Dastsooz H - Search Results

1

DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis.

Dastsooz H, Vahedi N, Fardaei M. Dastsooz H, et al. Iran J Basic Med Sci. 2013 Aug;16(8):946-9. Iran J Basic Med Sci. 2013. PMID: 24106601 Free PMC article.

2

A new ATP7B gene mutation with severe condition in two unrelated Iranian families with Wilson disease.

Dastsooz H, Dehghani SM, Imanieh MH, Haghighat M, Moini M, Fardaei M. Dastsooz H, et al. Gene. 2013 Feb 1;514(1):48-53. doi: 10.1016/j.gene.2012.10.085. Epub 2012 Nov 13. Gene. 2013. PMID: 23159873

3

Multiplex ARMS PCR to Detect 8 Common Mutations of ATP7B Gene in Patients With Wilson Disease.

Dastsooz H, Imanieh MH, Dehghani SM, Haghighat M, Moini M, Fardaei M. Dastsooz H, et al. Hepat Mon. 2013 May 16;13(5):e8375. doi: 10.5812/hepatmon.8375. eCollection 2013. Hepat Mon. 2013. PMID: 24003324 Free PMC article.

4

Family screening for a novel ATP7B gene mutation, c.2335T>G, in the South of Iran.

Manoochehri J, Masoumi Dehshiri R, Faraji H, Mohammadi S, Dastsooz H, Moradi T, Rezaei E, Sadeghi Kh, Fardaei M. Manoochehri J, et al. Among authors: dastsooz h. Iran J Ped Hematol Oncol. 2014;4(1):26-31. Epub 2014 Feb 20. Iran J Ped Hematol Oncol. 2014. PMID: 24734161 Free PMC article.

5

The same haplotype for two unrelated Wilson disease patients with new ATP7B mutation.

Dastsooz H, Dehghani SM, Fardaei M. Dastsooz H, et al. Arch Iran Med. 2014 Nov;17(11):755-8. Arch Iran Med. 2014. PMID: 25365615

6

Impact of KIF6 Polymorphism rs20455 on Coronary Heart Disease Risk and Effectiveness of Statin Therapy in 100 Patients from Southern Iran.

Hamidizadeh L, Haji Hosseini Baghdad Abadi R, Babaee Baigi MA, Dastsooz H, Khazaei Nejhad A, Fardaei M. Hamidizadeh L, et al. Among authors: dastsooz h. Arch Iran Med. 2015 Oct;18(10):683-7. Arch Iran Med. 2015. PMID: 26443250

7

VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran.

Nejabat M, Naghash P, Dastsooz H, Mohammadi S, Alipour M, Fardaei M. Nejabat M, et al. Among authors: dastsooz h. J Ophthalmic Vis Res. 2017 Apr-Jun;12(2):135-140. doi: 10.4103/jovr.jovr_97_16. J Ophthalmic Vis Res. 2017. PMID: 28540003 Free PMC article.

8

Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports.

Dastsooz H, Nemati H, Fard MAF, Fardaei M, Faghihi MA. Dastsooz H, et al. BMC Med Genet. 2017 Aug 18;18(1):87. doi: 10.1186/s12881-017-0439-y. BMC Med Genet. 2017. PMID: 28821231 Free PMC article.

9

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome.

Taghdiri M, Dastsooz H, Fardaei M, Mohammadi S, Farazi Fard MA, Faghihi MA. Taghdiri M, et al. Among authors: dastsooz h. Front Pediatr. 2017 Aug 9;5:169. doi: 10.3389/fped.2017.00169. eCollection 2017. Front Pediatr. 2017. PMID: 28848724 Free PMC article.

10

TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis.

Bykhovskaya Y, Fardaei M, Khaled ML, Nejabat M, Salouti R, Dastsooz H, Liu Y, Inaloo S, Rabinowitz YS. Bykhovskaya Y, et al. Among authors: dastsooz h. Invest Ophthalmol Vis Sci. 2017 Dec 1;58(14):6462-6469. doi: 10.1167/iovs.17-22819. Invest Ophthalmol Vis Sci. 2017. PMID: 29261847 Free PMC article.

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