Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Biochemical Genetics|January 13, 2025
Spectrum of ARSA mutations in Iranian patients with metachromatic leukodystrophyMohadeseh Fathi, Sheyda Khalilian, Mohammad Miryounesi, et al.
Molecular Biology Reports|May 20, 2022
Evaluation of potential of miR-8073 and miR-642 as diagnostic markers in pancreatic cancerMohadeseh Fathi, Hamid Asadzadeh Aghdaie, Soudeh Ghafouri-Fard, et al.
Biomolecules|November 27, 2021
LncRNAs: Novel Biomarkers for Pancreatic CancerSoudeh Ghafouri-Fard, Mohadeseh Fathi, Tianyue Zhai, et al.
Neurogenetics|December 3, 2024
Neurodegeneration with brain iron accumulation 5: report of three casesSheyda Khalilian, Mohadeseh Fathi, Akram Ghahghaei-Nezamabadi, et al.
Neurogenetics|October 17, 2025
Gaucher syndrome: report of six cases and review of genetic mutations among Iranian patientsMohammad Miryounesi, Mohadeseh Fathi, Sheyda Khalilian, et al.
Cancer Treatment and Research Communications|April 10, 2025
HOXB and HOXD genes contribute to the carcinogenic processes in glioblastoma: evidence form a bioinformatics analysisMohsen Ahmadi, Maryam Bazrgar, Saeedeh Akhavan, et al.
Molecular and Cellular Probes|March 13, 2024
Impact of miRNAs in the pathoetiology of recurrent implantation failureMohadeseh Fathi, Mohammad Amin Omrani, Sepideh Kadkhoda, et al.
Molecular Genetics and Metabolism Reports|July 14, 2025
Overview of genetic mutations causing adrenoleukodystrophy: A case-series studyMohadeseh Fathi, Sheyda Khalilian, Arezou Sayad, et al.
Human Genomics|May 13, 2025
A survey on mutation spectrum in Iranian patients with limb-girdle muscular dystrophiesSheyda Khalilian, Mohadeseh Fathi, Raheleh Tangestani, et al.
BMC Medical Genomics|April 9, 2025
Spectrum of genetic alterations in patients with peroxisome biogenesis defects in the Iranian population: a case series studySheyda Khalilian, Mohadeseh Fathi, Sanaz Jamshidi, et al.
Pageof 3