Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
5T32DK007011-28
Application #
6380216
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Hyde, James F
Project Start
1975-07-01
Project End
2005-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
28
Fiscal Year
2001
Total Cost
$224,799
Indirect Cost
Name
University of Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Mimoto, Mizuho S; Oyler, Julie L; Davis, Andrew M (2018) Evaluation and Treatment of Hirsutism in Premenopausal Women. JAMA 319:1613-1614
Dickens, Laura T; Naylor, Rochelle N (2018) Clinical Management of Women with Monogenic Diabetes During Pregnancy. Curr Diab Rep 18:12
Mimoto, Mizuho S; Nadal, Angel; Sargis, Robert M (2017) Polluted Pathways: Mechanisms of Metabolic Disruption by Endocrine Disrupting Chemicals. Curr Environ Health Rep 4:208-222
Chou, Sharon H; Vokes, Tamara J; Ma, Siu-Ling et al. (2014) Simplified criteria for selecting patients for vertebral fracture assessment. J Clin Densitom 17:386-91
Chou, Sharon H; Hwang, Jessica; Ma, Siu-Ling et al. (2014) Utility of heel dual-energy X-ray absorptiometry in diagnosing osteoporosis. J Clin Densitom 17:16-24
Hwang, Jessica L; Weiss, Roy E (2014) Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment. Diabetes Metab Res Rev 30:96-102
Sriphrapradang, Chutintorn; German, Alina; Dumitrescu, Alexandra M et al. (2012) Consecutive mutational events in a TSHR allele of Arab families with resistance to thyroid stimulating hormone. Thyroid 22:252-7
Hermanns, Pia; Grasberger, Helmut; Refetoff, Samuel et al. (2011) Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis. J Clin Endocrinol Metab 96:E977-81
Hulur, Imge; Hermanns, Pia; Nestoris, Claudia et al. (2011) A single copy of the recently identified dual oxidase maturation factor (DUOXA) 1 gene produces only mild transient hypothyroidism in a patient with a novel biallelic DUOXA2 mutation and monoallelic DUOXA1 deletion. J Clin Endocrinol Metab 96:E841-5
Sriphrapradang, Chutintorn; Tenenbaum-Rakover, Yardena; Weiss, Mia et al. (2011) The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation. J Clin Endocrinol Metab 96:E1001-6

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