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Genetic screening in Iranian patients with retinoblastoma.
Shahraki K, Ahani A, Sharma P, Faranoush M, Bahoush G, Torktaz I, Gahl WA, Naseripour M, Behnam B. Shahraki K, et al. Among authors: ahani a. Eye (Lond). 2017 Apr;31(4):620-627. doi: 10.1038/eye.2016.289. Epub 2016 Dec 16. Eye (Lond). 2017. PMID: 27983729 Free PMC article.
Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development.
Shojaei A, Ebrahimzadeh-Vesal R, Ahani A, Razzaghy-Azar M, Khakpour G, Ghazi F, Tavakkoly-Bazzaz J. Shojaei A, et al. Among authors: ahani a. Rep Biochem Mol Biol. 2017 Oct;6(1):59-65. Rep Biochem Mol Biol. 2017. PMID: 29090230 Free PMC article.
Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.
Behnam B, Shakiba M, Ahani A, Razzaghy Azar M. Behnam B, et al. Hepat Mon. 2013 Jun 9;13(6):e10124. doi: 10.5812/hepatmon.10124. eCollection 2013. Hepat Mon. 2013. PMID: 24032041 Free PMC article.
Here, we report two siblings a girl and a boy with diabetes mellitus (DM) who presented in one and two months of age respectively. ...The second child visited was a 7.75 year old boy who had spondyloepiphyseal dysplasia and subclinical hypothyroidism besides …
Here, we report two siblings a girl and a boy with diabetes mellitus (DM) who presented in one and two months of age respectiv …
An ABCD1 Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree.
Mehrpour M, Gohari F, Dizaji MZ, Ahani A, Malicdan MC, Behnam B. Mehrpour M, et al. Among authors: ahani a. J Mol Genet Med. 2016 Jun;10(2):222. doi: 10.4172/1747-0862.1000222. Epub 2016 Jun 19. J Mol Genet Med. 2016. PMID: 27489563 Free PMC article.
The Association between TNF-alpha Gene Polymorphisms and Endometriosis in An Iranian Population.
Babaabasi B, Ahani A, Sadeghi F, Bashizade-Fakhar H, Khorram Khorshid HR. Babaabasi B, et al. Among authors: ahani a. Int J Fertil Steril. 2019 Apr;13(1):6-11. doi: 10.22074/ijfs.2019.5542. Epub 2019 Jan 6. Int J Fertil Steril. 2019. PMID: 30644238 Free PMC article.
Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma.
Soleimani E, Saliminejad K, Akbari MT, Kamali K, Ahani A. Soleimani E, et al. Among authors: ahani a. Ophthalmic Genet. 2016 Dec;37(4):384-387. doi: 10.3109/13816810.2015.1107596. Epub 2016 Feb 25. Ophthalmic Genet. 2016. PMID: 26914443
Methionine synthase A2756G variation is associated with the risk of retinoblastoma in Iranian children.
Akbari MT, Naderi A, Saremi L, Sayad A, Irani S, Ahani A. Akbari MT, et al. Cancer Epidemiol. 2015 Dec;39(6):1023-5. doi: 10.1016/j.canep.2015.11.002. Epub 2015 Nov 18. Cancer Epidemiol. 2015. PMID: 26595280
Our results showed that the "G" was the minor allele with a frequency of 31.7% and 20.3% in both retinoblastoma and control groups, respectively. ...Individual with the 2756GG genotype had a 2.99 fold increased risk for retinoblastoma. According to our results, the …
Our results showed that the "G" was the minor allele with a frequency of 31.7% and 20.3% in both retinoblastoma and control groups, r …
Rapid detection of RB1 recurrent mutations in retinoblastoma by ARMS-PCR.
Saliminejad K, Behnam B, Akbari MT, Khorshid HR, Ghassemi F, Amoli FA, Akhondi MM, Vosoogh P, Naseripour M, Ahani A. Saliminejad K, et al. J Genet. 2013 May 29;92(2):e36-40. J Genet. 2013. PMID: 23981928 No abstract available.
Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.
Ahani A, Akbari MT, Saliminejad K, Behnam B, Akhondi MM, Vosoogh P, Ghassemi F, Naseripour M, Bahoush G, Khorshid HR. Ahani A, et al. Mol Vis. 2013;19:454-62. Epub 2013 Feb 22. Mol Vis. 2013. PMID: 23441118 Free PMC article.
PURPOSE: To screen deletions/duplications of the RB1 gene in a large cohort of Iranian patients using the multiplex ligation-dependent probe amplification (MLPA) technique. METHODS: A total of 121 patients with retinoblastoma, involving 55 unilateral and 66 bilatera …
PURPOSE: To screen deletions/duplications of the RB1 gene in a large cohort of Iranian patients using the multiplex ligation-dependen …
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