Results 101 to 110 of about 1,006 (159)
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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   +2 more sources

Recurrent Pleural Effusion Associated with Dysgammaglobulinemia

Chest, 1973
A 45-year-old man presented with recurrent bilateral pleural effusions of undetermined etiology. This was associated with absence of IgM and a decreased IgA fraction. Possible associations are discussed.
W J, Godfrey, J W, Sokolowski
openaire   +2 more sources

"Asymptomatic" Type I Dysgammaglobulinemia in Siblings

Annals of Internal Medicine, 1968
Abstract A family with type I dysgammaglobulinemia is presented in which a brother and sister were affected.
J R, Durant   +3 more
openaire   +2 more sources

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
openaire   +1 more source

A NOVEL PATHOGENIC SH2D1A MUTATION CAUSES X-LINKED LYMPHOPROLIFERATIVE DISEASE MANIFESTED BY NON-HODGKIN LYMPHOMA AND DYSGAMMAGLOBULINEMIA

Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis, 2022
G. Gilad   +14 more
semanticscholar   +1 more source

AUTOIMMUNITY IN ACQUIRED DYSGAMMAGLOBULINEMIA OF CHICKENS

1979
Publisher Summary This chapter discusses the autoimmunity in acquired dysgammaglobulinemia of chickens. The development of a line of chickens with inherited immunodeficiency has been recently reported. Examination of serum Ig levels from previous generations helped trace the defect to a single-line 3 male, an ancestor common to both line 140 and 142.
John Montero   +3 more
openaire   +1 more source

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