Publications
Peer reviewed articles
1. Nimkarn S , Cerame BI, Wei JQ, Dumic M, Zunec R, Brkljacic L, Skrabic V, New MI, Wilson RC. Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations. J Clin Endocrinol Metab.Jan;84(1):378-81,1999.
2. Cerame BI, Newfield R, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC. Prenatal diagnosis and treatment of 11-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia. J Clin Endocrinol Metab. Sep;84(9):3129-34, 1999.
3. New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield R, Vandermeulen J, Barron N, Russo DL, Loriaux L, O’malley B. Partial resistance to several steroids in two sisters. J Clin Endocrinol Metab. Dec;84(12):4454-64, 1999
4. New MI, Obeid J, Wilson RC, Cabrera MS, Goseco A, Macapacal MC, Marshall I, Nimkarn S, Quintos JB, Ten S, Ugrasbul F, Vandermolen, Harbison MD. Profile of The Pediatric Endocrine Clinic at New York-Presbyterian Hospital, New York Weill Cornell Center. J Clin Endocrinol Metab. 1999 Dec;84(12):4444-9, 1999
5. New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield R, Vandermeulen J, Barron N, Russo DL, Loriaux L, O’malley B. Partial resistance to multiple steroids in two sisters. J Steroid Biochem Mol Biol. Jan-Mar;76(1-5):161-6, 2002
6. Sawathiparnich P, Likitmaskul S, Angsusingha K, Nimkarn S, Chaichanwatanakul K, Laohapansang M, Tuchinda C. Persistent Hyperinsulinemic Hypoglycemia of infancy (PHHI): Experience at the Department of Pediatrics, Siriraj Hospital. J Med Assoc Thai. Aug;85 Suppl 2:S506-12, 2002
7. Nimkarn S, Likitmaskul S, ,Sangacharoenkit P, Pathomvanich A, Sawathiparnich P,Wacharasindhu S, Punnakanta L,Angsusingha K , Tuchinda C. Ambiguous genitalia: An Overview of 22 Years Experience and the Diagnostic Approach in the Pediatric Department, Siriraj Hospital. J Med Assoc Thai. Aug;85 Suppl 2:S496-505, 2002
8. Likitmaskul S, Wekawanich J, Wongran R, Chaichanwatanakul K, Kiattisakthavee, Nimkarn S, Prayongklin S, Weerakulwattana, Markmaitree, Ritjarean Y, Pookpun, Punnakanta L, Angsusingha K, Tuchinda C. Intensive Diabetes Education Program and Multidisciplinary Team Approach in Management of Newly Diagnosed Type 1 Diabetes Mellitus: A Greater Patient Benefit, Experience at Siriraj Hospital. J Med Assoc Thai. Aug;85 Suppl 2:S488-95, 2002.
9. Nimkarn S, Su KL, Berglind N, Wilson RC., New MI. Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia J Clin Endocrinol Metab Jan;92(1):137-42, 2007
10. Wilson RC, Nimkarn S, Dumic M, Obeid J, Azar M, Najmabadi H, Saffari F, New MI. Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency, Mol Genet Metab. 2007 Apr; 90(4):414-21. Epub 2007 Feb 1, 2007
11. Karnsakul W, Sawathiparnich P, Nimkarn S, Likitmaskul S, Santiprabhob J, Aanpreung P. Anterior pituitary hormone effects on hepatic functions in infants with congenital hypopituitarism. Ann Hepatol. Apr-Jun;6(2):97-103, 2007
12. Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Nat Clin Pract Endocrinol Metab. 2007 May;3(5):405-13.
13. Trinh L, Nimkarn S, New MI, Lin-Su KGrowth and Pubertal Characteristics in Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. J Pediatr Endocrinol Metab. 2007 Aug;20(8):883-91
14. Dumic M, Lin-Su K, Leibel N, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, and New MI. Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development. J Clin Endo Metab 93 (1): 182-189, 2008.
15. Dumic M, Lin-Su K, Leibel NI, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, New MI. Report of fertility in woman with predominantly 46,XY karyotype in family with multiple disorders of sexual development: Review of Prismatic Case. Mt Sinai J Med. 2008 Mar;75(2):168-9.
16. Osuwannaratana P, Nimkarn S, Santiprabhob J, Likitmaskul S, Sawathiparnich P. The etiologies of adrenal insufficiency in 73 Thai children: 20 years experience. J Med Assoc Thai. 2008 Oct;91(10):1544-50.
Case Reports
17. Pitukcheewanont P, Nimkarn S, Austin J, Sack Z, Fisher LK. Salt-wasting 21-hydroxylase deficiency congenital adrenal hyperplasia and pyloric stenosis in two Hispanic brothers. J Pediatr. Aug;149(2):268-70, 2006
Invited Contributions
18. Wilson RC, Nimkarn S, New MI. Apparent Mineralocorticoid Excess Syndrome. Trends Endocrinol Metab. Apr;12(3):104-11, 2001. Review
19. Nimkarn S. Apparent Mineralocorticoid Excess. Siriraj Hosp Gazette 53(9):682-693, 2001
20. Nimkarn S. Premature puberty, an unignorable problem. Kao Tan Roke: The Praram 9 hospital journal, Aug; 28:4-6, 2001
21. Nimkarn S. Short stature. Ramkunhaeng hospital journal, Jan-Jul 20: 14-18, 2002
22. Nimkarn S. Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21 hydroxylase deficiency. Journal of Paediatrics,Obstetrics & Gynaecology, May/Jun; 31(3): 91-6, 2005
23. Nimkarn S, New MI Prenatal diagnosis and treatment of congenital adrenal hyperplasia, Pediatr Endocrinol Rev. Dec;4(2):99-105, 2006
24. Newfield RS, Nimkarn S, New MI Final height in congenital adrenal hyperplasia due to 21-hydorxylase deficiency: is it all hormonal? Electronic Letter to J Clin Endo Metab2006; 91: 3821-3825 published online Dec 19, 2006
25. Nimkarn S, New MI Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia, Horm Res 67:53-60, 2007
26. Nimkarn S, New MI Reviewer critique of "Apparent mineralocorticoid excess manifested in an elderly patient with hypothyroidism", Am J Hypertens. Jan;20(1):108, 2007
27. Nimkarn S, New MI. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia. Trends Endocrinol Metab. 2008 Apr;19(3):96-9. Epub 2008 Feb 21.
28. Lin-Su K, Nimkarn S, and New MI. Congenital adrenal hyperplasia in adolescents: diagnosis and management. Ann N Y Acad Sci. 2008 Jun;1135:95-8.
