Shotelersuk V - Search Results

1

Novel Variants and Phenotypes in NEUROG3-Associated Syndrome.

Wejaphikul K, Srilanchakon K, Kamolvisit W, Jantasuwan S, Santawong K, Tongkobpetch S, Theerapanon T, Damrongmanee A, Hongsawong N, Ukarapol N, Dejkhamron P, Supornsilchai V, Porntaveetus T, Shotelersuk V. Wejaphikul K, et al. Among authors: shotelersuk v. J Clin Endocrinol Metab. 2022 Dec 17;108(1):52-58. doi: 10.1210/clinem/dgac554. J Clin Endocrinol Metab. 2022. PMID: 36149814

2

FGFR2 mutations among Thai children with Crouzon and Apert syndromes.

Shotelersuk V, Mahatumarat C, Ittiwut C, Rojvachiranonda N, Srivuthana S, Wacharasindhu S, Tongkobpetch S. Shotelersuk V, et al. J Craniofac Surg. 2003 Jan;14(1):101-4; discussion 105-7. doi: 10.1097/00001665-200301000-00019. J Craniofac Surg. 2003. PMID: 12544231

3

ASA E382K disrupts a potential exonic splicing enhancer and causes exon skipping, but missense mutations in ASA are not associated with ESEs.

Shotelersuk V, Desudchit T, Tongkobpetch S. Shotelersuk V, et al. Int J Mol Med. 2004 Oct;14(4):683-9. Int J Mol Med. 2004. PMID: 15375602

4

MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population.

Tongkobpetch S, Siriwan P, Shotelersuk V. Tongkobpetch S, et al. Among authors: shotelersuk v. J Hum Genet. 2006;51(8):671. doi: 10.1007/s10038-006-0006-4. Epub 2006 Jul 26. J Hum Genet. 2006. PMID: 16868654

5

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. Among authors: shotelersuk v. 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

6

Nonsense mutations of the CYBB gene in two Thai families with X-linked chronic granulomatous disease.

Vilaiphan P, Chatchatee P, Ngamphaiboon J, Tongkobpetch S, Suphapeetiporn K, Shotelersuk V. Vilaiphan P, et al. Among authors: shotelersuk v. Asian Pac J Allergy Immunol. 2007 Dec;25(4):243-7. Asian Pac J Allergy Immunol. 2007. PMID: 18402298 Free article.

7

Expression of mammaglobins A and B in nasal polyps is similar in patients with and without allergic rhinitis.

Chusakul S, Phannaso C, Tongkobpetch S, Aeumjaturapat S, Poovorawan Y, Suphapeetiporn K, Shotelersuk V. Chusakul S, et al. Among authors: shotelersuk v. Am J Rhinol. 2008 Mar-Apr;22(2):135-8. doi: 10.2500/ajr.2008.22.3138. Am J Rhinol. 2008. PMID: 18416968

8

Identification of two novel aquaporin-2 mutations in a Thai girl with congenital nephrogenic diabetes insipidus.

Sahakitrungruang T, Wacharasindhu S, Sinthuwiwat T, Supornsilchai V, Suphapeetiporn K, Shotelersuk V. Sahakitrungruang T, et al. Among authors: shotelersuk v. Endocrine. 2008 Apr;33(2):210-4. doi: 10.1007/s12020-008-9074-x. Epub 2008 May 13. Endocrine. 2008. PMID: 18473191

9

Two novel EBP mutations in Conradi-Hünermann-Happle syndrome.

Ausavarat S, Tanpaiboon P, Tongkobpetch S, Suphapeetiporn K, Shotelersuk V. Ausavarat S, et al. Among authors: shotelersuk v. Eur J Dermatol. 2008 Jul-Aug;18(4):391-3. doi: 10.1684/ejd.2008.0433. Epub 2008 Jun 23. Eur J Dermatol. 2008. PMID: 18573709

10

Carbamazepine and phenytoin induced Stevens-Johnson syndrome is associated with HLA-B*1502 allele in Thai population.

Locharernkul C, Loplumlert J, Limotai C, Korkij W, Desudchit T, Tongkobpetch S, Kangwanshiratada O, Hirankarn N, Suphapeetiporn K, Shotelersuk V. Locharernkul C, et al. Among authors: shotelersuk v. Epilepsia. 2008 Dec;49(12):2087-91. doi: 10.1111/j.1528-1167.2008.01719.x. Epub 2008 Jul 14. Epilepsia. 2008. PMID: 18637831 Free article.

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