Sahebalzamani A - Search Results

1

Effect of the mechanical activation on size reduction of crystalline acetaminophen drug particles.

Biazar E, Beitollahi A, Rezayat SM, Forati T, Asefnejad A, Rahimi M, Zeinali R, Ardeshir M, Hatamjafari F, Sahebalzamani A, Heidari M. Biazar E, et al. Among authors: sahebalzamani a. Int J Nanomedicine. 2009;4:283-7. doi: 10.2147/ijn.s5895. Epub 2009 Dec 29. Int J Nanomedicine. 2009. PMID: 20054432 Free PMC article.

2

The healing effect of unrestricted somatic stem cells loaded in collagen-modified nanofibrous PHBV scaffold on full-thickness skin defects.

Keshel SH, Biazar E, Rezaei Tavirani M, Rahmati Roodsari M, Ronaghi A, Ebrahimi M, Rad H, Sahebalzamani A, Rakhshan A, Afsordeh K. Keshel SH, et al. Among authors: sahebalzamani a. Artif Cells Nanomed Biotechnol. 2014 Jun;42(3):210-6. doi: 10.3109/21691401.2013.800080. Epub 2013 Aug 2. Artif Cells Nanomed Biotechnol. 2014. PMID: 23909504

3

A Novel VPS13B Mutation Identified by Whole-Exome Sequencing in Iranian Patients with Cohen Syndrome.

Karimzadeh MR, Omidi F, Sahebalzamani A, Saeidi K. Karimzadeh MR, et al. Among authors: sahebalzamani a. J Mol Neurosci. 2021 Dec;71(12):2566-2574. doi: 10.1007/s12031-021-01852-4. Epub 2021 May 26. J Mol Neurosci. 2021. PMID: 34041686

4

Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.

Kannan-Sundhari A, Yan D, Saeidi K, Sahebalzamani A, Blanton SH, Liu XZ. Kannan-Sundhari A, et al. Among authors: sahebalzamani a. Genet Test Mol Biomarkers. 2020 Oct;24(10):674-680. doi: 10.1089/gtmb.2020.0153. Epub 2020 Sep 29. Genet Test Mol Biomarkers. 2020. PMID: 32991204 Free PMC article.

5

Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.

Shang H, Yan D, Tayebi N, Saeidi K, Sahebalzamani A, Feng Y, Blanton S, Liu X. Shang H, et al. Among authors: sahebalzamani a. Biomed Res Int. 2018 Jan 15;2018:3103986. doi: 10.1155/2018/3103986. eCollection 2018. Biomed Res Int. 2018. PMID: 29568747 Free PMC article.

6

A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome.

Dehghani M, Mojarad M, Ghayoor Karimiani E, Vahidi Mehrjardi MY, Sahebalzamani A, Ashrafzadeh F, Beiraghi Toosi M, Eslahi A, Ahangari N, Yassini SM, Hassanbeigi A, Rasti A, Kalantar SM, Maroofian R. Dehghani M, et al. Among authors: sahebalzamani a. Public Health Genomics. 2017;20(3):188-193. doi: 10.1159/000477560. Epub 2017 Jul 19. Public Health Genomics. 2017. PMID: 28719906

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