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Neurogenetics|May 25, 2023
COLQ-related congenital myasthenic syndrome: An integrative viewTina Eshaghian, Bahareh Rabbani, Reza Shervin Badv, et al.Indian Journal of Medical Microbiology|May 16, 2024
Evaluation of the presence of integrons, sul and smqnr genes and the prevalence of antibiotic resistance in Stenotrophomonas maltophilia clinical isolatesMaryam Mokhtari Bibalan, Ali Mojtahedi, Nejat Mahdieh, et al.Scientific Reports|February 6, 2021
Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variantsNejat Mahdieh, Mahdieh Soveizi, Ali Reza Tavasoli, et al.Stem Cells and Development|May 3, 2021
Patient-Specific Induced Pluripotent Stem Cell-Derived Hepatocyte-Like Cells as a Model to Study Autosomal Recessive HypercholesterolemiaParisa Nikasa, Tine Tricot, Nejat Mahdieh, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 22, 2020
Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analysesBahareh Rabbani, Mohammad Kazem Bakhshandeh, Mohammad Reza Navaeifar, et al.Genetic Testing and Molecular Biomarkers|June 10, 2025
Association of Obstructive Sleep Apnea Syndrome with Leptin Receptor Gene Q223R and K109R Single Nucleotide Polymorphisms in the Iranian Kurdish PopulationAli Alizadeh Severi, Sharareh Rasouli, Mohammad Abdolsamadi, et al.International Journal of Endocrinology|July 28, 2020
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature PubarcheMahdieh Soveizi, Nejat Mahdieh, Aria Setoodeh, et al.Anti-Cancer Drugs|November 19, 2016
Construction, expression, and activity of a novel immunotoxin comprising a humanized antiepidermal growth factor receptor scFv and modified Pseudomonas aeruginosa exotoxin ABahman Akbari, Safar Farajnia, Nosratollah Zarghami, et al.Journal of Clinical Laboratory Analysis|March 2, 2018
Genotypic effect of a mutation of the MYBPC3 gene and two phenotypes with different patterns of inheritanceNejat Mahdieh, Maryam Hosseini Moghaddam, Mahsa Motavaf, et al.Human Genomics|February 21, 2023
Neurofibromatosis-Noonan syndrome and growth deficiency in an Iranian girl due to a pathogenic variant in NF1 geneSetila Dalili, Seyyedeh Azade Hoseini Nouri, Reza Bayat, et al.Pageof 10