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Barry Rich

AddressChicago IL 60637
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Qin K, Du X, Rich BH. An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome. Mol Genet Metab. 2007 Dec; 92(4):359-63. PMID: 17911039.
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    2. Germann JN, Kirschenbaum DS, Rich BH, O'Koon JC. Long-term evaluation of multi-disciplinary treatment of morbid obesity in low-income minority adolescents: La Rabida Children's Hospital's FitMatters program. J Adolesc Health. 2006 Oct; 39(4):553-61. PMID: 16982391.
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    3. Germann JN, Kirschenbaum DS, Rich BH. Child and parental self-monitoring as determinants of success in the treatment of morbid obesity in low-income minority children. J Pediatr Psychol. 2007 Jan-Feb; 32(1):111-21. PMID: 16775083.
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    4. Kirschenbaum DS, Germann JN, Rich BH. Treatment of morbid obesity in low-income adolescents: effects of parental self-monitoring. Obes Res. 2005 Sep; 13(9):1527-9. PMID: 16222054.
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    5. Faulkner MS, Quinn L, Rimmer JH, Rich BH. Cardiovascular endurance and heart rate variability in adolescents with type 1 or type 2 diabetes. Biol Res Nurs. 2005 Jul; 7(1):16-29. PMID: 15920000.
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    6. Lipton RB, Drum M, Burnet D, Rich B, Cooper A, Baumann E, Hagopian W. Obesity at the onset of diabetes in an ethnically diverse population of children: what does it mean for epidemiologists and clinicians? Pediatrics. 2005 May; 115(5):e553-60. PMID: 15867020.
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    7. Lipton R, Drum M, Burnet D, Mencarini M, Cooper A, Rich B. Self-reported social class, self-management behaviors, and the effect of diabetes mellitus in urban, minority young people and their families. Arch Pediatr Adolesc Med. 2003 Sep; 157(9):919-25. PMID: 12963599.
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    8. Pang S, Wang W, Rich B, David R, Chang YT, Carbunaru G, Myers SE, Howie AF, Smillie KJ, Mason JI. A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun; 87(6):2556-63. PMID: 12050213.
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    9. Lutfallah C, Wang W, Mason JI, Chang YT, Haider A, Rich B, Castro-Magana M, Copeland KC, David R, Pang S. Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency. J Clin Endocrinol Metab. 2002 Jun; 87(6):2611-22. PMID: 12050224.
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    10. Christian SL, Rich BH, Loebl C, Israel J, Vasa R, Kittikamron K, Spiro R, Rosenfield R, Ledbetter DH. Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus. J Pediatr. 1999 Jan; 134(1):42-6. PMID: 9880447.
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    11. Gokhale R, Favus MJ, Karrison T, Sutton MM, Rich B, Kirschner BS. Bone mineral density assessment in children with inflammatory bowel disease. Gastroenterology. 1998 May; 114(5):902-11. PMID: 9558278.
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    12. Brown MR, Parks JS, Adess ME, Rich BH, Rosenthal IM, Voss TC, VanderHeyden TC, Hurley DL. Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. Horm Res. 1998; 49(2):98-102. PMID: 9485179.
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    13. Rosenthal IM, Refetoff S, Rich B, Barnes RB, Sunthornthepvarakul T, Parma J, Rosenfield RL. Response to challenge with gonadotropin-releasing hormone agonist in a mother and her two sons with a constitutively activating mutation of the luteinizing hormone receptor--a clinical research center study. J Clin Endocrinol Metab. 1996 Oct; 81(10):3802-6. PMID: 8855841.
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    14. Lucky AW, McGuire J, Rosenfield RL, Lucky PA, Rich BH. Plasma androgens in women with acne vulgaris. J Invest Dermatol. 1983 Jul; 81(1):70-4. PMID: 6223099.
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    15. Rosenfield RL, Rich BH, Lucky AW. Adrenarche as a cause of benign pseudopuberty in boys. J Pediatr. 1982 Dec; 101(6):1005-9. PMID: 6216332.
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    16. Rich BH, Rosenfield RL, Moll GW, Lucky AW, Roche-Bender N, Fang V. Bioactive luteinizing hormone pituitary reserves during normal and abnormal male puberty. J Clin Endocrinol Metab. 1982 Jul; 55(1):140-6. PMID: 7042735.
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    17. Rich BH, Rosenfield RL, Lucky AW, Helke JC, Otto P. Adrenarche: changing adrenal response to adrenocorticotropin. J Clin Endocrinol Metab. 1981 Jun; 52(6):1129-36. PMID: 6262366.
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    18. Lucky AW, Rich BH, Rosenfield RL, Fang VS, Roche-Bender N. Bioactive LH: a test to discriminate true precocious puberty from premature thelarche and adrenarche. J Pediatr. 1980 Aug; 97(2):214-6. PMID: 7400888.
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    19. Lucky AW, Rich BH, Rosenfield RL, Fang VS, Roche-Bender N. LH bioactivity increases more than immunoreactivity during puberty. J Pediatr. 1980 Aug; 97(2):205-13. PMID: 7400887.
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    20. Rosenfield RL, Rich BH, Wolfsdorf JI, Cassorla F, Parks JS, Bongiovanni AM, Wu CH, Shackleton CH. Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiency. J Clin Endocrinol Metab. 1980 Aug; 51(2):345-53. PMID: 6249838.
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    21. Schwartz SS, Rich BH, Lucky AW, Straus FH, Gonen B, Wolfsdorf J, Thorp FW, Burrington JD, Madden JD, Rubenstein AH, Rosenfield RL. Familial nesidioblastosis: severe neonatal hypoglycemia in two families. J Pediatr. 1979 Jul; 95(1):44-53. PMID: 383929.
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    22. Razdan AK, Fang VS, Rich BH, Britton H, Rosenfield RL. Gonadotropin-releasing hormone infusion test in the distinction of hypopituitary patients from normal subjects. Fertil Steril. 1979 May; 31(5):507-12. PMID: 376356.
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