Detalhe da pesquisa
1.
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.
Cell;
2024 May 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38701783
2.
Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria.
Cell;
186(23): 5114-5134.e27, 2023 11 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37875108
3.
Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency.
Nat Immunol;
25(5): 764-777, 2024 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38609546
4.
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
Nature;
623(7988): 803-813, 2023 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37938781
5.
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
J Clin Immunol;
43(8): 1941-1952, 2023 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37584719
6.
Hematologically important mutations: Leukocyte adhesion deficiency (second update).
Blood Cells Mol Dis;
99: 102726, 2023 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36696755
7.
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
8.
Chediak Higashi Syndrome with Hemophagocytic Lymphohistiocytosis.
Fetal Pediatr Pathol;
42(2): 259-262, 2023 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35608383
9.
Effective anti-mycobacterial treatment for BCG disease in patients with Mendelian Susceptibility to Mycobacterial Disease (MSMD): a case series.
Ann Clin Microbiol Antimicrob;
21(1): 8, 2022 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35232430
10.
Fatal invasive aspergillosis in a child with chronic granulomatous disease.
J Wound Care;
31(5): 427-431, 2022 May 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35579316
11.
Phenotypic analysis of pyrin-associated autoinflammation with neutrophilic dermatosis patients during treatment.
Rheumatology (Oxford);
60(11): 5436-5446, 2021 11 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33693560
12.
Serum sickness-like reactions in Iranian children: a registry-based study in a referral center.
Allergol Immunopathol (Madr);
48(5): 424-429, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32653225
13.
Vaccine-Derived Poliovirus Infection among Patients with Primary Immunodeficiency and Effect of Patient Screening on Disease Outcomes, Iran.
Emerg Infect Dis;
25(11): 2005-2012, 2019 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31625840
14.
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
15.
Novel CYBA mutation in a family with BCGitis.
Acta Microbiol Immunol Hung;
67(1): 56-60, 2019 Dec 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31847541
16.
Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.
Immunol Rev;
264(1): 103-20, 2015 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25703555
17.
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rß1 Deficiency.
J Clin Immunol;
38(5): 617-627, 2018 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29995221
18.
Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature.
J Clin Immunol;
42(8): 1618-1621, 2022 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35906326
19.
Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rß1 deficiencies.
Pediatr Blood Cancer;
64(6)2017 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27873456
20.
Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats' Disease and Literature Review.
J Clin Immunol;
40(6): 940-947, 2020 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32638195