Search Results - "Nekuie Moghadam, Tayebeh"

Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family by Moazzeni, Hamidreza, Javadi, Mohammad Ali, Asgari, Danial, Khani, Marzieh, Emami, Mohammad, Moghadam, Abolfazl, Panahi-Bazaz, Mahmoud-Reza, Hosseini Tehrani, Mehdi, Karimian, Farid, Hosseini, Bagher, Nekuie Moghadam, Tayebeh, Hassanpour, Hossein, Akbari, Mohammad Taghi, Elahi, Elahe

“…is the only known causative gene of congenital hereditary endothelial dystrophy (CHED). Mutation screenings have shown that most but not all patients with CHED…”
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Screening for MIR184 mutations in Iranian patients with keratoconus by Farzadfard, Azad, Nassiri, Nader, Moghadam, Tayebeh, Paylakhi, Seyed, Elahi, Elahe

“…Purpose: To investigate whether microRNA (MIR)-184 mutations make a substantial contribution to keratoconus (KCN) among affected Iranian patients. Methods: A…”
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