The challenges in the interpretation of genetic variants detected by genomics techniques in patients with congenital anomalies

por Vaseghi, Hajar, Akrami, Seyed Mohammad, Rashidi‐Nezhad, Ali
Publicado 2023

The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile

por Rashidi-Nezhad, Ali, Talebi, Saeed, Saebnouri, Homeira, Akrami, Seyed Mohammad, Reymond, Alexandre
Publicado 2014

A novel case report of spinal muscular atrophy with progressive myoclonic epilepsy from Iran

por Shervin Badv, Reza, Nilipour, Yalda, Rahimi-Dehgolan, Shahram, Rashidi-Nezhad, Ali, Ghahvechi Akbari, Masood
Publicado 2019

The c.1243T>C mutation in the PROC gene is linked with inherited protein C deficiency and severe purpura fulminans

por Nourbakhsh, Seyed Mohammad Kazem, Bahadoram, Mohammad, Rashidi‐Nezhad, Ali, Habibi, Laleh, Mansouri, Fatemeh, Akade, Esma'il
Publicado 2023

Utilization of Whole Exome Sequencing in Lethal Form of Multiple Pterygium Syndrome: Identification of Mutations in Embryonal Subunit of Acetylcholine Receptor

por Nazari, Tahere, Rashidi-Nezhad, Ali, Ganji, Maziar, Rezaei, Zahra, Talebi, Saeed, Ghasemi, Nasrin, Tavakkoly Bazzaz, Javad
Publicado 2019

Effects of cannabinoid receptor type 2 in respiratory syncytial virus infection in human subjects and mice

por Tahamtan, Alireza, Samieipoor, Yazdan, Nayeri, Fatemeh Sadat, Rahbarimanesh, Ali Akbar, Izadi, Anahita, Rashidi-Nezhad, Ali, Tavakoli-Yaraki, Masoumeh, Farahmand, Mohammad, Bont, Louis, Shokri, Fazel, Mokhatri-Azad, Talat, Salimi, Vahid
Publicado 2017