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Clinical and Experimental Immunology|April 1, 1979
Histochemical studies for 5'-nucleotidase and alpha-naphthyl (non-specific) esterase in lymphocytes from patients with primary immunoglobulin deficienciesN Matamoros, D A Horwitz, C Newton, et al.
Clinical Immunology and Immunopathology|September 1, 1995
Structural basis for X-linked agammaglobulinemia (XLA): mutations at interacting Btk residues R562, W563, and A582H S Maniar, M Vihinen, A D Webster, et al.
Clinical and Experimental Immunology|April 1, 1989
Defective DNA synthesis by T cells in acquired 'common-variable' hypogammaglobulinaemia on stimulation with mitogensM E North, G P Spickett, J Allsop, et al.
Clinical and Experimental Immunology|September 6, 2000
Deficiency in circulating natural killer (NK) cell subsets in common variable immunodeficiency and X-linked agammaglobulinaemiaR M Aspalter, W A Sewell, K Dolman, et al.
Clinical and Experimental Immunology|February 1, 1987
Increased half-life of gammaglobulin after prolonged intravenous replacement therapyA M Lever, P L Yap, B Cuthbertson, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|July 24, 2015
Getting it right! Enhancing youth involvement in mental health researchLauren Mawn, Patrick Welsh, Lauren Kirkpatrick, et al.
Clinical and Experimental Immunology|September 1, 1989
Recovery of antibody production after HIV infection in 'common' variable hypogammaglobulinaemiaA D Webster, A Lever, G Spickett, et al.
The Journal of Investigative Dermatology|October 1, 1984
Cutaneous basophil hypersensitivity to inhalant allergens in atopic dermatitis patients: elicitation of delayed responses containing basophils following local transfer of immune serum but not IgE antibodyE B Mitchell, J Crow, S Rowntree, et al.
Gut|February 1, 1981
Coeliac disease with severe hypogammaglobulinaemiaA D Webster, G Slavin, M Shiner, et al.
The Journal of Infection|June 7, 2000
Detection of Mycoplasma fermentans in healthy students and patients with congenital immunodeficiencyJ G Ainsworth, S Hourshid, A D Webster, et al.
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