29. Lin-Su K, Nimkarn S, and New MI. “Treatment and Management of Congenital Adrenal Hyperplasia in Adults.” Expert Review of Endocrinology and Metabolism. Future Drugs (In Press, online doi:10.106/j.mce.2008.11.027)
30. Nimkarn S, New MI. “Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia” Proceedings of Adrenal 2008. Mol Cell Endocrinol. (In Press, Dec 3. [Epub ahead of print])
Books and Chapters in Books
31. Nimkarn S. “Insulin Therapy: pediatric aspects” in Practical Diabetes Mellitus, Siriraj, Bangkok, Thailand: 96-103, 2002
32. Nimkarn S. "Management of Congenital Adrenal Hyperplasia” in Guideline Management & Case Illustration in Pediatric Endocrinology. Wacharasindhu S, Jaruratsirikul S, Likitmaskul S. Bangkok, Text and Journal Publication: 124-144, 2002
33. Nimkarn S. “Chronic corticosteroid therapy: endocrine complications” in Challenging issues in adolescent endocrinology. Panamonta O, Jarurattanasirikul S , Santipraphob J. Bangkok, Reunkaew Karnpim: 183-195, 2004
34. Nimkarn S. “Persistent hyperinsulinemic hypoglycemia” in Metabolic genetic disorders in children, Wasant P. Bangkok, Bangkok Publication; vol 1: 123-139, 2003
35. Nimkarn S, New MI. “Congenital Adrenal Hyperplasia.” In: RE Weiss, S Refetoff (eds), Genetic Diagnosis of Endocrine Disease, 1st Edition. San Diego: Elsevier. (in Press)
36. Lin-Su K, Nimkarn S, New MI. “Diagnosis and Management of Congenital Adrenal Hyperplasia” in Pediatric, Adolescent, and Young Adult Gynecology Textbook, Altchek & Deligdisch, Wiley-Blackwell, Oxford: 25-35 (in press)
Media Resource Educational Material
37. Nimkarn S, New M, (updated November 2008) 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia in: GeneReviewsat GeneTests: Medical Genetics Information Resource [database online]. Copyright, University of Washington, Seattle. 1997-2006. Available at http://www.genetests.org.
38. Nimkarn S, Lin-Su K, Kaltman J, and New MI. “Congenital Adrenal Hyperplasia.” British Medical Journal. (In Press)
39. Nimkarn S, New MI “Chapter 8 Adrenal Disorder in website WWW.ENDOTEXT.ORG” version of May 20, 2008: New MI, section, published by MDTEXT.COM,INC, S.DARTMOUTH,MA. Available at http://endotext.org/pediatrics/pediatrics8/pediatricsframe8.htm
Abstracts (Optional, not encouraged)
1. Cerame BI, Nimkarn S, Roe TF, New MI, Wilson RC “A Single Basepair Deletion of CYP11B1 Gene Causing Classic 11-Hydroxylase Deficiency Congenital Adrenal Hyperplasia” The 80th Annual Meeting of The Endocrine Society, New Orleans, June 24-27, Abstract No. P1-272, p. 177, 1998.
2. New MI, Vandermeulen J, zzzzzNimkarn S, Cunningham-Rundles S, Wilson RC, Newfield RS “Global Steroid Resistance with Hypertension.” The 80th Annual Meeting of The Endocrine Society, New Orleans, June 24-27, Abstract No. O19-4, p. 78, 1998.
3. New MI, Vandermeulen J, Nimkarn S, Cunningham-Rundles S, Wilson RC, Newfield RS “Global Steroid Resistance with Hypertension.” The Association for Patient-Oriented Research, Atlantic City, April 30-May 2, 1999.
4. Nimkarn S, Lane JM, Harbison MD, “Bisphosphonate Therapy for Debilitating Idiopathic Juvenile Osteoporosis.” National Coopertive Growth Study Meeting, Charleston, South Carolina, Sep 30- Oct 3, 1999
5. Quintos JB, Nimkarn S, Ugrasbul F, Harbison MD.2000“Persistence of Vitamin D Deficiency Rickets in The 1990’s: Risk Factors and Clinical Characteristics” The 2000 PAS/AAP Joint Annual Meeting ,Boston, May 12-16, Pediatric Research 47 (4), suppl, p 138A, 2000
6. Nimkarn S, Quintos JB, Novogroder M, Gertner JM, Harbison MD 2000“Albright Hereditary Osteodystrophy Associated with Male Pseudohermaphroditism” The 2000 PAS/AAP Joint Annual Meeting, Boston, May 12-16, Pediatric Research 47 (4), suppl, p 136A, 2000
7. Nimkarn S, Lane JM, Harbison MD 2000 “Bisphosphonate Therapy for Debilitating Idiopathic Juvenile Osteoporosis.” The 2000 PAS/AAP Joint Annual Meeting in Boston, May 12-16, Pediatric Research 47 (4), suppl, p 136A, 2000
8. Nimkarn S, Wei JQ., Likitmaskul S., Chaichanwatanakul K, Kiattisakthavee P, Song D, New MI, Wilson RC, “Molecular Genotyping of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia in Thailand”, Endo 2000 The Endocrine Society 82nd Annual Meeting, Toronto, June 21-24 Abstract No. 531, p.516,2000 .
9. Nimkarn S, Bradlow L, Quintos JBQ, Pryor ND, Shackelton CHL., New MI, Wilson RC, “A New Case of Mild Apperent Mineralocorticoid Excess Syndrome”, Endo 2000 The Endocrine Society 82nd Annual Meeting, Toronto, June 21-24 Abstract No. 541, p.518, 2000.
10. Pitukcheewanont P, Nimkarn S, Fisher LK, Silverstein A, New MI, “Salt Wasting 21-Hydroxylase Deficiency Congential Adrenal Hyperplasia and Congential Pyrolic Stenosis in two Hispanic brothers”, 11th International Congress of Endocrinology (ICE 2000), Sydney, Australia, October 29-November2, Abstract No. P943, p.330, 2000
11. Nimkarn S, Wei JQ, Likitmaskul S, Chaichanwatanakul K, Kiattisakthavee P, Song D, New MI, Wilson RC, “Molecular Genotyping of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia in Thailand”, 52th Thai Congress of Pediatrics, Trang, Thailand, April 25-27, Abstract No.C-7, p.68, 2001
13. Marshall I, Nimkarn S, Wei JQ, Guazzarotti L, New MI, Wilson RC: “Detection of Mutation in the 21-hydroxylase gene”, Endo 2001 The Endocrine Society 83th Annual Meeting, Denver, June 20-23, Abstract No. P2-7, 2001
14. Nimkarn S “Management of Diabetes Mellitus on the sick days” Diabetes Mellitus From up to date knowledge to a better clinical practice, Bangkok, Thailand, Oct 17-19, p 127-131, 2001.
