Novel Homozygous Nonsense Mutation in the LRP5 Gene in Two Siblings with Osteoporosis-pseudoglioma Syndrome

by Abolfazl Heidari, Ali Homaei, Fatemeh Saffari
Published 2023-09-01

Identification of a Novel Mutation in an Iranian Family With 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Series

by Abolfazl Heidari, Ali Homaei, Fatemeh Saffari
Published 2022-04-01

Diagnostic value of NIPT assay for fetal aneuploidy screening in pregnant women with moderate risk of trisomy in first stage screening

by Fatemeh Lalooha, Shokouh Sadat Haji Seyed Abotorabi, Farideh Movahed, Farzaneh Bahrami, Abolfazl Heidari, Monirsadat Mirzadeh
Published 2022-06-01

Adolescent metabolic syndrome and its components associations with incidence of type 2 diabetes in early adulthood: Tehran lipid and glucose study

by Golaleh Asghari, Mitra Hasheminia, Abolfazl Heidari, Parvin Mirmiran, Kamran Guity, Mohammad Karim Shahrzad, Fereidoun Azizi, Farzad Hadaegh
Published 2021-01-01

CTLA-4 Gene Polymorphisms (-318C/T, +49A/G, +6230A/G) in Iranian Patients with Multiple Sclerosis

by Abolfazl Heidari, Mohammad Keramatipour, Ali Akbar Amirzargar, Ali Rashidinezhad, Ahmad Ali Sahmani, Hossein Mozhdehipanah, Mohammad Reza Noori Daloii
Published 2010-12-01