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.
Genetic and immunologic evaluation of children with inborn errors of immunity and severe or critical COVID-19.
J Allergy Clin Immunol
; 150(5): 1059-1073, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36113674
3.
Comparison of the Onset and End of Specific and Major Side Effects in Iranian Teenage Participants Vaccinated With COVID-19 Vaccine: Sinopharm and Soberana.
Med J Islam Repub Iran
; 37: 15, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37123336
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.
Pediatric and adolescent COVID-19 vaccination side effects: A retrospective cohort study of the Iranian teenage group in 2021.
J Med Virol
; 94(10): 4890-4900, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35758760
6.
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
7.
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
8.
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
9.
The effect of opium on severity of COVID-19 infection:An original study from Iran.
Med J Islam Repub Iran
; 35: 115, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34956961
10.
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
11.
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
12.
The role of molecular diagnosis in anaphylactic patients with dual or triple-sensitization to Hymenoptera venoms.
Allergy Asthma Clin Immunol
; 20(1): 22, 2024 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38521942
13.
Immune endotyping and gene expression profile of patients with chronic rhinosinusitis with nasal polyps in the aspirin-exacerbated respiratory disease (AERD) and the non-AERD subgroups.
Allergy Asthma Clin Immunol
; 20(1): 14, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38360807
14.
Doxycycline Improves Quality of Life and Anosmia in Chronic Rhinosinusitis With Nasal Polyposis: A Randomized Controlled Trial.
Am J Rhinol Allergy
; 37(4): 384-390, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-36740870
15.
Immunologic response, Efficacy, and Safety of Vaccines against COVID-19 Infection in Healthy and immunosuppressed Children and Adolescents Aged 2 - 21 years old: A Systematic Review and Meta-analysis.
J Clin Virol
; 153: 105196, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35716417
16.
The Uncomplicated Course of COVID-19 in Primary Immunodeficiency Patients: A Report of 14 Common Variable Immunodeficiency Patients.
Iran J Allergy Asthma Immunol
; 21(5): 594-599, 2022 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36341567
17.
Progressive multifocal leukoencephalopathy in a patient with novel mutation in the RAC2 gene: a case report.
J Med Case Rep
; 16(1): 235, 2022 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689244
18.
Neonatal Onset of Hemophagocytic Lymphohistiocytosis Due to Prenatal Varicella-Zoster Infection in a Neonate with Griscelli Syndrome Type 2.
Iran J Allergy Asthma Immunol
; 21(4): 488-493, 2022 Aug 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36243938
19.
Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency.
J Invest Dermatol
; 142(9): 2435-2445, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35276224
20.
Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions.
JCI Insight
; 7(8)2022 04 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-35316210