Results 251 to 260 of about 18,379 (288)
Some of the next articles are maybe not open access.
Pediatric Transplantation, 2019
X‐linked agammaglobulinemia (XLA) is a primary antibody disorder due to a mutation in the Bruton tyrosine kinase gene that requires lifelong immunoglobulin replacement resulting in a significant economic burden and treatment abandonment.
V. Vellaichamy Swaminathan +7 more
semanticscholar +1 more source
X‐linked agammaglobulinemia (XLA) is a primary antibody disorder due to a mutation in the Bruton tyrosine kinase gene that requires lifelong immunoglobulin replacement resulting in a significant economic burden and treatment abandonment.
V. Vellaichamy Swaminathan +7 more
semanticscholar +1 more source
International Archives of Allergy and Immunology, 1961
M, DIAMANT, P, KALLOS, G, RUBENSOHN
openaire +2 more sources
M, DIAMANT, P, KALLOS, G, RUBENSOHN
openaire +2 more sources
Current Spectrum of Infections in Patients with X-Linked Agammaglobulinemia
Journal of Clinical Immunology, 2021O. Paccoud +12 more
semanticscholar +1 more source
TCF3 Dominant Negative Variant Causes an Early Block in B-Lymphopoiesis and Agammaglobulinemia
Journal of Clinical Immunology, 2021Ebtehal Al Sheikh +4 more
semanticscholar +1 more source
Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia
Journal of Clinical Immunology, 2020Kento Inoue +6 more
semanticscholar +1 more source
Expression of the Gene Defect in X-Linked Agammaglobulinemia
New England Journal of Medicine, 1986Jack W Singer
exaly