Saleh-Gohari N - Search Results

1

A family with the 619 bp deletion on the beta-globin gene found in Kerman Province, Iran.

Saleh-Gohari N, Mashizi AK. Saleh-Gohari N, et al. Hemoglobin. 2009;33(6):515-8. doi: 10.3109/03630260903335935. Hemoglobin. 2009. PMID: 19958199

2

Spectrum of α-globin gene mutations in the Kerman Province of Iran.

Saleh-Gohari N, Khosravi-Mashizi A. Saleh-Gohari N, et al. Hemoglobin. 2010;34(5):451-60. doi: 10.3109/03630269.2010.511587. Hemoglobin. 2010. PMID: 20854119

3

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.

4

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.

5

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.

6

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.

7

Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers.

Saleh-Gohari N, Khademi Bami M, Nikbakht R, Karimi-Maleh H. Saleh-Gohari N, et al. J Clin Pathol. 2015 Jul;68(7):562-6. doi: 10.1136/jclinpath-2014-202825. Epub 2015 May 2. J Clin Pathol. 2015. PMID: 25935548

8

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

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

Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome.

Haghighi A, Tiwari A, Piri N, Nürnberg G, Saleh-Gohari N, Haghighi A, Neidhardt J, Nürnberg P, Berger W. Haghighi A, et al. Among authors: saleh gohari n. PLoS One. 2014 Nov 13;9(11):e112747. doi: 10.1371/journal.pone.0112747. eCollection 2014. PLoS One. 2014. PMID: 25392994 Free PMC article.

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