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Page 1
Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Neehus AL, Carey B, Landekic M, Panikulam P, Deutsch G, Ogishi M, Arango-Franco CA, Philippot Q, Modaresi M, Mohammadzadeh I, Corcini Berndt M, Rinchai D, Le Voyer T, Rosain J, Momenilandi M, Martin-Fernandez M, Khan T, Bohlen J, Han JE, Deslys A, Bernard M, Gajardo-Carrasco T, Soudée C, Le Floc'h C, Migaud M, Seeleuthner Y, Jang MS, Nikolouli E, Seyedpour S, Begueret H, Emile JF, Le Guen P, Tavazzi G, Colombo CNJ, Marzani FC, Angelini M, Trespidi F, Ghirardello S, Alipour N, Molitor A, Carapito R, Mazloomrezaei M, Rokni-Zadeh H, Changi-Ashtiani M, Brouzes C, Vargas P, Borghesi A, Lachmann N, Bahram S, Crestani B, Fayon M, Galode F, Pahari S, Schlesinger LS, Marr N, Bogunovic D, Boisson-Dupuis S, Béziat V, Abel L, Borie R, Young LR, Deterding R, Shahrooei M, Rezaei N, Parvaneh N, Craven D, Gros P, Malo D, Sepulveda FE, Nogee LM, Aladjidi N, Trapnell BC, Casanova JL, Bustamante J. Neehus AL, et al. Among authors: mohammadzadeh i. Cell. 2024 Jan 18;187(2):390-408.e23. doi: 10.1016/j.cell.2023.11.036. Epub 2023 Dec 28. Cell. 2024. PMID: 38157855 Free PMC article.
BCGitis as the primary manifestation of chronic granulomatous disease.
Khalili N, Mohammadzadeh I, Khalili N, Heredia RJ, Zoghi S, Boztug K, Rezaei N. Khalili N, et al. Among authors: mohammadzadeh i. IDCases. 2020 Dec 29;23:e01038. doi: 10.1016/j.idcr.2020.e01038. eCollection 2021. IDCases. 2020. PMID: 33425681 Free PMC article.
Severe primary antibody deficiency due to a novel mutation of mu heavy chain.
Mohammadzadeh I, Yeganeh M, Aghamohammadi A, Parvaneh N, Behniafard N, Abolhassani H, Tabassomi F, Hemmat M, Kanegane H, Miyawaki T, Ohara O, Rezaei N. Mohammadzadeh I, et al. J Investig Allergol Clin Immunol. 2012;22(1):78-9. J Investig Allergol Clin Immunol. 2012. PMID: 22448464 Free article. No abstract available.
Primary immunodeficiency diseases in Northern Iran.
Mohammadzadeh I, Moazzami B, Ghaffari J, Aghamohammadi A, Rezaei N. Mohammadzadeh I, et al. Allergol Immunopathol (Madr). 2017 May-Jun;45(3):244-250. doi: 10.1016/j.aller.2016.11.001. Epub 2017 Feb 22. Allergol Immunopathol (Madr). 2017. PMID: 28237128
Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients.
Momtazmanesh S, Rayzan E, Zoghi S, Shahkarami S, Molatefi R, Mohammadzadeh I, Ghaffari J, Mahmoudi H, Dmytrus J, Segarra-Roca A, Somekh I, Witzel M, Hauck F, Boztug K, Klein C, Rezaei N. Momtazmanesh S, et al. Among authors: mohammadzadeh i. Endocr Metab Immune Disord Drug Targets. 2022;22(1):159-168. doi: 10.2174/1871530321666210226143912. Endocr Metab Immune Disord Drug Targets. 2022. PMID: 33634762
Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients.
Aghamohammadi A, Abolhassani H, Latif A, Tabassomi F, Shokuhfar T, Torabi Sagvand B, Shahinpour S, Mirminachi B, Parvaneh N, Movahedi M, Gharagozlou M, Sherkat R, Amin R, Aleyasin S, Faridhosseini R, Jabbari-Azad F, Cheraghi T, Eslamian MH, Khalili A, Kalantari N, Shafiei A, Dabbaghzade A, Khayatzadeh A, Ebrahimi M, Razavinejad D, Bazregari S, Ebrahimi M, Ghaffari J, Bemanian MH, Behniafard N, Kashef S, Mohammadzadeh I, Hammarström L, Rezaei N. Aghamohammadi A, et al. Among authors: mohammadzadeh i. Expert Rev Clin Immunol. 2014 Oct;10(10):1405-17. doi: 10.1586/1744666X.2014.958469. Expert Rev Clin Immunol. 2014. PMID: 25225775
Clinical and immunological features of 65 Iranian patients with common variable immunodeficiency.
Aghamohammadi A, Farhoudi A, Moin M, Rezaei N, Kouhi A, Pourpak Z, Yaseri N, Movahedi M, Gharagozlou M, Zandieh F, Yazadni F, Arshi S, Mohammadzadeh I, Ghazi BM, Mahmoudi M, Tahaei S, Isaeian A. Aghamohammadi A, et al. Among authors: mohammadzadeh i. Clin Diagn Lab Immunol. 2005 Jul;12(7):825-32. doi: 10.1128/CDLI.12.7.825-832.2005. Clin Diagn Lab Immunol. 2005. PMID: 16002630 Free PMC article.
59 results