Detalhe da pesquisa
1.
From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature.
BMC Pediatr
; 24(1): 116, 2024 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38350907
2.
The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation Stages.
J Clin Immunol
; 43(4): 819-834, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36790564
3.
Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients.
Pediatr Allergy Immunol
; 34(7): e13990, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37492921
4.
Investigation of the Relationship between Aspirin-Sensitivity and Poor Response to Medical Management in NSAIDs-exacerbated Respiratory Disease Patients with Sinonasal Polyposis.
Med J Islam Repub Iran
; 37: 63, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37457420
5.
Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations).
Immunol Invest
; 51(1): 170-181, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32896191
6.
Oral Immunotherapy in Patients with IgE Mediated Reactions to Egg White: A Clinical Trial Study.
Immunol Invest
; 51(3): 630-643, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34309462
7.
The Effectiveness of Oral Immunotherapy in Patients with Sesame Anaphylaxis using Omalizumab.
Clin Med Res
; 2022 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35998948
8.
Adverse reactions in a large cohort of patients with inborn errors of immunity receiving intravenous immunoglobulin.
Clin Immunol
; 230: 108826, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34418548
9.
Impact of SARS-CoV-2 Pandemic on Patients with Primary Immunodeficiency.
J Clin Immunol
; 41(2): 345-355, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33263173
10.
Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity.
Pediatr Allergy Immunol
; 32(6): 1335-1348, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33774840
11.
Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity.
Int Arch Allergy Immunol
; 181(9): 706-714, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32615565
12.
A newly found homozygous mutation in recombination activating gene 1 in a patient with leaky severe combined immunodeficiency disorder.
Mol Biol Rep
; 46(6): 6571-6575, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31520268
13.
Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1.
J Pediatr Hematol Oncol
; 41(1): e3-e6, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29750748
14.
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease.
J Pediatr Hematol Oncol
; 40(5): e268-e272, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29702544
15.
Phenotyping and follow up of forty-seven Iranian patients with common variable immunodeficiency.
Allergol Immunopathol (Madr)
; 44(3): 226-31, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26232306
16.
Aspirin desensitization for patients with aspirin-exacerbated respiratory disease: A randomized double-blind placebo-controlled trial.
Clin Immunol
; 160(2): 349-57, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26083948
17.
Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia.
J Clin Immunol
; 35(1): 22-5, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25491289
18.
Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome.
Pediatr Blood Cancer
; 67(2): e28084, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31749288
19.
Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation.
J Clin Immunol
; 39(2): 138-141, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30796585
20.
Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.
J Clin Immunol
; 34(4): 478-90, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24659230