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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 2 |
2021 | 1 |
2022 | 2 |
2023 | 3 |
2024 | 0 |
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7 results
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Page 1
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Neurogenetics. 2023 Oct;24(4):279-289. doi: 10.1007/s10048-023-00730-y. Epub 2023 Aug 19.
Neurogenetics. 2023.
PMID: 37597066
Evaluating the correlation between migraine and subclinical atherosclerosis.
Esmaeili S, Alizadeh M, Abdi Y, Allahdadian S, Chaibakhsh S, Naderkhani M, Farzad Maroufi S, Baharvand F, Mirzaasgari Z, Taghi Joghataei M.
Esmaeili S, et al.
J Clin Neurosci. 2022 Dec;106:27-31. doi: 10.1016/j.jocn.2022.07.024. Epub 2022 Oct 12.
J Clin Neurosci. 2022.
PMID: 36242871
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Intravitreal recombinant tPA before vitrectomy for diabetic tractional retinal detachment: A randomized controlled trial.
Falavarjani KG, Anvari P, Shad E, Dehghan Niri MH, Sedaghat A, Abdi F, Parvaresh MM, Saeidian B, Gordiz A, Amirfarhangi Anbardan A.
Falavarjani KG, et al.
Eur J Ophthalmol. 2022 Nov;32(6):3522-3526. doi: 10.1177/11206721221116013. Epub 2022 Jul 21.
Eur J Ophthalmol. 2022.
PMID: 35861974
Clinical Trial.
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BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes.
Khani M, Shamshiri H, Taheri H, Hardy J, Bras JT, Carmona S, Moazzeni H, Alavi A, Heshmati A, Taghizadeh P, Nilipour Y, Ghazanfari T, Shahabi M, Okhovat AA, Rohani M, Valle G, Boostani R, Abdi S, Eshghi S, Nafissi S, Elahi E.
Khani M, et al.
Neurobiol Aging. 2021 Mar;99:102.e1-102.e10. doi: 10.1016/j.neurobiolaging.2020.09.021. Epub 2020 Oct 5.
Neurobiol Aging. 2021.
PMID: 33189404
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Endocrine Abnormalities in a Case of Neurodegeneration with Brain Iron Accumulation.
Haeri G, Akhoundi FH, Alavi A, Abdi S, Rohani M.
Haeri G, et al.
Mov Disord Clin Pract. 2020 Jun 24;7(6):706-707. doi: 10.1002/mdc3.12990. eCollection 2020 Aug.
Mov Disord Clin Pract. 2020.
PMID: 32775522
Free PMC article.
No abstract available.
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Impact of first eye cataract surgery on falls among patients of advanced age: a comparative study.
Akbari-Kamrani M, Heidarzadeh H, Naderan M, Gordiz A, Hemmati S, Chaibakhsh S, Mohammadi SS, Farsani MK, Zand A, Abdi F.
Akbari-Kamrani M, et al.
J Int Med Res. 2023 Dec;51(12):3000605231216685. doi: 10.1177/03000605231216685.
J Int Med Res. 2023.
PMID: 38069864
Free PMC article.
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Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Ashrafi M, Kameli R, Hosseinpour S, Razmara E, Zamani Z, Rezaei Z, Mashayekhi R, Pak N, Barzegar M, Azizimalamiri R, Kashani MR, Khosroshahi N, Rasulinezhad M, Heidari M, Amanat M, Abdi A, Mohammadi B, Mohammadi M, Zamani GR, Badv RS, Omrani A, Nikbakht S, Bereshneh AH, Movahedinia M, Moghaddam HF, Ardakani HS, Akbari MG, Tousi MB, Shahi MV, Hosseini F, Amouzadeh MH, Hosseini SA, Nikkhah A, Khajeh A, Alizadeh H, Yarali B, Rohani M, Karimi P, Elahi HML, Hosseiny SMM, Sadeghzadeh MS, Mohebbi H, Moghadam MH, Aryan H, Vahidnezhad H, Soveizi M, Rabbani B, Rabbani A, Mahdieh N, Garshasbi M, Tavasoli AR.
Ashrafi M, et al.
Neurogenetics. 2023 Oct;24(4):317-318. doi: 10.1007/s10048-023-00733-9.
Neurogenetics. 2023.
PMID: 37668767
No abstract available.
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