Faculty

Perrin C. White, M.D.
Bryan A. Dickson, M.D.
Melissa R. Ham, M.D.
Michele R. Hutchison, M.D., Ph.D.
Ellen C. Kaizer, M.D.
Bassil M. Kublaoui, M.D., Ph.D.
D. Randy McMillan, Ph.D.
Sudha L. Mootha, M.D.
Jon D. Oden, M.D.
Grace M. Tannin, M.D.

Fellows

Soumya Adhikari, M.D.
Jill Ann Goldfarb, M.D.
Shuchi Shah, M.D.

Research Staff

Kelli A. Black
Daniela C. Rogoff, M.D., Ph.D.

Faculty

Perrin C. White, M.D.

Selected Peer Reviewed Publications (from 114 Publications)

• Agarwal AK, Mune T, Monder C, White PC. NAD( )-dependent isoform of 11 beta-hydroxysteroid dehydrogenase. Cloning and characterization of cDNA from sheep kidney. Journal of Biological Chemistry 1994; 269(42):25959-25962.
• Mune T, Rogerson FM, Nikkila H, Agarwal AK, White PC. Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase. Nature Genetics 1995; 10(4):394-399.
• Kupari M, Hautanen A, Lankinen L, Koskinen P, Virolainen J, Nikkila H et al. Associations between human aldosterone synthase (CYP11B2) gene polymorphisms and left ventricular size, mass, and function. Circulation 1998; 97(6):569-575.
• Willcutts MD, Felner E, White PC. Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin. Human Molecular Genetics 1999; 8(7):1303-1307.
• Nunez BS, Rogerson FM, Mune T, Igarashi Y, Nakagawa Y, Phillipov G et al. Mutants of 11beta-hydroxysteroid dehydrogenase (11-HSD2) with partial activity: improved correlations between genotype and biochemical phenotype in apparent mineralocorticoid excess. Hypertension 1999; 34(4:Pt 1):638-642.
• Hautanen A, Toivanen P, Manttari M, Tenkanen L, Kupari M, Manninen V et al. Joint effects of an aldosterone synthase (CYP11B2) gene polymorphism and classic risk factors on risk of myocardial infarction. Circulation 1999; 100(22):2213-2218.
• Nikkila H, McMillan DR, Nunez BS, Pascoe L, Curnow KM, White PC. Sequence similarities between a novel putative G protein-coupled receptor and Na /Ca2 exchangers define a cation binding domain. Molecular Endocrinology 2000; 14(9):1351-1364.
• Felner EI, White PC. Improving management of diabetic ketoacidosis in children. Pediatrics 2001; 108(3):735-740.
• McMillan DR, Kayes-Wandover KM, Richardson JA, White PC. Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system. Journal of Biological Chemistry 2002; 277(1):785-792.
• Mune T, Morita H, Suzuki T, Takahashi Y, Isomura Y, Tanahashi T et al. Role of local 11 beta-hydroxysteroid dehydrogenase type 2 expression in determining the phenotype of adrenal adenomas. Journal of Clinical Endocrinology & Metabolism 2003; 88(2):864-870.
• Draper N, Walker EA, Bujalska IJ, Tomlinson JW, Chalder SM, Arlt W et al. Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency. Nature Genetics 2003; 34(4):434-439.
• Bassett M, Suzuki T, Sasano H, White PC, Rainey WE. The orphan nuclear receptors NURR1 and NGFIB regulate adrenal aldosterone production. Molecular Endocrinology 2004; 18(2):279-290.
• Felner EI, Dickson BA, White PC. Hypothyroidism in siblings due to a homozygous mutation of the TSH-beta subunit gene. Journal of Pediatric Endocrinology and Metabolism 2004; 17(4):669-672.
• Ham MR, Okada P, White PC. Bedside ketone determination in diabetic children with hyperglycemia and ketosis in the acute care setting. Pediatric Diabetes 2004; 5(1):39-43.
• McMillan DR, White PC. Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice. Molecular & Cellular Neuroscience 2004; 26(2):322-329.
• Stewart SM, Rao U, Emslie GJ, Diane Klein D, White PC. Depressive symptoms predict hospitalization in adolescents with Type I diabetes. Pediatrics 2005; 115(5):1315-1320.
• Isaji M, Mune T, Takada N, Yamamoto Y, Suwa T, Morita H, et al. Correlation between left ventricular mass and urinary sodium excretion in specific genotypes of CYP11B2. Journal of Hypertension 2005; 23(6):1149-1157.
• Bujalska IJ, Draper N, Michailidou Z, Tomlinson JW, White PC, Chapman K et al. Hexose-6-phosphate dehydrogenase confers oxo-reductase activity upon 11b-hydroxysteroid dehydrogenase type 1. Journal of Molecular Endocrinology 2005; 34(3):675-684.
• Gibert Y, McMillan DR, Kayes-Wandover K, Meyer A, Begemann G, White PC. Analysis of the very large G-protein coupled receptor gene (Vlgr1/Mass1/USH2C) in zebrafish. Gene 2005; 353(2):200-206.
• Stewart SM, Emslie GJ, Klein D, Haus S, White P. Self-care and glycemic control in adolescents with type1 diabetes. Children’s Health Care 2005;34:235-244.
• Bassett MH, Mayhew B, Rehman K, White PC, Mantero F, Arnaldi G et al. Expression profiles for steroidogenic enzymes in adrenocortical disease. Journal of Clinical Endocrinology and Metabolism 2005; 90(9):5446-5455.
• Felner EI, Klitz W, Ham M, Lazaro AM, Stastny P, Dupont B et al. Interaction of Age of Onset with Genetic Risk Factors for Type 1 Diabetes. Journal of Pediatric Diabetes 2005; 6(4):213-220.
• White PC.  Genotypes at HSD11B1 and H6PD loci are not risk factors for apparent cortisone reductase deficiency in a large population-based sample. Journal of Clinical Endocrinology and Metabolism 2005; 90(10):5880-5883.
• Tanahashi H, Mune T, Takahashi Y, Isaji M, Suwa T, Morita H et al. Association of Lys173Arg polymorphism with CYP11B2 expression in normal adrenal glands and aldosterone-producing adenomas. Journal of Clinical Endocrinology and Metabolism 2005; 90(11):6226-6231.
• Saner-Amigh KS, Mayhew BA, Mantero F, Schiavi F, White PC, Rao C et al. Elevated expression of luteinizing hormone receptor in aldosterone-producing adenomas. Journal of Clinical Endocrinology and Metabolism 2006; 91(3):1136-1142
• Lavery GG, Walker EA, Draper N, Jeyasuria P, Marcos J, Shackleton CH et al. Hexose-6-phosphate dehydrogenase knockout mice lack 11beta -hydroxysteroid dehydrogenase type 1-mediated glucocorticoid generation. Journal of Biological Chemistry 2006; 281(10):6546-6551
• McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG et al. The Very Large G-Protein Coupled Receptor, VLGR1, a component of the ankle link complex required for the normal development of auditory hair bundles. Journal of Neuroscience 2006; 26(24):6543-6553.

