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Page 1
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: ghorbani f. Iran J Child Neurol. 2019 Summer;13(3):25-34. Iran J Child Neurol. 2019. PMID: 31327966 Free PMC article.
Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia.
Ghorbani F, de Boer-Bergsma J, Verschuuren-Bemelmans CC, Pennings M, de Boer EN, Kremer B, Vanhoutte EK, de Vries JJ, van de Berg R, Kamsteeg EJ, van Diemen CC, Westers H, van de Warrenburg BP, Verbeek DS. Ghorbani F, et al. J Neurol. 2022 Nov;269(11):6086-6093. doi: 10.1007/s00415-022-11275-9. Epub 2022 Jul 21. J Neurol. 2022. PMID: 35864213 Free PMC article.
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance.
Ghorbani F, Alimohamed MZ, Vilacha JF, Van Dijk KK, De Boer-Bergsma J, Fokkens MR, Lemmink H, Sijmons RH, Sikkema-Raddatz B, Groves MR, Verschuuren-Bemelmans CC, Verbeek DS, Van Diemen CC, Westers H. Ghorbani F, et al. Front Genet. 2022 Mar 25;13:782685. doi: 10.3389/fgene.2022.782685. eCollection 2022. Front Genet. 2022. PMID: 35401678 Free PMC article.
MRONJ: reporting challenges.
Ghorbani F. Ghorbani F. Br Dent J. 2025 Jan;238(1):35. doi: 10.1038/s41415-025-8288-0. Br Dent J. 2025. PMID: 39794579 No abstract available.
262 results