Detalhe da pesquisa
1.
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
2.
Study of NLRP3 Single Nucleotide Polymorphisms in Juvenile Systemic Lupus Erythematosus (JSLE).
Immunol Invest
; 52(5): 598-615, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37262326
3.
DNA Methylation of CD70 Promoter in Juvenile Systemic Lupus Erythematosus.
Fetal Pediatr Pathol
; 41(1): 58-67, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32427516
4.
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
5.
Multimodality imaging of constrictive pericarditis in H syndrome.
Echocardiography
; 38(6): 1021-1032, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33899966
6.
Multisystem inflammatory syndrome associated with SARS-CoV-2 infection in 45 children: a first report from Iran.
Epidemiol Infect
; 148: e196, 2020 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32854812
7.
PTPN22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus.
Fetal Pediatr Pathol
; 39(1): 13-20, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31232672
8.
Farber disease: report of three cases with joint involvement mimicking juvenile idiopathic arthritis.
J Musculoskelet Neuronal Interact
; 19(4): 521-525, 2019 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31789304
9.
Direct Immunofluorescence Results of the Skin Biopsy and Frequency of Systemic Involvement in Children with Henoch-Schonlein Purpura.
Fetal Pediatr Pathol
; 38(2): 121-126, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30600750
10.
The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series.
BMC Med Genet
; 19(1): 87, 2018 05 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-29801470
11.
The Farsi version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR).
Rheumatol Int
; 38(Suppl 1): 171-178, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29637366
12.
Lack of Association between STAT4 Single Nucleotide Polymorphisms and Iranian Juvenile Rheumatoid Arthritis Patients.
Fetal Pediatr Pathol
; 36(3): 177-183, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28524764
13.
Association Study of MECP2 Gene Single Nucleotide Polymorphisms in Juvenile-Onset Systemic Lupus Erythematosus Patients from Iran.
Fetal Pediatr Pathol
; 36(6): 423-431, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29199882
14.
Association of PTPN22 Gene Polymorphisms with Susceptibility to Juvenile Idiopathic Arthritis in Iranian Population.
Fetal Pediatr Pathol
; 36(1): 42-48, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27732119
15.
Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA).
J Clin Immunol
; 40(4): 637-642, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32170523
16.
Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency.
J Clin Immunol
; 34(1): 123-6, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24177804
17.
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis.
J Clin Immunol
; 39(1): 11-14, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30612220
18.
Sensitivity and specificity of adenosine deaminase in diagnosis of juvenile idiopathic arthritis.
Med J Islam Repub Iran
; 28: 113, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25678992
19.
[99m Tc] Tc-MDP bone SPECT/CT diagnosing unstable slipped capital femoral epiphysis with secondary AVN in a patient with misleading knee pain.
Clin Case Rep
; 11(7): e7594, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37397570
20.
Multisystem inflammatory syndrome in children and Kawasaki disease; comparison of their clinical findings and one-year follow-up-a cross-sectional study.
Ital J Pediatr
; 49(1): 90, 2023 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37475054