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1.
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
2.
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
3.
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
4.
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
5.
Cardiac Assessment in Children with MIS-C: Late Magnetic Resonance Imaging Features.
Pediatr Cardiol;
44(1): 44-53, 2023 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-35916926
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
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
13.
ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients.
Allergy;
75(4): 921-932, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31596517
14.
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
15.
Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review.
Rheumatol Int;
40(1): 161-168, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31273456
16.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30506560
17.
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Immunol Rev;
264(1): 103-20, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25703555
18.
Anti-ß2 Glycoprotein I Antibodies in Children with Rheumatologic Disorders.
Indian J Clin Biochem;
34(1): 95-100, 2019 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-30728679
19.
In vitro T lymphocyte proliferation by carboxyfluorescein diacetate succinimidyl ester method is helpful in diagnosing and managing primary immunodeficiencies.
J Clin Lab Anal;
32(1)2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-28383134
20.
Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant.
J Allergy Clin Immunol;
147(2): 775-778.e8, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-32858082