Specialties:
Endocrinologist, Pediatric Endocrinologist, Pediatrician
Address:
5 East 98Th Street, 10Th Floor, New York, NY 10029
Education:
Medical School - University of Pennsylvania, MD
New York Presbyterian Hospital (Residency - Pediatrics)
Bellevue Hospital (Internship - Internal Medicine)
New York Presbyterian - Weill Cornell Medical Center (Fellowship - Pediatrics)
Cornell University (Degree: B.A. )
Languages:
English, Spanish, Italian
Awards and Publications:
New MI, Wilson RC. Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess. . Proc Natl Acad Sci 1999.; 96:: 12790-12797., Lin-Su K, Zhou P, Arora N, Betensky B, New MI, Wilson RC. In Vitro Expression Studies Of A Novel Mutation ?299 In A Patient Affected With Apparent Mineralocorticoid Excess (AME). . J Clin Endocrinol Metab. 2004; 89: 2024-2027., Nimkarn S, Lin-Su K, New MI, Wilson R, Berglind N. Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Congenital Adrenal Hyperplasia. J Clin Endo Metab 2007 January; 92(1): 137-142., Wilson RC, Nimkarn S, Dumic M, New MI, Azar M, Najmabadi H, Saffari F, Obeid J. Ethnic Specific Distribution of Mutations in 716 Patients with Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency. Mol Genet Metab 2007 Jan; E-Pub ., Trinh L, Lin-Su K, New MI, Nimkarn S. Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Ped Endocrinol Metab;., New MI. Extensive Personal Experience: Nonclassical 21-Hydroxylase Deficiency. J Clin Endo Metab 2006; 91: 4222-4231., Meyer-Bahlburg HL, Dolezal C, New MI, Kessler SJ, Schober JM, Zucker KJ. The Recalled Gender Questionnaire-Revised: A Psychometric Analysis in a Sample of Women with Congenital Adrenal Hyperplasia. J Sex Res 2006; 43(4): 364-367., Bhangoo A, Ten S, New MI, Wilson R. Donor splice mutation in the 11?-hydroxylase (CYP11B1) gene resulting in sex reversal: a case report and review of the literature. J Pediatr Endrocinol Metab 2006; 19: 1267-1282., Ergun-Longmire B, Auchus R, New MI, Tansil S, Wilson RC, Papri-Zareei M. Two novel mutations found in a patient with 17?-hydroxylase deficiency. J Clin Endocrinol Metab 2006; 91(10): 4179-4182., Meyer-Bahlburg HF, Dolezal C, New MI, Ehrhardt AA, Baker SW. Gender Development in Women with Congenital Adrenal Hyperplasia as a Function of Disorder Severity. Arch Sex Behav 2006; 35: 667-684., Ergun-Longmire B, Vinci G, Alonso L, New MI, Lin-Su K, McElreavey K, Tansil S. Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature. J Pediatr Endocrinol Metab 2005; 23(8): 739-748., Lin-Su K, Vogiatzi MG, Marshall I, New MI, Macapagal MC, Betensky B, Tansil S, Harbison MD. Treatment with Growth Hormone and LHRH Analogue Improves Final Adult Height in Children with Congenital Adrenal Hyperplasia. J Clin Endocrinol Metab 2005; 90: 3318-3325.
Board certifications:
American Board of Pediatrics