15. Nimkarn S, Likitmaskul S, Wei JQ, Chaichanwatanakul K, Kiattisakthavee P, New MI, Wilson RC “Genotypic analysis of 21 hydroxylase deficiency congenital adrenal hyperplasia in Thai patients”, The Endocrine Society of Thailand 13th Annual Meeting, Bangkok, Thailand, November 1-2, free paper III, p.33, 2001
16. Nimkarn S, “Congenital Adrenal Hyperplasia; A New Perspective of the Disease you know”,The 42th Siriraj Scientific Congress, Bangkok, Thailand, March 4-8, Abstract No L12, p.70-71, 2002
17. Sawathiparnich P, Likitmaskul S, Angsusingha K, Nimkarn S, Chaichanwatanakul K, Laohapansang M, Tuchinda C “Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI): Experience at the Department of Pediatrics, Siriraj Hospital”, 54th Thai Congress of Pediatrics, Cha-am, Thailand, April 24-26, Abstract No C-02, p 57, 2002
18. Keamseng C, Likitmaskul S, Kiattisakthavee P, Weerakulwatana L, Nimkarn S, Sawathiparnich P, Tuchinda C “Metabolic Disturbance in Obese Children in Siriraj Hospital”, 54th Thai Congress of Pediatrics, Cha-am, Thailand, April, 24-26, Abstract No C-03, p.58-9, 2002
19. Komtornrut C, Kittisangwara L, Yaiquawong M, Mahamaytakit N, Sundaraketu K, Nimkarn S “Growth Pattern of Turner Syndrome Patients at Siriraj Hospital” 54th Thai Congress of Pediatrics, Cha-am, Thailand, April 24-26, Abstract No C-04, p.60-1, 2002
20. Nimkarn S, Sawathiparnich P, Likitmaskul S “Cleft Palate in Combination with Salt-Wasting Congenital Adrenal Hyperplasia in Two Patients. More than a Co-incidence?”, 54th Thai Congress of Pediatrics, Cha-am, Thailand, April, 24-26, Abstract No C-08, p 66-7, 2002
21. Nimkarn S, Wei JQ, Likitmaskul S, Chaichanwatanakul K, Kiattisakthavee P, New MI, Wilson RC “Genotypic analysis of 21 hydroxylase deficiency congenital adrenal hyperplasia in Thai patients” The Ramathibodi Annual Scientific Meeting, Bangkok, Thailand, May 1-3, Abstract No 72, Ramathibodi Medical Journal 25, suppl, p 105, 2002
22. Macapagal MC, Slowinska BS, Nimkarn S, De BP, Licholai T, Marshall I, Hackett N, Crystal RG, New MI, Wilson RC “Gene Therapy of 21-hydroxylase Deficient Mice Utilizing an Adeno-associated Virus Vector” Endo 2002 The Endocrine Society 84th Annual Meeting, San Francisco, June 19-22, Abstract No P1-503, p 270, 2002
24. Nimkarn S, Weerakulwattana L, Wei JQ, Wilson RC, Kiattisakthavee P, Likitmaskul S, Chaichanwatanakul K Kumpornsin K, Limwongse C “Genotypic Analysis of 21 hydroxylase Deficiency Congenital Adrenal Hyperplasia in Thai patients, and the Genotype/ Phenotype Correlation” The 4th HUGO Pacific Meeting& 5th Asia Pacific Conference on Human Genetics, October 27-30, Pattaya, Thailand, Abstract No SG-20, 2002
25. Keamseng C, Likitmaskul S, Kiattisakthavee P, Weerakulwatana L, Nimkarn S, Sawathiparnich P, Tuchinda C “Risk of metabolic disturbance and diabetes development in Thai Obese Children”, The Endocrine Society of Thailand 14th Annual Meeting, Bangkok, Thailand, November 7-8, free paper I, p.23, 2002
26. Nimkarn S, Weerakulwattana L, Panamonta O, Sriwijitkamol A, Chaichanwatanakul K, Kiattisakthavee P, Likitmaskul S, Kumpornsin K, Wei JQ, Licholai T, Wilson RC, Limwongse C “Study of Congenital Adrenal Hyperplasia, a Steroid Disorder of Various Etiologies among Thai Patients”, The Endocrine Society of Thailand 14th Annual Meeting, Bangkok, Thailand, November 7-8, free paper III, p.34, 2002
27. Ukarapong S, Weerakulwattana L, Kiattisakthavee P, Nimkarn S “Efficacy of Determining Mid-parental Target Height by Paretnal Perception or by Standardized Measurement”, The Endocrine Society of Thailand 14th Annual Meeting, Bangkok, Thailand, November 7-8, free paper III, p.40, 2002
28. Osuwannaratana P, Nimkarn S, Kijnarong N, Shotelersuk V, Weerakulwattana L, Likitmaskul S. “ Hypophosphatemic Rickets as a Presentation of Renal Fanconi Syndrome due to Hereditary Cystinosis in Three Cambodian Siblings”, APPES 2002 The Asian Pacific Paediatric Endocrine Society second biennial scientific meeting , Cairns, Australia, Nov 11-13, Abstract No B4, p. 179, 2002
29. Numbenjapon N, Likitmaskul S, Kiattisakthavee P, Nimkarn S, Sawathiparnich P, Tuchinda C , “Clinical Picture of Type 2 Diabetes Mellitus in Thai Youth”, APPES 2002 The Asian Pacific Paediatric Endocrine Society second biennial scientific meeting , Cairns, Australia, Nov 11-13, Abstract No D17, p. 141, 2002
30. Nimkarn S, Harinsoot, Nunloi S, Likitmaskul S “Cleft Palate in Combination with Salt Wasting Congenital Adrenal Hyperplasia in Two Patients. More Than a Co-incidence?”, APPES 2002 The Asian Pacific Paediatric Endocrine Society second biennial scientific meeting , Cairns, Australia, Nov 11-13, Concurrent Oral Session A, p30, 2002
31. Komtornrut C, Kittisangwara L, Yaiquawong M, Mahamaytakit N, Sundaraketu K, Nimkarn S “Growth Pattern of Turner Syndrome Patients at Siriraj Hospital” The 43th Siriraj Scientific Congress, Bangkok, Thailand, March 3-7, Siriraj Hosp Gaz, 55 (1): p90-1, 200
32. Ukarapong S, Weerakulwattana L, Kiattisakthavee P, Nimkarn S “Efficacy of Determining Mid-parental Target Height by Paretnal Perception or by Standardized Measurement”, The 43th Siriraj Scientific Congress, Bangkok, Thailand, March 3-7, Siriraj Hosp Gaz, 55 (1): p96-7, 2003
33. Keamseng C, Likitmaskul S, Kiattisaktavee P, Weerakulwattana L, Nimkarn S, Sawathiparnich P, Tuchinda C “Risk of metabolic disturbance and diabetes development in Thai obese children” , The 43th Siriraj Scientific Congress, Bangkok, Thailand, March 3-7, Siriraj Hosp Gaz, 55(1): p 94-5
34. Numbenjaporn N, Likitmaskul S, Nimkarn S, Sawathiparnich P, Santipraphob J, Kiattisaktavee P, Wongarn R “Succesful strategy to improve glucose tolerance in obese youngsters” , 56th Thai Congress of Pediatrics, Pattaya, Thailand, April 23-25. Abstract No B-1, p36, 2003
35. Osuwannaratana P, Nimkarn S, Likitmaskul S, Santipraphob J, Sawathiparnich P “The etiologies of adrenal insufficiency in Thai children” , 56th Thai Congress of Pediatrics, Pattaya, Thailand, April 23-25. Abstract No B-2, p37, 2003
36. Somnuke PH, Likitmaskul S, Santipraphob J, Nimkarn S, Sawathiparnich “Treatment outcome of Graves disease in Thai children”, 56th Thai Congress of Pediatrics, Pattaya, Thailand, April 23-25. Abstract No P3-3, p73, 2003
37. Somnuke PH, Likitmaskul S, Santipraphob J, Nimkarn S, Sawathiparnich “Treatment outcome of Graves disease in Thai”, 12th Annual Meeting and Clinical Congress, American Association of Clinical Endocrinologists, San Diego, CA, May 12-14, Abstract No. 106, p 329, 2003
38. Numbenjaporn N, Likitmaskul, Nimkarn S, Sawathiparnich P, Santipraphob J, Kiattisakthavee P, Wongarn R, Punnakanta L “Sucessful strategy to improve glucose tolerance in obese youngsters”, 29th annual meeting of the International Society for Pediatric and Adolescent Diabetes (ISPAD), Saint-Malo, France. September 3-6, Abstract No O-15, Journal of Pediatric Endocrinology & Metabolism. 16 Suppl 4:919-55, 2003
