Detalles de la búsqueda
1.
Clinical heterogeneity in families with multiple cases of inborn errors of immunity.
Clin Immunol
; 259: 109896, 2024 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-38184287
2.
Genomic Testing Identifies Monogenic Causes in Patients with Very Early-Onset Inflammatory Bowel Disease: A Multi-center Survey in an Iranian Cohort.
Clin Exp Immunol
; 2024 Apr 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-38651248
3.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-37584719
4.
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry.
Clin Immunol
; 244: 109131, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36179983
5.
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency.
J Clin Immunol
; 42(3): 634-652, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35079916
6.
Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency.
Blood
; 136(23): 2638-2655, 2020 12 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-32603431
7.
Prevalence of nephrocalcinosis in children with congenital adrenal hyperplasia.
J Res Med Sci
; 27: 16, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35342446
8.
Epidemiology, Sociodemographic Factors and Comorbidity for Allergic Rhinitis, Asthma, and Rhinosinusitis Among 15 to 65-year-Old Iranian Patients.
Med J Islam Repub Iran
; 36: 128, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36620471
9.
Impact of SARS-CoV-2 Pandemic on Patients with Primary Immunodeficiency.
J Clin Immunol
; 41(2): 345-355, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33263173
10.
Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity.
Pediatr Allergy Immunol
; 32(6): 1335-1348, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-33774840
11.
Congenital disorders of glycosylation with defective fucosylation.
J Inherit Metab Dis
; 44(6): 1441-1452, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34389986
12.
Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity.
Int Arch Allergy Immunol
; 181(9): 706-714, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32615565
13.
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency.
J Allergy Clin Immunol
; 141(4): 1450-1458, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-28916186
14.
Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis.
J Clin Immunol
; 38(7): 816-832, 2018 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30302726
15.
An unusual cause of facial wound in a child: Hyper IgE syndrome-associated Noma neonatorum.
Int Wound J
; 19(8): 2226-2228, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35474291
16.
Metformin-Induced Generalized Bullous Fixed-Drug Eruption with a Positive Dechallenge-Rechallenge Test: A Case Report and Literature Review.
Case Rep Dermatol Med
; 2023: 6353919, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37034844
17.
Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity.
Biology (Basel)
; 12(5)2023 Apr 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-37237458
18.
The Effectiveness of Synbiotic on the Improvement of Clinical Symptoms in Children with Eosinophilic Esophagitis.
Int J Pediatr
; 2022: 4211626, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35295822
19.
Clinical and Epidemiological Features of Patients with Drug-Induced Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Iran: Different Points of Children from Adults.
Int J Pediatr
; 2022: 8163588, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35178096
20.
Assessment of the Effect of Short-Term Combined High-Intensity Interval Training on TLR4, NF-κB and IRF3 Expression in Young Overweight and Obese Girls.
Public Health Genomics
; 23(1-2): 26-36, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32101857