Rohani M - Search Results

1

Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients.

Alavi A, Nafissi S, Rohani M, Zamani B, Sedighi B, Shamshiri H, Fan JB, Ronaghi M, Elahi E. Alavi A, et al. Among authors: rohani m. Neurobiol Aging. 2013 May;34(5):1516.e1-8. doi: 10.1016/j.neurobiolaging.2012.09.006. Epub 2012 Oct 9. Neurobiol Aging. 2013. PMID: 23062701

2

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

Chitsazian F, Tusi BK, Elahi E, Saroei HA, Sanati MH, Yazdani S, Pakravan M, Nilforooshan N, Eslami Y, Mehrjerdi MA, Zareei R, Jabbarvand M, Abdolahi A, Lasheyee AR, Etemadi A, Bayat B, Sadeghi M, Banoei MM, Ghafarzadeh B, Rohani MR, Rismanchian A, Thorstenson Y, Sarfarazi M. Chitsazian F, et al. Among authors: rohani mr. J Mol Diagn. 2007 Jul;9(3):382-93. doi: 10.2353/jmoldx.2007.060157. J Mol Diagn. 2007. PMID: 17591938 Free PMC article.

3

Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C exist.

Narooie-Nejad M, Chitsazian F, Khoramian Tusi B, Mousavi F, Houshmand M, Rohani MR, Hosseinipour AS, Rismanchian A, Elahi E. Narooie-Nejad M, et al. Among authors: rohani mr. Mol Vis. 2009 Oct 22;15:2155-61. Mol Vis. 2009. PMID: 19898634 Free PMC article.

4

Evaluation of cerebral vasomotor reactivity in Parkinson's disease: is there any association with orthostatic hypotension?

Zamani B, Mehrabani M, Fereshtehnejad SM, Rohani M. Zamani B, et al. Among authors: rohani m. Clin Neurol Neurosurg. 2011 Jun;113(5):368-72. doi: 10.1016/j.clineuro.2010.12.014. Epub 2011 Jan 17. Clin Neurol Neurosurg. 2011. PMID: 21247685

5

PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.

Ghazavi F, Fazlali Z, Banihosseini SS, Hosseini SR, Kazemi MH, Shojaee S, Parsa K, Sadeghi H, Sina F, Rohani M, Shahidi GA, Ghaemi N, Ronaghi M, Elahi E. Ghazavi F, et al. Among authors: rohani m. Mov Disord. 2011 Jan;26(1):80-9. doi: 10.1002/mds.23417. Epub 2010 Nov 8. Mov Disord. 2011. PMID: 21322020

6

A study of factors associated with cerebral venous thrombosis.

Jalili M, Ghourchian S, Shahidi GA, Rohani M, Rezvani M, Zamani B. Jalili M, et al. Among authors: rohani m. Neurol Sci. 2013 Mar;34(3):321-6. doi: 10.1007/s10072-012-0997-x. Epub 2012 Mar 7. Neurol Sci. 2013. PMID: 22395946

7

Restless legs syndrome in Iranian patients with multiple sclerosis.

Miri S, Rohani M, Sahraian MA, Zamani B, Shahidi GA, Sabet A, Moradi-Lakeh M, Bodaghabadi M. Miri S, et al. Among authors: rohani m. Neurol Sci. 2013 Jul;34(7):1105-8. doi: 10.1007/s10072-012-1186-7. Epub 2012 Sep 9. Neurol Sci. 2013. PMID: 22960874

8

PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation.

Dezfouli MA, Alavi A, Rohani M, Rezvani M, Nekuie T, Klotzle B, Tonekaboni SH, Shahidi GA, Elahi E. Dezfouli MA, et al. Among authors: rohani m. Mov Disord. 2013 Feb;28(2):228-32. doi: 10.1002/mds.25271. Epub 2012 Nov 19. Mov Disord. 2013. PMID: 23166001

9

The novel mutation p.Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine.

Jaberi E, Chitsazian F, Ali Shahidi G, Rohani M, Sina F, Safari I, Malakouti Nejad M, Houshmand M, Klotzle B, Elahi E. Jaberi E, et al. Among authors: rohani m. J Hum Genet. 2013 Aug;58(8):526-30. doi: 10.1038/jhg.2013.45. Epub 2013 Jun 13. J Hum Genet. 2013. PMID: 23759946

10

Prevalence and associated features of restless legs syndrome in a population of Iranian women during pregnancy.

Vahdat M, Sariri E, Miri S, Rohani M, Kashanian M, Sabet A, Zamani B. Vahdat M, et al. Among authors: rohani m. Int J Gynaecol Obstet. 2013 Oct;123(1):46-9. doi: 10.1016/j.ijgo.2013.04.023. Epub 2013 Jul 22. Int J Gynaecol Obstet. 2013. PMID: 23886452

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