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Page 1
Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation.
Nabavi M, Shahrooei M, Rokni-Zadeh H, Vrancken J, Changi-Ashtiani M, Darabi K, Manian M, Seif F, Meyts I, Voet A, Moens L, Bossuyt X. Nabavi M, et al. J Clin Immunol. 2019 Feb;39(2):138-141. doi: 10.1007/s10875-019-00599-3. Epub 2019 Feb 22. J Clin Immunol. 2019. PMID: 30796585 No abstract available.
Frequency and clinical manifestations of patients with primary immunodeficiency disorders in Iran: update from the Iranian Primary Immunodeficiency Registry.
Rezaei N, Aghamohammadi A, Moin M, Pourpak Z, Movahedi M, Gharagozlou M, Atarod L, Ghazi BM, Isaeian A, Mahmoudi M, Abolmaali K, Mansouri D, Arshi S, Tarash NJ, Sherkat R, Akbari H, Amin R, Alborzi A, Kashef S, Farid R, Mohammadzadeh I, Shabestari MS, Nabavi M, Farhoudi A. Rezaei N, et al. Among authors: nabavi m. J Clin Immunol. 2006 Nov;26(6):519-32. doi: 10.1007/s10875-006-9047-x. Epub 2006 Oct 6. J Clin Immunol. 2006. PMID: 17024564
Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia.
Esmaeilzadeh H, Bemanian MH, Nabavi M, Arshi S, Fallahpour M, Fuchs I, zur Stadt U, Warnatz K, Ammann S, Ehl S, Lehmberg K, Rezaei N. Esmaeilzadeh H, et al. Among authors: nabavi m. J Clin Immunol. 2015 Jan;35(1):22-5. doi: 10.1007/s10875-014-0119-z. Epub 2014 Dec 10. J Clin Immunol. 2015. PMID: 25491289
LPS-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal IgM Phenotype and Low Number of B Cells.
Shokri S, Nabavi M, Hirschmugl T, Aghamohammadi A, Arshi S, Bemanian MH, Fallahpour M, Molatefi R, Rekabi M, Eslami N, Ahmadian J, Darabi K, Sedighi GR, Monajemzadeh M, Modaresi M, Parvaneh N, Boztug K, Rezaei N. Shokri S, et al. Among authors: nabavi m. Acta Med Iran. 2016 Oct;54(10):620-623. Acta Med Iran. 2016. PMID: 27888588 Free article.
A gain-of-function mutation of STAT1: A novel genetic factor contributing to chronic mucocutaneous candidiasis.
Eslami N, Tavakol M, Mesdaghi M, Gharegozlou M, Casanova JL, Puel A, Okada S, Arshi S, Bemanian MH, Fallahpour M, Molatefi R, Seif F, Zoghi S, Rezaei N, Nabavi M. Eslami N, et al. Among authors: nabavi m. Acta Microbiol Immunol Hung. 2017 Jun 1;64(2):191-201. doi: 10.1556/030.64.2017.014. Epub 2017 Jun 9. Acta Microbiol Immunol Hung. 2017. PMID: 28597685 Free article.
DOCK2 Deficiency in a Patient with Hyper IgM Phenotype.
Alizadeh Z, Mazinani M, Shakerian L, Nabavi M, Fazlollahi MR. Alizadeh Z, et al. Among authors: nabavi m. J Clin Immunol. 2018 Jan;38(1):10-12. doi: 10.1007/s10875-017-0468-5. Epub 2017 Dec 4. J Clin Immunol. 2018. PMID: 29204803 No abstract available.
Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report.
Pourvali A, Arshi S, Nabavi M, Bemanian MH, Shokri S, Shahrooei M, Rezaei N, Fallahpour M. Pourvali A, et al. Among authors: nabavi m. Iran J Immunol. 2019 Dec;16(4):334-338. doi: 10.22034/IJI.2019.80285. Iran J Immunol. 2019. PMID: 31885011 Free article.
184 results