Add to ORKGSummary: Two patients with lymphoedema of the legs developed recurrent respiratory infections and were found to have panhypogammaglobulinaemia. The early recognition and treatment of this form of immunity deficiency in patients with lymphoedema is important in order to prevent recurrent infections which could cause pulmonary damage and further lymphatic stasis
An abnormally low concentration of serum gamma globulin occurs in association with a wide variety of...
found in the lymphoid or solid organs of patients with common variable immunodeficiency. Objective: ...
AbstractCommon variable immunodeficiency is a primary immune deficiency characterized by heterogeneo...
Item does not contain fulltextIn this paper, clinical data of 49 adult patients with agammaglobulina...
Panhypogammaglobulinaemia is a rare complication of systemic lupus erythematosus (SLE), but its caus...
hypogammaglobulinaemia in a small percentage of patients with thymoma.1 GS is a rare, adult-onset, i...
manifestations of hypogammaglobulinaemia. Fifty-five patients with late-onset idiopathic immunoglobu...
Hypogammaglobulinemia is the most common chronic immune defect in patients with lymphoproliferative ...
Lymphoedema is a condition of localized fluid retention and tissue swelling caused by a compromised ...
Patients with hypogammaglobulinemia who do not fulfill all the classical diagnostic criteria for com...
THE ASSOCIATION of primary acquired hypo-gammaglobulinemia and a thymic tumor was first described by...
Hyper-IgM syndrome is a rare combined immune deficiency linked to a mutation most frequently found i...
Patients with hypogammaglobulinemia are susceptible to recurrent bacterial, viral, fungal, and paras...
Idiopathic hypogammaglobulinaemia, including common variable immune deficiency (CVID), has a heterog...
Background: Immunodeficiency with a thymoma (Good’s syndrome) is a rare condition occurring in patie...
An abnormally low concentration of serum gamma globulin occurs in association with a wide variety of...
found in the lymphoid or solid organs of patients with common variable immunodeficiency. Objective: ...
AbstractCommon variable immunodeficiency is a primary immune deficiency characterized by heterogeneo...
Item does not contain fulltextIn this paper, clinical data of 49 adult patients with agammaglobulina...
Panhypogammaglobulinaemia is a rare complication of systemic lupus erythematosus (SLE), but its caus...
hypogammaglobulinaemia in a small percentage of patients with thymoma.1 GS is a rare, adult-onset, i...
manifestations of hypogammaglobulinaemia. Fifty-five patients with late-onset idiopathic immunoglobu...
Hypogammaglobulinemia is the most common chronic immune defect in patients with lymphoproliferative ...
Lymphoedema is a condition of localized fluid retention and tissue swelling caused by a compromised ...
Patients with hypogammaglobulinemia who do not fulfill all the classical diagnostic criteria for com...
THE ASSOCIATION of primary acquired hypo-gammaglobulinemia and a thymic tumor was first described by...
Hyper-IgM syndrome is a rare combined immune deficiency linked to a mutation most frequently found i...
Patients with hypogammaglobulinemia are susceptible to recurrent bacterial, viral, fungal, and paras...
Idiopathic hypogammaglobulinaemia, including common variable immune deficiency (CVID), has a heterog...
Background: Immunodeficiency with a thymoma (Good’s syndrome) is a rare condition occurring in patie...
An abnormally low concentration of serum gamma globulin occurs in association with a wide variety of...
found in the lymphoid or solid organs of patients with common variable immunodeficiency. Objective: ...
AbstractCommon variable immunodeficiency is a primary immune deficiency characterized by heterogeneo...