Showing results (1-10 of 16) with videos related to
Sort By:
Pageof 2
Molecules (Basel, Switzerland)|April 26, 2025
Determination and Disposition of the Aromatase Inhibitor Exemestane in CYP3A-Deficient MiceHanieh Taheri, Eman Ahmed, Peng Hu, et al.Journal of Medical Genetics|July 25, 2022
Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigreeMarzieh Khani, Shahriar Nafissi, Hosein Shamshiri, et al.Research in Pharmaceutical Sciences|May 21, 2026
The effects of Vitex agnus-castus supplementation on inflammatory markers in women with PCOS: a randomized, double-blind, placebocontrolled trialAniseh Hatami, Hanieh Taheri, Ali Khosrowbeygi, et al.JBRA Assisted Reproduction|February 27, 2026
Effects of Arctium lappa L. Root Powder on Some Markers of Oxidative Stress and Inflammation in Women with Polycystic Ovary Syndrome: A Randomized, Double-Blind Controlled Clinical Trial StudyHanieh Taheri, Fatemeh Seydi, Farideh Jalali-Mashayekhi, et al.Clinical Case Reports|January 8, 2024
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe diseaseMarzieh Khani, Hosein Shamshiri, Shahriar Nafissi, et al.Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|April 18, 2024
Quantification of the aromatase inhibitor letrozole and its carbinol metabolite in mouse plasma by UHPLC-MS/MSHanieh Taheri, Yan Jin, Eman Ahmed, et al.American Journal of Medical Genetics. Part A|May 22, 2019
Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot-Marie-Tooth patients with TFG mutationMarzieh Khani, Hanieh Taheri, Hosein Shamshiri, et al.Neuromuscular Disorders : NMD|April 7, 2021
A case of adult onset Sandhoff disease that mimics Brown-Vialetto-Van Laere syndromeMarzieh Khani, Hosein Shamshiri, Hamidreza Moazzeni, et al.European Journal of Neurology|August 23, 2022
Identification of UBA1 as the causative gene of an X-linked non-Kennedy spinal-bulbar muscular atrophyMarzieh Khani, Shahriar Nafissi, Hosein Shamshiri, et al.Journal of Neurology|September 8, 2020
Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutationMarzieh Khani, Hanieh Taheri, Hosein Shamshiri, et al.Pageof 2