberto Del Rio, Daniela Pollutri, Daniela Pollutri, Fraia Melchionda, Andrea Pession, Marina Lanciotti, Carlo Dufour, Giuseppe Gaipa, Lorenzo Montanaro, Lorenzo Montanaro, Marianna Penzo, Marianna Penzo

    Diterbitkan 2022-11-01
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  12. 12
    Impaired Mitochondrial Function and Marrow Failure in Patients Carrying a Variant of the <i>SRSF4</i> Gene

    Impaired Mitochondrial Function and Marrow Failure in Patients Carrying a Variant of the <i>SRSF4</i> Gene oleh Maurizio Miano, Nadia Bertola, Alice Grossi, Gianluca Dell’Orso, Stefano Regis, Marta Rusmini, Paolo Uva, Diego Vozzi, Francesca Fioredda, Elena Palmisani, Michela Lupia, Marina Lanciotti, Federica Grilli, Fabio Corsolini, Luca Arcuri, Maria Carla Giarratana, Isabella Ceccherini, Carlo Dufour, Enrico Cappelli, Silvia Ravera

    Diterbitkan 2024-02-01
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  13. 13
    Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?

    Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities? oleh Elena Palmisani, Maurizio Miano, Alice Grossi, Marina Lanciotti, Michela Lupia, Paola Terranova, Isabella Ceccherini, Eugenia Montanari, Michaela Calvillo, Filomena Pierri, Concetta Micalizzi, Rosario Maggiore, Daniela Guardo, Sabrina Zanardi, Elena Facchini, Angela Maggio, Elena Mastrodicasa, Paola Corti, Giovanna Russo, Marta Pillon, Piero Farruggia, Simone Cesaro, Angelica Barone, Francesca Tosetti, Ugo Ramenghi, Nicoletta Crescenzio, Jack Bleesing, Carlo Dufour, Francesca Fioredda

    Diterbitkan 2023-03-01
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  14. 14
    Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia

    Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia oleh Amy L. Sherborne, Kari Hemminki, Rajiv Kumar, Claus R. Bartram, Martin Stanulla, Martin Schrappe, Eleni Petridou, Ágnes F. Semsei, Csaba Szalai, Daniel Sinnett, Maja Krajinovic, Jasmine Healy, Marina Lanciotti, Carlo Dufour, Stefania Indaco, Eman A El-Ghouroury, Ruchchadol Sawangpanich, Suradej Hongeng, Samart Pakakasama, Anna Gonzalez-Neira, Evelia L. Ugarte, Valeria P. Leal, Juan P.M. Espinoza, Azza M. Kamel, Gamal T.A. Ebid, Eman R. Radwan, Serap Yalin, Erdinc Yalin, Mehmet Berkoz, Jill Simpson, Eve Roman, Tracy Lightfoot, Fay J. Hosking, Jayaram Vijayakrishnan, Mel Greaves, Richard S. Houlston

    Diterbitkan 2011-07-01
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