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Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis.
Mamishi S, Shahmahmoudi S, Tabatabaie H, Teimourian S, Pourakbari B, Gheisari Y, Yeganeh M, Salavati A, Esteghamati AR, Gooya MM, Nategh R, Parvaneh N. Mamishi S, et al. Among authors: pourakbari b. Eur J Pediatr. 2008 Nov;167(11):1335-8. doi: 10.1007/s00431-008-0674-5. Epub 2008 Mar 4. Eur J Pediatr. 2008. PMID: 18317803
Hydatid disease in Iranian children.
Mamishi S, Sagheb S, Pourakbari B. Mamishi S, et al. Among authors: pourakbari b. J Microbiol Immunol Infect. 2007 Oct;40(5):428-31. J Microbiol Immunol Infect. 2007. PMID: 17932603
Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency.
Parvaneh N, Teimourian S, Jacomelli G, Badalzadeh M, Bertelli M, Zakharova E, Tabatabaei P, Parvaneh L, Pourakbari B, Yeganeh M, Tamizifar B, Mamishi S, Micheli V. Parvaneh N, et al. Among authors: pourakbari b. Clin Biochem. 2008 Mar;41(4-5):350-2. doi: 10.1016/j.clinbiochem.2007.11.007. Epub 2007 Nov 21. Clin Biochem. 2008. PMID: 18067860 No abstract available.
Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspot.
Mamishi S, Modarressi MH, Pourakbari B, Tamizifar B, Mahjoub F, Fahimzad A, Alyasin S, Bemanian MH, Hamidiyeh AA, Fazlollahi MR, Ashrafi MR, Isaeian A, Khotaei G, Yeganeh M, Parvaneh N. Mamishi S, et al. Among authors: pourakbari b. J Clin Immunol. 2008 Jul;28(4):384-9. doi: 10.1007/s10875-008-9192-5. Epub 2008 Mar 19. J Clin Immunol. 2008. PMID: 18350256
160 results