Zobrazeno 1 - 5
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pro vyhledávání: '"Ross S. Kendall"'
Autor:
Barbara I. Brown, Ross S. Kendall, Eduardo J. Yunis, A. G. Tzakis, S. Todo, Thomas E. Starzl, Robert R. Selby
Publikováno v:
European Journal of Pediatrics. 152:71-76
Progressive liver failure or hepatic complications of the primary disease led to orthotopic liver transplantation in eight children with glycogen storage disease over a 9-year period. One patient had glycogen storage disease (GSD) type I (von Gierke
Autor:
Barbara I. Brown, Rick Selby, Thomas E. Starzl, Eduardo J. Yunis, Andreas G. Tzakis, Ross S. Kendall
Publikováno v:
New England Journal of Medicine. 324:39-42
Type IV glycogen storage disease is a rare autosomal recessive disorder (also called Andersen’s disease1 or amylopectinosis) in which the activity of branching enzyme alpha-1, 4-glucan: alpha-1, 4-glucan 6-glucosyltransferase is deficient in the li
Publikováno v:
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 36(4)
1 d rgan, stem-cell, small-intestinal, and bone-marrow translants have all documented diarrhea to be one of the major auses of post-operative morbidity and has led to longer hosital stays, increased diagnostic and treatment costs, and ven death (Cox
Publikováno v:
Gastroenterology. 80:380-383
A 3-yr 8-mo-old female was diagnosed as having a congenital stricture of the common hepatic duct. She demonstrated hepatomegaly with marked elevations of serum transaminases, alkaline phosphatase, and bile acids without clinical jaundice or hyperbili
Publikováno v:
American journal of diseases of children (1960). 134(9)
• A 13-year-old boy had obstructive jaundice following several episodes of blunt abdominal trauma. At surgery, a stricture of the common bile duct, for which no other cause could be found, was identified and corrected. We describe our approach to t