39. Nimkarn S, Weerakulwattana L, Panamonta O, Kumpornsin K, Limwongse C “Standardized biochemical diagnosis of 21 hydroxylase deficiency congenital adrenal hyperplasia, the forgotten essentials”, The Endocrine Society of Thailand 15th Annual Meeting, Bangkok, Thailand, October 30-1, p.12-3, 2003
40. Nimkarn S, Weerakulwattana L, Chaichanwatanakul K, Panamonta O, Kumpornsin K, Limwongse C “Comprehensive study of congenital adrenal hyperplasia due to 21 hydroxylase deficiency in 92 Thai patients”, 11th Asian Congress of Pediatrics, Bangkok, Thailand, November 2-7, Abstract No. FO-V-5, p. 80, 2003
41. Nimkarn S, Sanguanjin Y, Ttanvijit P, Weerakulwattana L, Chaichanwatanakul K, Panamonta O, Kumpornsin K, Limwongse C. “Standardized biochemical diagnosis of 21 hydroxylase, the forgotten essentials”, 44 th Siriraj Scientific Congress, Bangkok, Thailand, Mar 15-19, Siriraj hosp gazette;56 (supp 1) 2004
42. Nimkarn S “Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency”, 3rd Biennia Scientific Meeting Asia Pacific Paediatric Endocrine Society, Kobe, Japan. September 24-26, Clinical Pediatric Endocrinology; 13 (2) suppl, p 6, 2004
43. Nimkarn S, Weerakulwattana L, Panamonta O Chaichanwatanakul K, , Kumpornsin K, Limwongse C. “Comprehensive study of congenital adrenal hyperplasia due to 21 hydroxylase deficiency in 90Thai patients”, 12th Congress of the Asian Federation of Endocrine Societies, 7th Asia and Oeceania Thyroid Association Congress, Singapore, Nov 30-Dec 4, Journal of the ASEAN Federation of Endocrine Societies (JAFES); Jan/Jul 21(1/2), suppl, 2003
44. Nimkarn S, Weerakulwattana L, Panamonta O Chaichanwatanakul K, , Kumpornsin K, Limwongse C, “Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia (21OHD CAH) in 93 Thai patients, from genotypes to phenotypes”, ESPE/ LWPES 7th Joint Meeting Paediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, Lyon, France, Sep 21-24, Abstract No. P3-1152, Hormone Research Vol. 64, Suppl. 1, p. 334, 2005
45. Lin-Su K, Nimkarn S, Obeid J, Wilson RC, New MI“Degree of genital ambiguity according to genptype in females with classical 21-hydroxylase deficiency”, oral presentation, 4th Annual Meeting of Androgen Excess Society (AES), Boston, Massachusetts, June 23, 2006
46. Nimkarn S, New MI, Wilson RC “Ethnic specific distribution of mutations in 784 patients affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency” 88th Annual Meeting of the Endocrine Society ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P3-483, p. 758-9, 2006
47. Nimkarn S, Wilson RC, Harbison MD, New MI, “Trend of aldosterone to plasma renin activity ratio in 21-hydroxylase deficiency congenital adrenal hyperplasia” 88th Annual Meeting of the Endocrine Society ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P1-796, p.366, 2006
48. Nimkarn S, Wilson RC, Harbison MD, New MI, “Sodium to potassium ratio as a diagnostic tool to identify sodium conservation in 21-hydroxylase deficiency congenital adrenal hyperplasia” 88th Annual Meeting of the Endocrine Society, ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P1-797, p.367, 2006
49. Trinh LN, Nimkarn S, Obeid J, New MI, Su KL “Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency” 88th Annual Meeting of the Endocrine Society, ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P1-802, p. 368, 2006
50. Karnsakul W, Sawathiparnich P, Nimkarn S, Likitmaskul S, Santiprabhob J, Aanpreung P “Anterior pituitary hormone effects on hepatic functions in infants with congenital hypopituitarism”North American Society for Pediatric Gastroenterology, Hepatology and Nutrition 19th Annual Meeting, Orlando, Florida, October 19-22, Abstract No 82 (poster of distinction), J Pediatr Gastroenterol Nutr, Vol 43, No.4, page E39, 2006
51. Nimkarn S, New MI. “Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency.” The 2nd World Congress on Gender-specific Medicine & Aging, the Endocrine Impact. Rome, Italy, Mar 8-11, online http://www.gendermedicine.com/Uploads/assets/new.pdf, 2007
52. Nimkarn S, Wilson RC, Lin-Su K, Harbison MD, New MI. “Long-term follow up in Apparent Mineralocorticoid Excess patients.” 33rd International Aldosterone Conference. Toronto, Canada. May 31-June 1, Poster number 9, p.35-36, 2007
53. Trinh L, Cobb E, Azar MR, Nimkarn S, New MI, Wilson R. “CYP11B1 mutations in Iranian patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.” 89th Annual Meeting of the Endocrine Society, ENDO 07, Toronto, Canada, June 15-18, Abstract No P4-25, 2007
54. Guevarra FM, Su KL, Nimkarn S, New MI. “Long term growth hormone therapy in an adolescent male with 45,X/46,XidicY(p11)” 89th Annual Meeting of the Endocrine Society, ENDO 07, Toronto, Canada, June 15-18, Abstract No P1-452, 2007
55. Guevarra FM, Nimkarn S, Wilson RC, New MI. “Family study of patients with 21-hydroxylase deficiency demonstrates affected parents.” 89th Annual Meeting of the Endocrine Society, ENDO 07, Toronto, Canada, June 15-18, Abstract No P1-451, 2007
56. Guevarra FM, Nimkarn S, New MI. Family study of 3 patients with 21-hydroxylase deficiency demonstrates affected parents. 5th Annual Meeting of Androgen Excess Society (AES). Toronto, Canada. June 1, 2007.
57. Nimkarn S, Guevarra FM, Wilson RC, Lin-Su K, Harbison MD, New MI. “Long-term follow up in Apparent Mineralocorticoid Excess patients.” Conference on Clinical Research of Rare Diseases. Bethesda, Maryland. September 5, Poster number31, p.16, 2007
58. Guevarra FM, Su KL, Nimkarn S, New MI “Serum 17 Hydroxyprogesterone and androgen levels in mothers with 21-hydroxylase deficiency during pregnancy” 10th Annual Pediatric Research Day, Mount Sinai School of Medicine, April 10, p.45, 2008
59. Berry TB, Nimkarn S, Zavilowitz B, Wilson RC, New MI, Satlin LM “Loss of salt wasting in classical congenital adrenal hyperplasia secondary to aldosterone-independent Na conservation” 10th Annual Pediatric Research Day, Mount Sinai School of Medicine, April 10, p.61, 2008
60. Lekarev O, Guevarra FM, Nimkarn S, New MI “Adrenal and ovarian masses in an adult 21 hydroxylase deficiency congenital adrenal hyperplasia” Pediatric Academic Societies and Asian Society of Pediatric Research 2008 Joint Meeting, May 3-6, Poster Number 684, p 14, Publication 4496.4, 2008
61. Guevarra FM, Nimkarn S, New MI “Family study of 8 patients with 21 hydroxylase deficiency demonstrates affected parents” Pediatric Academic Societies and Asian Society of Pediatric Research 2008 Joint Meeting, May 3-6, Poster Number 685, p 14, Publication 4496.5, 2008
Original peer-reviewed articles
1. Nimkarn S, Cerame BI, Wei JQ, Dumic M, Zunec R, Brkljacic L, Skrabic V, New MI, Wilson RC. Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutations. J Clin Endocrinol Metab.Jan;84(1):378-81,1999.
2. Cerame BI, Newfield R, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC. Prenatal diagnosis and treatment of 11-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia. J Clin Endocrinol Metab. Sep;84(9):3129-34, 1999.