Selected Book Chapters and Review Articles (from 96 Publications)

• White PC, Speiser PW. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocrine Reviews 2000; 21(3):245-291.
• Felner EI, White PC. Management of diabetic ketoacidosis. Recent Advances in Paediatrics 2003; 20:113-124.
• White PC. Aldosterone: direct effects on and production by the heart. Journal of Endocrinology and Metabolism 2003; 88(6):2376-2383.
• Speiser PW, White PC. Congenital adrenal hyperplasia. New England Journal of Medicine 2003; 349(8):776-788.
• Levine LS, White PC. Disorders of the adrenal glands. In: Behrman RE, Kliegman RM, Jenson HB, editors. Nelson Textbook of Pediatrics. Philadelphia, PA: Saunders, 2004: 1898-1921.
• White PC. Aldosterone synthase deficiency and related disorders. Molecular and Cellular Endocrinology 2004; 217(1-2):81-87.
• White PC, Rainey WE.  Polymorphisms in CYP11B genes and 11-hydroxylase activity. Journal of Clinical Endocrinology and Metabolism 2005; 90(2):1252-1255.
• Stewart SM, Rao U, White PC. Depression and diabetes in children and adolescents. Current Opinion in Pediatrics 2005; 17:626-631.
• White PC. Ontogeny of adrenal steroid biosynthesis: why girls will be girls. Journal of Clinical Investigation 2006;116(4):872-874.

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Bryan A. Dickson, M.D.

