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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

92 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Novel SOX10 Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis.
Thongpradit S, Jinawath N, Javed A, Jensen LT, Chunsuwan I, Rojnueangnit K, Tim-Aroon T, Lertsukprasert K, Shiao MS, Sirachainan N, Wattanasirichaigoon D. Thongpradit S, et al. Among authors: wattanasirichaigoon d. Front Genet. 2020 Dec 9;11:589784. doi: 10.3389/fgene.2020.589784. eCollection 2020. Front Genet. 2020. PMID: 33362852 Free PMC article.
A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency.
Pongphitcha P, Sirachainan N, Khongkraparn A, Tim-Aroon T, Songdej D, Wattanasirichaigoon D. Pongphitcha P, et al. Among authors: wattanasirichaigoon d. BMC Pediatr. 2022 Apr 29;22(1):233. doi: 10.1186/s12887-022-03291-5. BMC Pediatr. 2022. PMID: 35488219 Free PMC article.
Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years.
Mongkollarp N, Tim-Aroon T, Okascharoen C, Wichajarn K, Phosuwattanakul J, Chongviriyaphan N, Wattanasirichaigoon D. Mongkollarp N, et al. Among authors: wattanasirichaigoon d. Orphanet J Rare Dis. 2020 May 6;15(1):111. doi: 10.1186/s13023-020-01388-7. Orphanet J Rare Dis. 2020. PMID: 32375863 Free PMC article.
Comprehensive and long-term outcomes of enzyme replacement therapy followed by stem cell transplantation in children with Gaucher disease type 1 and 3.
Anurathapan U, Tim-Aroon T, Zhang W, Sanpote W, Wongrungsri S, Khunin N, Chutipongtanate S, Chirdkiatgumchai V, Ngiwsara L, Jaovisidha S, Khongkraparn A, Pakakasama S, Svasti J, Setchell KDR, Wattanasirichaigoon D, Hongeng S. Anurathapan U, et al. Among authors: wattanasirichaigoon d. Pediatr Blood Cancer. 2023 Mar;70(3):e30149. doi: 10.1002/pbc.30149. Epub 2022 Dec 23. Pediatr Blood Cancer. 2023. PMID: 36562549
92 results