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Page 1
Identification of homogeneously staining regions in leukemia patients.
Moghadam MH, Movafagh A, Omrani M, Ghanati K, Hashemi M, Poursafavi F, Darvish H, Abdolahi DZ, Gholami M, Heidari Rostamy MR, Safari S, Haghnejad L, Darehgazani R, Naeini NS, Motlagh MG, Amani D. Moghadam MH, et al. Among authors: darvish h. J Res Med Sci. 2013 Apr;18(4):363-5. J Res Med Sci. 2013. PMID: 24124438 Free PMC article.
Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease.
Darvish H, Heidari A, Hosseinkhani S, Movafagh A, Khaligh A, Jamshidi J, Noorollahi-Moghaddam H, Heidari-Rostami HR, Karkheiran S, Shahidi GA, Togha M, Paknejad SM, Ashrafian H, Abdi S, Firouzabadi SG, Jamaldini SH, Ohadi M. Darvish H, et al. J Mol Neurosci. 2013 Oct;51(2):389-93. doi: 10.1007/s12031-013-0021-9. Epub 2013 May 4. J Mol Neurosci. 2013. PMID: 23640536
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. 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
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: darvish h. 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.
Monoamine oxidase a gene polymorphisms and bipolar disorder in Iranian population.
Eslami Amirabadi MR, Rajezi Esfahani S, Davari-Ashtiani R, Khademi M, Emamalizadeh B, Movafagh A, Sadr S, Arabgol F, Darvish H, Razjoyan K. Eslami Amirabadi MR, et al. Among authors: darvish h. Iran Red Crescent Med J. 2015 Feb 21;17(2):e23095. doi: 10.5812/ircmj.23095. eCollection 2015 Feb. Iran Red Crescent Med J. 2015. PMID: 25793118 Free PMC article.
Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population.
Haghnejad L, Emamalizadeh B, Jamshidi J, Bidoki AZ, Ghaedi H, Ahmadi E, Abdollahi S, Shahmohammadibeni N, Taghavi S, Fazeli A, Motallebi M, Zarneh AE, Mohammadihosseinabad S, Abbaszadegan MR, Torkamandi S, Gavenaroudi MA, Pedram N, Shahidi GA, Tafakhori A, Darvish H, Movafagh A. Haghnejad L, et al. Among authors: darvish h. J Neurol Sci. 2015 Aug 15;355(1-2):72-4. doi: 10.1016/j.jns.2015.05.020. Epub 2015 May 27. J Neurol Sci. 2015. PMID: 26070653
No Evidence for Association Between Norepinephrine Transporter-3081 (A/T) Polymorphism and Attention Deficit Hyperactivity Disorder in Iranian Population.
Eslami Amirabadi MR, Davari-Ashtiani R, Khademi M, RajeziEsfahani S, Emamalizadeh B, Movafagh A, Arabgol F, Sadr S, Darvish H, Razjouyan K. Eslami Amirabadi MR, et al. Among authors: darvish h. Iran Red Crescent Med J. 2015 Jul 23;17(7):e22996. doi: 10.5812/ircmj.229961v2. eCollection 2015 Jul. Iran Red Crescent Med J. 2015. PMID: 26421175 Free PMC article.
121 results