Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 7

1.

Stiff person case misdiagnosed as conversion disorder: A case report.

Razmeh S, Habibi AH, Sina F, Alizadeh E, Eslami M.

Caspian J Intern Med. 2017 Fall;8(4):329-331. doi: 10.22088/cjim.8.4.329.

2.

Migraine headache in patients with idiopathic intracranial hypertension.

Sina F, Razmeh S, Habibzadeh N, Zavari A, Nabovvati M.

Neurol Int. 2017 Oct 2;9(3):7280. doi: 10.4081/or.2017.7280. eCollection 2017 Aug 29.

3.

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.

J Hum Genet. 2013 Aug;58(8):526-30. doi: 10.1038/jhg.2013.45. Epub 2013 Jun 13.

PMID:
23759946
4.

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.

Mov Disord. 2011 Jan;26(1):80-9. doi: 10.1002/mds.23417. Epub 2010 Nov 8.

PMID:
21322020
5.

Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients.

Shojaee S, Fazlali Z, Ghazavi F, Banihosseini SS, Kazemi MH, Parsa K, Sadeghi H, Sina F, Shahidi GA, Ronaghi M, Elahi E.

Neurosci Lett. 2009 Dec 25;467(2):53-7. doi: 10.1016/j.neulet.2009.09.058. Epub 2009 Oct 1.

PMID:
19800393
6.

A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.

Shojaee S, Sina F, Farboodi N, Fazlali Z, Ghazavi F, Ghorashi SA, Parsa K, Sadeghi H, Shahidi GA, Ronaghi M, Elahi E.

Mov Disord. 2009 May 15;24(7):1023-7. doi: 10.1002/mds.22503.

PMID:
19353692
7.

Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.

Shojaee S, Sina F, Banihosseini SS, Kazemi MH, Kalhor R, Shahidi GA, Fakhrai-Rad H, Ronaghi M, Elahi E.

Am J Hum Genet. 2008 Jun;82(6):1375-84. doi: 10.1016/j.ajhg.2008.05.005.

Supplemental Content

Loading ...
Support Center