3. New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield R, Vandermeulen J, Barron N, Russo DL, Loriaux L, O’malley B. Partial resistance to several steroids in two sisters. J Clin Endocrinol Metab. Dec;84(12):4454-64, 1999
4. New MI, Obeid J, Wilson RC, Cabrera MS, Goseco A, Macapacal MC, Marshall I, Nimkarn S, Quintos JB, Ten S, Ugrasbul F, Vandermolen, Harbison MD. Profile of The Pediatric Endocrine Clinic at New York-Presbyterian Hospital, New York Weill Cornell Center. J Clin Endocrinol Metab. 1999 Dec;84(12):4444-9, 1999
5. New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield R, Vandermeulen J, Barron N, Russo DL, Loriaux L, O’malley B. Partial resistance to multiple steroids in two sisters. J Steroid Biochem Mol Biol. Jan-Mar;76(1-5):161-6, 2002
6. Sawathiparnich P, Likitmaskul S, Angsusingha K, Nimkarn S, Chaichanwatanakul K, Laohapansang M, Tuchinda C. Persistent Hyperinsulinemic Hypoglycemia of infancy (PHHI): Experience at the Department of Pediatrics, Siriraj Hospital. J Med Assoc Thai. Aug;85 Suppl 2:S506-12, 2002
7. Nimkarn S, Likitmaskul S, ,Sangacharoenkit P, Pathomvanich A, Sawathiparnich P, Wacharasindhu S, Punnakanta L, Angsusingha K , Tuchinda C. Ambiguous genitalia: An Overview of 22 Years Experience and the Diagnostic Approach in the Pediatric Department, Siriraj Hospital. J Med Assoc Thai. Aug;85 Suppl 2:S496-505, 2002
8. Likitmaskul S, Wekawanich J, Wongran R, Chaichanwatanakul K, Kiattisakthavee, Nimkarn S, Prayongklin S, Weerakulwattana, Markmaitree, Ritjarean Y, Pookpun, Punnakanta L, Angsusingha K, Tuchinda C. Intensive Diabetes Education Program and Multidisciplinary Team Approach in Management of Newly Diagnosed Type 1 Diabetes Mellitus: A Greater Patient Benefit, Experience at Siriraj Hospital. J Med Assoc Thai. Aug;85 Suppl 2:S488-95, 2002.
9. Nimkarn S, Su KL, Berglind N, Wilson RC., New MI. Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia J Clin Endocrinol Metab Jan;92(1):137-42, 2007
10. Wilson RC, Nimkarn S, Dumic M, Obeid J, Azar M, Najmabadi H, Saffari F, New MI. Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency, Mol Genet Metab. 2007 Apr; 90(4):414-21. Epub 2007 Feb 1, 2007
11. Karnsakul W, Sawathiparnich P, Nimkarn S, Likitmaskul S, Santiprabhob J, Aanpreung P. Anterior pituitary hormone effects on hepatic functions in infants with congenital hypopituitarism. Ann Hepatol. Apr-Jun;6(2):97-103, 2007
12. Nimkarn S, New MI. Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Nat Clin Pract Endocrinol Metab. 2007 May;3(5):405-13.
13. Trinh L, Nimkarn S, New MI, Lin-Su K Growth and Pubertal Characteristics in Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. J Pediatr Endocrinol Metab. 2007 Aug;20(8):883-91
14. Dumic M, Lin-Su K, Leibel N, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, and New MI. Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development. J Clin Endo Metab 93 (1): 182-189, 2008.
15. Dumic M, Lin-Su K, Leibel NI, Ciglar S, Vinci G, Lasan R, Nimkarn S, Wilson JD, McElreavey K, New MI. Report of fertility in woman with predominantly 46,XY karyotype in family with multiple disorders of sexual development: Review of Prismatic Case. Mt Sinai J Med. 2008 Mar;75(2):168-9.
16. Osuwannaratana P, Nimkarn S, Santiprabhob J, Likitmaskul S, Sawathiparnich P. The etiologies of adrenal insufficiency in 73 Thai children: 20 years experience. J Med Assoc Thai. 2008 Oct;91(10):1544-50.
Case Reports
17. Pitukcheewanont P, Nimkarn S, Austin J, Sack Z, Fisher LK. Salt-wasting 21-hydroxylase deficiency congenital adrenal hyperplasia and pyloric stenosis in two Hispanic brothers. J Pediatr. Aug;149(2):268-70, 2006
Invited Contributions
18. Wilson RC, Nimkarn S, New MI. Apparent Mineralocorticoid Excess Syndrome. Trends Endocrinol Metab. Apr;12(3):104-11, 2001. Review
19. Nimkarn S. Apparent Mineralocorticoid Excess. Siriraj Hosp Gazette 53(9):682-693, 2001
20. Nimkarn S. Premature puberty, an unignorable problem. Kao Tan Roke: The Praram 9 hospital journal, Aug; 28:4-6, 2001
21. Nimkarn S. Short stature. Ramkunhaeng hospital journal, Jan-Jul 20: 14-18, 2002
22. Nimkarn S. Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21 hydroxylase deficiency. Journal of Paediatrics,Obstetrics & Gynaecology, May/Jun; 31(3): 91-6, 2005
23. Nimkarn S, New MI Prenatal diagnosis and treatment of congenital adrenal hyperplasia, Pediatr Endocrinol Rev. Dec;4(2):99-105, 2006
24. Newfield RS, Nimkarn S, New MI Final height in congenital adrenal hyperplasia due to 21-hydorxylase deficiency: is it all hormonal? Electronic Letter to J Clin Endo Metab2006; 91: 3821-3825 published online Dec 19, 2006
25. Nimkarn S, New MI Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia, Horm Res 67:53-60, 2007
26. Nimkarn S, New MI Reviewer critique of "Apparent mineralocorticoid excess manifested in an elderly patient with hypothyroidism", Am J Hypertens. Jan;20(1):108, 2007
27. Nimkarn S, New MI. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia. Trends Endocrinol Metab. 2008 Apr;19(3):96-9. Epub 2008 Feb 21.
28. Lin-Su K, Nimkarn S, and New MI. Congenital adrenal hyperplasia in adolescents: diagnosis and management. Ann N Y Acad Sci. 2008 Jun;1135:95-8.
29. Lin-Su K, Nimkarn S, and New MI. “Treatment and Management of Congenital Adrenal Hyperplasia in Adults.” Expert Review of Endocrinology and Metabolism. Future Drugs (In Press, online doi:10.106/j.mce.2008.11.027)
30. Nimkarn S, New MI. “Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia” Proceedings of Adrenal 2008. Mol Cell Endocrinol. (In Press, Dec 3. [Epub ahead of print])
Books and Chapters in Books
31. Nimkarn S. “Insulin Therapy: pediatric aspects” in Practical Diabetes Mellitus, Siriraj, Bangkok, Thailand: 96-103, 2002
32. Nimkarn S. "Management of Congenital Adrenal Hyperplasia” in Guideline Management & Case Illustration in Pediatric Endocrinology. Wacharasindhu S, Jaruratsirikul S, Likitmaskul S. Bangkok, Text and Journal Publication: 124-144, 2002
33. Nimkarn S. “Chronic corticosteroid therapy: endocrine complications” in Challenging issues in adolescent endocrinology. Panamonta O, Jarurattanasirikul S , Santipraphob J. Bangkok, Reunkaew Karnpim: 183-195, 2004
34. Nimkarn S. “Persistent hyperinsulinemic hypoglycemia” in Metabolic genetic disorders in children, Wasant P. Bangkok, Bangkok Publication; vol 1: 123-139, 2003
35. Nimkarn S, New MI. “Congenital Adrenal Hyperplasia.” In: RE Weiss, S Refetoff (eds), Genetic Diagnosis of Endocrine Disease, 1st Edition. San Diego: Elsevier. (in Press)
36. Lin-Su K, Nimkarn S, New MI. “Diagnosis and Management of Congenital Adrenal Hyperplasia” in Pediatric, Adolescent, and Young Adult Gynecology Textbook, Altchek & Deligdisch, Wiley-Blackwell, Oxford: 25-35 (in press)
Media Resource Educational Material
36. Marshall I, Nimkarn S, New MI. (updated March 2006) Chapter 9 Hypertension in Childhood. In WWW.ENDOTEXT.ORG website, version of March 1,2006: New MI, section, published by MDTEXT.COM,INC, S.DARTMOUTH,MA. Available at http://endotext.com/pediatrics/pediatrics9/pediatricsframe9.htm
37. Nimkarn S, New M, (updated November 2008) 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia in: GeneReviews at GeneTests: Medical Genetics Information Resource [database online]. Copyright, University of Washington, Seattle. 1997-2006. Available at http://www.genetests.org.
