TCF3 Dominant Negative Variant Causes an Early Block in B-Lymphopoiesis and Agammaglobulinemia [PDF]
, 2021 Al Shiekh, Ebtehal +4 more
core +1 more source
A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase
The Turkish Journal of Pediatrics, 2006 X-linked agammaglobulinemia (XLA) is a primary B cell immunodeficiency disorder, caused by a defect in the Bruton tyrosine kinase (BTK) gene. Here, we describe a novel four base pair mutation (838delGAGT) in intron 9 of the BTK gene leading to the
Lütfiye Mesci +5 more
doaj
Drug reaction to ceftriaxone in a child with X-linked agammaglobulinemia [PDF]
, 2002 Vandana Kudva-Patel +4 more
openalex +1 more source
Radionuclides in the postoperative management of orthotopic human organ transplantation. [PDF]
, 1969 Brown, DW, Starzl, TE
core +1 more source
Phenotypic variability: clinical presentation between the 6th year and the 60th year in a family with X-linked agammaglobulinemia [PDF]
, 2004 Karen Morwood +5 more
openalex +1 more source
Two case reports of B-cell lymphopenia associated with IGLL1 variants identified through newborn screening in Ukraine. [PDF]
Front PediatrBoyarchuk O +5 more
europepmc +1 more source
Immunodeficiency Diseases and Tumor Immunobiology [PDF]
, 1974 Abramoff, Peter A., Duquesnoy, Rene J.
core +1 more source
Membranous Glomerulonephritis in an Individual with X-linked Agammaglobulinemia on Intravenous Immunoglobulin [PDF]
, 2006 L.M. Endo +4 more
openalex +1 more source
A Rapid Point-of-Care Ultrasound Diagnosis and Treatment of Tamponade in a Patient With Rare and Lethal Purulent Pericarditis: A Case Report. [PDF]
CureusBass AN, Lynch S, Derr C, Gillen J.
europepmc +1 more source