Publications by authors named "Nima Parvaneh"

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Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants.
Russell Donis, Matthew N Wakeling, Nicola Jeffery, Molly Govier, Matthew B Johnson, Nima Parvaneh

Diabet Med· November 2025

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The neurologic face of X-linked lymphoproliferative syndrome type 1: a systematic review.
Erta Rajabi, Saber Gharagozlou, Kousha Farhadi, Moeinadin Safavi, Fatemeh Zamani, Nima Parvaneh

Orphanet J Rare Dis· October 2025

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Thrombocytopenia in patients with inborn errors of immunity.
Saba Fekrvand, Maryam Mohtashami, Negin Sanadgol, Helia Salehi, Najmeh Nameh Goshay Fard, Nima Parvaneh

BMC Immunol· September 2025

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Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel cases.
Erta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, Anne Molitor, Mohadese Sadat Mousavi Khorshidi, Nima Parvaneh

BMC Immunol· July 2025

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Two different forms of inherited human TCRα chain deficiency.
Marie Materna, Simin Seyedpour, Tom Le Voyer, Nima Parvaneh, Niloufar Yazdanpanah

J Hum Immun· July 2025

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Safety of MMR vaccination evaluated in children with food and gelatin allergy in Iran.
Mehdi Shokri, Masoud Movahedi, Nima Parvaneh, Mohammad Gharagozlou, Mohadese Sadat Mousavi Khorshidi

BMC Pediatr· April 2025

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Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature.
Marita Bosticardo, Kerry Dobbs, Ottavia M Delmonte, Andrew J Martins, Francesca Pala, Nima Parvaneh

Sci Immunol· January 2025

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How Hospitalizations Can Be Effective in Subsequent Care of Children with Asthma?
Samin Sharafian, Ghasem Barjouei Fard, Maryam Atabakzadeh, Masoud Movahedi, Nima Parvaneh

Iran J Allergy Asthma Immunol· December 2024

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Three cases of autoinflammatory disease with novel NLRC4 mutations, and the first mutation reported in the CARD domain of NLRC4 associated with autoinflammatory infantile enterocolitis (AIFEC).
Kosar Asna Ashari, Nima Parvaneh, Kayvan Mirnia, Mehri Ayati, Maryam Saeedi

Pediatr Rheumatol Online J· October 2024

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Hematopoietic Stem Cell Transplantation for C1q Deficiency: A Study on Behalf of the EBMT Inborn Errors Working Party.
Helena Buso, Etai Adam, Peter D Arkwright, Sagar Bhattad, Amir Ali Hamidieh, Nima Parvaneh

J Clin Immunol· October 2024

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A pleiotropic recurrent dominant variant causes a complex multisystemic disease.
Anne Molitor, Alexandre Lederle, Mirjana Radosavljevic, Vinay Sapuru, Megan E Zavorka Thomas, Nima Parvaneh

Sci Adv· September 2024

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Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room.
Sareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, Maryam Bemanalizadeh, Masood Ghahvechi Akbari, Nima Parvaneh

Iran J Child Neurol· September 2024

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Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, Samuel C C Chiang, Gudrun Thoulass, Nima Parvaneh

J Exp Med· July 2024

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Correction: Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.
Tamara Kögl, Hsin-Fang Chang, Julian Staniek, Samuel C C Chiang, Gudrun Thoulass, Nima Parvaneh

J Exp Med· July 2024

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Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Anna-Lena Neehus, Brenna Carey, Marija Landekic, Patricia Panikulam, Gail Deutsch, Nima Parvaneh

Cell· June 2024

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Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency.
Hirotsugu Oda, Kalpana Manthiram, Pallavi Pimpale Chavan, Eva Rieser, Önay Veli, Nima Parvaneh

Nat Immunol· May 2024

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FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.
Mana Momenilandi, Romain Lévy, Steicy Sobrino, Jingwei Li, Chantal Lagresle-Peyrou, Nima Parvaneh

Cell· May 2024

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Antibody Response Before and After the Booster Dose of Inactivated Corona Vaccine in Antibody Deficient Patients.
Mahshid Movahedi, Masoud Movahedi, Nima Parvaneh, Hassan Abolhassani, Mohadese Mahdavi

Iran J Allergy Asthma Immunol· April 2024

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The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants.
Marie Materna, Ottavia M Delmonte, Marita Bosticardo, Mana Momenilandi, Peyton E Conrey, Nima Parvaneh

Science· March 2024

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Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Anna-Lena Neehus, Brenna Carey, Marija Landekic, Patricia Panikulam, Gail Deutsch, Nima Parvaneh

Cell· January 2024

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Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Mohadese Sadat Mousavi Khorshidi, Yoann Seeleuthner, Zahra Chavoshzadeh, Maryam Behfar, Amir Ali Hamidieh, Nima Parvaneh

J Clin Immunol· November 2023

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Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria.
Jonathan Bohlen, Qinhua Zhou, Quentin Philippot, Masato Ogishi, Darawan Rinchai, Nima Parvaneh

Cell· November 2023

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Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
Tom Le Voyer, Audrey V Parent, Xian Liu, Axel Cederholm, Adrian Gervais, Nima Parvaneh

Nature· November 2023

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Association between IL-10 (at position -592) and IL-4 (at position -589) genotype polymorphism with atopic and non-atopic asthma in children.
Anahita Razaghian, Nima Parvaneh, Ali Akbar Amirzargar, Matineh Nirouei, Mohammad Gharagozlou

Am J Clin Exp Immunol· October 2023

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Tumor Necrosis Factor-α (-308G>A) Gene Polymorphism and Its Association with Asthma and Atopy Status.
Anahita Razaghian, Nima Parvaneh, Ali Akbar Amirzargar, Mohammad Gharagozlou

Iran J Allergy Asthma Immunol· September 2023

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