Results 171 to 180 of about 19,833 (230)

HYPOGAMMAGLOBULINEMIA

Pediatrics, 1960
An unusual patient, characterized by recurrent infections, hepatosplenomegaly, low levels of gamma-globulin in the serum (400 mg/100 ml) and lymphocytosis, is described. The patient had pneumonia due to Nocardia asteroides followed by chronic Salmonella newport infection of 16 months' duration, kept in check by continuous antibiotic ...
Thomas F. Dolan, Norman B. McCullough, Lewis E. Gibson   +2 more
openaire   +1 more source

Hypogammaglobulinemia and steatorrhea

The American Journal of Digestive Diseases, 1965
1. A patient with acquired idiopathic hypogammaglobulinemia and steatorrhea is described. Jejunal and ileal biopsies were histologically normal.
C F, McCarthy, W I, Austad, A E, Read
openaire   +2 more sources

Transient hypogammaglobulinemia and unclassified hypogammaglobulinemia: 'similarities and differences'.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2010
Transient hypogammaglobulinemia of infancy (THI) is characterized by recurrent infections and one or more reduced serum immunoglobulin (Ig) levels. Usually, this clinical picture resolves spontaneously by 3 yr of age. However, hypogammaglobulinemia persists until adolescence in some patients.
Keleş, Sevgi, Artaç, Hasibe, Kara, Reyhan, Göktürk, Bahar, Özen, Ahmet, Reisli, İsmail   +5 more
openaire   +2 more sources

DIAGNOSIS OF HYPOGAMMAGLOBULINEMIA

JAMA, 1962
Prompt, accurate diagnosis of gamma globulin deficiency as a cause of unusual susceptibility to infection is extremely important for several reasons: first, replacement therapy with pooled normal gamma globulin is effective in the prevention of serious infections if initiated before structural damage has occurred; second, supplies of gamma globulin ...
openaire   +2 more sources

The Genetics of Hypogammaglobulinemia

Current Allergy and Asthma Reports, 2004
Etiologies for human hypogammaglobulinemias are diverse and include genetic and nongenetic causes. Although recent reviews focus on the complex genetics of common variable immunodeficiency, in this review, we survey different causes of hypogammaglobulinemias and discuss possible mechanisms.
Grimbacher, Bodo, Schäffer, Alejandro A., Peter, Hans-Hartmut   +2 more
openaire   +3 more sources

Heterogeneity of hypogammaglobulinemia

American Journal of Hematology, 1980
AbstractIn 1952, Ogden Bruton described the first patient with recurrent infections and hypogammaglobulinemia [1]. For many years thereafter, hypogammaglobulinemia (or agammaglobulinemia) was believed to result from a deficiency (or absence) of the antibody‐producing cells, or “B” cell line of the lymphoid system.
openaire   +2 more sources

[Hypogammaglobulinemia].

Nordisk medicin, 1998
R H, RAMSEY, P, MURPHY, G O, BROUN, L Y, DAVIS   +3 more
  +6 more sources

XLID-Hypogammaglobulinemia

2011
Abstract This chapter provides pictures and clinical details of XLID ...
Roger E. Stevenson, Charles E. Schwartz, R. Curtis Rogers   +2 more
openaire   +1 more source

Gingivitis in Hypogammaglobulinemia

Journal of Periodontology, 1973
R W, Barrickman, M L, Callerame, J J, Condemi   +2 more
openaire   +2 more sources

Hypogammaglobulinemia

2011
  +4 more sources