Saleh Gohari N - Search Results

1

A Novel Splice Site Mutation of the ATM Gene Associated with Ataxia Telangiectasia.

Saeidi K, Saleh Gohari N, Mansouri Nejad SE. Saeidi K, et al. Among authors: saleh gohari n. Iran J Child Neurol. 2018 Fall;12(4):111-119. Iran J Child Neurol. 2018. PMID: 30279714 Free PMC article.

2

A novel homozygous frameshift mutation in the FUCA1 gene causes both severe and mild fucosidosis.

Saleh-Gohari N, Saeidi K, Zeighaminejad R. Saleh-Gohari N, et al. J Clin Pathol. 2018 Sep;71(9):821-824. doi: 10.1136/jclinpath-2018-205074. Epub 2018 Mar 27. J Clin Pathol. 2018. PMID: 29588375

3

Quantification of circulating miR-517c-3p and miR-210-3p levels in preeclampsia.

Nejad RMA, Saeidi K, Gharbi S, Salari Z, Saleh-Gohari N. Nejad RMA, et al. Among authors: saleh gohari n. Pregnancy Hypertens. 2019 Apr;16:75-78. doi: 10.1016/j.preghy.2019.03.004. Epub 2019 Mar 11. Pregnancy Hypertens. 2019. PMID: 31056162

4

Haplotype Analysis in Carriers of β-Globin Gene Mutation Facilitates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran.

Saleh-Gohari N, Saeidi K, Ziaadini-Dashtkhaki S. Saleh-Gohari N, et al. Iran J Public Health. 2020 Apr;49(4):791-799. Iran J Public Health. 2020. PMID: 32548060 Free PMC article.

5

A Study of Associations Between rs9349379 (PHACTR1), rs2891168 (CDKN2B-AS), rs11838776 (COL4A2) and rs4880 (SOD2) Polymorphic Variants and Coronary Artery Disease in Iranian Population.

Yari A, Saleh-Gohari N, Mirzaee M, Hashemi F, Saeidi K. Yari A, et al. Among authors: saleh gohari n. Biochem Genet. 2022 Feb;60(1):106-126. doi: 10.1007/s10528-021-10089-0. Epub 2021 Jun 9. Biochem Genet. 2022. PMID: 34109516

6

Comparing PCR With High-resolution Melting Analysis for Apolipoprotein E Genotyping in Alzheimer's: A Case-control Study.

Pourshaikhali S, Saleh-Gohari N, Saeidi K, Fekri Soofiabadi M. Pourshaikhali S, et al. Among authors: saleh gohari n. Basic Clin Neurosci. 2024 Jan-Feb;15(1):37-48. doi: 10.32598/bcn.2022.206.2. Epub 2024 Jan 1. Basic Clin Neurosci. 2024. PMID: 39291089 Free PMC article.

7

Co-inheritance of sickle cell trait and thalassemia mutations in South central iran.

Saleh-Gohari N, Mohammadi-Anaie M. Saleh-Gohari N, et al. Iran J Public Health. 2012;41(10):81-6. Epub 2012 Oct 1. Iran J Public Health. 2012. PMID: 23304665 Free PMC article.

8

BRCA1 Gene Mutations in Breast Cancer Patients from Kerman Province, Iran.

Saleh-Gohari N, Mohammadi-Anaie M, Kalantari-Khandani B. Saleh-Gohari N, et al. Iran J Cancer Prev. 2012 Fall;5(4):210-5. Iran J Cancer Prev. 2012. PMID: 25352972 Free PMC article.

9

A novel homozygous splice-site mutation in SCARB2 is associated with progressive myoclonic epilepsy with renal failure.

Yari A, Ali-Nejad RM, Saleh-Gohari N. Yari A, et al. Among authors: saleh gohari n. Neurol Sci. 2021 Dec;42(12):5077-5085. doi: 10.1007/s10072-021-05196-0. Epub 2021 Mar 26. Neurol Sci. 2021. PMID: 33772352

10

Distribution of β-Globin Gene Mutations in Thalassemia Minor Population of Kerman Province, Iran.

Saleh-Gohari N, Bazrafshani M. Saleh-Gohari N, et al. Iran J Public Health. 2010;39(2):69-76. Epub 2010 Jun 30. Iran J Public Health. 2010. PMID: 23113009 Free PMC article.

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