Thiti Snabboon

Summary

Affiliation: Chulalongkorn University
Country: Thailand

Publications

  1. ncbi request reprint A novel germline mutation, 1793delG, of the MEN1 gene underlying multiple endocrine neoplasia type 1
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand
    Jpn J Clin Oncol 35:280-2. 2005
  2. ncbi request reprint A germline mutation in a Thai family with familial multiple endocrine neoplasia type 1
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand
    J Med Assoc Thai 88:191-5. 2005
  3. ncbi request reprint A novel SPINK1 gene mutation, c.206C>T, in a Thai patient with chronic alcoholic pancreatitis
    Rungsun Rerknimitr
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University Bangkok, Thailand
    JOP 9:33-6. 2008
  4. ncbi request reprint A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    Horm Res 69:60-4. 2008
  5. doi request reprint Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy
    Thiti Snabboon
    Division of Endocrine and Metabolism, Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Patumwan, Bangkok, 10330, Thailand
    Endocrine 37:261-4. 2010
  6. doi request reprint Bilateral pheochromocytoma during the postpartum period
    Lalita Wattanachanya
    Department of Internal Medicine, Chulalongkorn University, Patumwan, Bangkok, Thailand
    Arch Gynecol Obstet 280:1055-8. 2009
  7. ncbi request reprint Adrenal hemorrhage as the first presentation of hepatocellular carcinoma
    Padiporn Vasinanukorn
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok
    Intern Med 46:1779-82. 2007
  8. ncbi request reprint Normal reference range of serum insulin-like growth factor (IGF)-I in healthy Thai adults
    Wanee Plengpanich
    Division of Endocrine and Metabolism, Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Rama IV Rd, Patumwan, Bangkok 10330, Thailand
    J Med Assoc Thai 91:1681-4. 2008
  9. ncbi request reprint A SPINK1 gene mutation in a Thai patient with fibrocalculous pancreatic diabetes
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    Southeast Asian J Trop Med Public Health 37:559-62. 2006
  10. doi request reprint A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis
    Wallaya Jongjaroenprasert
    Endocrine and Metabolism Unit, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Rama 6 Road, Mahidol University, Bangkok, Thailand
    J Hum Genet 57:301-4. 2012

