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Scientific Reports|September 29, 2021
Expression and clinical significance of IL7R, NFATc2, and RNF213 in familial and sporadic multiple sclerosisSeyedeh Zahra Hosseini Imani, Zohreh Hojati, Sheyda Khalilian, et al.Biochemical Genetics|April 2, 2025
Spectrum of Genetic Mutations Among Iranian Patients with GangliosidosisSheyda Khalilian, Mohadeseh Fathi, Mona Alizadeh, et al.Scientific Reports|April 9, 2021
Gene expression profiles of YAP1, TAZ, CRB3, and VDR in familial and sporadic multiple sclerosis among an Iranian populationSheyda Khalilian, Zohreh Hojati, Fariba Dehghanian, et al.BMC Research Notes|May 12, 2025
The investigation of apoptosis-related genes in periodontitisArezou Sayad, Fatemeh Hashemian, Leila Gholami, et al.Brain & Development|June 22, 2026
Aspartoacylase (ASPA) gene mutations and neuroimaging features in Iranian patients with Canavan disease: a descriptive studyElham Rahimian, Majid R Tahsini, Parvaneh Karimzadeh, et al.Journal of Molecular Neuroscience : MN|June 12, 2026
Exploratory Analysis of Neuroimaging and Molecular Findings in a Cohort of Neuronal Ceroid Lipofuscinosis: a Descriptive studyElham Rahimian, Majid R Tahsini, Mohadeseh Fathi, et al.Molecular Cytogenetics|December 20, 2024
Performance of cell free DNA as a screening tool based on the results of first trimester screeningMahtab Motevasselian, Mohammad Amin Omrani, Soraya Saleh Gargari, et al.Neuromolecular Medicine|July 2, 2024
A Comprehensive Overview of NF1 Mutations in Iranian PatientsShahram Savad, Mohammad-Hossein Modarressi, Sarang Younesi, et al.Pageof 4