Hosseinpour S - Search Results

1

Homozygous in-frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family.

Heidari E, Razmara E, Hosseinpour S, Tavasoli AR, Garshasbi M. Heidari E, et al. Among authors: hosseinpour s. Ann Hum Genet. 2020 Jul;84(4):315-323. doi: 10.1111/ahg.12378. Epub 2020 Feb 20. Ann Hum Genet. 2020. PMID: 32077500

2

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: hosseinpour s. 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

3

Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients.

Rezaei Z, Hosseinpour S, Ashrafi MR, Mahdieh N, Alizadeh H, Mohammadpour M, Khosroshahi N, Amanat M, Tavasoli AR. Rezaei Z, et al. Among authors: hosseinpour s. Neuropediatrics. 2019 Apr;50(2):130-134. doi: 10.1055/s-0039-1679911. Epub 2019 Feb 21. Neuropediatrics. 2019. PMID: 30791064

4

Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review.

Rostami P, Hosseinpour S, Ashrafi MR, Alizadeh H, Garshasbi M, Tavasoli AR. Rostami P, et al. Among authors: hosseinpour s. Acta Neurol Belg. 2020 Jun;120(3):511-516. doi: 10.1007/s13760-019-01168-6. Epub 2019 Jun 20. Acta Neurol Belg. 2020. PMID: 31222513 Review.

5

Deep brain stimulation in status dystonicus caused by anti-NMDA receptor encephalitis.

Tavasoli AR, Shahidi G, Parvaresh M, Fasano A, Ashrafi MR, Hosseinpour S, Lang AE, Rohani M. Tavasoli AR, et al. Among authors: hosseinpour s. Parkinsonism Relat Disord. 2019 Sep;66:255-257. doi: 10.1016/j.parkreldis.2019.07.023. Epub 2019 Jul 20. Parkinsonism Relat Disord. 2019. PMID: 31345707 No abstract available.

6

Persistent dystonia and basal ganglia involvement following metronidazole induced encephalopathy.

Omrani A, Rohani M, Hosseinpour S, Tavasoli AR. Omrani A, et al. Among authors: hosseinpour s. 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.

7

Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome Sequencing.

Zamani GR, Mohammadi MF, Tavasoli AR, Ashrafi MR, Hosseinpour S, Ghabeli H, Pourbakhtyaran E, Haghighi R, Hosseiny SMM, Mohammadi P, Heidari M. Zamani GR, et al. Among authors: hosseinpour s. J Mol Neurosci. 2022 May;72(5):1098-1107. doi: 10.1007/s12031-022-01980-5. Epub 2022 Feb 26. J Mol Neurosci. 2022. PMID: 35218518

8

Follow-up of 25 patients with treatable ataxia: A comprehensive case series study.

Ashrafi MR, Pourbakhtyaran E, Rohani M, Shalbafan B, Tavasoli AR, Hosseinpour S, Rasulinezhad M, Rezaei Z, Zare Dehnavi A, Hosseiny SMM, Haghighi R, Ghabeli H, Heidari M. Ashrafi MR, et al. Among authors: hosseinpour s. Clin Case Rep. 2022 Apr 20;10(4):e05777. doi: 10.1002/ccr3.5777. eCollection 2022 Apr. Clin Case Rep. 2022. PMID: 35474986 Free PMC article.

9

Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy.

Zamani G, Hosseinpour S, Ashrafi MR, Mohammadi M, Badv RS, Tavasoli AR, Akbari MG, Bereshneh AH, Malamiri RA, Heidari M. Zamani G, et al. Among authors: hosseinpour s. BMC Neurol. 2022 May 2;22(1):162. doi: 10.1186/s12883-022-02687-1. BMC Neurol. 2022. PMID: 35501714 Free PMC article.

10

Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.

Ashrafi MR, Mohammadi P, Tavasoli AR, Heidari M, Hosseinpour S, Rasulinejad M, Rohani M, Akbari MG, Malamiri RA, Badv RS, Fathi D, Dehnavi AZ, Savad S, Rabbani A, Synofzik M, Mahdieh N, Rezaei Z. Ashrafi MR, et al. Among authors: hosseinpour s. Cerebellum. 2023 Aug;22(4):640-650. doi: 10.1007/s12311-022-01430-3. Epub 2022 Jun 22. Cerebellum. 2023. PMID: 35731353

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