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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: klein c. Blood. 2023 Feb 9;141(6):645-658. doi: 10.1182/blood.2022016783. Blood. 2023. PMID: 36223592 Free PMC article.
The clinical, immunohematological, and molecular study of Iranian patients with severe congenital neutropenia.
Rezaei N, Moin M, Pourpak Z, Ramyar A, Izadyar M, Chavoshzadeh Z, Sherkat R, Aghamohammadi A, Yeganeh M, Mahmoudi M, Mahjoub F, Germeshausen M, Grudzien M, Horwitz MS, Klein C, Farhoudi A. Rezaei N, et al. Among authors: klein c. J Clin Immunol. 2007 Sep;27(5):525-33. doi: 10.1007/s10875-007-9106-y. Epub 2007 Jun 21. J Clin Immunol. 2007. PMID: 17587155
Neutropenia and primary immunodeficiency diseases.
Rezaei N, Moazzami K, Aghamohammadi A, Klein C. Rezaei N, et al. Among authors: klein c. Int Rev Immunol. 2009;28(5):335-66. doi: 10.1080/08830180902995645. Int Rev Immunol. 2009. PMID: 19811314 Review.
Genetic etiologies of severe congenital neutropenia.
Boztug K, Klein C. Boztug K, et al. Among authors: klein c. Curr Opin Pediatr. 2011 Feb;23(1):21-6. doi: 10.1097/MOP.0b013e32834262f8. Curr Opin Pediatr. 2011. PMID: 21206270 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: klein c. 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.
Myeloperoxidase deficiency: the secret under the flag of unstained cell.
Patıroğlu T, Eke Güngör H, Belohradsky JS, Unal E, Klein C. Patıroğlu T, et al. Among authors: klein c. Turk J Haematol. 2013 Jun;30(2):232-3. doi: 10.4274/Tjh.2012.0012. Epub 2013 Jun 5. Turk J Haematol. 2013. PMID: 24385801 Free PMC article. No abstract available.
Inherited biallelic CSF3R mutations in severe congenital neutropenia.
Triot A, Järvinen PM, Arostegui JI, Murugan D, Kohistani N, Dapena Díaz JL, Racek T, Puchałka J, Gertz EM, Schäffer AA, Kotlarz D, Pfeifer D, Díaz de Heredia Rubio C, Ozdemir MA, Patiroglu T, Karakukcu M, Sánchez de Toledo Codina J, Yagüe J, Touw IP, Unal E, Klein C. Triot A, et al. Among authors: klein c. Blood. 2014 Jun 12;123(24):3811-7. doi: 10.1182/blood-2013-11-535419. Epub 2014 Apr 21. Blood. 2014. PMID: 24753537 Free PMC article.
3,906 results