Banihosseini SS - Search Results

1

Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients.

Alavi A, Elahi E, Tehrani MH, Amoli FA, Javadi MA, Rafati N, Chiani M, Banihosseini SS, Bayat B, Kalhor R, Amini SS. Alavi A, et al. Among authors: banihosseini ss. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4490-7. doi: 10.1167/iovs.07-0264. Invest Ophthalmol Vis Sci. 2007. PMID: 17898270

2

Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.

Elahi E, Kalhor R, Banihosseini SS, Torabi N, Pour-Jafari H, Houshmand M, Amini SS, Ramezani A, Loeys B. Elahi E, et al. Among authors: banihosseini ss. J Invest Dermatol. 2006 Jul;126(7):1506-9. doi: 10.1038/sj.jid.5700247. Epub 2006 May 11. J Invest Dermatol. 2006. PMID: 16691202 Free article.

3

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. Shojaee S, et al. Among authors: banihosseini ss. Am J Hum Genet. 2008 Jun;82(6):1375-84. doi: 10.1016/j.ajhg.2008.05.005. Am J Hum Genet. 2008. PMID: 18513678 Free PMC article.

4

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. Shojaee S, et al. Among authors: banihosseini ss. Neurosci Lett. 2009 Dec 25;467(2):53-7. doi: 10.1016/j.neulet.2009.09.058. Epub 2009 Oct 1. Neurosci Lett. 2009. PMID: 19800393

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: banihosseini ss. Mov Disord. 2011 Jan;26(1):80-9. doi: 10.1002/mds.23417. Epub 2010 Nov 8. Mov Disord. 2011. PMID: 21322020

6

Variation in plasma leptin levels in young Iranian children with cystic fibrosis.

Monajemzadeh M, Ashtiani MT, Sadrian E, Shams S, Motamed F, Sani MN, Banihosseini SS, Abbasi A. Monajemzadeh M, et al. Among authors: banihosseini ss. Arch Med Sci. 2013 Oct 31;9(5):883-7. doi: 10.5114/aoms.2013.38683. Epub 2013 Nov 5. Arch Med Sci. 2013. PMID: 24273574 Free PMC article.

7

Applying a neural network to predict the thermodynamic parameters for an expanded nearest-neighbor model.

Najafabadi HS, Goodarzi H, Torabi N, Banihosseini SS. Najafabadi HS, et al. Among authors: banihosseini ss. J Theor Biol. 2006 Feb 7;238(3):657-65. doi: 10.1016/j.jtbi.2005.06.014. Epub 2005 Aug 2. J Theor Biol. 2006. PMID: 16061260

8

Lipid profile, thyroid function, and serum magnesium level in type I diabetic children.

Derakhshan R, Balaee P, Darakhshan S, Masoodpoor N, Banihosseini SS. Derakhshan R, et al. Among authors: banihosseini ss. Minerva Pediatr. 2011 Feb;63(1):27-33. Minerva Pediatr. 2011. PMID: 21311427

9

Corticosteroid regimens for treatment of acute and chronic graft versus host disease (GvHD) after allogenic stem cell transplantation.

Salmasian H, Rohanizadegan M, Banihosseini S, Rahimi Darabad R, Rabbani-Anari M, Shakiba A, Ferrara JL. Salmasian H, et al. Cochrane Database Syst Rev. 2010 Jan 20;2010(1):CD005565. doi: 10.1002/14651858.CD005565.pub2. Cochrane Database Syst Rev. 2010. PMID: 20091579 Free PMC article. Review.

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