about
IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and TurkeyInherited and acquired immunodeficiencies underlying tuberculosis in childhood.Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisThe extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.Eponym. Kostmann disease.DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.Purine nucleoside phosphorylase deficiency with fatal course in two sisters.HLA-haploidentical transplantations for primary immunodeficiencies: a single-center experience.A novel G6PC3 gene mutation in a patient with severe congenital neutropenia.An unconditioned bone marrow transplantation in a child with purine nucleoside phosphorylase deficiency and its unique complication.Selective IgA deficiency: clinical and laboratory features of 118 children in Turkey.Complete deficiency of the IL-12 receptor beta1 chain: three unrelated Turkish children with unusual clinical features.Kostmann disease with developmental delay in three patients.Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiencyHuman IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Caner Aytekin
@ast
Caner Aytekin
@en
Caner Aytekin
@es
Caner Aytekin
@nl
type
label
Caner Aytekin
@ast
Caner Aytekin
@en
Caner Aytekin
@es
Caner Aytekin
@nl
prefLabel
Caner Aytekin
@ast
Caner Aytekin
@en
Caner Aytekin
@es
Caner Aytekin
@nl
P106
P31
P496
0000-0002-2921-5270