Rasoulinezhad M - Search Results

1

Geoprocess of geospatial urban data in Tallinn, Estonia.

Eslamirad N, De Luca F, Lylykangas KS, Ben Yahia S, Rasoulinezhad M. Eslamirad N, et al. Among authors: rasoulinezhad m. Data Brief. 2023 Apr 22;48:109172. doi: 10.1016/j.dib.2023.109172. eCollection 2023 Jun. Data Brief. 2023. PMID: 37383820 Free PMC article.

2

Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report.

Zardadi S, Razmara E, Rasoulinezhad M, Babaei M, Ashrafi MR, Pak N, Garshasbi M, Tavasoli AR. Zardadi S, et al. Among authors: rasoulinezhad m. BMC Pediatr. 2022 Jul 13;22(1):412. doi: 10.1186/s12887-022-03468-y. BMC Pediatr. 2022. PMID: 35831840 Free PMC article.

3

CEP104 gene may involve in the pathogenesis of a new developmental disorder other than joubert syndrome.

Badv RS, Mahdiannasser M, Rasoulinezhad M, Habibi L, Rashidi-Nezhad A. Badv RS, et al. Among authors: rasoulinezhad m. Mol Biol Rep. 2022 Aug;49(8):7231-7237. doi: 10.1007/s11033-022-07353-w. Epub 2022 Mar 31. Mol Biol Rep. 2022. PMID: 35359234

4

Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 Gene.

Tavasoli AR, Memar EHE, Ashrafi MR, Hosseini SMM, Haghighi R, Ghabeli H, Pourbakhtyaran E, Rasoulinezhad M, Mohammadi P, Heidari M. Tavasoli AR, et al. Among authors: rasoulinezhad m. J Mol Neurosci. 2022 Apr;72(4):719-729. doi: 10.1007/s12031-021-01955-y. Epub 2022 Jan 4. J Mol Neurosci. 2022. PMID: 34982360

5

Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy.

Heidari E, Rasoulinezhad M, Pak N, Reza Ashrafi M, Heidari M, Banwell B, Garshasbi M, Reza Tavasoli A. Heidari E, et al. Among authors: rasoulinezhad m. Mitochondrion. 2021 Sep;60:12-20. doi: 10.1016/j.mito.2021.07.001. Epub 2021 Jul 9. Mitochondrion. 2021. PMID: 34252606

6

Leukoencephalopathy in Al-Raqad syndrome: Expanding the clinical and neuroimaging features caused by a biallelic novel missense variant in DCPS.

Masoudi M, Bereshneh AH, Rasoulinezhad M, Ashrafi MR, Garshasbi M, Tavasoli AR. Masoudi M, et al. Among authors: rasoulinezhad m. Am J Med Genet A. 2020 Oct;182(10):2391-2398. doi: 10.1002/ajmg.a.61776. Epub 2020 Aug 7. Am J Med Genet A. 2020. PMID: 32770650

7

Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8.

Hosseini Bereshneh A, Hosseipour S, Rasoulinezhad MS, Pak N, Garshasbi M, Tavasoli AR. Hosseini Bereshneh A, et al. Among authors: rasoulinezhad ms. Eur J Med Genet. 2020 May;63(5):103868. doi: 10.1016/j.ejmg.2020.103868. Epub 2020 Jan 28. Eur J Med Genet. 2020. PMID: 32004679

8

Prevalence of cryptococcal antigen positivity among HIV infected patient with CD4 cell count less than 100 of Imam Khomeini Hospital, Tehran, Iran.

Hajiabdolbaghi M, Kalantari S, Jamshidi-Makiani M, Shojaei E, Abbasian L, Rasoulinezhad M, Tayeri K. Hajiabdolbaghi M, et al. Among authors: rasoulinezhad m. Iran J Microbiol. 2017 Apr;9(2):119-121. Iran J Microbiol. 2017. PMID: 29214004 Free PMC article.

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