Localized ocular crystal-storing histiocytosis and associated lymphoma - Report of two cases and review of literature

por Eslami, Maryam, Rossman, David, Rasmussen, Steve, Chae, Tony
Publicado 2022

Evaluation of the Anti-Metastatic Effect of Foeniculum Vulgare on the Protein Expression of HSP 70 & 90 in Balb/c Mice with 4t1 Model of Breast Cancer

por Sadegh Roudbari, Leila, Eslami, Maryam, Movahedi, Monireh, Golab, Fereshteh
Publicado 2023

Expression of COLLAGEN 1 and ELASTIN Genes in Mitral Valvular Interstitial Cells within Microfiber Reinforced Hydrogel

por Eslami, Maryam, Javadi, Gholamreza, Agdami, Nasser, Shokrgozar, Mohammad Ali
Publicado 2015

Genetic Investigation of 261 Cases of Turner Syndrome Patients Referred to the Genetic Clinic

por Farhud, Dariush, Asgarian, Rojiar, Seifalian, Amelia, Mostafaeinejad, Paria, Eslami, Maryam
Publicado 2021

Some Notes on Stem Cell Therapy in Cardiovascular Diseases

por Reza Mohammadhasani, Mohammad, Hasanzad, Mandana, Mohammadhasani, Amirreza, Samzadeh, Mohammad, Eslami, Maryam
Publicado 2010

Case Report: Use of Amniotic Membrane for Tectonic Repair of Peripheral Ulcerative Keratitis With Corneal Perforation

por Eslami, Maryam, Benito-Pascual, Blanca, Goolam, Saadiah, Trinh, Tanya, Moloney, Greg
Publicado 2022

Delayed Topographical and Refractive Changes Following Corneal Cross-Linking for Keratoconus

por Eslami, Maryam, Ghaseminejad, Farhad, Dubord, Paul J., Yeung, Sonia N., Iovieno, Alfonso
Publicado 2022

A Case Report of Genetic Cascade Screening in Dilated Cardiomyopathy: A Perspective for Preventive Cardiology

por Barati, Zeinab, Farhoud, Dariush, Nixdorff, Uwe, Mohammadhasani, Mohammadreza, Eslami, Maryam, Nayernia, Karim
Publicado 2021

Effect of ghrelin on serum metabolites in Alzheimer’s disease model rats; a metabolomics studies based on 1H-NMR technique

por Goshadrou, Fatemeh, Arefi Oskouie, Afsaneh, Eslami, Maryam, Nobakht Mothlagh Ghoochani, BiBi Fatemeh
Publicado 2018

Endothelial Nitric Oxide Synthase 4a/B Polymorphism and Its Interaction with Enos G894T Variants in Type 2 Diabetic Patients: Modifying the Risk of Diabetic Nephropathy

por Mohammadi, Mahsa, Yaghooti, Hamid, Adibmanesh, Azim, Mohammadtaghvaie, Narges, Akhormeh, Ali Karimi, Eslami, Maryam
Publicado 2022

Gjb3 Gene Mutations in Non-Syndromic Hearing Loss of Bloch, Kurd, and Turkmen Ethnicities in Iran

por ALIAZAMI, Farnoush, FARHUD, Dariush, ZARIF-YEGANEH, Marjan, SALEHI, Siamak, HOSSEINIPOUR, Azam, SASANFAR, Roxana, ESLAMI, Maryam
Publicado 2020