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Genetic Testing and Molecular Biomarkers|December 4, 2024
The Association Between the C-Reactive Protein Gene Variants rs1130864 and rs2794521 and Obstructive Sleep Apnea in the Iranian Kurdish PopulationSharareh Rasouli, Ali Alizadeh Severi, Mohammad Abdolsamadi, et al.
Neuropediatrics|February 22, 2019
Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated PatientsZahra Rezaei, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
Developmental Neuroscience|September 1, 2021
Nonsyndromic Early-Onset Epileptic Encephalopathies: Two Novel KCTD7 Pathogenic Variants and a Literature ReviewSima Binaafar, Masoud Garshasbi, Ali Reza Tavasoli, et al.
Cardiovascular Toxicology|May 20, 2018
Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary InterventionNejat Mahdieh, Ahmad Rabbani, Ata Firouzi, et al.
Genetic Testing and Molecular Biomarkers|March 11, 2011
Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variantNejat Mahdieh, Bahareh Rabbani, Atefeh Shirkavand, et al.
Cardiovascular Toxicology|August 11, 2018
Correction to: Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary InterventionNejat Mahdieh, Ahmad Rabbani, Ata Firouzi, et al.
Genetic Testing and Molecular Biomarkers|October 25, 2011
Mutation analysis of the CYP21A2 gene in the Iranian populationBahareh Rabbani, Nejat Mahdieh, Mohammad Tahgi Haghi Ashtiani, et al.
Journal of Molecular Neuroscience : MN|March 11, 2022
Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to TherapyMahmoud Reza Ashrafi, Roya Haghighi, Reza Shervin Badv, et al.
Clinical Laboratory|September 25, 2012
Design of a biological method for rapid detection of presence of PCR inhibitors in aged bone DNAAkram Ghasemi, Nejat Mahdieh, Mahmood Tavallaei, et al.
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