Novel Homozygous Missense Mutation in RYR1 Leads to Severe Congenital Ptosis, Ophthalmoplegia, and Scoliosis in the Absence of Myopathy

Por Dilaver, Nafi, Mazaheri, Neda, Maroofian, Reza, Zeighami, Jawaher, Seifi, Tahere, Zamani, Mina, Sedaghat, Alireza, Shariati, Gholam Reza, Galehdari, Hamid
Publicado no Mol Syndromol (2017)

Construction and Development of a Cardiac Tissue-Specific and Hypoxia-Inducible Expression Vector

Por Ghaderi, Shahrooz, Alidadiani, Neda, Soleimani Rad, Jafar, Heidari, Hamid Reza, Dilaver, Nafi, Mansoori, Behzad, Rhabarghazi, Reza, Parvizi, Rezayat, Khaze Shahgoli, Vahid, Baradaran, Behzad
Publicado no Adv Pharm Bull (2018)

Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis

Por Hashemian, Somayyeh, Eshraghi, Peyman, Dilaver, Nafi, Galehdari, Hamid, Shalbafan, Bita, Vakili, Rahim, Ghaemi, Nosrat, Ahangari, Najmeh, Rezazadeh Varaghchi, Jamileh, Zeighami, Jawaher, Sedaghat, Alireza, Aminzadeh, Majid, Hamid, Mohammad, Saberi, Alihossein, Ashtari, Fereshteh, Ghayoor Karimiani, Ehsan, Shariati, Gholamreza
Publicado no Iran J Child Neurol (2019)