Vitamin D can be effective on the prevention of COVID-19 complications: A narrative review on molecular aspects AA Shiravi, M Saadatkish, Z Abdollahi, P Miar, H Khanahmad, ... International Journal for Vitamin and Nutrition Research, 2020 | 28 | 2020 |
Nervous system involvement in COVID-19: a review of the current knowledge M Norouzi, P Miar, S Norouzi, P Nikpour Molecular Neurobiology 58, 3561-3574, 2021 | 18 | 2021 |
Vitamin D can be effective against COVID19 and other similar viral infections: a review on molecular aspects AA Shiravi, M Saadat, Z Abdollahi, P Miar, H Khanahmad, M Zeinalian Zenodo, 2020 | 3 | 2020 |
Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian … S Nasrniya, P Miar, S Narrei, M Sepehrnejad, MH Nilforoush, H Abtahi, ... Laboratory Medicine 53 (2), 111-122, 2022 | 2 | 2022 |
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family M Norouzi, M Shafiei, Z Abdollahi, P Miar, H Galehdari, MH Emami, ... Frontiers in Oncology 11, 648649, 2021 | 2 | 2021 |
A Simplified Protocol for Microsatellite Instability Evaluation in Iranian Patients at Risk for Lynch Syndrome Z Abdollahi, MA Tabatabaiefar, M Noruzi, P Miar, M Kazemi, A Naimi, ... Laboratory Medicine 53 (3), 235-241, 2022 | | 2022 |
BAT25, ACVR2, and TGFBR2 Mononucleotide STR Markers: A Triplex Panel for Microsatellite Instability Testing in Colorectal Tumors P Miar, MA Tabatabaiefar, Z Abdollahi, M Noruzi, M Kazemi, A Naimi, ... Advanced Biomedical Research 11 (1), 79, 2022 | | 2022 |
A Novel Stop-Gain Mutation in MSH2 Gene Among a Persian Family Fulfilling Classic Amsterdam Criteria for Lynch Syndrome P Miar, S Narrei, MA Tabatabaiefar, MR Pourreza, ... | | 2021 |
WRN is a Possible Genetic Cause of Hereditary Cancer Syndrome in an Iranian Family with Different Cancer Types M Norouzi, Z Abdollahi, P Miar, H Galehdari, MH Emami, M Zeinalian, ... Frontiers in Oncology 11, 1921, 2021 | | 2021 |