نتائج البحث - Andrew McLean‐Tooke

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  1. 1
    Adrenaline in the treatment of anaphylaxis: what is the evidence?

    Adrenaline in the treatment of anaphylaxis: what is the evidence? حسب Andrew McLean‐Tooke

    منشور في 2003
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  2. 2
    Immunodeficiency and Autoimmunity in 22q11.2 Deletion Syndrome

    Immunodeficiency and Autoimmunity in 22q11.2 Deletion Syndrome حسب Andrew McLean‐Tooke, Gavin P Spickett, Andrew R. Gennery

    منشور في 2007
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  3. 3
    Immunologic defects in 22q11.2 deletion syndrome

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

    منشور في 2008
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  4. 4
    Methotrexate, rheumatoid arthritis and infection risk--what is the evidence?

    Methotrexate, rheumatoid arthritis and infection risk--what is the evidence? حسب Andrew McLean‐Tooke, Catherine Aldridge, Sheila Waugh, Gavin P Spickett, Lesley Kay

    منشور في 2009
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  5. 5
    Anti‐tissue transglutaminase antibodies in the follow‐up of adult coeliac disease

    Anti‐tissue transglutaminase antibodies in the follow‐up of adult coeliac disease حسب Chris R. Dipper, Sohom Maitra, Reena Thomas, Christopher A Lamb, Andrew McLean‐Tooke, Rachel Ward, DOUGLAS W. SMITH, G Spickett, John Mansfield

    منشور في 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 حسب 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

    منشور في 2008
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  7. 7
    Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

    Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes حسب Ulrich Salzer, Chiara Bacchelli, Sylvie Buckridge, Qiang Pan‐Hammarström, Stephanie Jennings, V Lougaris, Astrid Bergbreiter, Tina Hagena, Jennifer Birmelin, Alessandro Plebani, A. David B. Webster, Hans-Hartmut Peter, Daniel Suez, Helen Chapel, Andrew McLean‐Tooke, Gavin P Spickett, Stephanie Añover-Sombke, Hans D. Ochs, Simon Urschel, Bernd H. Belohradsky, Sanja Ugrinović, Dinakantha Kumararatne, Tatiana Lawrence, Are Martin Holm, José Luis Franco, Ilka Schulze, Pascal Schneider, E. Michael Gertz, Alejandro A. Schäffer, Lennart Hammarström, Adrian J. Thrasher, H. Bobby Gaspar, Bodo Grimbacher

    منشور في 2008
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