Results 71 to 80 of about 215 (110)
Dysgammaglobulinemia in the Presence of Plasma Cells
New England Journal of Medicine, 1965 AS information about the gamma globulins has increased, it has become apparent that these are a heterogeneous group of proteins, varying in molecular size, antigenicity and electrophoretic mobility...
John J Condemi +2 more
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Inherited Dysgammaglobulinemia of Chickens
, 1981 Disorders of the immune system leading to hypogammaglobulinemia are considered to be either primary defects in stem cell precursors of B lymphocytes or disorders in the maturation of B cells. In the X-linked form of immunodeficiency B cells are usually absent; however, patients with the form of immunodeficiency referred to as varied immunodeficiency ...
Albert A. Benedict +2 more
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Vitiligo and dysgammaglobulinemia. A case report and family study
Clinical Genetics, 1975 This report concerns an 8 year old female with vitiligo and a dysgammaglobulinemia characterized by absent IgA, very low IgG, and normal TgM. The t‐cell immune system was intact but other family members had low levels or absence of IgA. The possible relationship of dysgammaglobulinemia and vitiligo is discussed along with the classification and ...
W E Nance
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THE GASTROINTESTINAL TRACT IN DYSGAMMAGLOBULINEMIA
, 1969 Marvin H Sleisenger, Graham H Jeffries
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Dysgammaglobulinemia associated with malabsorption and tetany
The American Journal of Digestive Diseases, 1970 A patient is reported with a malabsorption syndrome associated with nodular lymphoid hyperplasia of the small intestine and dysgammaglobulinemia characterized by virtual absence of IgA and IgM, with a reduced concentration of IgG. Prominent clinical features were severe steatorrhea and tetany.
F L, Anderson +2 more
openaire +3 more sources
B AND T LYMPHOCYTES IN DYSGAMMAGLOBULINEMIA
, 1975 B.Q. Lanier, A.S. Goldman, N.S. Harris
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Correction of Neutropenia Associated With Dysgammaglobulinemia
Pediatrics, 1974Dysgammaglobulinemia type I (deficiency of IgG and IgA with normal or elevated IgM) is frequently associated with severe neutropenia, undue susceptibility to infection and recurrent or persistent mouth ulcers.1 The mechanism underlying the neutropenia is unclear and gamma-globulin treatment has in all but two cases2,3 failed to increase absolute ...
C H, Rieger, J W, Moohr, R M, Rothberg
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HISTIOCYTIC REACTION IN DYSGAMMAGLOBULINEMIA AND CONGENITAL RUBELLA
Pediatrics, 1970A girl was born of a mother who had rubella during the first trimester of pregnancy. The child showed failure to thrive, hepatosplenomegaly, lymphadenopathy, glaucoma, and nerve deafness. She also developed a dysgammaglobulinemia with low serum γM, low to absent γA, and high (19s) γM.
H N, Claman +3 more
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Annals of Internal Medicine, 1968
Excerpt To the Editor:I would like to disagree with a statement made by the authors of the paper entitled, "'Asymptomatic' Type I Dysgammaglobulinemia in Siblings" (Ann. Intern. Med.
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Excerpt To the Editor:I would like to disagree with a statement made by the authors of the paper entitled, "'Asymptomatic' Type I Dysgammaglobulinemia in Siblings" (Ann. Intern. Med.
exaly +2 more sources