ArleneBasaMercadoMD

PubMed

• Continuous monitoring of blood pressure in children and adolescents,a review of the literature.
  Arlene B Mercado> ;Pediatric Endocrinology Reviews. 2008 Aug 1
• 7 citations
  The prevalence of metabolic syndrome in inner city obese African-American youth.
  Jose Bernardo Quintos, Hiren Muzumdar, Minu George, Arlene B Mercado, Haiyan Lu, Alex Sternberg, Madu Rao, Salvador Castells> ;Pediatric Endocrinology Reviews. 2006 Dec 1
• 4 citations
  Pancreatic beta-cell hyperactivity in morbidly obese adolescents.
  Arlene B Mercado, Salvador Castells> ;Pediatric Endocrinology Reviews. 2006 Dec 1
• 18 citations
  Estimates of body fat in children by Hologic QDR-2000 and QDR-4500A dual-energy X-ray absorptiometers compared with deuterium dilution.
  Delphine R. Robotham, Dale A. Schoeller, Arlene B. Mercado, Margaret C. Mirch, Kelly R. Theim, James C. Reynolds, Jack A. Yanovski> ;Journal of Pediatric Gastroenterology and Nutrition. 2006 Mar 1
• 39 citations
  Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot
  Phyllis W. Speiser, Perrin C. White, Jacob Dupont, Deguang Zhu, A. B. Mercado, Maria I. New> ;Human Genetics. 1994 Apr 1
• 3 citations
  Molecular genetic prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization.
  Phyllis W. Speiser, Perrin C. White, Jakob Dupont, Deguang Zhu, A. B. Mercado, Maria I. New> ;Recent Progress in Hormone Research. 1994 Jan 1
• 17 citations
  Prenatal diagnosis/treatment in families at risk for infants with steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia)
  Lefke P. Karaviti, A. B. Mercado, Myra B. Mercado, Phyllis W. Speiser, Mimi Buegeleisen, Christopher Crawford, Lida Antonian, Perrin C. White, Maria I. New> ;The Journal of Steroid Biochemistry and Molecular Biology. 1992 Mar 1
• 110 citations
  Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene.
  Robert C. Wilson, Ji-Qing Wei, K. C. Cheng, A. B. Mercado, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 1995 May 1
• 233 citations
  Steroid 21-hydroxylase deficiency : genotype may not predict phenotype
  Robert C. Wilson, A. B. Mercado, K. C. Cheng, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 1995 Aug 1
• 130 citations
  Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency.
  A. B. Mercado, Robert C. Wilson, K. C. Cheng, Ji-Qing Wei, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 1995 Jul 1
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