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Page 1
c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.
Safarpour Lima B, Ghaedi H, Daftarian N, Ahmadieh H, Jamshidi J, Khorrami M, Noroozi R, Sohrabifar N, Assarzadegan F, Hesami O, Taghavi S, Ahmadifard A, Atakhorrami M, Rahimi-Aliabadi S, Shahmohammadibeni N, Alehabib E, Andarva M, Darvish H, Emamalizadeh B. Safarpour Lima B, et al. Among authors: darvish h. Eur J Med Genet. 2016 Feb;59(2):65-9. doi: 10.1016/j.ejmg.2016.01.001. Epub 2016 Jan 7. Eur J Med Genet. 2016. PMID: 26773575
Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.
Pouya AR, Abedini SS, Mansoorian N, Behjati F, Nikzat N, Mohseni M, Nieh SE, Abbasi Moheb L, Darvish H, Monajemi GB, Banihashemi S, Kahrizi K, Ropers HH, Najmabadi H. Pouya AR, et al. Among authors: darvish h. Eur J Med Genet. 2009 Jul-Aug;52(4):170-3. doi: 10.1016/j.ejmg.2009.03.014. Epub 2009 Apr 8. Eur J Med Genet. 2009. PMID: 19361583
A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.
Darvish H, Esmaeeli-Nieh S, Monajemi GB, Mohseni M, Ghasemi-Firouzabadi S, Abedini SS, Bahman I, Jamali P, Azimi S, Mojahedi F, Dehghan A, Shafeghati Y, Jankhah A, Falah M, Soltani Banavandi MJ, Ghani M, Garshasbi M, Rakhshani F, Naghavi A, Tzschach A, Neitzel H, Ropers HH, Kuss AW, Behjati F, Kahrizi K, Najmabadi H. Darvish H, et al. J Med Genet. 2010 Dec;47(12):823-8. doi: 10.1136/jmg.2009.076398. Epub 2010 Oct 26. J Med Genet. 2010. PMID: 20978018
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.
HLA-DRA is associated with Parkinson's disease in Iranian population.
Jamshidi J, Movafagh A, Emamalizadeh B, Zare Bidoki A, Manafi A, Ghasemi Firouzabadi S, Shahidi GA, Kazeminasab S, Petramfar P, Fazeli A, Motallebi M, Mortazavi-Tabatabaei SA, Kowsari A, Jafarian Z, Darvish H. Jamshidi J, et al. Among authors: darvish h. Int J Immunogenet. 2014 Dec;41(6):508-11. doi: 10.1111/iji.12151. Epub 2014 Oct 15. Int J Immunogenet. 2014. PMID: 25319953
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.
119 results