Peer Reviewed Publications

• Dickson BA, Franks RC. Aldosterone-producing adenoma presenting with hypokalemic myopathy. Clinical Pediatrics 1988; 27(7):344-347.
• Smith EP, Dickson BA, Chernausek SD. Insulin-like growth factor binding protein-3 secretion from cultured rat sertoli cells: dual regulation by follicle stimulating hormone and insulin-like growth factor-I. Endocrinology 1990; 127(6):2744-2751.
• Chernausek SD, Dickson BA, Smith EP, Hoath SB. Suppression of insulin-like growth factor I during epidermal growth factor-induced growth retardation. American Journal of Physiology 1991; 260(3 Pt 1):E416-E421.
• Murray MA, Dickson BA, Smith EP, Hoath SB, Chernausek SD. Epidermal growth factor stimulates insulin-like growth factor-binding protein-1 expression in the neonatal rat. Endocrinology 1993; 133(1):159-165.
• Meier DE, Snyder WH 3rd, Dickson BA, Margraf LR, Guzzetta PC Jr. Parathyroid carcinoma in a child. Journal of Pediatric Surgery 1999; 34(4):606-608.
• Felner EI, Thompson MT, Ratliff AF, White PC, Dickson BA. Time course of recovery of adrenal function in children treated for leukemia. Journal of Pediatrics 2000; 137(1):21-24.

Book Chapters and Review Articles

• Dickson BA. Thyrotoxic crisis and euthroid sick syndrome. In: Levin DL, Morriss FC, editors. Essentials of Pediatric Intensive Care. New York: Churchill Livingstone, Inc., 1997: 577-580.
• Dickson BA. Syndrome of inappropriate antidiuretic hormone secretion. In: Levin DL, Morriss FC, editors. Essentials of Pediatric Intensive Care. New York: Churchill Livingstone, Inc., 1997: 581-583.

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Melissa R. Ham, M.D.

Peer Reviewed Publications

• Ham MR, Okada P, White PC. Bedside ketone determination in diabetic children with hyperglycemia and ketosis in the acute care setting. Pediatric Diabetes 2004; 5(1):39-43.
• Felner EI, Klitz W, Ham M, Lazaro AM, Stastny P, Dupont B et al. Interaction of Age of Onset with Genetic Risk Factors for Type 1 Diabetes. Journal of Pediatric Diabetes 2005; 6(4):213-220.

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Michele R. Hutchison, M.D., Ph.D.

Peer Reviewed Publications

• Wolfson AJ, Hutchison MR, Andrews JS, Merriam KJ. Effects of charcoal on dissociation kinetics of nuclear and cytosolic steroid-receptor complexes from hen oviduct. Journal of Receptor Research 1990; 10(3-4):137-148.
• Gama Sosa MA, Rosas DH, DeGasperi R, Morita E, Hutchison MR, Ruprecht RM. Negative regulation of the 5' long terminal repeat (LTR) by the 3' LTR in the murine proviral genome. Journal of Virology 1994; 68(4):2662-2670.
• Cobb MH, Xu S, Hepler JE, Hutchison M, Frost J, Robbins DJ. Regulation of the MAP kinase cascade. Cellular & Molecular Biology Research 1994; 40(3):253-256.
• Polverino A, Frost J, Yang P, Hutchison M, Neiman AM, Cobb MH et al. Activation of mitogen-activated protein kinase cascades by p21-activated protein kinases in cell-free extracts of Xenopus oocytes. Journal of Biological Chemistry 1995; 270(44):26067-26070.
• Frost JA, Xu S, Hutchison MR, Marcus S, Cobb MH. Actions of Rho family small G proteins and p21-activated protein kinases on mitogen-activated protein kinase family members. Molecular & Cellular Biology 1996; 16(7):3707-3713.
• Hutchison M, Berman KS, Cobb MH. Isolation of TAO1, a protein kinase that activates MEKs in stress-activated protein kinase cascades. Journal of Biological Chemistry 1998; 273(44):28625-28632.
• Chen Z, Hutchison M, Cobb MH. Isolation of the protein kinase TAO2 and identification of its mitogen-activated protein kinase/extracellular signal-regulated kinase kinase binding domain. Journal of Biological Chemistry 1999; 274(40):28803-28807.
• Berman, KS, Hutchison M, Avery L, Cobb MH. kin-18, a C. elegans protein kinase involved in feeding. Gene 2001; 279(2):137-147.

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Ellen C. Kaizer, M.D.

