Detalhe da pesquisa
1.
Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity.
Blood
; 2024 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38579284
2.
Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier.
Blood
; 141(26): 3226-3230, 2023 06 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36745868
3.
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages.
Scand J Immunol
; 89(2): e12737, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30506560
4.
Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation.
J Allergy Clin Immunol
; 138(5): 1384-1394.e2, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27350570
5.
A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacity.
Clin Immunol
; 153(2): 288-91, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24845792
6.
Three different classifications, B lymphocyte subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene mutations, CTLA-4 and ICOS gene polymorphisms in Turkish patients with common variable immunodeficiency.
J Clin Immunol
; 32(6): 1165-79, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22699762
7.
Immunoglobulin light chain levels can be used to determine disease stage in children with juvenile idiopathic arthritis.
Clin Lab Sci
; 24(2): 93-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21657141
8.
Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.
Inflamm Bowel Dis
; 23(12): 2109-2120, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28930861
9.
Human soluble tumor necrosis factor receptor I (sTNF-RI) and interleukin-I receptor antagonist (IL-I Ra) in different stages of acute rheumatic fever.
Anadolu Kardiyol Derg
; 8(2): 139-42, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18400635
10.
Progressive morphea of early childhood tracing Blaschko's lines on the face: involvement of X chromosome monosomy in pathogenesis and clinical prognosis.
Int J Dermatol
; 50(11): 1406-1410, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22004499