Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

por Zardadi, Safoura, Rayat, Sima, Hassani Doabsari, Maryam, Keramatipour, Mohammad, Morovvati, Saeid
Publicado 2021

Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population

por Rayat, Sima, Ramezanidoraki, Nasim, Kazemi, Nima, Modarressi, Mohammad H., Falah, Masoumeh, Zardadi, Safoura, Morovvati, Saeid
Publicado 2022

Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

por Zardadi, Safoura, Rayat, Sima, Doabsari, Maryam Hassani, Alishiri, Aliagha, Keramatipour, Mohammad, Shahri, Zeynab Javanfekr, Morovvati, Saeid
Publicado 2021

Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

por Zardadi, Safoura, Razmara, Ehsan, Asgaritarghi, Golareh, Jafarinia, Ehsan, Bitarafan, Fatemeh, Rayat, Sima, Almadani, Navid, Morovvati, Saeid, Garshasbi, Masoud
Publicado 2020

Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report

por Zardadi, Safoura, Razmara, Ehsan, Rasoulinezhad, Maryam, Babaei, Meisam, Ashrafi, Mohammad Reza, Pak, Neda, Garshasbi, Masoud, Tavasoli, Ali Reza
Publicado 2022