Add to ORKGX-linked hyper-IgM syndrome (XHIM) is a primary immunodeficiency with absent IgG, IgA, IgE and normal/elevated IgM due to defects in the CD40 ligand (CD40L) gene. CD40L is expressed on T-lymphocytes and is essential in the interaction between B and T cells that induces class switch recombination
When caring for patients with life-limiting diseases, improving survival and optimizing quality of l...
Type 1, X-linked Hyper-IgM syndrome (HIGM1) is caused by mutations in the gene encoding the CD154 pr...
B lymphocytes from patients with X chromosome-linked immunoglobulin deficiency with normal or elevat...
X-linked hyper-IgM syndrome (XHIM) is a primary immunodeficiency with absent IgG, IgA, IgE and norm...
X-linked hyper-IgM syndrome (XHIM) is a primary immunodeficiency due to defects in immunoglobulin c...
X-linked hyper-IgM syndrome is characterized by absent IgG, IgA, and IgE with normal/elevated IgM d...
Hyper-immunoglobulin M (IgM) syndrome (HIGM) is a rare primary immunodeficiency characterized by ele...
X-linked hyper IgM syndrome (XHIM) is a primary immunode-ficiency disorder caused by mutations of th...
X-linked hyper-lgM (HIGM-1) syndrome is a rare disorder resulting from mutations in the CD40-ligand ...
X-linked hyper-immunoglobulin M (hyper-IgM) syndrome (XHIM) is a primary immunodeficiency due to mut...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
Immunocompetence requires cognate cell-cell communication that is mediated through cell surface liga...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
When caring for patients with life-limiting diseases, improving survival and optimizing quality of l...
Type 1, X-linked Hyper-IgM syndrome (HIGM1) is caused by mutations in the gene encoding the CD154 pr...
B lymphocytes from patients with X chromosome-linked immunoglobulin deficiency with normal or elevat...
X-linked hyper-IgM syndrome (XHIM) is a primary immunodeficiency with absent IgG, IgA, IgE and norm...
X-linked hyper-IgM syndrome (XHIM) is a primary immunodeficiency due to defects in immunoglobulin c...
X-linked hyper-IgM syndrome is characterized by absent IgG, IgA, and IgE with normal/elevated IgM d...
Hyper-immunoglobulin M (IgM) syndrome (HIGM) is a rare primary immunodeficiency characterized by ele...
X-linked hyper IgM syndrome (XHIM) is a primary immunode-ficiency disorder caused by mutations of th...
X-linked hyper-lgM (HIGM-1) syndrome is a rare disorder resulting from mutations in the CD40-ligand ...
X-linked hyper-immunoglobulin M (hyper-IgM) syndrome (XHIM) is a primary immunodeficiency due to mut...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
Immunocompetence requires cognate cell-cell communication that is mediated through cell surface liga...
X-linked hyper-IgM syndrome (X-HIM) is an immunodeficiency caused by mutations in the gene encoding ...
When caring for patients with life-limiting diseases, improving survival and optimizing quality of l...
Type 1, X-linked Hyper-IgM syndrome (HIGM1) is caused by mutations in the gene encoding the CD154 pr...
B lymphocytes from patients with X chromosome-linked immunoglobulin deficiency with normal or elevat...