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Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome.
Nasiri J, Salehi M, Hosseinzadeh M, Zamani M, Fattahpour S, Aryani O, Fazel Najafabadi E, Jabarzadeh M, Asadi S, Gholamrezapour T, Sedghi M, Ghorbani F. Nasiri J, et al. Among authors: aryani o. Iran J Child Neurol. 2019 Summer;13(3):25-34. Iran J Child Neurol. 2019. PMID: 31327966 Free PMC article.
A Novel Mutation in Aspartoacylase Gene; Canavan Disease.
Ashrafi M, Tavasoli A, Katibeh P, Aryani O, Vafaee-Shahi M. Ashrafi M, et al. Among authors: aryani o. Iran J Child Neurol. 2015 Fall;9(4):54-7. Iran J Child Neurol. 2015. PMID: 26664442 Free PMC article.
Effects of miglustat on stabilization of neurological disorder in niemann-pick disease type C: Iranian pediatric case series.
Karimzadeh P, Tonekaboni SH, Ashrafi MR, Shafeghati Y, Rezayi A, Salehpour S, Ghofrani M, Taghdiri MM, Rahmanifar A, Zaman T, Aryani O, Shoar BN, Shiva F, Tavasoli A, Houshmand M. Karimzadeh P, et al. Among authors: aryani o. J Child Neurol. 2013 Dec;28(12):1599-606. doi: 10.1177/0883073812464526. Epub 2012 Nov 8. J Child Neurol. 2013. PMID: 23143717
42 results