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Items: 17

1.

Hypokalemic Periodic Paralysis as the First Manifestation of Thyrotropin-Secreting Pituitary Adenoma.

Kaewkrasaesin C, Buranasupkajorn P, Piriyawat P, Sunthornyothin S, Snabboon T.

Case Rep Endocrinol. 2019 Oct 16;2019:5913194. doi: 10.1155/2019/5913194. eCollection 2019.

2.

Antiretroviral-naïve HIV-infected patients had lower bone formation markers than HIV-uninfected adults.

Wattanachanya L, Jantrapakde J, Avihingsanon A, Ramautarsing R, Kerr S, Trachunthong D, Pussadee K, Teeratakulpisarn N, Jadwattanakul T, Chaiwatanarat T, Buranasupkajorn P, Phanuphak N, Sunthornyothin S, Phanuphak P; TNT 003 study team.

AIDS Care. 2019 May 28:1-10. doi: 10.1080/09540121.2019.1622631. [Epub ahead of print]

PMID:
31137948
3.

Loss-of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes.

Jungtrakoon P, Shirakawa J, Buranasupkajorn P, Gupta MK, De Jesus DF, Pezzolesi MG, Panya A, Hastings T, Chanprasert C, Mendonca C, Kulkarni RN, Doria A.

Diabetes. 2019 May;68(5):1084-1093. doi: 10.2337/db17-0821. Epub 2019 Mar 4.

4.

The coexistence of Cushing syndrome and gynecomastia as the manifestations of adrenocortical carcinoma.

Umphonsathien M, Srichomkwun P, Buranasupkajorn P, Snabboon T.

Kaohsiung J Med Sci. 2018 Dec;34(12):705-706. doi: 10.1016/j.kjms.2018.06.004. Epub 2018 Jul 4. No abstract available.

5.

Genetic Tools for Coronary Risk Assessment in Type 2 Diabetes: A Cohort Study From the ACCORD Clinical Trial.

Morieri ML, Gao H, Pigeyre M, Shah HS, Sjaarda J, Mendonca C, Hastings T, Buranasupkajorn P, Motsinger-Reif AA, Rotroff DM, Sigal RJ, Marcovina SM, Kraft P, Buse JB, Wagner MJ, Gerstein HC, Mychaleckyj JC, Parè G, Doria A.

Diabetes Care. 2018 Nov;41(11):2404-2413. doi: 10.2337/dc18-0709. Epub 2018 Sep 27.

6.

Cowden syndrome and pituitary tumours.

Srichomkwun P, Houngngam N, Boonchaya-Anant P, Chutinet A, Buranasupkajorn P, Snabboon T.

QJM. 2018 Oct 1;111(10):735-736. doi: 10.1093/qjmed/hcy133. No abstract available.

PMID:
29931205
7.

Genetic Predictors of Cardiovascular Mortality During Intensive Glycemic Control in Type 2 Diabetes: Findings From the ACCORD Clinical Trial.

Shah HS, Gao H, Morieri ML, Skupien J, Marvel S, Paré G, Mannino GC, Buranasupkajorn P, Mendonca C, Hastings T, Marcovina SM, Sigal RJ, Gerstein HC, Wagner MJ, Motsinger-Reif AA, Buse JB, Kraft P, Mychaleckyj JC, Doria A.

Diabetes Care. 2016 Nov;39(11):1915-1924. Epub 2016 Aug 15.

8.

Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.

Prudente S, Jungtrakoon P, Marucci A, Ludovico O, Buranasupkajorn P, Mazza T, Hastings T, Milano T, Morini E, Mercuri L, Bailetti D, Mendonca C, Alberico F, Basile G, Romani M, Miccinilli E, Pizzuti A, Carella M, Barbetti F, Pascarella S, Marchetti P, Trischitta V, Di Paola R, Doria A.

Am J Hum Genet. 2015 Jul 2;97(1):177-85. doi: 10.1016/j.ajhg.2015.05.011. Epub 2015 Jun 11.

9.

Genetic Variant at the GLUL Locus Predicts All-Cause Mortality in Patients With Type 2 Diabetes.

Prudente S, Shah H, Bailetti D, Pezzolesi M, Buranasupkajorn P, Mercuri L, Mendonca C, De Cosmo S, Niewczas M, Trischitta V, Doria A.

Diabetes. 2015 Jul;64(7):2658-63. doi: 10.2337/db14-1653. Epub 2015 Feb 12.

10.

Joint effect of insulin signaling genes on all-cause mortality.

Menzaghi C, Fontana A, Copetti M, Rizza S, Spoto B, Buranasupkajorn P, Tripepi G, Marucci A, Bailetti D, Hastings T, Testa A, Mendonca C, Mallamaci F, De Cosmo S, Bacci S, Federici M, Doria A, Zoccali C, Trischitta V.

Atherosclerosis. 2014 Dec;237(2):639-44. doi: 10.1016/j.atherosclerosis.2014.10.005. Epub 2014 Oct 24.

11.

Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy.

Snabboon T, Plengpanich W, Houngngam N, Buranasupkajorn P, Plengvidhya N, Sereepapong W, Sunthornyothin S, Shotelersuk V.

Endocrine. 2010 Apr;37(2):261-4. doi: 10.1007/s12020-009-9292-x. Epub 2010 Jan 5.

PMID:
20960261
12.

Multiple lobulated cystic lesions in suprasellar cistern.

Pittayanon R, Buranasupkajorn P, Snabboon T.

Intern Med. 2009;48(24):2151-2. No abstract available.

13.

Bilateral pheochromocytoma during the postpartum period.

Wattanachanya L, Bunworasate U, Plengpanich W, Houngngam N, Buranasupkajorn P, Sunthornyothin S, Shotelersuk V, Snabboon T.

Arch Gynecol Obstet. 2009 Dec;280(6):1055-8. doi: 10.1007/s00404-009-1057-5. Epub 2009 Apr 2.

PMID:
19340440
14.

Erdheim-Chester disease.

Vanichaniramol N, Kingpetch K, Buranasupkajorn P, Sunthornyothin S, Snabboon T.

Intern Med. 2008;47(18):1633-4. Epub 2008 Sep 16. No abstract available.

15.

A novel SPINK1 gene mutation, c.206C>T, in a Thai patient with chronic alcoholic pancreatitis.

Rerknimitr R, Shotelersuk V, Buranasupkajorn P, Plengpanich W, Snabboon T.

JOP. 2008 Jan 8;9(1):33-6.

16.

A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.

Snabboon T, Plengpanich W, Buranasupkajorn P, Khwanjaipanich R, Vasinanukorn P, Suwanwalaikorn S, Khovidhunkit W, Shotelersuk V.

Horm Res. 2008;69(1):60-4. Epub 2007 Dec 4.

PMID:
18059085
17.

Thyrotoxic periodic paralysis induced by pulse methylprednisolone.

Wongraoprasert S, Buranasupkajorn P, Sridama V, Snabboon T.

Intern Med. 2007;46(17):1431-3. Epub 2007 Sep 3.

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