Familial hypogammaglobulinemia with variable serum immunoglobulins. Concordance with lymphocyte ecto-5'-nucleotidase deficiency.
暂无分享,去创建一个
H. Sampson | K. Rich | I. Fox | L. N. Edwards
[1] J. Cassidy,et al. Lymphocyte 5'-nucleotidase deficiency in hypogammaglobulinemia: clinical characteristics. , 1980, Clinical immunology and immunopathology.
[2] P. Daddona,et al. Immunoreconstitution by peripheral blood leukocytes in adenosine deaminase-deficient severe combined immunodeficiency. , 1980, The Journal of clinical investigation.
[3] B. Mitchell,et al. Purinogenic immunodeficiency diseases: clinical features and molecular mechanisms. , 1980, Annals of internal medicine.
[4] T. Waldmann,et al. Ecto-5'-nucleotidase activity in T and B lymphocytes from normal subjects and patients with congenital X-linked agammaglobulinemia. , 1979, Journal of immunology.
[5] T. Palella,et al. Cellular immune deficiency with autoimmune hemolytic anemia in purine nucleoside phosphorylase deficiency. , 1979, The American journal of medicine.
[6] E. Gelfand,et al. Distribution of 5'-nucleotidase in human lymphoid tissues. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[7] J. Cassidy,et al. Lymphocyte ecto-5'-nucleotidase deficiency in agammaglobulinemia. , 1978, Science.
[8] R. Good,et al. Role of helper, suppressor and B-cell defects in the pathogenesis of the hypogammaglobulinemias. , 1978, The New England journal of medicine.
[9] E. Gelfand,et al. Partial deficiency of purine nucleoside phosphorylase: studies of purine and pyrimidine metabolism. , 1978, The Journal of laboratory and clinical medicine.
[10] G. Asherson,et al. Purine metabolism in lymphocytes from patients with primary hypogammaglobulinaemia. , 1978, Clinical and experimental immunology.
[11] G. Asherson,et al. LYMPHOCYTE PURINE 5'-NUCLEOTIDASE DEFICIENCY IN PRIMARY HYPOGAMMAGLOBULINÆMIA , 1977, The Lancet.
[12] K. Bloch,et al. Familial variable immunodeficiency: autosomal dominant pattern of inheritance with variable expression of the defect(s). , 1975, The Journal of pediatrics.
[13] T. Waldmann,et al. Role of suppressor T cells in pathogenesis of common variable hypogammaglobulinaemia. , 1974, Lancet.
[14] R. Goldblum,et al. X-linked B lymphocyte deficiencyI. Panhypo-?-globulinemia and dys-?-globulinemia in siblings , 1974 .
[15] R. Geha,et al. Heterogeneity of "acquired" or common variable agammaglobulinemia. , 1974, The New England journal of medicine.
[16] R. Buckley,et al. Molecular form of adenosine deaminase in severe combined immunodeficiency. , 1974, Biochemical and biophysical research communications.
[17] R. Gilbertsen,et al. Membrane receptors and in vitro responsiveness of lymphocytes in human immunodeficiency. , 1974, Journal of immunology.
[18] R. Good,et al. B and T lymphocytes in primary immunodeficiency disease in man. , 1973, The Journal of clinical investigation.
[19] R. Buckley,et al. Hereditary Alterations in the Immune Response: Coexistence of ‘Agammaglobulinemia', Acquired Hypogammaglobulinemia and Selective Immunoglobulin Deficiency in a Sibship , 1968, Pediatric Research.
[20] N. Edwards,et al. Normal levels of 5'-nucleotidase activity in lymphocytes from patients with x-linked agammaglobulinemia. , 1979, Science.
[21] T. Waldmann,et al. Suppressor cells in the regulation of the immune response. , 1977, Progress in clinical immunology.