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Chemmedchem|February 16, 2022
Design, Synthesis and X-Ray Structural Studies of Potent HIV-1 Protease Inhibitors Containing C-4 Substituted Tricyclic Hexahydro-Furofuran Derivatives as P2 LigandsArun K Ghosh, Satish Kovela, Ashish Sharma, et al.
American Heart Journal|March 10, 2021
Comparison of Outcomes with Midodrine and Fludrocortisone for Objective Recurrence in Treating Syncope (COMFORTS trial): Rationale and design for a multi-center randomized controlled trialArya Aminorroaya, Hamed Tavolinejad, Saeed Sadeghian, et al.
Obesity Surgery|February 25, 2025
Bariatric Surgery and Remission of Metabolic Syndrome: A Meta-analysis of Randomised Controlled Trials and Prospective StudiesYomna E Dean, Mohamed I Mohamed, Abdulrahman Shokri, et al.
Nature Biomedical Engineering|February 17, 2018
Macrogenomic engineering via modulation of the scaling of chromatin packing densityLuay M Almassalha, Greta M Bauer, Wenli Wu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 28, 2026
Prevalence of dementia in selected Middle East and North Africa (MENA) countries: A systematic review and meta-analysisMohsen Sedighi, Mohammad Hasan Shahabi, Alireza Amanollahi, et al.
ARYA Atherosclerosis|January 27, 2018
Persian Registry Of cardioVascular diseasE (PROVE): Design and methodologyMahshid Givi, Nizal Sarrafzadegan, Mohammad Garakyaraghi, et al.
Neurobiology of Aging|November 15, 2020
BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genesMarzieh Khani, Hosein Shamshiri, Hanieh Taheri, et al.
Mucosal Immunology|June 25, 2015
Increased levels of inflammatory cytokines in the female reproductive tract are associated with altered expression of proteases, mucosal barrier proteins, and an influx of HIV-susceptible target cellsKelly B Arnold, Adam Burgener, Kenzie Birse, et al.
Clinical Cardiology|March 16, 2018
Rationale, design, and preliminary results of the Quebec Warfarin Cohort StudySylvie Perreault, Payman Shahabi, Robert Côté, et al.
Archives of Neurology|January 12, 2005
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sampleSilvia Buervenich, Andrea Carmine, Dagmar Galter, et al.
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