Resultados de búsqueda - L. D. Notarangelo

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  1. 1
    Immunohistologic analysis of ineffective CD40-CD40 ligand interaction in lymphoid tissues from patients with X-linked immunodeficiency with hyper-IgM. Abortive germinal center cell reaction and severe depletion of follicular dendritic cells.

    Immunohistologic analysis of ineffective CD40-CD40 ligand interaction in lymphoid tissues from patients with X-linked immunodeficiency with hyper-IgM. Abortive germinal center cell... por Fabio Facchetti, C Appiani, Lucia Salvi, J Levy, L. D. Notarangelo

    Publicado 1995
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  2. 2
    Studies of the expression of the Wiskott-Aldrich syndrome protein.

    Studies of the expression of the Wiskott-Aldrich syndrome protein. por Donn M. Stewart, S. Treiber-Held, Carole C. Kurman, Fabio Facchetti, L. D. Notarangelo, David L. Nelson

    Publicado 1996
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  3. 3
    Common Polymorphisms of the Growth Hormone (GH) Receptor Do Not Correlate with the Growth Response to Exogenous Recombinant Human GH in GH-Deficient Children

    Common Polymorphisms of the Growth Hormone (GH) Receptor Do Not Correlate with the Growth Response to Exogenous Recombinant Human GH in GH-Deficient Children por Alba Pilotta, Patrizia Mella, M. Filisetti, Barbara Felappi, Elena Prandi, Gaspare Parrinello, L. D. Notarangelo, Fabio Buzi

    Publicado 2006
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  4. 4
    X-chromosome inactivation analysis in a female carrier of FOXP3 mutation

    X-chromosome inactivation analysis in a female carrier of FOXP3 mutation por Alberto Tommasini, Sérgio Ferrari, Daniele Moratto, Raffaele Badolato, Michele Boniotto, Doroti Pirulli, L. D. Notarangelo, M Andolina

    Publicado 2002
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  5. 5
    Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.

    Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease. por Mauno Vihinen, David Vetrie, Hina S. Maniar, HD Ochs, Qili Zhu, Igor Vor̆echovský, A D Webster, L. D. Notarangelo, Lennart Nilsson, Janusz M. Sowadski

    Publicado 1994
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  6. 6
    Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005

    Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest,... por L. D. Notarangelo, Jean‐Laurent Casanova, Mary Ellen Conley, Helen Chapel, Albert Fischer, Jennifer M. Puck, Chaim M. Roifman, Reinhard Seger, Raif S. Geha

    Publicado 2006
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  7. 7
    PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients

    PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patients por Marcho Chiarini, Cristiano Sabelli, Paola Melotti, Cecília Garlanda, Gianfranco Savoldi, Cinzia Mazza, Rita Padoan, Alessandro Plebani, Alberto Mantovani, L. D. Notarangelo, B.M. Assael, Raffaele Badolato

    Publicado 2010
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  8. 8
    Signaling via IL-2 and IL-4 in JAK3-Deficient Severe Combined Immunodeficiency Lymphocytes: JAK3-Dependent and Independent Pathways

    Signaling via IL-2 and IL-4 in JAK3-Deficient Severe Combined Immunodeficiency Lymphocytes: JAK3-Dependent and Independent Pathways por Scott A. Oakes, Fabio Candotti, James A. Johnston, Yiqing Chen, John J. Ryan, Naomi Taylor, Xiuwen Liu, Lothar Hennighausen, L. D. Notarangelo, William E. Paul, R. Michael Blaese, John J. O'Shea

    Publicado 1996
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  9. 9
    Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis

    Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis por Alessandra Santoro, Sonia Cannella, Giovanna Bossi, Federico Gallo, Antonino Trizzino, Daniela Pende, Francesco Dieli, Giuseppa Bruno, Jane C. Stinchcombe, Concetta Micalizzi, Carmela Fusco, Cesare Danesino, Lorenzo Moretta, L. D. Notarangelo, Gillian M. Griffiths, Maurizio Aricò

    Publicado 2006
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  10. 10
    V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations

    V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations por Anna Villa, Cristina Sobacchi, L. D. Notarangelo, Fabio Bozzi, Mario Abinun, Tore G. Abrahamsen, Peter D. Arkwright, Michal Baniyash, Edward G. Brooks, Mary Ellen Conley, Patricia Cortés, Marzia Duse, Anders Fasth, Alexandra M. Filipovich, Anthony J. Infante, Alison Jones, Evelina Mazzolari, Susanna Müller, Srdjan Pašić, Gideon Rechavi, Maria Grazia Sacco, Sandro Santagata, Marlis L. Schroeder, Reinhard Seger, Dario Strina, Alberto G. Ugazio, Jouni Väliaho, Mauno Vihinen, Larry B. Vogler, Hans D. Ochs, Paolo Vezzoni, Wilhelm Friedrich, Klaus Schwarz

    Publicado 2001
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