Detalhe da pesquisa
1.
Familial clustering of nonalcoholic fatty liver disease in first-degree relatives of adults with lean nonalcoholic fatty liver disease.
Liver Int
; 43(12): 2713-2726, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37804066
2.
How do we translate gaps and unmet needs of blood management for thalassemia into a collaborative implementation framework?
Transfus Med
; 33(6): 497-502, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37775960
3.
Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias.
Clin Chem
; 68(6): 794-802, 2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35262663
4.
Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency Syndrome.
Neuropediatrics
; 53(2): 129-132, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34674205
5.
Association study identifies genetic determinants and non-genetic factors on steady-state plasma and therapeutic outcome of galantamine in mixed dementia.
Eur J Clin Pharmacol
; 78(8): 1249-1259, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35633386
6.
Effect of gene polymorphisms in ADAM33, TGFß1, VEGFA, and PLAUR on asthma in Thai population.
Asian Pac J Allergy Immunol
; 40(1): 39-46, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31586488
7.
Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes: implication to Asian population testing.
Breast Cancer Res Treat
; 188(1): 237-248, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33649982
8.
Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes.
Int Ophthalmol
; 41(1): 121-134, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32869108
9.
Incidence and risk factors of vascular dementia in Thai stroke patients.
J Stroke Cerebrovasc Dis
; 29(8): 104878, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32417242
10.
Skewed X chromosome inactivation in girls and female adolescents with autoimmune thyroid disease.
Clin Endocrinol (Oxf)
; 89(6): 863-869, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30229980
11.
Medical genetic services in a developing country: lesson from Thailand.
Curr Opin Pediatr
; 29(6): 634-639, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28922317
12.
Influence of genetic and non-genetic factors on phenytoin-induced severe cutaneous adverse drug reactions.
Eur J Clin Pharmacol
; 73(7): 855-865, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391407
13.
A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.
Mol Vis
; 22: 342-51, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27122965
14.
Liddle's Syndrome: A Case Report.
J Med Assoc Thai
; 98(10): 1035-40, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26638596
15.
Effects of PCSK1 genetic variants on obesity among Thai children and their family members: in relation to health risk, and biochemical and anthropometric parameters.
Southeast Asian J Trop Med Public Health
; 45(1): 214-25, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24964673
16.
Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in Thailand.
J Neuromuscul Dis
; 11(1): 191-199, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-37927275
17.
Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in Thailand.
NPJ Genom Med
; 9(1): 9, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38355628
18.
Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand.
Clin Chem Lab Med
; 51(8): 1605-14, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23525874
19.
STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.
Cureus
; 15(2): e34495, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36874343
20.
Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel.
Cureus
; 15(5): e39067, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37323311