Salimeh Gohari - Search Results

Year	Number of Results
2003	1
2004	2
2005	1
2007	2
2008	1
2009	2
2010	2
2011	1
2012	4
2013	5
2014	2
2015	1
2018	2
2019	1
2020	1
2021	2
2022	1

1

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

2

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

3

Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients.

Haghighi A, Haack TB, Atiq M, Mottaghi H, Haghighi-Kakhki H, Bashir RA, Ahting U, Feichtinger RG, Mayr JA, Rötig A, Lebre AS, Klopstock T, Dworschak A, Pulido N, Saeed MA, Saleh-Gohari N, Holzerova E, Chinnery PF, Taylor RW, Prokisch H. Haghighi A, et al. Among authors: saleh gohari n. Orphanet J Rare Dis. 2014 Aug 20;9:119. doi: 10.1186/s13023-014-0119-3. Orphanet J Rare Dis. 2014. PMID: 25208612 Free PMC article. Review.

4

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

5

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.

6

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.

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

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.

9

Congenital insensitivity to pain with anhidrosis in an Iranian patient.

Saleh-Gohari N, Mohammadi-Anaie M. Saleh-Gohari N, et al. Basic Clin Neurosci. 2013 Winter;4(1):88-90. Basic Clin Neurosci. 2013. PMID: 25337332 Free PMC article.

10

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

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