Peer Reviewed Publications

• Ressler C, Tatake JG, Kaizer E, Putnam DH. Neurotoxins in a vetch food: stability to cooking and removal of γ-glutamyl-β-cyanoalanine and β-cyanoalanine and acute toxicity from common vetch (vicia sativa l.) legumes. Journal of Agricultural Food Chemistry 1997; 45(1):189-194.
• Borel MJ, Williams PE, Jabbour K, Levenhagen D, Kaizer E, Flakoll PJ. Parenteral glutamine infusion alters insulin-mediated glucose metabolism. Journal of Parenteral & Enteral Nutrition 1998; 22(5):280-285.
• Kachur SP, Khatib RA, Kaizer E, Fox SS, Abdulla SM, Bloland PB. Adherence to antimalarial combination therapy with sulfadoxine-pyrimethamine and artesunate in rural Tanzania. American Journal of Tropical Medicine and Hygiene 2004; 71(6):715-722.

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Bassil M. Kublaoui, M.D., Ph.D.

Peer Reviewed Publications

• Kublaoui B, Lee J, Pilch PF. Dynamics of signaling during insulin-stimulated endocytosis of its receptor in adipocytes. Journal of Biological Chemistry 1995; 270(1):59-65.
• Liu H, Kublaoui B, Pilch PF, Lee J. Insulin activation of mitogen-activated protein (MAP) kinase and Akt is phosphatidylinositol 3-kinase-dependent in rat adipocytes. Biochemical & Biophysical Research Communications 2000; 274(3):845-851.
• Holder JL, Zhang L, Kublaoui BM, DiLeone RJ, Oz OK, Bair CH, Lee YH, Zinn AR. Sim1 gene dosage modulates the homeostatic feeding response to increase dietary fat in mice. American Journal of Physiology: Endocrinology and Metabolism 2004; 287(1):E105-E113.
• Kublaoui BM, Holder JL Jr, Gemelli T, Zinn AR. Sim1 haploinsufficiency impairs melanocortin-mediated anorexia and activation of paraventricular nucleus neurons. Molecular Endocrinology 2006;20(10):2483-2492.
• Kublaoui BM, Holder JL Jr, Tolson KP, Gemelli T, Zinn AR. SIM1 overexpression partially rescues agouti yellow and diet-induced obesity by normalizing food intake. Endocrinology 2006;147(10):4542-4549.

Book Chapters and Review Articles

• Kublaoui BM, Zinn AR. Editorial: MC4R mutations--weight before screening! Journal of Clinical Endocrinology and Metabolism 2006;91(5):1671-1672.

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D. Randy McMillan, Ph.D.

Peer Reviewed Publications

• McMillan DR, Faust C. The expression and characterization of rat IgE produced by construction of the epsilon-heavy chain gene from exon modules. Journal of Biological Chemistry 1992; 267(7):4904-4910.
• McMillan DR, Xiao X, Shao L, Graves K, Benjamin IJ. Targeted disruption of heat shock transcription factor 1 abolishes thermotolerance and protection against heat-inducible apoptosis. Journal of Biological Chemistry 1998; 273(13):7523-7528.
• Xiao X, Zuo X, Davis AA, McMillan DR, Curry BB, Richardson JA et al. HSF1 is required for extra-embryonic development, postnatal growth and protection during inflammatory responses in mice. EMBO Journal 1999; 18(21):5943-5952.
• Nikkila H, McMillan DR, Nunez BS, Pascoe L, Curnow KM, White PC. Sequence similarities between a novel putative G protein-coupled receptor and Na /Ca² exchangers define a cation binding domain. Molecular Endocrinology 2000; 14(9):1351-1364.
• McMillan DR, Kayes-Wandover KM, Richardson JA, White PC. Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system. Journal of Biological Chemistry 2002; 277(1):785-792.
• McMillan DR, Christians E, Forster M, Xiao X, Connell P, Plumier JC. et al. Heat shock transcription factor 2 is not essential for embryonic development, fertility, or adult cognitive and psychomotor function in mice. Molecular & Cellular Biology 2002; 22(22):8005-8014.
• McMillan DR, White PC. Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice. Molecular & Cellular Neuroscience 2004; 26(2):322-329.
• Gibert Y, McMillan DR, Kayes-Wandover K, Meyer A, Begemann G, White PC. Analysis of the very large G-protein coupled receptor gene (Vlgr1/Mass1/USH2C) in zebrafish. Gene 2005; 353(2):200-206.
• McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG et al. The Very Large G-Protein Coupled Receptor, VLGR1, a component of the ankle link complex required for the normal development of auditory hair bundles. Journal of Neuroscience 2006; 26(24):6543-6553.

