Search Results - L. D. Notarangelo

  • Showing 1 - 10 results of 10
Refine Results
  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... by Fabio Facchetti, C Appiani, Lucia Salvi, J Levy, L. D. Notarangelo

    Published 1995
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Studies of the expression of the Wiskott-Aldrich syndrome protein.

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

    Published 1996
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by Alba Pilotta, Patrizia Mella, M. Filisetti, Barbara Felappi, Elena Prandi, Gaspare Parrinello, L. D. Notarangelo, Fabio Buzi

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    X-chromosome inactivation analysis in a female carrier of FOXP3 mutation

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

    Published 2002
    Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.

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

    Published 1994
    Get full text
    Artigo
    Save to List
    Saved in:
  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,... by L. D. Notarangelo, Jean‐Laurent Casanova, Mary Ellen Conley, Helen Chapel, Albert Fischer, Jennifer M. Puck, Chaim M. Roifman, Reinhard Seger, Raif S. Geha

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2010
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 1996
    Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2006
    Get full text
    Carta
    Save to List
    Saved in:
  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 by 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

    Published 2001
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: