Showing results (761-770 of 1,205) with videos related to
Sort By:
Pageof 121
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Tumor necrosis factor increases serum leptin levels in humansM S Zumbach, M W Boehme, P Wahl, et al.Statistical Analysis and Data Mining|April 5, 2011
Controlling the False Discovery Rate for Feature Selection in High-resolution NMR SpectraSeoung Bum Kim, Victoria C P Chen, Youngja Park, et al.Physics in Medicine and Biology|December 23, 2008
Investigation of detection limits for diffuse optical tomography systems: I. Theory and experimentR Ziegler, B Brendel, A Schipper, et al.Endocrinology|June 30, 1998
Intestinal adaptation after extensive small bowel resection: differential changes in growth and insulin-like growth factor system messenger ribonucleic acids in jejunum and ileumT R Ziegler, M P Mantell, J C Chow, et al.Diabetes|April 1, 1991
Implication of specific DQB1 alleles in genetic susceptibility and resistance by identification of IDDM siblings with novel HLA-DQB1 allele and unusual DR2 and DR1 haplotypesH A Erlich, R L Griffith, T L Bugawan, et al.Journal of Prosthetics and Orthotics : JPO|September 9, 2008
Comparison of Rectified and Unrectified Sockets for Transtibial AmputeesJack R Engsberg, S Wayne Sprouse, Mary L Uhrich, et al.Annals of Surgery|September 1, 1995
A new treatment for patients with short-bowel syndrome. Growth hormone, glutamine, and a modified dietT A Byrne, R L Persinger, L S Young, et al.The American Journal of Physiology|November 1, 1996
Gut adaptation and the insulin-like growth factor system: regulation by glutamine and IGF-I administrationT R Ziegler, M P Mantell, J C Chow, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Severe osteoporosis in familial Hajdu-Cheney syndrome: progression of acro-osteolysis and osteoporosis during long-term follow-upG Leidig-Bruckner, J Pfeilschifter, N Penning, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[Aspartylglucosaminuria. Clinical description of 2 German patients]R Ziegler, H Schmidt, A C Sewell, et al.Pageof 121