Ngā hua rapu - 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? mā Andrew McLean‐Tooke

    I whakaputaina 2003
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  2. 2
    Immunodeficiency and Autoimmunity in 22q11.2 Deletion Syndrome

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

    I whakaputaina 2007
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    Revisão
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  3. 3
    Immunologic defects in 22q11.2 deletion syndrome

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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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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? mā Andrew McLean‐Tooke, Catherine Aldridge, Sheila Waugh, Gavin P Spickett, Lesley Kay

    I whakaputaina 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 mā Chris R. Dipper, Sohom Maitra, Reena Thomas, Christopher A Lamb, Andrew McLean‐Tooke, Rachel Ward, DOUGLAS W. SMITH, G Spickett, John Mansfield

    I whakaputaina 2009
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa
    Artigo
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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 mā 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

    I whakaputaina 2008
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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