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The Yale Journal of Biology and Medicine|December 1, 1974
Variation in hepatic bile composition following cholecystectomy in patients with previous gallstonesJ L Boyer, J R Bloomer, W C Maddrey, et al.
Gastroenterology|March 1, 1977
Serum alpha-fetoprotein in patients with massive hepatic necrosisJ R Bloomer, T A Waldmann, K R McIntire, et al.
JAMA|July 7, 1975
alpha-fetoprotein in noneoplastic hepatic disordersJ R Bloomer, T A Waldmann, K R McIntire, et al.
The Journal of Clinical Investigation|November 1, 1975
Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblastsH L Bonkowsky, J R Bloomer, P S Ebert, et al.
Lancet (London, England)|July 31, 1976
Inheritance in protoporphyria. Comparison of haem synthetase activity in skin fibroblasts with clinical featuresJ R Bloomer, H L Bonkowsky, P S Ebert, et al.
Gastroenterology|September 1, 1983
Enzymatic formation of zinc-protoporphyrin by rat liver and its potential effect on hepatic heme metabolismJ R Bloomer, R J Reuter, K O Morton, et al.
The American Journal of Medicine|June 1, 1975
Hepatic disease in erythropoietic protoporphyriaJ R Bloomer, M J Phillips, D L Davidson, et al.
Biochimica Et Biophysica Acta|October 24, 1998
A novel stop codon mutation (X417L) of the ferrochelatase gene in bovine protoporphyria, a natural animal model of the human diseaseM M Jenkins, R D LeBoeuf, G R Ruth, et al.
American Journal of Veterinary Research|July 1, 1990
Comparison of bile porphyrin concentrations in cattle and human beings with protoporphyriaJ R Bloomer, J G Straka, H Hill, et al.
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