Nima Parvaneh
Tehran University of Medical Sciences
H-index: 42
Asia-Iran
Top articles of Nima Parvaneh
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Human inherited CCR2 deficiency underlies progressive polycystic lung disease | Cell | Anna-Lena Neehus Brenna Carey Marija Landekic Patricia Panikulam Gail Deutsch | 2024/1/18 |
Immune reconstitution after hematopoietic stem cell transplantation with reduced intensity conditioning for inborn errors of immunity | Paolo A Muraro Maria T Cencioni | 2021/11/17 | |
Antibody Response before and after the Booster Dose of Inactivated Corona Vaccine in Antibody Deficient Patients | Iranian Journal of Allergy, Asthma and Immunology | Mahshid Movahedi Masoud Movahedi Nima Parvaneh Hassan Abolhassani Mohadese Mahdavi | 2024/4/14 |
Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency | Nature Immunology | Hirotsugu Oda Kalpana Manthiram Pallavi Pimpale Chavan Eva Rieser Önay Veli | 2024/4/12 |
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants | Science | Marie Materna Ottavia M Delmonte Marita Bosticardo Mana Momenilandi Peyton E Conrey | 2024/3/1 |
Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian … | Journal of Clinical Immunology | Mohadese Sadat Mousavi Khorshidi Yoann Seeleuthner Zahra Chavoshzadeh Maryam Behfar Amir Ali Hamidieh | 2023/11 |
Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria | Science immunology | Quentin Philippot Masato Ogishi Jonathan Bohlen Julia Puchan Andrés Augusto Arias | 2023/2/10 |
Novel RAG2 Mutation in a Patient with Leaky Severe Combined Immunodeficiency | Immunology and Genetics Journal | Salar Pashangzadeh Reza Yazdani Samaneh Delavari Hassan Abolhassani Nima Parvaneh | 2023/5/22 |
Tumor Necrosis Factor-α (-308G> A) Gene Polymorphism and Its Association with Asthma and Atopy Status | Iranian Journal of Allergy, Asthma and Immunology | Anahita Razaghian Nima Parvaneh Ali Akbar Amirzargar Mohammad Gharagozlou | 2023/9/10 |
Impaired thymic AIRE expression underlies autoantibodies against type I IFNs in humans with inborn errors of the alternative NF-kB pathway | Authorea Preprints | Tom Le Voyer Adrian Gervais Jérémie Rosain Audrey Parent Axel Cederholm | 2023/1/9 |
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease | Journal of Experimental Medicine | Mehul Sharma Daniel Leung Mana Momenilandi Lauren CW Jones Lucia Pacillo | 2023/3/8 |
Clinical and immunological characteristics of 69 leukocyte adhesion deficiency‐I patients | Pediatric Allergy and Immunology | Mohammad Reza Fazlollahi Amir Ali Hamidieh Leila Moradi Raheleh Shokouhi Shoormati Nastaran Sabetkish | 2023/7 |
Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect | Journal of investigational allergology & clinical immunology | F Tofighi Zavareh A Mirshafiey R Yazdani AA Keshtkar H Abolhassani | 2023/12/14 |
Association between IL-10 (at position-592) and IL-4 (at position-589) genotype polymorphism with atopic and non-atopic asthma in children | American Journal of Clinical and Experimental Immunology | Anahita Razaghian Nima Parvaneh Ali Akbar Amirzargar Matineh Nirouei Mohammad Gharagozlou | 2023 |
Chediak Higashi syndrome with hemophagocytic lymphohistiocytosis | Fetal and Pediatric Pathology | Moeinadin Safavi Nima Parvaneh | 2023/3/4 |
Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling | Nature Communications | Cristiane J Nunes-Santos HyeSun Kuehn Brigette Boast SuJin Hwang Douglas B Kuhns | 2023/6/22 |
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency | NATURE | Stéphanie Boisson-Dupuis Eric Oksenhendler Satoshi Okada Oana Caluseriu Mathilde Valeria Ursini | 2023/11/8 |
Analysis of Lymphocyte and Clinical Profile among Non-monogenic Common Variable Immunodeficiency Patients with and without Class Switch Recombination Defect | J Investig Allergol Clin Immunol | Abbas Mirshafiey Asghar Aghamohammadi | 2023 |
Hematologically important mutations: Leukocyte adhesion deficiency (second update) | Blood Cells, Molecules, and Diseases | Dirk Roos Karin Van Leeuwen Manisha Madkaikar Priyanka M Kambli Maya Gupta | 2023/3/1 |
Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A) | Frontiers in Immunology | Nina Brauer Yuto Maruta Miriam Lisci Katharina Strege Ilske Oschlies | 2023/6/14 |
