Detalhe da pesquisa
1.
Clinical heterogeneity in families with multiple cases of inborn errors of immunity.
Clin Immunol
; 259: 109896, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38184287
2.
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
3.
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
4.
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
5.
Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran.
Int Arch Allergy Immunol
; 180(1): 52-63, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31117086
6.
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency.
J Allergy Clin Immunol
; 141(4): 1450-1458, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28916186
7.
Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis.
J Clin Immunol
; 38(7): 816-832, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30302726
8.
The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran.
J Clin Immunol
; 41(4): 811-813, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33442788
9.
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
10.
BAK, BAX, and NBK/BIK proapoptotic gene alterations in Iranian patients with ataxia telangiectasia.
J Clin Immunol
; 30(1): 132-7, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19898928
11.
Behavior abnormality following intravenous immunoglobulin treatment in patients with primary antibody deficiencies.
Hum Psychopharmacol
; 25(5): 419-22, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20589928
12.
IgA deficiency: correlation between clinical and immunological phenotypes.
J Clin Immunol
; 29(1): 130-6, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18683032
13.
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.
J Allergy Clin Immunol Pract
; 7(3): 864-878.e9, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30240888
14.
Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease.
Br J Haematol
; 141(6): 848-51, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18422995
15.
Chromosomal radiosensitivity in patients with common variable immunodeficiency.
Immunobiology
; 213(5): 447-54, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18472053
16.
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.
Expert Rev Clin Immunol
; 12(4): 479-86, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26910880
17.
Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients.
Expert Rev Clin Immunol
; 10(10): 1405-17, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25225775
18.
Prevention and control of infections in patients with severe congenital neutropenia; a follow up study.
Iran J Allergy Asthma Immunol
; 11(1): 51-6, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22427476
19.
Cutaneous granulomas in common variable immunodeficiency: case report and review of literature.
Acta Dermatovenerol Croat
; 18(2): 107-13, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20624361
20.
Common causes of anaphylaxis in children: the first report of anaphylaxis registry in iran.
World Allergy Organ J
; 3(1): 9-13, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23282381