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

15 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Investigating the expression level of miR-17-3p, miR-101-3p, miR-335-3p, and miR-296-3p in the peripheral blood of patients with acute myocardial infarction.
Bakhshi A, Khani M, Alipour Parsa S, Khaheshi I, Namazi MH, Mazouri A, Bidram P, Safi M, Vakili H, Eslami V, Saadat H, Heidari L, Sohrabifar N. Bakhshi A, et al. Among authors: sohrabifar n. Mol Cell Biochem. 2024 Apr;479(4):859-868. doi: 10.1007/s11010-023-04766-4. Epub 2023 May 24. Mol Cell Biochem. 2024. PMID: 37222878
The Association Between Hematologic Indices With TIMI Flow In STEMI Patients Who Undergo primary percutaneous coronary intervention.
Parsa SA, Nourian S, Safi M, Namazi MH, Saadat H, Vakili H, Eslami V, Salehi A, Kiaee FH, Sohrabifar N, Khaheshi I. Parsa SA, et al. Among authors: sohrabifar n. Cardiovasc Hematol Disord Drug Targets. 2022 Sep 13. doi: 10.2174/1871529X22666220913122046. Online ahead of print. Cardiovasc Hematol Disord Drug Targets. 2022. PMID: 36100995
Association between leukocyte telomere length and COVID-19 severity.
Mahmoodpoor A, Sanaie S, Eskandari M, Behrouzi N, Taghizadeh M, Roudbari F, Emamalizadeh B, Sohrabifar N, Kazeminasab S. Mahmoodpoor A, et al. Among authors: sohrabifar n. Egypt J Med Hum Genet. 2023;24(1):37. doi: 10.1186/s43042-023-00415-z. Epub 2023 May 29. Egypt J Med Hum Genet. 2023. PMID: 37273887 Free PMC article.
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: sohrabifar n. 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
15 results