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Items: 1 to 20 of 64

1.

Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease.

Santiwatana S, Mahachoklertwattana P, Limwongse C, Khlairit P, Pongratanakul S, Roothumnong E, Prangphan K, Choubtum L, Songdej D, Poomthavorn P.

Clin Endocrinol (Oxf). 2018 Sep 19. doi: 10.1111/cen.13857. [Epub ahead of print]

PMID:
30229980
2.

Medical genetic services in a developing country: lesson from Thailand.

Limwongse C.

Curr Opin Pediatr. 2017 Dec;29(6):634-639. doi: 10.1097/MOP.0000000000000544. Review.

PMID:
28922317
3.

Role of Urinary Neutrophil Gelatinase-Associated Lipocalin for Predicting the Severity of Renal Functions in Patients With Autosomal-Dominant Polycystic Kidney Disease.

Vareesangthip K, Vareesangthip K, Limwongse C, Reesukumal K.

Transplant Proc. 2017 Jun;49(5):950-954. doi: 10.1016/j.transproceed.2017.03.061.

PMID:
28583565
4.

Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.

Jinda W, Taylor TD, Suzuki Y, Thongnoppakhun W, Limwongse C, Lertrit P, Trinavarat A, Atchaneeyasakul LO.

Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2413-2420. doi: 10.1167/iovs.16-21322.

PMID:
28453600
5.

Influence of genetic and non-genetic factors on phenytoin-induced severe cutaneous adverse drug reactions.

Yampayon K, Sukasem C, Limwongse C, Chinvarun Y, Tempark T, Rerkpattanapipat T, Kijsanayotin P.

Eur J Clin Pharmacol. 2017 Jul;73(7):855-865. doi: 10.1007/s00228-017-2250-2. Epub 2017 Apr 8.

PMID:
28391407
6.

A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.

Jinda W, Poungvarin N, Taylor TD, Suzuki Y, Thongnoppakhun W, Limwongse C, Lertrit P, Suriyaphol P, Atchaneeyasakul LO.

Mol Vis. 2016 Apr 21;22:342-51. eCollection 2016.

7.

Genetic variant screening of MC3R and MC4R genes in early-onset obese children and their relatives among a Thai population: family-based study.

Wannaiampikul S, Phonrat B, Tungtrongchitr A, Limwongse C, Chongviriyaphan N, Santiprabhob J, Tungtrongchitr R.

Genet Mol Res. 2015 Dec 22;14(4):18090-102. doi: 10.4238/2015.December.22.35.

8.

Liddle's Syndrome: A Case Report.

Phoojaroenchanachai M, Buranakitjaroen P, Limwongse C.

J Med Assoc Thai. 2015 Oct;98(10):1035-40.

PMID:
26638596
9.

Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita.

Panichareon B, Seedapan T, Thongnoppakhun W, Limwongse C, Pithukpakorn M, Limjindaporn T.

Case Rep Dermatol. 2015 Aug 12;7(2):212-9. doi: 10.1159/000439042. eCollection 2015 May-Aug.

10.

Association between rs155971 in the PCSK1 gene and the lipid profile of obese Thai children: a family-based study.

Kulanuwat S, Santiprabhob J, Phonrat B, Limwongse C, Tungtrongchitr A, Chongviriyaphan N, Tungtrongchitr R.

Genet Mol Res. 2015 Aug 7;14(3):9136-44. doi: 10.4238/2015.August.7.23.

11.

Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancer.

Korphaisarn K, Pongpaibul A, Limwongse C, Roothumnong E, Klaisuban W, Nimmannit A, Jinawath A, Akewanlop C.

World J Gastroenterol. 2015 Jan 21;21(3):926-34. doi: 10.3748/wjg.v21.i3.926.

12.

Common variations in the FTO gene and obesity in Thais: a family-based study.

Chuenta W, Phonrat B, Tungtrongchitr A, Limwongse C, Chongviriyaphan N, Santiprabhob J, Tungtrongchitr R.

Gene. 2015 Mar 1;558(1):75-81. doi: 10.1016/j.gene.2014.12.050. Epub 2014 Dec 24.

PMID:
25542809
13.

Effects of PCSK1 genetic variants on obesity among Thai children and their family members: in relation to health risk, and biochemical and anthropometric parameters.

Kulanuwat S, Phonrat B, Tungtrongchitr A, Limwongse C, Chongviriyaphan N, Tungtrongchitr R, Santiprabhob J.

Southeast Asian J Trop Med Public Health. 2014 Jan;45(1):214-25.

PMID:
24964673
14.

Genetics and genomics in Thailand: challenges and opportunities.

Shotelersuk V, Limwongse C, Mahasirimongkol S.

Mol Genet Genomic Med. 2014 May;2(3):210-6. doi: 10.1002/mgg3.83. Epub 2014 May 14. No abstract available.

15.

A Novel Mutation of the GNE Gene in Distal Myopathy with Rimmed Vacuoles: A Case with Inflammation.

Tanboon J, Rongsa K, Pithukpakorn M, Boonyapisit K, Limwongse C, Sangruchi T.

Case Rep Neurol. 2014 Mar 8;6(1):55-9. doi: 10.1159/000360730. eCollection 2014 Jan.

16.

Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes.

Jinda W, Taylor TD, Suzuki Y, Thongnoppakhun W, Limwongse C, Lertrit P, Suriyaphol P, Trinavarat A, Atchaneeyasakul LO.

Invest Ophthalmol Vis Sci. 2014 Apr 7;55(4):2259-68. doi: 10.1167/iovs.13-13567.

PMID:
24618324
17.

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand.

Viprakasit V, Limwongse C, Sukpanichnant S, Ruangvutilert P, Kanjanakorn C, Glomglao W, Sirikong M, Utto W, Tanphaichitr VS.

Clin Chem Lab Med. 2013 Aug;51(8):1605-14. doi: 10.1515/cclm-2013-0098.

PMID:
23525874
18.

Small Ancestry Informative Marker panels for complete classification between the original four HapMap populations.

Setsirichok D, Piroonratana T, Assawamakin A, Usavanarong T, Limwongse C, Wongseree W, Aporntewan C, Chaiyaratana N.

Int J Data Min Bioinform. 2012;6(6):651-74.

PMID:
23356013
19.

An omnibus permutation test on ensembles of two-locus analyses can detect pure epistasis and genetic heterogeneity in genome-wide association studies.

Setsirichok D, Tienboon P, Jaroonruang N, Kittichaijaroen S, Wongseree W, Piroonratana T, Usavanarong T, Limwongse C, Aporntewan C, Phadoongsidhi M, Chaiyaratana N.

Springerplus. 2013 May 19;2:230. doi: 10.1186/2193-1801-2-230. eCollection 2013.

20.

Activation of indoleamine 2,3-dioxygenase in patients with scrub typhus and its role in growth restriction of Orientia tsutsugamushi.

Prachason T, Konhan K, Pongnarin P, Chatsiricharoenkul S, Suputtamongkol Y, Limwongse C.

PLoS Negl Trop Dis. 2012;6(7):e1731. doi: 10.1371/journal.pntd.0001731. Epub 2012 Jul 31.

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