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

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

50 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Beta-synuclein gene alterations in dementia with Lewy bodies.
Ohtake H, Limprasert P, Fan Y, Onodera O, Kakita A, Takahashi H, Bonner LT, Tsuang DW, Murray IV, Lee VM, Trojanowski JQ, Ishikawa A, Idezuka J, Murata M, Toda T, Bird TD, Leverenz JB, Tsuji S, La Spada AR. Ohtake H, et al. Among authors: limprasert p. Neurology. 2004 Sep 14;63(5):805-11. doi: 10.1212/01.wnl.0000139870.14385.3c. Neurology. 2004. PMID: 15365127 Free PMC article.
Familial dementia with Lewy bodies with an atypical clinical presentation.
Bonner LT, Tsuang DW, Cherrier MM, Eugenio CJ, Du Jennifer Q, Steinbart EJ, Limprasert P, La Spada AR, Seltzer B, Bird TD, Leverenz JB. Bonner LT, et al. Among authors: limprasert p. J Geriatr Psychiatry Neurol. 2003 Mar;16(1):59-64. doi: 10.1177/0891988702250585. J Geriatr Psychiatry Neurol. 2003. PMID: 12641375 Free PMC article.
Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier.
Yamada K, Limprasert P, Ratanasukon M, Tengtrisorn S, Yingchareonpukdee J, Vasiknanonte P, Kitaoka T, Ghadami M, Niikawa N, Kishino T. Yamada K, et al. Among authors: limprasert p. Am J Med Genet. 2001 Apr 15;100(1):52-5. doi: 10.1002/1096-8628(20010415)100:1<52::aid-ajmg1214>3.0.co;2-b. Am J Med Genet. 2001. PMID: 11337749
Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder.
Wongpaiboonwattana W, Plong-On O, Hnoonual A, Limprasert P. Wongpaiboonwattana W, et al. Among authors: limprasert p. Medicine (Baltimore). 2020 Sep 4;99(36):e21946. doi: 10.1097/MD.0000000000021946. Medicine (Baltimore). 2020. PMID: 32899028 Free PMC article.
Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.
Hnoonual A, Thammachote W, Tim-Aroon T, Rojnueangnit K, Hansakunachai T, Sombuntham T, Roongpraiwan R, Worachotekamjorn J, Chuthapisith J, Fucharoen S, Wattanasirichaigoon D, Ruangdaraganon N, Limprasert P, Jinawath N. Hnoonual A, et al. Among authors: limprasert p. Sci Rep. 2017 Sep 21;7(1):12096. doi: 10.1038/s41598-017-12317-3. Sci Rep. 2017. PMID: 28935972 Free PMC article.
50 results