Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 2
2008 2
2011 1
2012 4
2013 4
2014 3
2015 2
2016 1
2017 4
2018 8
2019 7
2020 14
2021 12
2022 7
2023 13
2024 9
2025 8
2026 2

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

78 results

Results by year

Filters applied: . Clear all
Page 1
Familial Hypermanganesemia in Iran.
Tabatabaee SN, Effat Nejad S, Nikkhah A, Hashemi N, Alavi A, Lang AE, Rohani M, Emamikhah M. Tabatabaee SN, et al. Among authors: alavi a. Mov Disord Clin Pract. 2023 Mar 26;10(5):850-853. doi: 10.1002/mdc3.13723. eCollection 2023 May. Mov Disord Clin Pract. 2023. PMID: 37205251 Free PMC article. No abstract available.
Tremor-Dominant Pantothenate Kinase-associated Neurodegeneration.
Rohani M, Shahidi G, Alavi A, Lang AE, Yousefi N, Razme S, Fasano A. Rohani M, et al. Among authors: alavi a. Mov Disord Clin Pract. 2017 Jun 30;4(5):772-774. doi: 10.1002/mdc3.12512. eCollection 2017 Sep-Oct. Mov Disord Clin Pract. 2017. PMID: 30838286 Free PMC article.
Potential role of FKBP5 single-nucleotide polymorphisms in functional seizures.
Asadi-Pooya AA, Simani L, Asadollahi M, Rashidi FS, Ahmadipour E, Alavi A, Roozbeh M, Akbari N, Firouzabadi N. Asadi-Pooya AA, et al. Among authors: alavi a. Epilepsia Open. 2023 Jun;8(2):479-486. doi: 10.1002/epi4.12716. Epub 2023 Mar 21. Epilepsia Open. 2023. PMID: 36825897 Free PMC article.
MFSD8 gene mutations; evidence for phenotypic heterogeneity.
Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M, Effati J, Miratashi SAM, Dehani M, Jamali P, Khorram Khorshid HR. Zare-Abdollahi D, et al. Among authors: alavi a. Ophthalmic Genet. 2019 Apr;40(2):141-145. doi: 10.1080/13816810.2019.1592200. Epub 2019 Apr 22. Ophthalmic Genet. 2019. PMID: 31006324
White matter abnormalities in 15 subjects with SPG76.
Alkhalifa A, Chen S, Hasiloglu ZI, Filosto M, Cali E, Houlden H, Sgobbi de Souza P, Alavi A, Goizet C, Stevanin G, Taithe F, Nicita F, Vasco G, Tozza S, Cocozza S, Carboni N, Figus A, Wu J, Basak AN, Brais B, Rouleau G, La Piana R. Alkhalifa A, et al. Among authors: alavi a. J Neurol. 2023 Dec;270(12):5784-5792. doi: 10.1007/s00415-023-11918-5. Epub 2023 Aug 14. J Neurol. 2023. PMID: 37578488
78 results