38. Nimkarn S, Lin-Su K, Kaltman J, and New MI. “Congenital Adrenal Hyperplasia.” British Medical Journal. (In Press)
39. Nimkarn S, New MI “Chapter 8 Adrenal Disorder in website WWW.ENDOTEXT.ORG” version of May 20, 2008: New MI, section, published by MDTEXT.COM,INC, S.DARTMOUTH,MA. Available at http://endotext.org/pediatrics/pediatrics8/pediatricsframe8.htm
Abstracts (Optional, not encouraged)
1. Cerame BI, Nimkarn S, Roe TF, New MI, Wilson RC “A Single Basepair Deletion of CYP11B1 Gene Causing Classic 11-Hydroxylase Deficiency Congenital Adrenal Hyperplasia” The 80th Annual Meeting of The Endocrine Society, New Orleans, June 24-27, Abstract No. P1-272, p. 177, 1998.
2. New MI, Vandermeulen J, Nimkarn S, Cunningham-Rundles S, Wilson RC, Newfield RS “Global Steroid Resistance with Hypertension.” The 80th Annual Meeting of The Endocrine Society, New Orleans, June 24-27, Abstract No. O19-4, p. 78, 1998.
3. New MI, Vandermeulen J, Nimkarn S, Cunningham-Rundles S, Wilson RC, Newfield RS “Global Steroid Resistance with Hypertension.” The Association for Patient-Oriented Research, Atlantic City, April 30-May 2, 1999.
4. Nimkarn S, Lane JM, Harbison MD, “Bisphosphonate Therapy for Debilitating Idiopathic Juvenile Osteoporosis.” National Coopertive Growth Study Meeting, Charleston, South Carolina, Sep 30- Oct 3, 1999
5. Quintos JB, Nimkarn S, Ugrasbul F, Harbison MD.2000 “Persistence of Vitamin D Deficiency Rickets in The 1990’s: Risk Factors and Clinical Characteristics” The 2000 PAS/AAP Joint Annual Meeting ,Boston, May 12-16, Pediatric Research 47 (4), suppl, p 138A, 2000
6. Nimkarn S, Quintos JB, Novogroder M, Gertner JM, Harbison MD 2000 “Albright Hereditary Osteodystrophy Associated with Male Pseudohermaphroditism” The 2000 PAS/AAP Joint Annual Meeting, Boston, May 12-16, Pediatric Research 47 (4), suppl, p 136A, 2000
7. Nimkarn S, Lane JM, Harbison MD 2000 “Bisphosphonate Therapy for Debilitating Idiopathic Juvenile Osteoporosis.” The 2000 PAS/AAP Joint Annual Meeting in Boston, May 12-16, Pediatric Research 47 (4), suppl, p 136A, 2000
8. Nimkarn S, Wei JQ., Likitmaskul S., Chaichanwatanakul K, Kiattisakthavee P, Song D, New MI, Wilson RC, “Molecular Genotyping of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia in Thailand”, Endo 2000 The Endocrine Society 82nd Annual Meeting, Toronto, June 21-24 Abstract No. 531, p.516,2000 .
9. Nimkarn S, Bradlow L, Quintos JBQ, Pryor ND, Shackelton CHL., New MI, Wilson RC, “A New Case of Mild Apperent Mineralocorticoid Excess Syndrome”, Endo 2000 The Endocrine Society 82nd Annual Meeting, Toronto, June 21-24 Abstract No. 541, p.518, 2000.
10. Pitukcheewanont P, Nimkarn S, Fisher LK, Silverstein A, New MI, “Salt Wasting 21-Hydroxylase Deficiency Congential Adrenal Hyperplasia and Congential Pyrolic Stenosis in two Hispanic brothers”, 11th International Congress of Endocrinology (ICE 2000), Sydney, Australia, October 29-November2, Abstract No. P943, p.330, 2000
11. Nimkarn S, Wei JQ, Likitmaskul S, Chaichanwatanakul K, Kiattisakthavee P, Song D, New MI, Wilson RC, “Molecular Genotyping of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia in Thailand”, 52th Thai Congress of Pediatrics, Trang, Thailand, April 25-27, Abstract No.C-7, p.68, 2001
13. Marshall I, Nimkarn S, Wei JQ, Guazzarotti L, New MI, Wilson RC: “Detection of Mutation in the 21-hydroxylase gene”, Endo 2001 The Endocrine Society 83th Annual Meeting, Denver, June 20-23, Abstract No. P2-7, 2001
14. Nimkarn S “Management of Diabetes Mellitus on the sick days” Diabetes Mellitus From up to date knowledge to a better clinical practice, Bangkok, Thailand, Oct 17-19, p 127-131, 2001.
