Zobrazeno 1 - 10
of 51
pro vyhledávání: '"O. Rennert"'
Autor:
John B. Bodensteiner, D. Oshman, Bradley G. Schaefer, J. Wall, O. Rennert, S. Stein, Gary R. Thurnau, O. Brown
Publikováno v:
Clinical Genetics. 30:381-391
We describe a mother and her male infant affected with a craniotubular dysplasia characterized by severe craniofacial hyperostosis and sclerosis with obliteration of paranasal sinuses and foramina of the skull base. Subsequent severe bilateral hearin
Autor:
M, Raygada, O, Rennert
Publikováno v:
Clinical genetics. 67(1)
Congenital generalized Lipodystrophy (BSCL) or Berardinelli-Seip syndrome (Mendelian inheritance in man, catalog no. 269700) is a rare autosomal recessive syndrome characterized by paucity of body fat since birth and insulin resistance. The pathophys
Publikováno v:
Archives of Disease in Childhood. 47:830-833
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Publikováno v:
Kidney international. Supplement. 16
Eighteen uremic patients received i.v. infusions of a mixture of amino acids three times per week for 3 months in an effort to improve cellular amino acid imbalance and related cell bioactivities. They were a subset of 42 uremic patients stabilized b
Publikováno v:
Texas reports on biology and medicine. 34(1)
The effect of plasma or serum from homozygotes and heterozygotes for the cystic fibrosis (CF) gene on the active uptake of 3-0-14C-methyl-D-glucose (3-0-14C-MDG) by rat jejunal epithelium was studied. Furthermore, the role of the polyamine, spermidin
Publikováno v:
Blood. 47(4)
High-pressure liquid chromatography analysis of polyamines in bone narrow from leukemic and nonleukemic subjects demonstrated increased concentrations of putrescine, spermidine, and spermine associated with increased cellularity. The most striking ab
Autor:
A, Dekaban, O, Rennert
Publikováno v:
Journal of neuropathology and experimental neurology. 26(1)
Publikováno v:
The Journal of the Florida Medical Association. 57(9)