Detalhe da pesquisa
1.
International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome.
J Allergy Clin Immunol
; 149(1): 410-421.e7, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34033842
2.
Comprehensive Assessment of Skin Disorders in Patients with Common Variable Immunodeficiency (CVID).
J Clin Immunol
; 42(3): 653-664, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-35084691
3.
Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients.
J Clin Immunol
; 42(1): 72-84, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34628594
4.
T Cell Repertoire Abnormality in Immunodeficiency Patients with DNA Repair and Methylation Defects.
J Clin Immunol
; 42(2): 375-393, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34825286
5.
Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.
J Clin Immunol
; 42(8): 1748-1765, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-35947323
6.
Immunophenotypic and functional analysis of lymphocyte subsets in common variable immunodeficiency patients without monogenic defects.
Scand J Immunol
; 96(1): e13164, 2022 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-35305035
7.
Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature.
Immunol Invest
; 51(2): 331-342, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-33047643
8.
Evaluation of Expression of LRBA and CTLA-4 Proteins in Common Variable Immunodeficiency Patients.
Immunol Invest
; 51(2): 381-394, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-33191838
9.
The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS).
Immunol Invest
; 51(3): 644-659, 2022 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-33401995
10.
Adverse reactions in a large cohort of patients with inborn errors of immunity receiving intravenous immunoglobulin.
Clin Immunol
; 230: 108826, 2021 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34418548
11.
Variable Abnormalities in T and B Cell Subsets in Ataxia Telangiectasia.
J Clin Immunol
; 41(1): 76-88, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33052516
12.
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity.
J Clin Immunol
; 41(6): 1339-1351, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34052995
13.
Known and potential molecules associated with altered B cell development leading to predominantly antibody deficiencies.
Pediatr Allergy Immunol
; 32(8): 1601-1615, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34181780
14.
Clinical, immunological and genetic findings in patients with UNC13D deficiency (FHL3): A systematic review.
Pediatr Allergy Immunol
; 32(1): 186-197, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32679608
15.
Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like diseases: A systematic review.
Pediatr Allergy Immunol
; 32(7): 1519-1532, 2021 10.
Artigo
Inglês
| MEDLINE | ID: mdl-33963613
16.
The spectrum of ATM gene mutations in Iranian patients with ataxia-telangiectasia.
Pediatr Allergy Immunol
; 32(6): 1316-1326, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33547824
17.
Effect of Class Switch Recombination Defect on the Phenotype of Ataxia-Telangiectasia Patients.
Immunol Invest
; 50(2-3): 201-215, 2021 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32116070
18.
Evaluation of Radiation Sensitivity in Patients with Hyper IgM Syndrome.
Immunol Invest
; 50(5): 580-596, 2021 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-32584193
19.
Evaluation of miR-210 expression in common variable immunodeficiency: patients with unsolved genetic defect.
Allergol Immunopathol (Madr)
; 49(2): 84-93, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33641299
20.
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.
Artigo
Inglês
| MEDLINE | ID: mdl-31887391