UHealth - University of Miami Health System

Tossaporn Seeherunvong, M.D.

Información general

Tossaporn  Seeherunvong, M.D.

Contacto

Idiomas

  • English
  • Thai

Certificaciones

  • American Board of Pediatrics
  • American Board of Pediatrics-Pediatric Endocrinology

Especialidades

  • Pediatric Endocrinology (Pediatrics)
  • Pediatrics

Puestos

  • Assistant Professor of Clinical Pediatrics

Intereses clínicas

Growth disorders

Pubertal disorders

Thyroid disorders in children

Calcium disorders in children

Adrenal disorders in children

Glucose disorders in children

Sexual differentiation disorders

Intereses de
investigación

Hyperglycemia

Thyroid disorders in children

Premios

Super Doctor- Florida
Super Doctor- Florida
Super Doctor- Florida
Top Pediatrician

Educación

M.D.
Mahidol University, Ramathibodi Hospital
Residency
SUNY Upstate Medical University
Fellowship
Johns Hopkins University
Fellowship
University of Miami Miller School of Medicine

Publicaciones

  • Seeherunvong T, Diamantopoulos S, Berkovitz GD. A nine year old girl with thyrotoxicosis, ataxia, and chorea. Brain Dev 2007 Nov;29(10):660-1.
  • Seeherunvong T, Perera EM, McElreavey K, Bao Y, Berkovitz GD. Duplication of SOX9 is a Rare Cause of 46,XX Sex Reversal. Poster presentation presented in endocrine genetics session at the Endocrine Society’s 87th Annual Meeting in San Diego, June 4-7, 2005.
  • Seeherunvong T, Perera EM, Bao Y, Benke PJ, Benigno A, Donahue RP, Berkovitz GD. XX sex reversal with partial duplication of chromosome arm 22q. Am J Med Genet 2004 Jun 1;127(2):149-51.
  • Perera EM, Martin H, Seeherunvong T, Kos L, Hughes IA, Hawkins JR, Berkovitz GD. Tescalcin, a novel gene belonging to EF-hand Ca2+ binding proteins, Col9a3 and renin are expressed in the mouse testis during the early stages of gonadal differentiation. Endocrinology 2001 Jan;142(1):455-63
  • Seeherunvong T, Perera EM, Benke PJ, Benigno AB, Donahue RP, Berkovitz GD. 46, XX sex reversal with duplication of chromosome 22q. Oral presentation in endocrine genetics session at the Endocrine Society’s 82nd Annual Meeting in Toronto, Canada, June 21-24, 2000.
  • Bao Y, Hughes P, Seeherunvong T, Eidson M. Ataxia and chorea in a 9 year old female with graves disease. Poster presentation in meeting professor poster session at the Endocrine Society’s 82nd Annual Meeting in Toronto, Canada, June 21-24, 2000.
  • Seeherunvong T, Seeherunvong W, Leal D, Abitbol C, Berkovitz G, Eidson M. Intractable hypoglycemia in a patient with diabetes mellitus, bilateral nephrectomy, and chronic active hepatitis. Clin Pediatr (Phila). 2000 Sep;39(9):557-60.
  • Berkovitz GD, Seeherunvong T. Molecular basis of disorders of sexual differentiation. In:Handwerger S, eds. Molecular and cellular pediatric endocrinology. Humana Press, Totowa, NJ, 1999, pp. 1-9.
  • Berkovitz GD, Seeherunvong T. Abnormalities of gonadal differentiation. Baillieres Clin Endocrinol Metab 1998 Apr;12(1):133-42.
  • Seeherunvong T, Churesigaew S. Etiologic study of primary congenital hypothyroidism. J Med Assoc Thai 1998 Sep;81(9):653-7.
  • Seeherunvong T, Churesigaew S, Hemsrichart V. Multiple endocrine neoplasia type IIa: a case report. J Med Assoc Thai 1998 Oct;81(10):789-93.

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