Hereditary Autonomic Neuropathy of the Oral Cavity and its Management

por ESMAEILZADEH, Niloofar, ASHRAFI, Mahmoud Reza, SHOJAALDINI ARDAKANI, Hossein, SERAJ, Bahman, AREF, Parissa
Publicado 2022

FAM20A Mutations Can Cause Enamel-Renal Syndrome (ERS)

por Wang, Shih-Kai, Aref, Parissa, Hu, Yuanyuan, Milkovich, Rachel N., Simmer, James P., El-Khateeb, Mohammad, Daggag, Hinda, Baqain, Zaid H., Hu, Jan C-C.
Publicado 2013

Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

por Parry, David A., Mighell, Alan J., El-Sayed, Walid, Shore, Roger C., Jalili, Ismail K., Dollfus, Hélène, Bloch-Zupan, Agnes, Carlos, Roman, Carr, Ian M., Downey, Louise M., Blain, Katharine M., Mansfield, David C., Shahrabi, Mehdi, Heidari, Mansour, Aref, Parissa, Abbasi, Mohsen, Michaelides, Michel, Moore, Anthony T., Kirkham, Jennifer, Inglehearn, Chris F.
Publicado 2009