Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
International Journal of Pediatric Otorhinolaryngology|April 10, 2017
MYO15A splicing mutations in hearing loss: A review literature and report of a novel mutationMahsa Motavaf, Mahdieh Soveizi, Majid Maleki, et al.
Cellular and Molecular Neurobiology|October 10, 2022
Pathophysiology, Diagnosis, Treatment, and Genetics of Carpal Tunnel Syndrome: A ReviewMahshid Malakootian, Mahdieh Soveizi, Akram Gholipour, et al.
Medical Journal of the Islamic Republic of Iran|July 7, 2018
A novel PKP2 mutation and intrafamilial phenotypic variability in ARVC/DNejat Mahdieh, Sedigheh Saedi, Mahdieh Soveizi, et al.
International Journal of Cardiology|May 30, 2020
Genetic homozygosity in a diverse population: An experience of long QT syndromeNejat Mahdieh, Mohammadrafi Khorgami, Mahdieh Soveizi, et al.
Annals of Human Genetics|May 20, 2017
Autosomal Recessive Nonsyndromic Arrhythmogenic Right Ventricular Cardiomyopathy without Cutaneous Involvements: A Novel MutationMahdieh Soveizi, Bahareh Rabbani, Yousef Rezaei, et al.
ESC Heart Failure|June 14, 2024
Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac deathAmir Azimi, Mahdieh Soveizi, Alireza Salmanipour, et al.
Cardiology Research and Practice|September 5, 2025
Beyond the Beat, Next-Generation Sequencing Discovery of Novel RYR2 Gene Variant in Long QT SyndromeSamira Kalayinia, Amir Ghaffari Jolfayi, Amirali Soheili, 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.
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.
Journal of Cellular and Molecular Medicine|July 21, 2026
From Genotype to Phenotype: Investigating SLC22A5 Variants and Their Significance in Carnitine Deficiency: A Systematic Review StudyAmir Ghaffari Jolfayi, Mahdieh Soveizi, Niloofar Naderi, et al.
Pageof 2