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Acquired Hypogammaglobulinemia

Known as: Acquired Hypogammaglobulinemias, Hypogammaglobulinemias, Acquired, Acquired Agammaglobulinemia 
A primary immunodeficiency characterized by low levels or absence of all the immunoglobulin classes and lack of B-lymphocytes or plasma cells. It… Expand
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Severe combined immunodeficiency (SCID) and X-linked agammaglobulinemia (XLA) are inborn errors of immune function that require… Expand
Review
2002
Review
2002
Primary immune deficiencies have an estimated overall incidence of 1 in 10,000 individuals. These disorders are diverse… Expand
Highly Cited
1998
Highly Cited
1998
X-linked lymphoproliferative syndrome (XLP or Duncan disease) is characterized by extreme sensitivity to Epstein-Barr virus (EBV… Expand
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Highly Cited
1994
Highly Cited
1994
Partial albinism with immunodeficiency is a rare and fatal immunologic disorder characterized by pigmentary dilution and variable… Expand
Highly Cited
1981
Highly Cited
1981
Multiple methods, pedigree analysis, clinical evaluation, and Epstein-Barr virus (EBV)-specific serology, EBV DNA hybridization… Expand
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Highly Cited
1979
Highly Cited
1979
We studied a five-year-old girl with several autoimmune disorders and a 16-year-old boy with acquired agammaglobulinemia to… Expand
Review
1979
Review
1979
Haemophilus influenzae is an aerobic pleomorphic gram-negative coccobacillus that requires both X and V factors for growth. It… Expand
Review
1978
Review
1978
ABSTRACTBased on a study of 26 cases and a review of the literature, lymphoid hyperplasia of the gastrointestinal tract can be… Expand
Highly Cited
1972
Highly Cited
1972
Sheep red blood cells can surround, in vitro, some human peripheral blood lymphocytes in a formation called a rosette. The number… Expand
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Highly Cited
1966
Highly Cited
1966
1. Five patients with congenital or acquired agammaglobulinemia, lacking detectable IgA in serum or saliva, were transfused with… Expand