Collaborators

Detail Information

Publications23

  1. ncbi request reprint A novel germline mutation, 1793delG, of the MEN1 gene underlying multiple endocrine neoplasia type 1
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand
    Jpn J Clin Oncol 35:280-2. 2005
    ..This mutation is predicted to cause a loss of the second nuclear localization signal of the menin protein...
  2. ncbi request reprint A germline mutation in a Thai family with familial multiple endocrine neoplasia type 1
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Patumwan, Bangkok 10330, Thailand
    J Med Assoc Thai 88:191-5. 2005
    ..The newly available genetic test for patients with MEN1 in Thailand makes it possible to accurately DNA-based diagnose clinically suspected individuals and their presymptomatic members, which has important therapeutic impacts on them...
  3. ncbi request reprint A novel SPINK1 gene mutation, c.206C>T, in a Thai patient with chronic alcoholic pancreatitis
    Rungsun Rerknimitr
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University Bangkok, Thailand
    JOP 9:33-6. 2008
    ..In this regard, various genes involving an alcohol-metabolizing pathway or pancreatitis protecting factors have been extensively studied in order to identify genetic predisposition to alcoholic pancreatitis...
  4. ncbi request reprint A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    Horm Res 69:60-4. 2008
    ..Therefore, abnormalities of the POU1F1 gene are known to be responsible for a phenotype causing combined pituitary hormone deficiency (CPHD) involving growth hormone, prolactin and thyrotropin...
  5. doi request reprint Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy
    Thiti Snabboon
    Division of Endocrine and Metabolism, Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Patumwan, Bangkok, 10330, Thailand
    Endocrine 37:261-4. 2010
    ..482G>A in exon 3 of the VHL gene, indicating von Hippel-Lindau syndrome. Physicians who care for hypertensive pregnant patients should be aware of this condition as its diagnosis would probably lead to a better outcome...
  6. doi request reprint Bilateral pheochromocytoma during the postpartum period
    Lalita Wattanachanya
    Department of Internal Medicine, Chulalongkorn University, Patumwan, Bangkok, Thailand
    Arch Gynecol Obstet 280:1055-8. 2009
    ..Most cases of pheochromocytoma are sporadic but they can be part of hereditary autosomal dominant syndromes...
  7. ncbi request reprint Adrenal hemorrhage as the first presentation of hepatocellular carcinoma
    Padiporn Vasinanukorn
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok
    Intern Med 46:1779-82. 2007
    ..Spontaneous massive AH due to metastatic HCC is unusual. Considering the high incidence of HCC in Asia, clinicians should be aware of this atypical and fatal presentation...
  8. ncbi request reprint Normal reference range of serum insulin-like growth factor (IGF)-I in healthy Thai adults
    Wanee Plengpanich
    Division of Endocrine and Metabolism, Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Rama IV Rd, Patumwan, Bangkok 10330, Thailand
    J Med Assoc Thai 91:1681-4. 2008
    ..The diagnosis value of IGF-I is dependent on the establishment of an accurate reference ranges, which can be affected by parameters such as age, gender, ethnicity, medications, chronic illness, or assay methodologies...
  9. ncbi request reprint A SPINK1 gene mutation in a Thai patient with fibrocalculous pancreatic diabetes
    Thiti Snabboon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    Southeast Asian J Trop Med Public Health 37:559-62. 2006
    ..We describe a heterozygous mutation, IVS3+2 T>C, of SPINK1 gene in a young Thai female patient with typical presentation of FCPD. To our knowledge, this is the first report of the SPINK1 gene mutation in a FCPD patient in Southeast Asia...
  10. doi request reprint A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis
    Wallaya Jongjaroenprasert
    Endocrine and Metabolism Unit, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Rama 6 Road, Mahidol University, Bangkok, Thailand
    J Hum Genet 57:301-4. 2012
    ..44 × 10(-5), OR=5.13; 95% CI=1.87-14.1; combined-analysis P=3.71 × 10(-12), OR=5.47; 95% CI=3.04-9.83)...
  11. ncbi request reprint An extra-adrenal pheochromocytoma of the organ of Zuckerkandl: report of a case
    Supparerk Prichayudh
    Department of Surgery, Chutalongkorn University, Bangkok, Thailand
    J Med Assoc Thai 92:1532-7. 2009
    ..The patient remains normotensive and symptom free at 15-month follow-up. The authors also discuss the diagnostic modalities and surgical technique used in the presented patient...
  12. ncbi request reprint Bilateral pheochromocytoma during pregnancy
    Vorapong Phupong
    Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University, Pathumwan, Bangkok 10330, Thailand
    Arch Gynecol Obstet 271:276-9. 2005
    ..Pheochromocytoma is a rare disease of the chromaffin cells that secrete catecholamines. It may occur during pregnancy. Bilateral pheochromocytoma in pregnancy is even rarer...