15. Nimkarn S, Likitmaskul S, Wei JQ, Chaichanwatanakul K, Kiattisakthavee P, New MI, Wilson RC “Genotypic analysis of 21 hydroxylase deficiency congenital adrenal hyperplasia in Thai patients”, The Endocrine Society of Thailand 13th Annual Meeting, Bangkok, Thailand, November 1-2, free paper III, p.33, 2001
16. Nimkarn S, “Congenital Adrenal Hyperplasia; A New Perspective of the Disease you know”,The 42th Siriraj Scientific Congress, Bangkok, Thailand, March 4-8, Abstract No L12, p.70-71, 2002
17. Sawathiparnich P, Likitmaskul S, Angsusingha K, Nimkarn S, Chaichanwatanakul K, Laohapansang M, Tuchinda C “Persistent Hyperinsulinemic Hypoglycemia of Infancy (PHHI): Experience at the Department of Pediatrics, Siriraj Hospital”, 54th Thai Congress of Pediatrics, Cha-am, Thailand, April 24-26, Abstract No C-02, p 57, 2002
18. Keamseng C, Likitmaskul S, Kiattisakthavee P, Weerakulwatana L, Nimkarn S, Sawathiparnich P, Tuchinda C “Metabolic Disturbance in Obese Children in Siriraj Hospital”, 54th Thai Congress of Pediatrics, Cha-am, Thailand, April, 24-26, Abstract No C-03, p.58-9, 2002
19. Komtornrut C, Kittisangwara L, Yaiquawong M, Mahamaytakit N, Sundaraketu K, Nimkarn S “Growth Pattern of Turner Syndrome Patients at Siriraj Hospital” 54th Thai Congress of Pediatrics, Cha-am, Thailand, April 24-26, Abstract No C-04, p.60-1, 2002
20. Nimkarn S, Sawathiparnich P, Likitmaskul S “Cleft Palate in Combination with Salt-Wasting Congenital Adrenal Hyperplasia in Two Patients. More than a Co-incidence?”, 54th Thai Congress of Pediatrics, Cha-am, Thailand, April, 24-26, Abstract No C-08, p 66-7, 2002
21. Nimkarn S, Wei JQ, Likitmaskul S, Chaichanwatanakul K, Kiattisakthavee P, New MI, Wilson RC “Genotypic analysis of 21 hydroxylase deficiency congenital adrenal hyperplasia in Thai patients” The Ramathibodi Annual Scientific Meeting, Bangkok, Thailand, May 1-3, Abstract No 72, Ramathibodi Medical Journal 25, suppl, p 105, 2002
22. Macapagal MC, Slowinska BS, Nimkarn S, De BP, Licholai T, Marshall I, Hackett N, Crystal RG, New MI, Wilson RC “Gene Therapy of 21-hydroxylase Deficient Mice Utilizing an Adeno-associated Virus Vector” Endo 2002 The Endocrine Society 84th Annual Meeting, San Francisco, June 19-22, Abstract No P1-503, p 270, 2002
24. Nimkarn S, Weerakulwattana L, Wei JQ, Wilson RC, Kiattisakthavee P, Likitmaskul S, Chaichanwatanakul K Kumpornsin K, Limwongse C “Genotypic Analysis of 21 hydroxylase Deficiency Congenital Adrenal Hyperplasia in Thai patients, and the Genotype/ Phenotype Correlation” The 4th HUGO Pacific Meeting& 5th Asia Pacific Conference on Human Genetics, October 27-30, Pattaya, Thailand, Abstract No SG-20, 2002
25. Keamseng C, Likitmaskul S, Kiattisakthavee P, Weerakulwatana L, Nimkarn S, Sawathiparnich P, Tuchinda C “Risk of metabolic disturbance and diabetes development in Thai Obese Children”, The Endocrine Society of Thailand 14th Annual Meeting, Bangkok, Thailand, November 7-8, free paper I, p.23, 2002
26. Nimkarn S, Weerakulwattana L, Panamonta O, Sriwijitkamol A, Chaichanwatanakul K, Kiattisakthavee P, Likitmaskul S, Kumpornsin K, Wei JQ, Licholai T, Wilson RC, Limwongse C “Study of Congenital Adrenal Hyperplasia, a Steroid Disorder of Various Etiologies among Thai Patients”, The Endocrine Society of Thailand 14th Annual Meeting, Bangkok, Thailand, November 7-8, free paper III, p.34, 2002
27. Ukarapong S, Weerakulwattana L, Kiattisakthavee P, Nimkarn S “Efficacy of Determining Mid-parental Target Height by Paretnal Perception or by Standardized Measurement”, The Endocrine Society of Thailand 14th Annual Meeting, Bangkok, Thailand, November 7-8, free paper III, p.40, 2002
28. Osuwannaratana P, Nimkarn S, Kijnarong N, Shotelersuk V, Weerakulwattana L, Likitmaskul S. “ Hypophosphatemic Rickets as a Presentation of Renal Fanconi Syndrome due to Hereditary Cystinosis in Three Cambodian Siblings”, APPES 2002 The Asian Pacific Paediatric Endocrine Society second biennial scientific meeting , Cairns, Australia, Nov 11-13, Abstract No B4, p. 179, 2002
29. Numbenjapon N, Likitmaskul S, Kiattisakthavee P, Nimkarn S, Sawathiparnich P, Tuchinda C , “Clinical Picture of Type 2 Diabetes Mellitus in Thai Youth”, APPES 2002 The Asian Pacific Paediatric Endocrine Society second biennial scientific meeting , Cairns, Australia, Nov 11-13, Abstract No D17, p. 141, 2002
30. Nimkarn S, Harinsoot, Nunloi S, Likitmaskul S “Cleft Palate in Combination with Salt Wasting Congenital Adrenal Hyperplasia in Two Patients. More Than a Co-incidence?”, APPES 2002 The Asian Pacific Paediatric Endocrine Society second biennial scientific meeting , Cairns, Australia, Nov 11-13, Concurrent Oral Session A, p30, 2002
31. Komtornrut C, Kittisangwara L, Yaiquawong M, Mahamaytakit N, Sundaraketu K, Nimkarn S “Growth Pattern of Turner Syndrome Patients at Siriraj Hospital” The 43th Siriraj Scientific Congress, Bangkok, Thailand, March 3-7, Siriraj Hosp Gaz, 55 (1): p90-1, 200
32. Ukarapong S, Weerakulwattana L, Kiattisakthavee P, Nimkarn S “Efficacy of Determining Mid-parental Target Height by Paretnal Perception or by Standardized Measurement”, The 43th Siriraj Scientific Congress, Bangkok, Thailand, March 3-7, Siriraj Hosp Gaz, 55 (1): p96-7, 2003
33. Keamseng C, Likitmaskul S, Kiattisaktavee P, Weerakulwattana L, Nimkarn S, Sawathiparnich P, Tuchinda C “ Risk of metabolic disturbance and diabetes development in Thai obese children” , The 43th Siriraj Scientific Congress, Bangkok, Thailand, March 3-7, Siriraj Hosp Gaz, 55(1): p 94-5
34. Numbenjaporn N, Likitmaskul S, Nimkarn S, Sawathiparnich P, Santipraphob J, Kiattisaktavee P, Wongarn R “Succesful strategy to improve glucose tolerance in obese youngsters” , 56th Thai Congress of Pediatrics, Pattaya, Thailand, April 23-25. Abstract No B-1, p36, 2003
35. Osuwannaratana P, Nimkarn S, Likitmaskul S, Santipraphob J, Sawathiparnich P “The etiologies of adrenal insufficiency in Thai children” , 56th Thai Congress of Pediatrics, Pattaya, Thailand, April 23-25. Abstract No B-2, p37, 2003
36. Somnuke PH, Likitmaskul S, Santipraphob J, Nimkarn S, Sawathiparnich “Treatment outcome of Graves disease in Thai children”, 56th Thai Congress of Pediatrics, Pattaya, Thailand, April 23-25. Abstract No P3-3, p73, 2003
37. Somnuke PH, Likitmaskul S, Santipraphob J, Nimkarn S, Sawathiparnich “Treatment outcome of Graves disease in Thai”, 12th Annual Meeting and Clinical Congress, American Association of Clinical Endocrinologists, San Diego, CA, May 12-14, Abstract No. 106, p 329, 2003
38. Numbenjaporn N, Likitmaskul, Nimkarn S, Sawathiparnich P, Santipraphob J, Kiattisakthavee P, Wongarn R, Punnakanta L “Sucessful strategy to improve glucose tolerance in obese youngsters”, 29th annual meeting of the International Society for Pediatric and Adolescent Diabetes (ISPAD), Saint-Malo, France. September 3-6, Abstract No O-15, Journal of Pediatric Endocrinology & Metabolism. 16 Suppl 4:919-55, 2003