Book Chapters and Review Articles

• McMillan DR, Gething MJ, Sambrook J. The cellular response to unfolded proteins: intercompartmental signaling. Current Opinion in Biotechnology 1994; 5(5):540-545.
• Benjamin IJ, McMillan DR. Stress (heat shock) proteins: molecular chaperones in cardiovascular biology and disease. Circulation Research 1998; 83(2):117-132.

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Sudha L. Mootha, M.D.

Peer Reviewed Publications

• Mootha SL, Barkovich AJ, Grumbach MM, Edwards MS, Gitelman SE, Kaplan SL et al. Idiopathic hypothalamic diabetes insipidus, pituitary stalk thickening, and the occult intracranial germinoma in children and adolescents. Journal of Clinical Endocrinology and Metabolism 1997;82(5):1362-1367.

• Mootha SL, Riley WJ, Brosnan PG. Hypothalamic-pituitary dysfunction associated with Moyamoya disease in children. Journal of  Pediatric Endocrinology and Metabolism 1999; 12(3):449-53.

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Jon D. Oden, M.D.

Peer Reviewed Publications

• Oden J, Bourgeois M. Neonatal endocrinology. Indian Journal of Pediatrics 2000; 67(3):217-223.
• Freemark M, Avril I, Fleenor D, Driscoll P, Petro A, Opara E et al. Targeted deletion of the PRL receptor: effects on islet development, insulin production, and glucose tolerance. Endocrinology 2002; 143(4):1378-1385.
• Oden J, Freemark M. Thyroxine supplementation in preterm infants: critical analysis. Current Opinion in Pediatrics 2002; 14(4):447-452.
• Oden J, Fleenor D, Driscoll P, Freemark M. Leptin in the newborn mouse. Plasma concentrations, characterization of the circulating hormone, and tissue source. Biology of the Neonate 2002; 82(2):109-116.
• Litton J, Rice A, Friedman N, Oden J, Lee MM, Freemark M. Insulin pump therapy in toddlers and preschool children with type 1 diabetes mellitus. Journal of Pediatrics 2002; 141(4):490-495.
• Oden J, Cheifetz IM. Neonatal Thyrotoxicosis and Persistent Pulmonary Hypertension Necessitating Extracorporeal Life Support. Pediatrics 2005; 115:e105-e108. 

Book Chapters and Review Articles

• Oden J, Treem WR. Inborn errors of fasting adaptation. In: Walker WA, Watkins JR, Duggan C, editors. Nutrition in Pediatrics:  Basic Science and Clinical Applications. Hamilton, Ontario: BC Decker Inc., 2004: 591-608.

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Grace M. Tannin, M.D.

Peer Reviewed Publications

• Lorberboym M, Sarker SD, Speiser P, Tannin G, New MI. Bilateral adrenal uptake of gallium-67 citrate in a patient with congenital adrenal hyperplasia. Clinical Nuclear Medicine 1990; 15:849.
• Tannin GM, Agarwal AK, Monder C, New MI, White PC. The human gene for 11 beta-hydroxysteroid dehydrogenase. Structure, tissue distribution, and chromosomal localization. Journal of Biological Chemistry 1991; 266(25):16653-16658.
• Speiser PW, New MI, Tannin GM, Pickering D, Yang SY, White PC. Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Human Genetics 1992; 88(6):647-648.
• Nikkila H, Tannin GM, New MI, Taylor NF, Kalaitzoglou G, Monder C et al. Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency. Journal of Clinical Endocrinology & Metabolism 1993; 77(3):687-691.
• Cuttler L, Silvers JB, Singh J, Marrero U, Finkelstein B, Tannin G et al. Short stature and growth hormone therapy. A national study of physician recommendation patterns. JAMA 1996; 276(7):531-537.
• Kayes-Wandover KM, Tannin GM, Shulman D, Peled D, Jones KL, Karaviti L et al. Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene. Journal of Clinical Endocrinology & Metabolism 2001; 86(11):5379-5382.

