Vafaee Shahi M - Search Results

1

The first febrile seizure; predisposing factors and recurrence rate.

Kazemi A, Shervin Badv R, Fallah R, Piri A, Tahernia L, Vafaee Shahi M. Kazemi A, et al. Among authors: vafaee shahi m. Iran J Child Neurol. 2021 Spring;15(2):69-76. doi: 10.22037/ijcn.v15i1.15644. Epub 2021 Mar 1. Iran J Child Neurol. 2021. PMID: 36213155 Free PMC article.

2

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: vafaee shahi m. Iran J Child Neurol. 2015 Fall;9(4):54-7. Iran J Child Neurol. 2015. PMID: 26664442 Free PMC article.

3

Cerebellar Infarction in a 9 Year Old Child Presenting with Fever and Ataxia: A Case Report.

Vafaeeshahi M, Azizishalbaf N, Tahernia L. Vafaeeshahi M, et al. Iran J Child Neurol. 2019 Winter;13(1):107-114. Iran J Child Neurol. 2019. PMID: 30598678 Free PMC article.

4

Bilateral horizontal gaze palsy in an 8-year-old girl: A rare case with NDUFS4 gene mutation.

Vafaee-Shahi M, Ghasemi S, Beiraghi Toosi M, Ashrafi MR, Badv RS, Tavasoli AR, Tahernia L. Vafaee-Shahi M, et al. Clin Case Rep. 2021 Aug 30;9(9):e04748. doi: 10.1002/ccr3.4748. eCollection 2021 Sep. Clin Case Rep. 2021. PMID: 34484776 Free PMC article.

5

Lessons from Ten Years' the Prevalence of Congenital Rubella Syndrome (CRS) in the Young Population Living in a Developing Country, Tehran; Iran.

Noorbakhsh S, Vafaee-Shahi M, Tahernia L, Ashouri S, Riahi A. Noorbakhsh S, et al. Among authors: vafaee shahi m. Infect Disord Drug Targets. 2022;22(3):e131221198861. doi: 10.2174/1871526521666211213161712. Infect Disord Drug Targets. 2022. PMID: 34961468

6

Methenyltetrahydrofolate synthease deficiency (MTHFS deficiency): Novel mutation and brain MRI findings: A case report and glance to other cases.

Vafaee-Shahi M, Amirkashani D, Ashrafi MR, Tahernia L, Riahi A. Vafaee-Shahi M, et al. Clin Neurol Neurosurg. 2022 Apr;215:107153. doi: 10.1016/j.clineuro.2022.107153. Epub 2022 Jan 31. Clin Neurol Neurosurg. 2022. PMID: 35219051

7

Sexual Dimorphism in Telomere Length in Childhood Autism.

Panahi Y, Salasar Moghaddam F, Babaei K, Eftekhar M, Shervin Badv R, Eskandari MR, Vafaee-Shahi M, Pezeshk H, Pedram M. Panahi Y, et al. Among authors: vafaee shahi m. J Autism Dev Disord. 2023 May;53(5):2050-2061. doi: 10.1007/s10803-022-05486-2. Epub 2022 Feb 27. J Autism Dev Disord. 2023. PMID: 35220523

8

Intracranial angiomatoid fibrous histiocytoma: report of a rare case.

Tabibkhooei A, Asgarzadeh L, Sadeghipour A, Vafaee Shahi M. Tabibkhooei A, et al. Among authors: vafaee shahi m. Iran J Child Neurol. 2022 Summer;16(3):205-212. doi: 10.22037/ijcn.v15i4.26805. Epub 2022 Jul 16. Iran J Child Neurol. 2022. PMID: 36204427 Free PMC article.

9

A rare presentation of Carnitine palmitoyltransferase II (CPT-2) deficiency with normal acylcarnitine profile in a 10-year-old boy with muscle weakness and bilateral hearing loss; a case report.

Vafaee Shahi M, Ghasemi S, Tahernia L, Riahi A. Vafaee Shahi M, et al. Iran J Child Neurol. 2022 Fall;16(4):65-74. doi: 10.22037/ijcn.v17i1.27609. Epub 2022 Oct 23. Iran J Child Neurol. 2022. PMID: 36478999 Free PMC article.

10

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. 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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