| Partial Defect in the Cholesterol Side-Chain Cleavage Enzyme P450scc (CYP11A1) Resembling Nonclassic Congenital Lipoid Adrenal Hyperplasia T Sahakitrungruang, MK Tee, PR Blackett, WL Miller The Journal of Clinical Endocrinology & Metabolism 96 (3), 792-798, 2011 | 110 | 2011 |
| Clinical, genetic, and functional characterization of four patients carrying partial loss-of-function mutations in the steroidogenic acute regulatory protein (StAR) T Sahakitrungruang, RE Soccio, M Lang-Muritano, JM Walker, ... The Journal of Clinical Endocrinology & Metabolism 95 (7), 3352-3359, 2010 | 89 | 2010 |
| Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients T Sahakitrungruang, N Huang, MK Tee, V Agrawal, WE Russell, P Crock, ... The Journal of Clinical Endocrinology & Metabolism 94 (12), 4992-5000, 2009 | 88 | 2009 |
| Germline and Somatic DICER1 Mutations in a Pituitary Blastoma Causing Infantile-Onset Cushing's Disease T Sahakitrungruang, C Srichomthong, S Pornkunwilai, J Amornfa, ... The Journal of Clinical Endocrinology & Metabolism 99 (8), E1487-E1492, 2014 | 79 | 2014 |
| Obesity, metabolic syndrome, and insulin dynamics in children after craniopharyngioma surgery T Sahakitrungruang, T Klomchan, V Supornsilchai, S Wacharasindhu European journal of pediatrics 170, 763-769, 2011 | 42 | 2011 |
| Clinical and molecular review of atypical congenital adrenal hyperplasia T Sahakitrungruang Annals of pediatric endocrinology & metabolism 20 (1), 1-7, 2015 | 41 | 2015 |
| Identification of mutations in the SRD5A2 gene in Thai patients with male pseudohermaphroditism T Sahakitrungruang, S Wacharasindhu, P Yeetong, T Snabboon, ... Fertility and sterility 90 (5), 2015. e11-2015. e15, 2008 | 40 | 2008 |
| Cardio-metabolic risk factors in youth with classical 21-hydroxylase deficiency K Ariyawatkul, S Tepmongkol, S Aroonparkmongkol, T Sahakitrungruang European journal of pediatrics 176, 537-545, 2017 | 34 | 2017 |
| Expanding clinical spectrum of non‐autoimmune hyperthyroidism due to an activating germline mutation, p. M453T, in the thyrotropin receptor gene V Supornsilchai, T Sahakitrungruang, N Wongjitrat, S Wacharasindhu, ... Clinical endocrinology 70 (4), 623-628, 2009 | 31 | 2009 |
| A novel homozygous Q334X mutation in the HSD3B2 gene causing classic 3β-hydroxysteroid dehydrogenase deficiency: an unexpected diagnosis after a positive newborn screen for 21 … DD Jeandron, T Sahakitrungruang Hormone research in paediatrics 77 (5), 334-338, 2012 | 27 | 2012 |
| DKA with severe hypertriglyceridemia and cerebral edema in an adolescent boy: a case study and review of the literature T Saengkaew, T Sahakitrungruang, S Wacharasindhu, V Supornsilchai Case Reports in Endocrinology 2016 (1), 7515721, 2016 | 25 | 2016 |
| Novel CYP11B2 mutation causing aldosterone synthase (P450c11AS) deficiency T Klomchan, V Supornsilchai, S Wacharasindhu, V Shotelersuk, ... European journal of pediatrics 171, 1559-1562, 2012 | 23 | 2012 |
| Novel mutations of the SRD5A2 and AR genes in Thai patients with 46, XY disorders of sex development C Ittiwut, J Pratuangdejkul, V Supornsilchai, S Muensri, Y Hiranras, ... Journal of Pediatric Endocrinology and Metabolism 30 (1), 19-26, 2017 | 21 | 2017 |
| The prevalence of nonalcoholic fatty liver disease and its risk factors in children and young adults with type 1 diabetes mellitus J Sae-Wong, B Chaopathomkul, T Phewplung, N Chaijitraruch, ... The Journal of Pediatrics 230, 32-37. e1, 2021 | 20 | 2021 |
| Novel P450c17 mutation H373D causing combined 17α-hydroxylase/17, 20-lyase deficiency T Sahakitrungruang, MK Tee, PW Speiser, WL Miller The Journal of Clinical Endocrinology & Metabolism 94 (8), 3089-3092, 2009 | 20 | 2009 |
| Type 1 diabetes management and outcomes: a multicenter study in Thailand P Dejkhamron, J Santiprabhob, S Likitmaskul, C Deerochanawong, ... Journal of Diabetes Investigation 12 (4), 516-526, 2021 | 17 | 2021 |
| Factors associated with glycemic control in children and adolescents with type 1 diabetes mellitus at a tertiary-care center in Thailand: a retrospective observational study T Dumrisilp, V Supornsilchai, S Wacharasindhu, S Aroonparkmongkol, ... Asian Biomed 11 (6), 443-450, 2017 | 17 | 2017 |
| Identification and Functional Analysis of Six DAX1 Mutations in Patients With X-Linked Adrenal Hypoplasia Congenita C Suthiworachai, R Tammachote, C Srichomthong, R Ittiwut, ... Journal of the Endocrine Society 3 (1), 171-180, 2019 | 16 | 2019 |
| Functional characterization of vasopressin receptor 2 mutations causing partial and complete congenital nephrogenic diabetes insipidus in Thai families T Sahakitrungruang, MK Tee, N Rattanachartnarong, V Shotelersuk, ... Hormone research in paediatrics 73 (5), 349-354, 2010 | 16 | 2010 |
| Implementation of diabetes care and educational program via telemedicine in patients with COVID‐19 in home isolation in Thailand: A real‐world experience T Harindhanavudhi, C Areevut, T Sahakitrungruang, T Tharavanij, ... Journal of Diabetes Investigation 13 (8), 1448-1457, 2022 | 12 | 2022 |
