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

Results by year

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

Year Number of Results
2002 1
2003 2
2004 1
2006 4
2007 3
2008 1
2009 3
2010 1
2011 3
2012 8
2013 6
2014 1
2015 2
2016 1
2017 6
2018 1
2019 7
2020 13
2021 6
2022 11
2023 7
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

74 results

Results by year

Filters applied: . Clear all
Page 1
Enhancing Equitable Access to Rare Disease Diagnosis and Treatment around the World: A Review of Evidence, Policies, and Challenges.
Adachi T, El-Hattab AW, Jain R, Nogales Crespo KA, Quirland Lazo CI, Scarpa M, Summar M, Wattanasirichaigoon D. Adachi T, et al. Among authors: wattanasirichaigoon d. Int J Environ Res Public Health. 2023 Mar 8;20(6):4732. doi: 10.3390/ijerph20064732. Int J Environ Res Public Health. 2023. PMID: 36981643 Free PMC article. Review.
Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients.
Phetthong T, Tim-Aroon T, Khongkraparn A, Noojarern S, Kuptanon C, Wichajarn K, Sathienkijkanchai A, Suphapeetiporn K, Charoenkwan P, Tantiworawit A, Noentong N, Wattanasirichaigoon D. Phetthong T, et al. Among authors: wattanasirichaigoon d. Orphanet J Rare Dis. 2021 Dec 20;16(1):519. doi: 10.1186/s13023-021-02151-2. Orphanet J Rare Dis. 2021. PMID: 34930372 Free PMC article.
Two infants with abetalipoproteinemia: Classic versus atypical presentation.
Prachasitthisak N, Tanpowpong P, Tim-Aroon T, Treepongkaruna S, Chongviriyaphan N, Vithayasai N, Iamopas O, Wattanasirichaigoon D. Prachasitthisak N, et al. Among authors: wattanasirichaigoon d. Pediatr Int. 2019 May;61(5):508-509. doi: 10.1111/ped.13822. Epub 2019 May 14. Pediatr Int. 2019. PMID: 31087595 No abstract available.
Klinefelter Syndrome Mosaicism 46,XX/47,XXY: A New Case and Literature Review.
Tangshewinsirikul C, Dulyaphat W, Tim-Aroon T, Parinayok R, Chareonsirisuthigul T, Korkiatsakul V, Waisayarat J, Sirisreetreerux P, Tingthanatikul Y, Wattanasirichaigoon D. Tangshewinsirikul C, et al. Among authors: wattanasirichaigoon d. J Pediatr Genet. 2020 Dec;9(4):221-226. doi: 10.1055/s-0040-1713002. Epub 2020 Jun 17. J Pediatr Genet. 2020. PMID: 32733741 Free PMC article.
A generation of human induced pluripotent stem cell line (MUi031-A) from a type-3 Gaucher disease patient carrying homozygous mutation on GBA1 gene.
Pornsukjantra T, Kangboonruang K, Tong-Ngam P, Tim-Aroon T, Wattanasirichaigoon D, Anurathapan U, Hongeng S, Tubsuwan A, Bhukhai K, Asavapanumas N. Pornsukjantra T, et al. Among authors: wattanasirichaigoon d. Stem Cell Res. 2022 Apr;60:102698. doi: 10.1016/j.scr.2022.102698. Epub 2022 Feb 2. Stem Cell Res. 2022. PMID: 35151019 Free article.
74 results