Yeetong P - Search Results

1

TTTCA repeat insertions in an intron of YEATS2 in benign adult familial myoclonic epilepsy type 4.

Yeetong P, Pongpanich M, Srichomthong C, Assawapitaksakul A, Shotelersuk V, Tantirukdham N, Chunharas C, Suphapeetiporn K, Shotelersuk V. Yeetong P, et al. Brain. 2019 Nov 1;142(11):3360-3366. doi: 10.1093/brain/awz267. Brain. 2019. PMID: 31539032

2

Identification of mutations in the SRD5A2 gene in Thai patients with male pseudohermaphroditism.

Sahakitrungruang T, Wacharasindhu S, Yeetong P, Snabboon T, Suphapeetiporn K, Shotelersuk V. Sahakitrungruang T, et al. Among authors: yeetong p. Fertil Steril. 2008 Nov;90(5):2015.e11-5. doi: 10.1016/j.fertnstert.2008.01.019. Epub 2008 Mar 7. Fertil Steril. 2008. PMID: 18314109 Free article.

3

Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome.

Yeetong P, Mahatumarat C, Siriwan P, Rojvachiranonda N, Suphapeetiporn K, Shotelersuk V. Yeetong P, et al. Am J Med Genet A. 2009 Nov;149A(11):2489-92. doi: 10.1002/ajmg.a.33048. Am J Med Genet A. 2009. PMID: 19842205

4

Two novel CTNS mutations in cystinosis patients in Thailand.

Yeetong P, Tongkobpetch S, Kingwatanakul P, Deekajorndech T, Bernardini IM, Suphapeetiporn K, Gahl WA, Shotelersuk V. Yeetong P, et al. Gene. 2012 May 15;499(2):323-5. doi: 10.1016/j.gene.2012.03.047. Epub 2012 Mar 16. Gene. 2012. PMID: 22450360 Free PMC article.

5

A newly identified locus for benign adult familial myoclonic epilepsy on chromosome 3q26.32-3q28.

Yeetong P, Ausavarat S, Bhidayasiri R, Piravej K, Pasutharnchat N, Desudchit T, Chunharas C, Loplumlert J, Limotai C, Suphapeetiporn K, Shotelersuk V. Yeetong P, et al. Eur J Hum Genet. 2013 Feb;21(2):225-8. doi: 10.1038/ejhg.2012.133. Epub 2012 Jun 20. Eur J Hum Genet. 2013. PMID: 22713812 Free PMC article.

6

Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2.

Tammachote R, Kingsuwannapong N, Tongkobpetch S, Srichomthong C, Yeetong P, Kingwatanakul P, Monico CG, Suphapeetiporn K, Shotelersuk V. Tammachote R, et al. Among authors: yeetong p. Am J Med Genet A. 2012 Sep;158A(9):2124-30. doi: 10.1002/ajmg.a.35495. Epub 2012 Jul 20. Am J Med Genet A. 2012. PMID: 22821680

7

Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy.

Puangsricharern V, Yeetong P, Charumalai C, Suphapeetiporn K, Shotelersuk V. Puangsricharern V, et al. Among authors: yeetong p. Br J Ophthalmol. 2014 Oct;98(10):1460-2. doi: 10.1136/bjophthalmol-2014-305584. Epub 2014 Aug 19. Br J Ophthalmol. 2014. PMID: 25138764 No abstract available.

8

A Frameshift Mutation in PEN-2 Causes Familial Comedones Syndrome.

Panmontha W, Rerknimitr P, Yeetong P, Srichomthong C, Suphapeetiporn K, Shotelersuk V. Panmontha W, et al. Among authors: yeetong p. Dermatology. 2015;231(1):77-81. doi: 10.1159/000382122. Epub 2015 May 30. Dermatology. 2015. PMID: 26044244

9

Adaptive immune defects in a patient with leukocyte adhesion deficiency type III with a novel mutation in FERMT3.

Suratannon N, Yeetong P, Srichomthong C, Amarinthnukrowh P, Chatchatee P, Sosothikul D, van Hagen PM, van der Burg M, Wentink M, Driessen GJ, Suphapeetiporn K, Shotelersuk V. Suratannon N, et al. Among authors: yeetong p. Pediatr Allergy Immunol. 2016 Mar;27(2):214-7. doi: 10.1111/pai.12485. Epub 2015 Oct 22. Pediatr Allergy Immunol. 2016. PMID: 26359933 No abstract available.

10

Splicing analysis of CYP11B1 mutation in a family affected with 11β-hydroxylase deficiency: case report.

Charnwichai P, Yeetong P, Suphapeetiporn K, Supornsilchai V, Sahakitrungruang T, Shotelersuk V. Charnwichai P, et al. Among authors: yeetong p. BMC Endocr Disord. 2016 Jun 17;16(1):37. doi: 10.1186/s12902-016-0118-6. BMC Endocr Disord. 2016. PMID: 27316665 Free PMC article.

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