1. Investigating the association of Lamotrigine and Phenytoin‐induced Stevens‐Johnson syndrome/Toxic Epidermal Necrolysis with HLA‐B*1502 in Iranian population. Issue 2 (4th December 2020) Authors: Sabourirad, Sara; Mortezaee, Reza; Mojarad, Majid; Eslahi, Atieh; Shahrokhi, Yahya; Kiafar, Bita; Jarahi, Lida; Afkhami Ardakani, Saman; Farrokhi, Shima Journal: Experimental dermatology Issue: Volume 30:Issue 2(2021) Page Start: 284 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss. (15th April 2021) Authors: Farjami, Mahsa; Fathi, Mozhgan; Ghasemi, Mohammad Mehdi; Rajati, Mohsen; Eslahi, Atieh; Alimardani, Malihe; Mojarrad, Majid Journal: Fetal and pediatric pathology Issue: Volume 40:Number 2(2021) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. NR1H4-related Progressive Familial Intrahepatic Cholestasis 5: Further Evidence for Rapidly Progressive Liver Failure. Issue 6 (June 2020) Authors: Himes, Ryan W.; Mojarrad, Majid; Eslahi, Atieh; Finegold, Milton J.; Maroofian, Reza; Moore, David D. Journal: Journal of pediatric gastroenterology and nutrition Issue: Volume 70:Issue 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. (4th March 2019) Authors: Alimardani, Maliheh; Hosseini, Seyed Mojtaba; Khaniani, Mahmoud Shekari; Haghi, Mohsen Rajati; Eslahi, Atieh; Farjami, Mashsa; Chezgi, Javad; Derakhshan, Sima Mansoori; Mojarrad, Majid Journal: Fetal and pediatric pathology Issue: Volume 38:Number 2(2019) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