Book Chapters and Review Articles

• White PC, Pascoe L, Curnow KM, Tannin G, Rysler A. Molecular biology of 11β-hydroxylase and 11β-hydroxysteroid dehydrogenase enzymes. Journal of Steroid Biochemistry and Molecular Biology 1992; 43(8):827-835.
• White PC, Tannin GM, Obeid J, Curnow KM, Pascoe L. Aldosterone synthesis and receptor specificity: 11β-hydroxylase ad 11β-dehydrogenase. In: Saez JM, Brownie AC, Capponi A, Chambaz EM, Mantero F, editors. Cellular and Molecular Biology of the Adrenal Cortex. Montrogue, France: John Libbey Eurotext Ltd., 1992: 163-173.
• New MI, Tannin G, Curtis JA, Vogiatzi M. Enzyme defects and adrenal insufficiency. In: Bhatt HR, James VHT, Besser GM, Bottazzo GF, Keen H, editors. Advances in Thomas Addison's Diseases. Bristol, UK: Journal of Endocrinology, Ltd., 1994: 163-164.
• White PC, Obeid J, Agarwal AK, Tannin GM, Nikkila H. Genetic analysis of 11β-hydroxysteroid dehydrogenase. Steroids 1994; 59(2):111-115.

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Fellows

Soumya Adhikari, M.D.

Peer Reviewed Publications

• Dunstan CA, Salafranca MN, Adhikari S, Xia Y, Feng L, Harrison JK. Identification of two rat genes orthologous to the human interleukin-8 receptors. Journal of Biological Chemistry 1996; 271(51):32770-32776.
• Jiang Y, Salafranca MN, Adhikari S, Xia Y, Feng L, Sonntag MK et al. Chemokine receptor expression in cultured glia and rat experimental allergic encephalomyelitis. Journal of Neuroimmunology 1998; 86(1):1-12.
• http://www.utsouthwestern.edu/utsw/mytask/wrapper/0,2457,,00.htmlHarrison JK, Jiang Y, Chen S, Xia Y, Maciejewski D, McNamara RK et al. Role for neuronally derived fractalkine in mediating interactions between neurons and CX3CR1-expressing microglia. Proceedings of the National Academy of Sciences of the United States of America 1998; 95(18):10896-10901.

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Jill Ann Goldfarb, M.D.

Book Chapters and Review Articles

• Goldfarb JA. For parents: Treating Type 2 diabetes in children. Diabetes Self Management 2005; 22(4):80-83.

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Shuchi Shah, M.D.

Peer Reviewed Publications

• Shah S, Miller PR, Meredith JW, Chang MC. Elevated Admission White Blood Cell Count in Pregnant Trauma Patients: An Indicator of Ongoing Placental Abruption.  The American Surgeon 2002; 68(7):644-647.
• Shah S, Doyle K, Lange EM, Shen P, Pennell T, Ferree C et al. Breast Cancer Recurrences in Elderly Patients after Lumpectomy. The American Surgeon 2002; 68(8):735-739.

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Research Staff

Kelli A. Black

Peer Reviewed Publications

• Hong YS, Hogan JR, Wang X, Sarkar A, Sim C, Loftus BJ et al. Construction of a BAC library and generation of BAC end sequence-tagged connectors for genome sequencing of the African malaria mosquito Anopheles gambiae. Molecular Genetics and Genomics 2003; 268(6):720-728.

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Daniela C. Rogoff, M.D., Ph.D.

Peer Reviewed Publications

• Rogoff D, Smolenicka Z, Bergadá I, Vallejo G, Barontini M, Heinrich JJ et al. The Codon 213 of the 11β-Hydroxysteroid Dehydrogenase Type 2 Gene Is a Hot Spot for Mutations in Apparent Mineralocorticoid Excess. Journal of Clinical Endocrinology and Metabolism 1998; 83(12):4391-4393.
• Rogoff D, Bergadá I, Venara M, Chemes H, Heinrich JJ,Barontini M. Intermittent hyperaldosteronism in a child due to an adrenal adenoma. European Journal of Pediatrics 2001; 160(2):114-116.
• Rogoff D, Gomez-Sanchez CE, Foecking MF, Wortsman J, Slominski A. Steroidogenesis in the human skin: 21-hydroxylation in cultured keratinocytes. Journal of Steroid Biochemistry and Molecular Biology 2001; 78(1):77-81.

Book Chapters and Review Articles

• Barontini M, Rogoff D. Hipertensión de origen endocrino. In: Beas F editor. Endocrinología del niño y el adolescente - 2ª edición. Santiago, Chile: Editorial Mediterránea, 2002: 334-350.

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