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Cell Death & Disease|August 27, 2024
Drp1 depletion protects against ferroptotic cell death by preserving mitochondrial integrity and redox homeostasisStephan Tang, Anneke Fuß, Zohreh Fattahi, et al.Archives of Iranian Medicine|October 8, 2015
Genetic Investigation of an Iranian Supercentenarian by Whole Exome SequencingTara Akhtarkhavari, Mohammad Taghi Joghataei, Zohreh Fattahi, et al.European Journal of Medical Genetics|October 26, 2018
SZT2 mutation in a boy with intellectual disability, seizures and autistic featuresAriana Kariminejad, Hilda Yazdan, Elham Rahimian, et al.Journal of Human Genetics|May 23, 2014
Mutation profile of BBS genes in Iranian patients with Bardet-Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genesZohreh Fattahi, Parvin Rostami, Amin Najmabadi, et al.Archives of Iranian Medicine|February 1, 2024
Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian CohortFarzane Zare Ashrafi, Tara Akhtarkhavari, Zohreh Fattahi, et al.Archives of Iranian Medicine|February 1, 2024
Expanding the Molecular Spectrum of HK1-Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in IranMasoumeh Goleyjani Moghadam, Zohreh Elahi, Mohamad Soveyzi, et al.Archives of Iranian Medicine|January 6, 2015
Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathyZohreh Fattahi, Kimia Kahrizi, Shahriar Nafissi, et al.American Journal of Medical Genetics. Part A|December 15, 2018
GPR126: A novel candidate gene implicated in autosomal recessive intellectual disabilityMasoumeh Hosseini, Zohreh Fattahi, Seyedeh Sedigheh Abedini, et al.Molecular Genetics & Genomic Medicine|January 6, 2023
Bi-allelic loss of function variant in the NRCAM gene is associated with motor-predominant axonal polyneuropathy; the second reportZohreh Elahi, Mohamad Soveyzi, Shahriar Nafissi, et al.Neuromuscular Disorders : NMD|March 30, 2016
Report of limb girdle muscular dystrophy type 2a in 6 Iranian patients, one with a novel deletion in CAPN3 geneMahsa Fadaee, Ariana Kariminejad, Zohreh Fattahi, et al.Pageof 5