Teimourian S - Search Results

1

Identification of eleven different mutations including six novel, in the arylsulfatase B gene in Iranian patients with mucopolysaccharidosis type VI.

Jafaryazdi R, Shams S, Isaian A, Setoodeh A, Teimourian S. Jafaryazdi R, et al. Among authors: teimourian s. Mol Biol Rep. 2019 Jun;46(3):3417-3426. doi: 10.1007/s11033-019-04804-9. Epub 2019 Apr 13. Mol Biol Rep. 2019. PMID: 30982216

2

Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease.

Teimourian S, Zomorodian E, Badalzadeh M, Pouya A, Kannengiesser C, Mansouri D, Cheraghi T, Parvaneh N. Teimourian S, et al. Br J Haematol. 2008 Jun;141(6):848-51. doi: 10.1111/j.1365-2141.2008.07148.x. Epub 2008 Apr 18. Br J Haematol. 2008. PMID: 18422995 Free article.

3

Serum selenium concentration in healthy children living in Tehran.

Safaralizadeh R, Sirjani M, Pourpak Z, Kardar G, Teimourian S, Shams S, Namdar Z, Kazemnejad A, Moin M. Safaralizadeh R, et al. Among authors: teimourian s. Biofactors. 2007;31(2):127-31. doi: 10.1002/biof.5520310203. Biofactors. 2007. PMID: 18806316

4

Mutation characterization and heterodimer analysis of patients with leukocyte adhesion deficiency: Including one novel mutation.

Teimourian S, De Boer M, Roos D, Isaian A, Moghanloo E, Lashkary S, Hassani B, Mollanoori H, Babaei V, Azarnezhad A. Teimourian S, et al. Immunol Lett. 2017 Jul;187:7-13. doi: 10.1016/j.imlet.2017.04.012. Epub 2017 Apr 23. Immunol Lett. 2017. PMID: 28445705

5

Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease.

Teimourian S, Sazgara F, de Boer M, van Leeuwen K, Roos D, Lashkary S, Chavoshzadeh Z, Nabavi M, Bemanian MH, Isaian A. Teimourian S, et al. J Pediatr Hematol Oncol. 2018 Jul;40(5):e268-e272. doi: 10.1097/MPH.0000000000001189. J Pediatr Hematol Oncol. 2018. PMID: 29702544

6

Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1.

Teimourian S, De Boer M, Roos D, Isaian A, Bemanian MH, Lashkary S, Nabavi M, Arshi S, Nateghian A, Sayyahfar S, Sazgara F, Taheripak G, Alipour Fayez E. Teimourian S, et al. J Pediatr Hematol Oncol. 2019 Jan;41(1):e3-e6. doi: 10.1097/MPH.0000000000001221. J Pediatr Hematol Oncol. 2019. PMID: 29750748

7

Effects of Oral Probiotic Feeding on Toll-Like Receptor Gene Expression of the Chicken's Cecal Tonsil.

Asgari F, Falak R, Teimourian S, Pourakbari B, Ebrahimnezhad S, Shekarabi M. Asgari F, et al. Among authors: teimourian s. Rep Biochem Mol Biol. 2018 Apr;6(2):151-157. Rep Biochem Mol Biol. 2018. PMID: 29765997 Free PMC article.

8

Filaggrin gene polymorphisms in Iranian ichthyosis vulgaris and atopic dermatitis patients.

Hassani B, Isaian A, Shariat M, Mollanoori H, Sotoudeh S, Babaei V, Ziaali A, Teimourian S. Hassani B, et al. Among authors: teimourian s. Int J Dermatol. 2018 Dec;57(12):1485-1491. doi: 10.1111/ijd.14213. Epub 2018 Sep 23. Int J Dermatol. 2018. PMID: 30246302

9

The beta-thalassemia mutation spectrum in the Iranian population.

Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH. Najmabadi H, et al. Among authors: teimourian s. Hemoglobin. 2001 Aug;25(3):285-96. doi: 10.1081/hem-100105221. Hemoglobin. 2001. PMID: 11570721

10

Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemia.

Aghamohammadi A, Fiorini M, Moin M, Parvaneh N, Teimourian S, Yeganeh M, Goffi F, Kanegane H, Amirzargar AA, Pourpak Z, Rezaei N, Salavati A, Pouladi N, Abdollahzade S, Notarangelo LD, Miyawaki T, Plebani A. Aghamohammadi A, et al. Among authors: teimourian s. Int Arch Allergy Immunol. 2006;141(4):408-14. doi: 10.1159/000095469. Epub 2006 Aug 30. Int Arch Allergy Immunol. 2006. PMID: 16943681

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