Common variable immune deficiency (CVID) is the most common symptomatic primary
immune deficiency, affecting~ 1 in 25,000 persons. These patients suffer from impaired …

Using whole-exome sequencing to examine the genetic causes of immune deficiency in 235
common variable immunodeficiency (CVID) patients seen in the United States (Mount Sinai …

Common variable immunodeficiency disorder (CVID) is the most prevalent form of primary
idiopathic hypogammaglobulinemia. Identification of genetic defects in CVID is hampered by …

Common variable immunodeficiency (CVID) is considered to be a collection of genetic
immune defects with complex inheritance patterns. While the main phenotype is loss of B …

Common variable immune deficiency disorder (CVID) is the most clinically relevant cause of
antibody failure. It is a highly heterogeneous disease with different underlying etiologies …

Although common variable immunodeficiency (CVID) has long been considered as a group
of primary Ab deficiencies, growing experimental data now suggest a global disruption of the …

Common variable immunodeficiency (CVID), the most prevalent symptomatic primary
immunodeficiency, displays impaired terminal B-cell differentiation and defective antibody …

Common variable immunodeficiency (CVID) is the most frequently diagnosed symptomatic
primary immunodeficiency. CVID develops as a consequence of absence or malfunction of …

The role of CD4 T regulatory cells is well established in peripheral tolerance and the
pathogenesis of the murine model and human autoimmune diseases. CD4 T regulatory cells …

The molecular basis of common variable immunodeficiency (CVID) is unknown. To assess
humoral immunity in CVID, we selected 24 patients with early or late onset of disease. X …