Results 211 to 220 of about 12,870 (263)
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Pediatrics, 1952
A hitherto unrecognized entity manifested by complete absence of gamma globulin with otherwise normal serum proteins and recurrent pneumococcal sepsis is described in an 8 year old male. The patient appears to be normal in other respects and after extensive study no structural or functional change could be demonstrated in any body system although gamma
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A hitherto unrecognized entity manifested by complete absence of gamma globulin with otherwise normal serum proteins and recurrent pneumococcal sepsis is described in an 8 year old male. The patient appears to be normal in other respects and after extensive study no structural or functional change could be demonstrated in any body system although gamma
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Agammaglobulinemia and Regional Enteritis
Annals of Internal Medicine, 1969Abstract An 18-year-old white man with congenital agammaglobulinemia that was probably sex-linked developed clinically and pathologically typical regional enteritis.
Robert A. Good +2 more
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2014
Agammaglobulinemia is a rare form of primary immune deficiency characterized by absence of circulating B cells and low serum levels of all immunoglobulin classes, in the presence of normal T cell counts and function. Affected patients are particularly susceptible to infections, frequently severe ones.
Vassilios Lougaris, Alessandro Plebani
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Agammaglobulinemia is a rare form of primary immune deficiency characterized by absence of circulating B cells and low serum levels of all immunoglobulin classes, in the presence of normal T cell counts and function. Affected patients are particularly susceptible to infections, frequently severe ones.
Vassilios Lougaris, Alessandro Plebani
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C3 Activator in Agammaglobulinemia
International Archives of Allergy and Immunology, 1978C3 activator in sera of patients with agammaglobulinemia shows higher levels compared with age-matched healthy controls. This fact may be due to a compensatory function of the alternative pathway of the complement system to make up for the defect of production of antibody in these patients.
S. Nakajima, K. Nihei, Y. Hyodo
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A decade with agammaglobulinemia
The Journal of Pediatrics, 1962Summary This progress report is presented a decade after recognition of a patient with agammaglobulinemia. It includes a brief description and follow-up of the first recognized patient, a brief summary of significant advances in the elucidation of agammaglobulinemia as a disease entity, and some predictions on the type of advances which may be made ...
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Agammaglobulinemia: The Fundamental Defect
Science, 1964Addition of phytohemagglutinin and of streptolysin S to in vitro cultures of leukocytes of normal and agammaglobulinemic subjects resulted in mitosis of lymphocytes and their differentiation to plasma cells. In contrast, specific antigens induced mitosis and differentiation of lymphocytes of normal but not of agammaglobulinemic donors. The data suggest
H. Hugh Fudenberg, Kurt Hirschhorn
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The Journal of Pediatrics, 1957
Summary A case of agammaglobulinemia in a 5 1/2-year-old boy is presented. The gamma globulin level in the child's serum as determined by immunological method was extremely low, between 0.5 and 1 mg. per 100 ml. plasma, which is lower than in other cases reported in the literature.
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Summary A case of agammaglobulinemia in a 5 1/2-year-old boy is presented. The gamma globulin level in the child's serum as determined by immunological method was extremely low, between 0.5 and 1 mg. per 100 ml. plasma, which is lower than in other cases reported in the literature.
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Clinical Reviews in Allergy & Immunology, 2000
The identification of the gene responsible for XLA has made it possible to clarify the clinical and laboratory findings in this disorder. It has markedly improved our ability to provide informative genetic counseling for affected families and it has helped unmask disorders that are clinically similar to XLA but genotypically different.
Jurg Rohrer +2 more
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The identification of the gene responsible for XLA has made it possible to clarify the clinical and laboratory findings in this disorder. It has markedly improved our ability to provide informative genetic counseling for affected families and it has helped unmask disorders that are clinically similar to XLA but genotypically different.
Jurg Rohrer +2 more
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SUCCESSFUL HOMOGRAFT OF SKIN IN A CHILD WITH AGAMMAGLOBULINEMIA
Journal of the American Medical Association, 1955A substantial obstacle to current medical and surgical progress is the established fact that tissues and organs from one person transplanted to another will not survive. Although it has been suspected that rejection of homografts has an immunologic basis, proof of this concept is lacking.
Robert A. Good, Richard L. Vareo
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Pediatric Allergy and Immunology, 2020
Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently decreased immunoglobulin levels.
Saba Fekrvand +22 more
semanticscholar +1 more source
Congenital agammaglobulinemia is the first primary immunodeficiency disorder characterized by a defect in B lymphocyte development and subsequently decreased immunoglobulin levels.
Saba Fekrvand +22 more
semanticscholar +1 more source