  13. ncbi request reprint Functioning adrenocortical carcinoma with superior vena cava and upper airway obstructions
    Sathapakorn Siriwong
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    J Med Assoc Thai 89:1511-5. 2006
    ..Adrenocortical carcinoma (ACC) is one of the most aggressive endocrine malignancies with a dismal prognosis. Typically, the tumor is large and has regional invasion or distant metastasis at initial presentation...
  14. ncbi request reprint Adrenal crisis due to bilateral adrenal hemorrhage in primary antiphospholipid syndrome
    Usanee Ringkananon
    Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    J Med Assoc Thai 88:534-7. 2005
    ..The antiphospholipid syndrome should be suspected in a patient presenting with adrenal crisis without a distinct etiology...
  15. doi request reprint Identification of mutations in the SRD5A2 gene in Thai patients with male pseudohermaphroditism
    Taninee Sahakitrungruang
    Department of Pediatrics, Division of Pediatric Endocrinology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    Fertil Steril 90:2015.e11-5. 2008
    ..To describe two unrelated Thai patients with suspected 5alpha-reductase type 2 deficiency and perform mutation analysis of the SRD5A2 gene...
  16. pmc PTPRF is disrupted in a patient with syndromic amastia
    Surasawadee Ausavarat
    Interdepartment of Biomedical Sciences, Faculty of Graduate School, Chulalongkorn University, Bangkok 10330, Thailand
    BMC Med Genet 12:46. 2011
    ..1;q13.13). In addition to characterization of her clinical and cytogenetic features, we successfully identified the interrupted gene and studied its consequences...
  17. ncbi request reprint Asymptomatic bilateral giant adrenal myelolipomas: case report and review of literature
    Waraporn Polamaung
    Department of Internal Medicine, Chulalongkorn University, Bangkok, Thailand
    Endocr Pract 13:667-71. 2007
    ..To describe an unusual case of bilateral giant adrenal masses caused by a primary adrenal myelolipoma...
  18. ncbi request reprint Thyrotoxic periodic paralysis induced by pulse methylprednisolone
    Somporn Wongraoprasert
    Division of Endocrine and Metabolism, Department of Internal Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    Intern Med 46:1431-3. 2007
    ..We suggest that acute paralysis after the use of steroids should raise a suspicion of thyrotoxic periodic paralysis (TPP). The potential mechanisms of steroid-induced TPP are discussed...
  19. doi request reprint Association between genetic polymorphisms and sites of cervicocerebral artery atherosclerosis
    Aurauma Chutinet
    Division of Neurology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand
    J Stroke Cerebrovasc Dis 21:379-85. 2012
    ..The low prevalence of extracranial carotid stenosis in this population might result from low frequencies of the APOE ε4 allele...
  20. ncbi request reprint No association between an interleukin 4 gene promoter (-589) polymorphism and Graves' disease in Thai patients
    Jeerawat Nakkuntod
    Immunology Unit, Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Rama IV Rd, Bangkok 10330, Thailand
    J Med Assoc Thai 87:S123-8. 2004
    ..The -589T allele frequencies were similar between patients and control subjects (69% vs 69.3%) suggesting that this polymorphism can not be used as a genetic marker for GD susceptibility in Thais...
  21. ncbi request reprint A more appropriate algorithm of thyroid function test in diagnosis of hyperthyroidism for Thai patients
    Thiti Snabboon
    Department of Medicine, Faculty of Medicine, Chulalongkorn University, Rama IV Road, Patumwan, Bangkok 10330, Thailand
    J Med Assoc Thai 87:S19-21. 2004
    ..Thyroid function test is an essential tool in the diagnosis of thyroid dysfunction. To date, it is still controversial which diagnostic algorithm is best applicable to clinically hyperthyroidism patients...
  22. ncbi request reprint Association of TNF-alpha, TNF-beta, IFN-gamma and IL-1Ra gene polymorphisms with Graves' disease in the Thai population
    Jeerawat Nakkuntod
    Interdepartment of Medical Microbiology, Graduate School Chulalongkorn University, Bangkok, Thailand
    Asian Pac J Allergy Immunol 24:207-11. 2006
    ..01, OR = 2, 95% CI = 1.16 to 3.44). This polymorphism may be involved in the susceptibility to GD in part through its higher promoter activity of TNF-alpha production...
  23. ncbi request reprint Monogene and polygene therapy for the treatment of experimental prostate cancers by use of apoptotic genes bax and bad driven by the prostate-specific promoter ARR(2)PB
    Ye Zhang
    Department of Medicine, Baylor College of Medicine and Veterans Affairs Medical Center, 2002 Holcombe Boulevard, Houston, TX 77030, USA
    Hum Gene Ther 13:2051-64. 2002
    ..The data suggest that polygene therapy with apoptotic molecules is more effective in experimental models of androgen-dependent or -independent prostate cancer than monogene therapy...