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pro vyhledávání: '"Eric S. Orwoll"'
Autor:
Eric S. Orwoll
Publikováno v:
New England Journal of Medicine. 374:2514-2517
Funding for older scientists represents an increasingly large proportion of NIH dollars awarded, a trend with important consequences for the scientific workforce. But we can more actively encourage the transfer of knowledge and resources between gene
Autor:
Richard D. Smith, Tujin Shi, Kerry S Jones, Inez Schoenmakers, Joseph M. Zmuda, Christine G. Lee, Ann Prentice, Carrie M. Nielson, Yuqian Gao, Roger Bouillon, Jane A. Cauley, Christine M. Swanson, Dirk Vanderschueren, Eric S. Orwoll, Rene F. Chun, John S. Adams, Martin Hewison, Jon M. Jacobs, Ying Wang, Jodi Lapidus, Steven Pauwels
Publikováno v:
New England Journal of Medicine. 374:1695-1696
The choice of a vitamin D–binding protein assay is key in calculating free 25-hydroxyvitamin D levels. The results of this analysis support the use of total 25-hydroxyvitamin D as a marker of vitamin D status, regardless of race or GC genotype.
Autor:
Eric S. Orwoll
Publikováno v:
New England Journal of Medicine. 374:682-683
Aging is variably but inevitably accompanied by declines in health; concomitantly, in men, circulating sex-steroid levels fall with age.1 To what extent these two processes are causally linked and whether testosterone therapy can prevent or ameliorat
Autor:
Mark P. Ettinger, Silvano Adami, Stuart J. Weiss, Kristel Vandormael, Peter Pietschmann, John J. Graham, Eric S. Orwoll, David L. Kendler, Paul D. Miller, Antonio Lombardi, Roman S. Lorenc, K. Weber
Publikováno v:
New England Journal of Medicine. 343:604-610
Despite its association with disability, death, and increased medical costs, osteoporosis in men has been relatively neglected as a subject of study. There have been no large, controlled trials of treatment in men.In a two-year double-blind trial, we
Autor:
Eric S. Orwoll, Janet Reeder
Publikováno v:
New England Journal of Medicine. 355:e28
In adults with osteogenesis imperfecta, a wide spectrum of skeletal manifestations is apparent. Many mutations in the type I collagen gene are associated with this disorder.