Items where Author is "Parvaneh, N."

Article

(2024) Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room. Iranian Journal of Child Neurology. pp. 33-45. ISSN 1735-4668

(2024) The immunopathological landscape of human pre-TCRa deficiency: From rare to common variants. Science. ISSN 00368075 (ISSN)

(2024) The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants. Science. p. 19. ISSN 0036-8075

(2023) Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients. Pediatric Allergy and Immunology. p. 12. ISSN 0905-6157

(2023) Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG <i>RFXANK</i> Founder Mutation in the Iranian Population. Journal of Clinical Immunology. pp. 1941-1952. ISSN 0271-9142

(2023) Hematologically important mutations: Leukocyte adhesion deficiency (second update). Blood Cells Molecules and Diseases. p. 14. ISSN 1079-9796

(2023) A case series of ten plus one deficiency of adenosine deaminase 2 (DADA2) patients in Iran. Pediatric Rheumatology. p. 8.

(2022) Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency. Journal of Experimental Medicine. p. 33. ISSN 0022-1007

(2022) TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases. Pediatric Rheumatology. p. 8.

(2019) Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE. ISSN 2213-2201 (Electronic)

(2019) Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran. Immunology Letters. pp. 70-78. ISSN 0165-2478

(2018) Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency. The Journal of allergy and clinical immunology. pp. 1450-1458. ISSN 1097-6825 (Electronic) 0091-6749 (Linking)

(2018) Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis. Journal of Clinical Immunology. pp. 816-832. ISSN 0271-9142

(2017) New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiency. European Annals of Allergy and Clinical Immunology. pp. 235-239. ISSN 1764-1489

(2016) In silico analysis of deleterious single nucleotide polymorphisms in human BUB1 mitotic checkpoint serine/threonine kinase B gene. Meta Gene. pp. 142-150. ISSN 2214-5400

(2015) Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment. Journal of Investigational Allergology and Clinical Immunology. pp. 416-425. ISSN 1018-9068