39. Nimkarn S, Weerakulwattana L, Panamonta O, Kumpornsin K, Limwongse C “Standardized biochemical diagnosis of 21 hydroxylase deficiency congenital adrenal hyperplasia, the forgotten essentials”, The Endocrine Society of Thailand 15th Annual Meeting, Bangkok, Thailand, October 30-1, p.12-3, 2003
40. Nimkarn S, Weerakulwattana L, Chaichanwatanakul K, Panamonta O, Kumpornsin K, Limwongse C “Comprehensive study of congenital adrenal hyperplasia due to 21 hydroxylase deficiency in 92 Thai patients”, 11th Asian Congress of Pediatrics, Bangkok, Thailand, November 2-7, Abstract No. FO-V-5, p. 80, 2003
41. Nimkarn S, Sanguanjin Y, Ttanvijit P, Weerakulwattana L, Chaichanwatanakul K, Panamonta O, Kumpornsin K, Limwongse C. “Standardized biochemical diagnosis of 21 hydroxylase, the forgotten essentials”, 44 th Siriraj Scientific Congress, Bangkok, Thailand, Mar 15-19, Siriraj hosp gazette;56 (supp 1) 2004
42. Nimkarn S “Prenatal diagnosis and treatment of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency”, 3rd Biennia Scientific Meeting Asia Pacific Paediatric Endocrine Society, Kobe, Japan. September 24-26, Clinical Pediatric Endocrinology; 13 (2) suppl, p 6, 2004
43. Nimkarn S, Weerakulwattana L, Panamonta O Chaichanwatanakul K, , Kumpornsin K, Limwongse C. “Comprehensive study of congenital adrenal hyperplasia due to 21 hydroxylase deficiency in 90Thai patients”, 12th Congress of the Asian Federation of Endocrine Societies, 7th Asia and Oeceania Thyroid Association Congress, Singapore, Nov 30-Dec 4, Journal of the ASEAN Federation of Endocrine Societies (JAFES); Jan/Jul 21(1/2), suppl, 2003
44. Nimkarn S, Weerakulwattana L, Panamonta O Chaichanwatanakul K, , Kumpornsin K, Limwongse C, “Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia (21OHD CAH) in 93 Thai patients, from genotypes to phenotypes”, ESPE/ LWPES 7th Joint Meeting Paediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, Lyon, France, Sep 21-24, Abstract No. P3-1152, Hormone Research Vol. 64, Suppl. 1, p. 334, 2005
45. Lin-Su K, Nimkarn S, Obeid J, Wilson RC, New MI “Degree of genital ambiguity according to genptype in females with classical 21-hydroxylase deficiency”, oral presentation, 4th Annual Meeting of Androgen Excess Society (AES), Boston, Massachusetts, June 23, 2006
46. Nimkarn S, New MI, Wilson RC “Ethnic specific distribution of mutations in 784 patients affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency” 88th Annual Meeting of the Endocrine Society ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P3-483, p. 758-9, 2006
47. Nimkarn S, Wilson RC, Harbison MD, New MI, “Trend of aldosterone to plasma renin activity ratio in 21-hydroxylase deficiency congenital adrenal hyperplasia” 88th Annual Meeting of the Endocrine Society ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P1-796, p.366, 2006
48. Nimkarn S, Wilson RC, Harbison MD, New MI, “Sodium to potassium ratio as a diagnostic tool to identify sodium conservation in 21-hydroxylase deficiency congenital adrenal hyperplasia” 88th Annual Meeting of the Endocrine Society, ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P1-797, p.367, 2006
49. Trinh LN, Nimkarn S, Obeid J, New MI, Su KL “Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency” 88th Annual Meeting of the Endocrine Society, ENDO 06, Boston, Massachusetts, June 24-27, Abstract No P1-802, p. 368, 2006
50. Karnsakul W, Sawathiparnich P, Nimkarn S, Likitmaskul S, Santiprabhob J, Aanpreung P “Anterior pituitary hormone effects on hepatic functions in infants with congenital hypopituitarism”North American Society for Pediatric Gastroenterology, Hepatology and Nutrition 19th Annual Meeting, Orlando, Florida, October 19-22, Abstract No 82 (poster of distinction), J Pediatr Gastroenterol Nutr, Vol 43, No.4, page E39, 2006
51. Nimkarn S, New MI. “Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to 21-hydroxylase deficiency.” The 2nd World Congress on Gender-specific Medicine & Aging, the Endocrine Impact. Rome, Italy, Mar 8-11, online http://www.gendermedicine.com/Uploads/assets/new.pdf, 2007
52. Nimkarn S, Wilson RC, Lin-Su K, Harbison MD, New MI. “Long-term follow up in Apparent Mineralocorticoid Excess patients.” 33rd International Aldosterone Conference. Toronto, Canada. May 31-June 1, Poster number 9, p.35-36, 2007
53. Trinh L, Cobb E, Azar MR, Nimkarn S, New MI, Wilson R. “CYP11B1 mutations in Iranian patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.” 89th Annual Meeting of the Endocrine Society, ENDO 07, Toronto, Canada, June 15-18, Abstract No P4-25, 2007
54. Guevarra FM, Su KL, Nimkarn S, New MI. “Long term growth hormone therapy in an adolescent male with 45,X/46,XidicY(p11)” 89th Annual Meeting of the Endocrine Society, ENDO 07, Toronto, Canada, June 15-18, Abstract No P1-452, 2007
55. Guevarra FM, Nimkarn S, Wilson RC, New MI. “Family study of patients with 21-hydroxylase deficiency demonstrates affected parents.” 89th Annual Meeting of the Endocrine Society, ENDO 07, Toronto, Canada, June 15-18, Abstract No P1-451, 2007
56. Guevarra FM, Nimkarn S, New MI. Family study of 3 patients with 21-hydroxylase deficiency demonstrates affected parents. 5th Annual Meeting of Androgen Excess Society (AES). Toronto, Canada. June 1, 2007.
57. Nimkarn S, Guevarra FM, Wilson RC, Lin-Su K, Harbison MD, New MI. “Long-term follow up in Apparent Mineralocorticoid Excess patients.” Conference on Clinical Research of Rare Diseases. Bethesda, Maryland. September 5, Poster number31, p.16, 2007
58. Guevarra FM, Su KL, Nimkarn S, New MI “Serum 17 Hydroxyprogesterone and androgen levels in mothers with 21-hydroxylase deficiency during pregnancy” 10th Annual Pediatric Research Day, Mount Sinai School of Medicine, April 10, p.45, 2008
59. Berry TB, Nimkarn S, Zavilowitz B, Wilson RC, New MI, Satlin LM “Loss of salt wasting in classical congenital adrenal hyperplasia secondary to aldosterone-independent Na conservation” 10th Annual Pediatric Research Day, Mount Sinai School of Medicine, April 10, p.61, 2008
60. Lekarev O, Guevarra FM, Nimkarn S, New MI “Adrenal and ovarian masses in an adult 21 hydroxylase deficiency congenital adrenal hyperplasia” Pediatric Academic Societies and Asian Society of Pediatric Research 2008 Joint Meeting, May 3-6, Poster Number 684, p 14, Publication 4496.4, 2008
61. Guevarra FM, Nimkarn S, New MI “Family study of 8 patients with 21 hydroxylase deficiency demonstrates affected parents” Pediatric Academic Societies and Asian Society of Pediatric Research 2008 Joint Meeting, May 3-6, Poster Number 685, p 14, Publication 4496.5, 2008
62. Guevarra FM, Lin-Su K, Nimkarn S, New MI “Serum 17 hydroxyprogesterone and androgen levels in mothers with 21-hydroxylase deficiency during pregnancy”90th Annual Meeting of the Endocrine Society, ENDO 08, San Francisco, CA, , June 15-18, Abstract No P1-602, 2008
63. Berry TB, Lin-Su K, Nimkarn S, New MI“Inaccurate Estimation of Gestational Age Affects Outcome of Prenatal Treatment of Congenital Adrenal Hyperplasia” 90th Annual Meeting of the Endocrine Society, ENDO 08, San Francisco, CA, , June 15-18, Abstract No P2-581, 2008
