Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

46 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
The study of rs324420 (C385A) polymorphism of the FAAH gene of the endocannabinoid system in patients with epilepsy and ADHD.
Anvar LH, Alejafar A, Moosavi SE, Charsouei S, Zeynalzadeh N, Fanid LM, Emamalizadeh B, Aydinlou ZH, Vaezi H, Kashefi A, Tomaz C, Nikanfar M, Ahmadalipour A. Anvar LH, et al. Among authors: emamalizadeh b. Epilepsy Res. 2023 May;192:107100. doi: 10.1016/j.eplepsyres.2023.107100. Epub 2023 Feb 3. Epilepsy Res. 2023. PMID: 37018974
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: emamalizadeh b. 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
An interdependence between GAPVD1 gene polymorphism, expression level and response to interferon beta in patients with multiple sclerosis.
Khademi B, Khorrami M, Ayromlou H, Rikhtegar R, Moghadam EA, Tahmasebivand M, Mousavi SR, Kheirollahi M, Fakhr F, Alizadeh-Ghodsi M, Emamalizadeh B. Khademi B, et al. Among authors: emamalizadeh b. J Neuroimmunol. 2021 Apr 15;353:577507. doi: 10.1016/j.jneuroim.2021.577507. Epub 2021 Jan 30. J Neuroimmunol. 2021. PMID: 33548618
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: emamalizadeh b. 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.
RIT2 Polymorphisms: Is There a Differential Association?
Emamalizadeh B, Jamshidi J, Movafagh A, Ohadi M, Khaniani MS, Kazeminasab S, Biglarian A, Taghavi S, Motallebi M, Fazeli A, Ahmadifard A, Shahidi GA, Petramfar P, Shahmohammadibeni N, Dadkhah T, Khademi E, Tafakhori A, Khaligh A, Safaralizadeh T, Kowsari A, Mirabzadeh A, Zarneh AES, Khorrami M, Shokraeian P, Banavandi MJS, Lima BS, Andarva M, Alehabib E, Atakhorrami M, Darvish H. Emamalizadeh B, et al. Mol Neurobiol. 2017 Apr;54(3):2234-2240. doi: 10.1007/s12035-016-9815-4. Epub 2016 Mar 3. Mol Neurobiol. 2017. PMID: 26941103
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: emamalizadeh b. 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
46 results