Risultati della ricerca - D Barge

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  1. 1
    Lymphocyte subsets in term and significantly preterm UK infants in the first year of life analysed by single platform flow cytometry

    Lymphocyte subsets in term and significantly preterm UK infants in the first year of life analysed by single platform flow cytometry di Janet Berrington, D Barge, Alan Fenton, A J Cant, Gavin P Spickett

    Pubblicazione 2005
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  2. 2
    Immunologic defects in 22q11.2 deletion syndrome

    Immunologic defects in 22q11.2 deletion syndrome di Andrew McLean‐Tooke, D Barge, Gavin P Spickett, Andrew R. Gennery

    Pubblicazione 2008
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  3. 3
    Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome

    Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome di Andrew R. Gennery, D Barge, John O’Sullivan, Terry Flood, Mario Abinun, AJ Cant

    Pubblicazione 2002
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  4. 4
    Inflammatory and autoimmune manifestations in X-linked carriers of chronic granulomatous disease in the United Kingdom

    Inflammatory and autoimmune manifestations in X-linked carriers of chronic granulomatous disease in the United Kingdom di Alexandra Battersby, Helen Braggins, Mark S. Pearce, Catherine M. Cale, Siobhán O. Burns, Scott Hackett, Stephen Hughes, D Barge, David Goldblatt, Andrew R. Gennery

    Pubblicazione 2017
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  5. 5
    Unrelated donor and HLA‐identical sibling haematopoietic stem cell transplantation cure chronic granulomatous disease with good long‐term outcome and growth

    Unrelated donor and HLA‐identical sibling haematopoietic stem cell transplantation cure chronic granulomatous disease with good long‐term outcome and growth di Elena Soncini, Mary Slatter, Laura Jones, Stephen Hughes, Stephen Hodges, Terence Flood, D Barge, Gavin P Spickett, Graham Jackson, Matthew Collin, Mario Abinun, Andrew J. Cant, Andrew R. Gennery

    Pubblicazione 2009
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  6. 6
    Mutations in <i>CHD7</i> in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome

    Mutations in <i>CHD7</i> in patients with CHARGE syndrome cause T–B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome di Andrew R. Gennery, Mary Slatter, Jason Rice, Lies H. Hoefsloot, D Barge, Andrew McLean‐Tooke, Tara Montgomery, JA Goodship, Alastair D. Burt, Terry Flood, Mario Abinun, A J Cant, Diana Johnson

    Pubblicazione 2008
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  7. 7
    Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells

    Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells di Neil V. Morgan, Sarah Goddard, Tony S. Cardno, David McDonald, Fatimah Rahman, D Barge, A. Ciupek, Anna Straatman-Iwanowska, Shanaz Pasha, Mary Guckian, Graham Anderson, Aarnoud Huissoon, Andrew J. Cant, Warren P. Tate, Sophie Hambleton, Eamonn R. Maher

    Pubblicazione 2011
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  8. 8
    Hematopoietic stem cell transplantation for CTLA4 deficiency

    Hematopoietic stem cell transplantation for CTLA4 deficiency di Mary Slatter, Karin R. Engelhardt, Lauri M. Burroughs, Peter D. Arkwright, Zohreh Nademi, Suzanne Skoda‐Smith, David Hagin, Alan Kennedy, D Barge, Terence Flood, Mario Abinun, Robert Wynn, Andrew R. Gennery, Andrew J. Cant, David M. Sansom, Sophie Hambleton, Troy R. Torgerson

    Pubblicazione 2016
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  9. 9
    New graft manipulation strategies improve the outcome of mismatched stem cell transplantation in children with primary immunodeficiencies

    New graft manipulation strategies improve the outcome of mismatched stem cell transplantation in children with primary immunodeficiencies di Reem Elfeky, Ravi Shah, Mohamed Najib Mohamed Unni, Giorgio Ottaviano, Kanchan Rao, Robert Chiesa, Persis Amrolia, Austen Worth, Terry Flood, Mario Abinun, Sophie Hambleton, Andrew J. Cant, Kimberly Gilmour, Stuart Adams, Gul Ahsan, D Barge, Andrew R. Gennery, Waseem Qasim, Mary Slatter, Paul Veys

    Pubblicazione 2019
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  10. 10
    Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency

    Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency di Tarana Singh Dang, Joseph D. P. Willet, Helen Griffin, Neil V. Morgan, Graeme O’Boyle, Peter D. Arkwright, Stephen Hughes, Mario Abinun, Louise Tee, D Barge, Karin R. Engelhardt, Michael R. Jackson, Andrew J. Cant, Eamonn R. Maher, Mauro Santibáñez Koref, Louise N. Reynard, Simi Ali, Sophie Hambleton

    Pubblicazione 2016
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  11. 11
    T-cell receptor αβ+ and CD19+ cell–depleted haploidentical and mismatched hematopoietic stem cell transplantation in primary immune deficiency

    T-cell receptor αβ+ and CD19+ cell–depleted haploidentical and mismatched hematopoietic stem cell transplantation in primary immune deficiency di Ravi Shah, Reem Elfeky, Zohreh Nademi, Waseem Qasim, Persis Amrolia, Robert Chiesa, Kanchan Rao, Giovanna Lucchini, Juliana Silva, Austen Worth, D Barge, David G. Ryan, Jane Conn, Andrew J. Cant, Roderick Skinner, Intan Juliana Abd Hamid, Terence Flood, Mario Abinun, Sophie Hambleton, Andrew R. Gennery, Paul Veys, Mary Slatter

    Pubblicazione 2017
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