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Page 1
Neurodegeneration with Brain Iron Accumulation and a Brief Report of the Disease in Iran.
Can J Neurol Sci. 2022 May;49(3):338-351. doi: 10.1017/cjn.2021.124. Epub 2021 Jun 4.
Can J Neurol Sci. 2022.
PMID: 34082843
Review.
Late-Onset Mitochondrial Membrane Protein-Associated Neurodegeneration With Extensive Brain Iron Deposition.
Alavi A, Mokhtari M, Hajati R, Davarzani A, Fasano A, Lang AE, Rohani M.
Alavi A, et al. Among authors: hajati r.
Mov Disord Clin Pract. 2019 Nov 30;7(1):120-121. doi: 10.1002/mdc3.12868. eCollection 2020 Jan.
Mov Disord Clin Pract. 2019.
PMID: 31970231
Free PMC article.
No abstract available.
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Anticipation Can Be More Common in Hereditary Spastic Paraplegia with SPAST Mutations Than It Appears.
Hashemi SS, Hajati R, Davarzani A, Rohani M, DanaeeFard F, Rahimi Bidgoli MM, Fatehi F, Kariminejad A, Najmabadi H, Nafissi S, Alavi A.
Hashemi SS, et al. Among authors: hajati r.
Can J Neurol Sci. 2022 Sep;49(5):651-661. doi: 10.1017/cjn.2021.188. Epub 2021 Aug 6.
Can J Neurol Sci. 2022.
PMID: 34353391
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Giant axonal neuropathy: The first Iranian case with a variation in the gigaxonin gene and a glance to the other cases.
Vafaee-Shahi M, Ghasemi S, Ghahvechi-Akbar M, Tahernia L, Davarzani A, Hajati R, Zare-Abdollahi D, Alavi A.
Vafaee-Shahi M, et al. Among authors: hajati r.
Curr J Neurol. 2020 Oct 6;19(4):200-210. doi: 10.18502/cjn.v19i4.5548.
Curr J Neurol. 2020.
PMID: 38011432
Free PMC article.
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Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families.
Pashaei M, Davarzani A, Hajati R, Zamani B, Nafissi S, Larti F, Nilipour Y, Rohani M, Alavi A.
Pashaei M, et al. Among authors: hajati r.
J Neurogenet. 2021 Mar-Jun;35(2):84-94. doi: 10.1080/01677063.2021.1895146. Epub 2021 Mar 26.
J Neurogenet. 2021.
PMID: 33771085
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