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Search Results - Mojdeh Roghani
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Usher Syndrome Type 2 in An Iranian Family: A Novel Founder Variation in The USH2A Gene
by
Neissi, Mostafa
,
Mohammadi-Asl, Javad
,
Mohammadi-Asl, Misagh
,
Roghani, Mojdeh
,
Sheikh-Hosseini, Motahareh
,
Issa Al-Badran, Adnan
Published in
Cell journal (Yakhteh)
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Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis
by
Neissi, Mostafa
,
Misagh Mohammadi-Asl
,
Mojdeh Roghani
,
Issa Al-Badran, Adnan
,
Motahareh Sheikh-Hosseini
,
Mohammadi-Asl, Javad
Published in
Neurology Asia
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Identification and characterization of NMNAT1 gene mutations in an Iranian patient with Leber congenital amaurosis 9
by
Neissi, Mostafa
,
Sheikh‐Hosseini, Motahareh
,
Mohammadi‐Asl, Misagh
,
Al‐Badran, Adnan Issa
,
Roghani, Mojdeh
,
Mohammadi‐Asl, Javad
,
Jorfi, Kamele
Published in
Clinical case reports
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Clinical and genetic analysis of Niemann-Pick disease type C with a novel NPC1 variant
by
Neissi, Mostafa
,
Al-Badran, Adnan Issa
,
Mohammadi-Asl, Misagh
,
Al-Badran, Raed Abdulelah
,
Sheikh-Hosseini, Motahareh
,
Roghani, Mojdeh
,
Mohammadi-Asl, Javad
Published in
Journal of rare diseases (Berlin, Germany)
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Assessment of the protective effect of KN‐93 drug in systemic epilepsy disorders induced by pilocarpine in male rat
by
Ebrahimi, Fatemeh
,
Sadr, Seyed Shahabeddin
,
Roghani, Mehrdad
,
Khamse, Safoura
,
Mohammadian Haftcheshmeh, Saeed
,
Navid Hamidi, Mojdeh
,
Mohseni‐Moghaddam, Parvaneh
,
Zamani, Elham
Published in
Journal of cellular biochemistry
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The role of nitric oxide in the PKA inhibitor induced spatial memory deficits in rat: Involvement of choline acetyltransferase
by
Najafi, Sheyda
,
Payandemehr, Borna
,
Tabrizian, Kaveh
,
Shariatpanahi, Marjan
,
Nassireslami, Ehsan
,
Azami, Kian
,
Mohammadi, Mojdeh
,
Asadi, Farideh
,
Roghani, Ali
,
Sharifzadeh, Mohammad
Published in
European journal of pharmacology
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