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1.
Author Correction: DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation.
Nat Immunol
; 23(5): 815, 2022 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-35332329
2.
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation.
Nat Immunol
; 13(6): 612-20, 2012 May 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-22581261
3.
Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections.
Int Arch Allergy Immunol
; 185(4): 392-401, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38154455
4.
Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies.
Int Arch Allergy Immunol
; 185(4): 382-391, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38246144
5.
Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency.
J Allergy Clin Immunol
; 152(6): 1634-1645, 2023 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-37595759
6.
Analysis of IL-1ß, TGF-ß, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis.
Mol Biol Rep
; 51(1): 15, 2023 Dec 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-38085361
7.
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature.
Asian Pac J Allergy Immunol
; 41(4): 372-378, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-33638623
8.
Mid-Regional Proadrenomedullin Levels in Primary Immunodeficiencies Complicated with Pulmonary Manifestations.
Indian J Clin Biochem
; 38(4): 475-484, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37746537
9.
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry.
Clin Immunol
; 244: 109131, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36179983
10.
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants.
Scand J Immunol
; 95(6): e13163, 2022 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-35303369
11.
Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency.
Allergy
; 77(10): 3108-3123, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35491430
12.
Immunologic changes during desensitization with cow's milk: How it differs from natural tolerance or nonallergic state?
Ann Allergy Asthma Immunol
; 129(6): 751-757.e3, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35914664
13.
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity.
J Clin Immunol
; 41(6): 1339-1351, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34052995
14.
Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia.
J Clin Immunol
; 41(8): 1878-1892, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34477998
15.
A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia.
J Pediatr Hematol Oncol
; 43(6): e780-e784, 2021 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33843817
16.
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management.
Allergol Immunopathol (Madr)
; 49(1): 95-100, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33528935
17.
Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in IL-21R gene and successful treatment with hematopoietic stem cell transplantation.
Pediatr Hematol Oncol
; 38(8): 745-752, 2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-33966600
18.
Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.
J Allergy Clin Immunol
; 145(5): 1452-1463, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31887391
19.
Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation.
J Clin Immunol
; 40(4): 646, 2020 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-32367426
20.
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study.
Pediatr Allergy Immunol
; 31(5): 528-536, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32060950