Molecular analysis of T-B-NK+severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia [PDF]
Osama Alsmadi +8 more
openalex +1 more source
Corrigendum: Interleukin-2-Inducible T-Cell Kinase Deficiency—New Patients, New Insight?
Sujal Ghosh +7 more
doaj +1 more source
Approach to the child with recurrent infections
Children with a history of recurrent, severe, or unusual infections present a diagnostic challenge. It is important to maintain a high index of suspicion for the diagnosis of immunodeficiency, for early diagnosis and treatment can improve outcome ...
Suzan A AlKhater
doaj
Engrafted maternal T cells in human severe combined immunodeficiency: Evidence for a TH2 phenotype and a potential role of apoptosis on the restriction of T-cell receptor variable β repertoire [PDF]
Alessandro Plebani +10 more
openalex +1 more source
Targeted Next-Generation Sequencing in the Molecular Diagnosis of Severe Combined Immunodeficiency. [PDF]
Bakaros E +13 more
europepmc +1 more source
Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK. [PDF]
Keller B +13 more
europepmc +1 more source
Purine nucleoside metabolism in the erythrocytes of patients with adenosine deaminase deficiency and severe combined immunodeficiency. [PDF]
R. P. Agarwal +8 more
openalex +1 more source
A novel <i>de novo IL2RG</i> nonsense mutation in a pediatric patient with X-linked severe combined immunodeficiency. [PDF]
Wang L +9 more
europepmc +1 more source

