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Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.
Linder MI, Mizoguchi Y, Hesse S, Csaba G, Tatematsu M, Łyszkiewicz M, Ziȩtara N, Jeske T, Hastreiter M, Rohlfs M, Liu Y, Grabowski P, Ahomaa K, Maier-Begandt D, Schwestka M, Pazhakh V, Isiaku AI, Briones Miranda B, Blombery P, Saito MK, Rusha E, Alizadeh Z, Pourpak Z, Kobayashi M, Rezaei N, Unal E, Hauck F, Drukker M, Walzog B, Rappsilber J, Zimmer R, Lieschke GJ, Klein C. Linder MI, et al. Among authors: rezaei n. Blood. 2023 Feb 9;141(6):645-658. doi: 10.1182/blood.2022016783. Blood. 2023. PMID: 36223592 Free PMC article.
Severe combined immunodeficiency: a cohort of 40 patients.
Yeganeh M, Heidarzade M, Pourpak Z, Parvaneh N, Rezaei N, Gharagozlou M, Movahedi M, Shabestari MS, Mamishi S, Aghamohammadi A, Moin M. Yeganeh M, et al. Among authors: rezaei n. Pediatr Allergy Immunol. 2008 Jun;19(4):303-6. doi: 10.1111/j.1399-3038.2007.00647.x. Epub 2007 Dec 18. Pediatr Allergy Immunol. 2008. PMID: 18093084
Neutropenia and primary immunodeficiency diseases.
Rezaei N, Moazzami K, Aghamohammadi A, Klein C. Rezaei N, et al. Int Rev Immunol. 2009;28(5):335-66. doi: 10.1080/08830180902995645. Int Rev Immunol. 2009. PMID: 19811314 Review.
The phenotype of human STK4 deficiency.
Abdollahpour H, Appaswamy G, Kotlarz D, Diestelhorst J, Beier R, Schäffer AA, Gertz EM, Schambach A, Kreipe HH, Pfeifer D, Engelhardt KR, Rezaei N, Grimbacher B, Lohrmann S, Sherkat R, Klein C. Abdollahpour H, et al. Among authors: rezaei n. Blood. 2012 Apr 12;119(15):3450-7. doi: 10.1182/blood-2011-09-378158. Epub 2012 Jan 31. Blood. 2012. PMID: 22294732 Free PMC article.
1,582 results