about
Fc receptor-like proteins (FCRL): immunomodulators of B cell functionClinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis.Idiopathic CD4+ T cell lymphocytopenia with the absence of B cells and CD8+28+ cells in peripheral blood.Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries.Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans.Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.A Clinical and Laboratory Approach to the Evaluation of Innate Immunity in Pediatric CVID Patients.Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case reportNovel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency.Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications.Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency.Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN-γ receptor-1 deficiency.Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation.Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?Clinical and laboratory evaluation of periodically monitored Turkish children with IgG subclass deficiencies.Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis.Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey.Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever.A novel Y331X nonsense mutation in TNFRSF1A gene in two unrelated Turkish families with periodic fever syndrome.Human soluble tumor necrosis factor receptor I (sTNF-RI) and interleukin-I receptor antagonist (IL-I Ra) in different stages of acute rheumatic fever.Purine nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections.Inverse relationship between the ratio of ICAM-1 expressing lymphocytes and serum TGF-beta 1 concentrations in acute rheumatic fever.Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases.Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections.CD4+CD25+Foxp3+ T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency.Mannose-binding lectin may affect pregnancy outcome.Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report.Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections.Evaluation of transforming growth factor-beta 1 level in crevicular fluid of cyclosporin A-treated patients.A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity.IgG-anti-IgA antibodies: an autoimmune finding in patients with psoriasis vulgaris.Chronic inflammatory bowel disease in a patient with common variable immunodeficiency.Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study.Decreased ratio of CD4/CD8 lymphocytes might be predictive for successful interferon alpha and lamivudine combined therapy in childhood chronic hepatitis B infection: A preliminary study.Hyper-immunoglobulin M syndrome type 3 with normal CD40 cell surface expression.The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study.New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy.Maternally acquired varicella-zoster virus antibodies disappear at 6 months of age in prematurely born children.
P50
Q28291477-A3C7F2C5-2B93-444C-9DDF-779FE12956F3Q33359560-EDE881CA-D45B-47C8-A39E-40DF533DCD40Q34896014-A1E8687A-5558-4755-B7E5-99D76A423843Q35007146-34868A6F-F2AE-47AE-AF34-F5DA0DB7A5ADQ35086274-8ED7F693-FCD1-4FB1-B4FF-AA61F5D6FBABQ35105055-138E28A0-9D27-4F11-8510-F12A907CFD3DQ35510477-9A8D3758-CE7F-4CDB-98D7-D45538B3119EQ35541010-5775E8EE-665B-43ED-A308-4412361DD23AQ35831233-6AB7088B-6D61-4B5F-9D23-33487935184BQ36088237-4DA8B32B-5DA1-440B-AA34-EABC24E6298FQ36370643-E5A059D2-7828-4F0B-AC33-2D3E007EECF5Q36752187-F52EC1E7-2D3D-4DA1-8CF4-3D1E7A5AD2E1Q37056155-4B753DFA-CB08-4099-A968-BDC40746E655Q37215141-D5770C58-8C03-435E-82F3-21581FAD62FEQ37266580-0B761912-61FE-4D94-AD65-D128FB858635Q37528395-89850FE9-C77F-4D1C-8BC4-0429E46DA4A3Q37832971-615AA54A-E028-441D-98E0-DB01880C4FD9Q38880881-14F5DCE1-F11D-481F-B2FE-25761E5F2A2EQ40306826-98E8FC70-94D8-4A86-8533-9E690A26F530Q40322522-01690190-FFAB-470D-95B0-87594886A89CQ40377895-D3D17528-E0AF-4C8C-AEA4-4FAD68422A6AQ40422250-73DCB814-9893-47B8-8ADD-8BF66101EEEFQ40444190-79DA1609-0127-4EEB-AC24-02CE0DE749B2Q40503560-C86F1C4D-DE31-4DA2-B459-D1BC39FA95F8Q40518108-C58ED134-AAA6-4FC6-9193-089723EF5479Q40855800-1F72C9CC-D79C-4AF6-8450-48054A4BE34AQ40865167-26A44E33-E8C1-4AC4-98D2-C8B18FCBACA6Q40892317-03FFFD01-35F5-4599-94BC-8DB4D25D75DBQ42370719-D8C78B53-0137-40B9-9054-47EDF119B0AAQ43176149-EFA9ED77-616C-4C87-A91E-6D711299B98DQ43598371-5EBBA73F-B351-4C6F-BE50-8FABBB05F6BAQ43663999-43663656-65AE-413A-B19D-2D24715E3E4FQ43875737-20004E75-C853-42F3-A202-DD3038E27DC3Q43935626-39695AD8-5226-4FCA-8E3A-F062816E5E45Q44220803-C01AC8DF-90BC-4057-A7FB-7EBA7708ACC4Q44444933-9936F2EB-31EC-4D34-9692-8A9B98296E40Q44702040-4348D42A-EA59-40F0-9CCF-6F101AD56201Q44885671-DF11CBB9-9B83-42C9-A2BB-8D51A88AFDD3Q45180122-C01D7102-6FA0-4917-8F92-F17A1E052ADCQ45722652-F1556457-AD77-430A-82B1-783877D41F23
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Guzide Aksu
@ast
Guzide Aksu
@en
Guzide Aksu
@es
Guzide Aksu
@nl
Guzide Aksu
@sl
type
label
Guzide Aksu
@ast
Guzide Aksu
@en
Guzide Aksu
@es
Guzide Aksu
@nl
Guzide Aksu
@sl
prefLabel
Guzide Aksu
@ast
Guzide Aksu
@en
Guzide Aksu
@es
Guzide Aksu
@nl
Guzide Aksu
@sl
P106
P1153
7004014994
P21
P2798
P31
P496
0000-0003-2714-0903