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Page 1
Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients.
Darvish H, Movafagh A, Omrani MD, Firouzabadi SG, Azargashb E, Jamshidi J, Khaligh A, Haghnejad L, Naeini NS, Talebi A, Heidari-Rostami HR, Noorollahi-Moghaddam H, Karkheiran S, Shahidi GA, Paknejad SM, Ashrafian H, Abdi S, Kayyal M, Akbari M, Pedram N, Emamalizadeh B. Darvish H, et al. Among authors: akbari m. Neurosci Lett. 2013 Sep 13;551:75-8. doi: 10.1016/j.neulet.2013.07.013. Epub 2013 Jul 21. Neurosci Lett. 2013. PMID: 23880019
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population.
Fattahi Z, Kalhor Z, Fadaee M, Vazehan R, Parsimehr E, Abolhassani A, Beheshtian M, Zamani G, Nafissi S, Nilipour Y, Akbari MR, Kahrizi K, Kariminejad A, Najmabadi H. Fattahi Z, et al. Among authors: akbari mr. Clin Genet. 2017 Mar;91(3):386-402. doi: 10.1111/cge.12810. Epub 2016 Jul 21. Clin Genet. 2017. PMID: 27234031
When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS).
Mohseni M, Akbari M, Booth KT, Babanejad M, Azaiez H, Ardalani F, Arzhangi S, Jalalvand K, Nikzat N, Ghodratpour F, Jamali P, Adeli OA, Habibi H, Kahrizi K, Najmabadi H. Mohseni M, et al. Among authors: akbari m. J Hum Genet. 2020 Jul;65(7):609-617. doi: 10.1038/s10038-020-0740-z. Epub 2020 Mar 30. J Hum Genet. 2020. PMID: 32231217 Free PMC article.
RIT2, a susceptibility gene for Parkinson's disease in Iranian population.
Emamalizadeh B, Movafagh A, Akbari M, Kazeminasab S, Fazeli A, Motallebi M, Shahidi GA, Petramfar P, Mirfakhraie R, Darvish H. Emamalizadeh B, et al. Among authors: akbari m. Neurobiol Aging. 2014 Dec;35(12):e27-e28. doi: 10.1016/j.neurobiolaging.2014.07.013. Epub 2014 Jul 19. Neurobiol Aging. 2014. PMID: 25146456 No abstract available.
1,701 results