Tavasoli AR[au] - Search Results

Year	Number of Results
2013	1
2014	2
2015	1
2017	4
2018	3
2019	10
2020	16
2021	12
2022	8

1

An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.

Ashrafi MR, Amanat M, Garshasbi M, Kameli R, Nilipour Y, Heidari M, Rezaei Z, Tavasoli AR. Ashrafi MR, et al. Among authors: tavasoli ar. Expert Rev Neurother. 2020 Jan;20(1):65-84. doi: 10.1080/14737175.2020.1699060. Epub 2019 Dec 12. Expert Rev Neurother. 2020. PMID: 31829048 Review.

2

Nonsyndromic Early-Onset Epileptic Encephalopathies: Two Novel KCTD7 Pathogenic Variants and a Literature Review.

Binaafar S, Garshasbi M, Tavasoli AR, Badv RS, Hosseiny SMM, Samanta D, Rabbani B, Mahdieh N. Binaafar S, et al. Among authors: tavasoli ar. Dev Neurosci. 2021;43(6):348-357. doi: 10.1159/000519318. Epub 2021 Sep 1. Dev Neurosci. 2021. PMID: 34469883 Review.

3

Novel variants in critical domains of ATP8A2 and expansion of clinical spectrum.

Heidari E, Harrison AN, Jafarinia E, Tavasoli AR, Almadani N, Molday RS, Garshasbi M. Heidari E, et al. Among authors: tavasoli ar. Hum Mutat. 2021 May;42(5):491-497. doi: 10.1002/humu.24180. Epub 2021 Mar 14. Hum Mutat. 2021. PMID: 33565221

4

Persistent dystonia and basal ganglia involvement following metronidazole induced encephalopathy.

Omrani A, Rohani M, Hosseinpour S, Tavasoli AR. Omrani A, et al. Among authors: tavasoli ar. Neurol Sci. 2020 Apr;41(4):957-959. doi: 10.1007/s10072-019-04091-z. Epub 2019 Oct 25. Neurol Sci. 2020. PMID: 31654363 No abstract available.

5

A novel missense variant in the LMNB2 gene causes progressive myoclonus epilepsy.

Soleimanipour F, Razmara E, Rahbarizadeh F, Fallahi E, Khodaeian M, Tavasoli AR, Garshasbi M. Soleimanipour F, et al. Among authors: tavasoli ar. Acta Neurol Belg. 2021 Mar 30. doi: 10.1007/s13760-021-01650-0. Online ahead of print. Acta Neurol Belg. 2021. PMID: 33783721

6

ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants.

Dehnavi AZ, Heidari E, Rasulinezhad M, Heidari M, Ashrafi MR, Hosseini MM, Sadeghzadeh F, Fallah MS, Rostampour N, Bahraini A, Garshasbi M, Tavasoli AR. Dehnavi AZ, et al. Among authors: tavasoli ar. Hum Genomics. 2021 Jul 19;15(1):45. doi: 10.1186/s40246-021-00345-0. Hum Genomics. 2021. PMID: 34281620 Free PMC article.

7

Childhood leukodystrophies: A literature review of updates on new definitions, classification, diagnostic approach and management.

Ashrafi MR, Tavasoli AR. Ashrafi MR, et al. Among authors: tavasoli ar. Brain Dev. 2017 May;39(5):369-385. doi: 10.1016/j.braindev.2017.01.001. Epub 2017 Jan 20. Brain Dev. 2017. PMID: 28117190 Review.

8

A novel deletion variant in CLN3 with highly variable expressivity is responsible for juvenile neuronal ceroid lipofuscinoses.

Gilani N, Razmara E, Ozaslan M, Abdulzahra IK, Arzhang S, Tavasoli AR, Garshasbi M. Gilani N, et al. Among authors: tavasoli ar. Acta Neurol Belg. 2021 Jun;121(3):737-748. doi: 10.1007/s13760-021-01655-9. Epub 2021 Mar 30. Acta Neurol Belg. 2021. PMID: 33783722

9

Novel disease-causing variants in a cohort of Iranian patients with metachromatic leukodystrophy and in silico analysis of their pathogenicity.

Mahdieh N, Sharifi A, Rabbani A, Ashrafi M, Tavasoli AR, Badv RS, Bonkowsky JL, Rabbani B. Mahdieh N, et al. Among authors: tavasoli ar. Clin Neurol Neurosurg. 2021 Feb;201:106448. doi: 10.1016/j.clineuro.2020.106448. Epub 2020 Dec 22. Clin Neurol Neurosurg. 2021. PMID: 33385934

10

Leukoencephalopathy in RIN2 syndrome: Novel mutation and expansion of clinical spectrum.

Kameli R, Ashrafi MR, Ehya F, Alizadeh H, Hosseinpour S, Garshasbi M, Tavasoli AR. Kameli R, et al. Among authors: tavasoli ar. Eur J Med Genet. 2020 Jan;63(1):103629. doi: 10.1016/j.ejmg.2019.02.002. Epub 2019 Feb 13. Eur J Med Genet. 2020. PMID: 30769224

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