Funding Agency

Agency
National Institute of Health (NIH)
Institute
Food and Drug Administration (FDA)
Type
Research Project (R01)
Project #
5R01FD002568-02
Application #
7458123
Study Section
Special Emphasis Panel (ZFD1-SRC (99))
Program Officer
Lewis, Debra Y
Project Start
2004-09-30
Project End
2007-09-29
Budget Start
2005-09-30
Budget End
2006-09-29
Support Year
2
Fiscal Year
2005
Total Cost
Indirect Cost

  Institution

Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218

  Publications

Lin, Maria H; Numbenjapon, Nawaporn; Germain-Lee, Emily L et al. (2015) Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy. J Pediatr Endocrinol Metab 28:911-8
Muniyappa, Ranganath; Warren, Mary A; Zhao, Xiongce et al. (2013) Reduced insulin sensitivity in adults with pseudohypoparathyroidism type 1a. J Clin Endocrinol Metab 98:E1796-801
Joseph, Andrew W; Shoemaker, Ashley H; Germain-Lee, Emily L (2011) Increased prevalence of carpal tunnel syndrome in albright hereditary osteodystrophy. J Clin Endocrinol Metab 96:2065-73
Long, Dominique N; Levine, Michael A; Germain-Lee, Emily L (2010) Bone mineral density in pseudohypoparathyroidism type 1a. J Clin Endocrinol Metab 95:4465-75
Plagge, Antonius; Kelsey, Gavin; Germain-Lee, Emily L (2008) Physiological functions of the imprinted Gnas locus and its protein variants Galpha(s) and XLalpha(s) in human and mouse. J Endocrinol 196:193-214
Germain-Lee, Emily L (2006) Short stature, obesity, and growth hormone deficiency in pseudohypoparathyroidism type 1a. Pediatr Endocrinol Rev 3 Suppl 2:318-27