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… (More)
National Institutes of Health

Papers overview

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2018
2018
Fig. 1 An 8-year-old girl with history of transient protein-losing enteropathy (PLE) in infancy, but thereafter no diarrhea… (More)
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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… (More)
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Highly Cited
2009
Highly Cited
2009
Granulomatous disease occurs in 8-22% of patients with common variable immunodeficiency (CVID). We examined the clinical and… (More)
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2008
2008
Subcutaneous immunoglobulin G (SCIG) infusions as life-long replacement therapy in patients with primary antibody deficiences… (More)
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2007
2007
Common variable immunodeficiency (CVID) is a heterogeneous syndrome characterized by defective immunoglobulin production and high… (More)
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Highly Cited
2004
Highly Cited
2004
BACKGROUND Lung damage progression is the most frequent condition in patients with common variable immunodeficiency (CVID… (More)
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2000
2000
BACKGROUND Vitamin A has a broad range of immunological effects, and vitamin A deficiency is associated with recurrent infections… (More)
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Highly Cited
1998
Highly Cited
1998
X-linked lymphoproliferative syndrome (XLP or Duncan disease) is characterized by extreme sensitivity to Epstein-Barr virus (EBV… (More)
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Review
1997
Review
1997
Because the gastrointestinal tract is the largest lymphoid organ in the body, it is not surprising that patients with… (More)
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Highly Cited
1988
Highly Cited
1988
This first report of a Swiss registry includes 313 patients with primary immunodeficiency syndromes (PIDS) who were observed… (More)
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