Suphapeetiporn K - Search Results

1

Trinucleotide repeat expansion in the transcription factor 4 (TCF4) gene in Thai patients with Fuchs endothelial corneal dystrophy.

Okumura N, Puangsricharern V, Jindasak R, Koizumi N, Komori Y, Ryousuke H, Nakahara M, Nakano M, Adachi H, Tashiro K, Yoshii K, Chantaren P, Ittiwut R, Shotelersuk V, Suphapeetiporn K. Okumura N, et al. Among authors: suphapeetiporn k. Eye (Lond). 2020 May;34(5):880-885. doi: 10.1038/s41433-019-0595-8. Epub 2019 Sep 25. Eye (Lond). 2020. PMID: 31554942 Free PMC article.

2

PTEN c.511C>T nonsense mutation in a BRRS family disrupts a potential exonic splicing enhancer and causes exon skipping.

Suphapeetiporn K, Kongkam P, Tantivatana J, Sinthuwiwat T, Tongkobpetch S, Shotelersuk V. Suphapeetiporn K, et al. Jpn J Clin Oncol. 2006 Dec;36(12):814-21. doi: 10.1093/jjco/hyl107. Epub 2006 Oct 16. Jpn J Clin Oncol. 2006. PMID: 17043057

3

Expanding the phenotypic spectrum of Caffey disease.

Suphapeetiporn K, Tongkobpetch S, Mahayosnond A, Shotelersuk V. Suphapeetiporn K, et al. Clin Genet. 2007 Mar;71(3):280-4. doi: 10.1111/j.1399-0004.2007.00768.x. Clin Genet. 2007. PMID: 17309652

4

Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.

Leoyklang P, Suphapeetiporn K, Siriwan P, Desudchit T, Chaowanapanja P, Gahl WA, Shotelersuk V. Leoyklang P, et al. Among authors: suphapeetiporn k. Hum Mutat. 2007 Jul;28(7):732-8. doi: 10.1002/humu.20515. Hum Mutat. 2007. PMID: 17377962

5

An exceptionally low percentage of Thai expectant mothers and medical personnel with folic acid knowledge and peri-conceptional consumption urges an urgent education program and/or food fortification.

Vilaiphan P, Suphapeetiporn K, Phupong V, Shotelersuk V. Vilaiphan P, et al. Among authors: suphapeetiporn k. Int J Food Sci Nutr. 2007 Jun;58(4):297-303. doi: 10.1080/09637480701217131. Int J Food Sci Nutr. 2007. PMID: 17566891

6

TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population.

Suphapeetiporn K, Tongkobpetch S, Siriwan P, Shotelersuk V. Suphapeetiporn K, et al. Clin Genet. 2007 Nov;72(5):478-83. doi: 10.1111/j.1399-0004.2007.00891.x. Epub 2007 Sep 14. Clin Genet. 2007. PMID: 17868388

7

Risk factors associated with the occurrence of frontoethmoidal encephalomeningocele.

Suphapeetiporn K, Mahatumarat C, Rojvachiranonda N, Taecholarn C, Siriwan P, Srivuthana S, Shotelersuk V. Suphapeetiporn K, et al. Eur J Paediatr Neurol. 2008 Mar;12(2):102-7. doi: 10.1016/j.ejpn.2007.07.005. Epub 2007 Sep 14. Eur J Paediatr Neurol. 2008. PMID: 17869141

8

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: suphapeetiporn k. 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.

9

Three novel mutations in the PORCN gene underlying focal dermal hypoplasia.

Leoyklang P, Suphapeetiporn K, Wananukul S, Shotelersuk V. Leoyklang P, et al. Among authors: suphapeetiporn k. Clin Genet. 2008 Apr;73(4):373-9. doi: 10.1111/j.1399-0004.2008.00975.x. Epub 2008 Mar 3. Clin Genet. 2008. PMID: 18325042

10

Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.

Tongkobpetch S, Suphapeetiporn K, Siriwan P, Shotelersuk V. Tongkobpetch S, et al. Among authors: suphapeetiporn k. Int J Oral Maxillofac Surg. 2008 Jun;37(6):550-3. doi: 10.1016/j.ijom.2008.01.024. Epub 2008 Mar 19. Int J Oral Maxillofac Surg. 2008. PMID: 18356023

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