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J R Bloomer

Showing results (81-90 of 102) with videos related to

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The Journal of Pediatrics|March 1, 1987
Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantationM Tuchman, D K Freese, H L Sharp, et al.
The Journal of Biological Chemistry|January 15, 1987
The enzyme defect in bovine protoporphyria. Studies with purified ferrochelataseJ R Bloomer, H D Hill, K O Morton, et al.
The Journal of Clinical Investigation|September 1, 1972
Quantitative studies of the delivery of hepatic-synthesized bilirubin to plasma utilizing -aminolevulinic acid-4- 14 C and bilirubin- 3 H in manE A Jones, R Shrager, J R Bloomer, et al.
Gut|February 1, 1980
Benign recurrent intrahepatic cholestasis: studies of bilirubin kinetics, bile acids, and cholangiographyJ A Summerfield, J Scott, M Berman, et al.
The Journal of Pediatrics|January 1, 1991
Hematin therapy for the neurologic crisis of tyrosinemiaJ M Rank, A Pascual-Leone, W Payne, et al.
British Journal of Haematology|August 1, 1990
Hematin therapy in late onset congenital erythropoietic porphyriaJ M Rank, J G Straka, M K Weimer, et al.
Digestive Diseases (Basel, Switzerland)|November 1, 1995
Review of support systems used in the management of fulminant hepatic failureB M McGuire, T D Sielaff, S L Nyberg, et al.
JAMA|January 2, 1987
Red blood cell porphobilinogen deaminase in the evaluation of acute intermittent porphyriaC A Pierach, M K Weimer, R A Cardinal, et al.
The American Journal of Surgical Pathology|January 1, 1987
Liver allograft rejection. An analysis of the use of biopsy in determining outcome of rejectionD C Snover, D K Freese, H L Sharp, et al.
Gastroenterology|July 1, 1989
Liver transplantation in a patient with protoporphyriaJ R Bloomer, M K Weimer, I C Bossenmaier, et al.
Pageof 11

Showing results (81-90 of 102) with videos related to

Sort By:
Pageof 11
The Journal of Pediatrics|March 1, 1987
Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantationM Tuchman, D K Freese, H L Sharp, et al.
The Journal of Biological Chemistry|January 15, 1987
The enzyme defect in bovine protoporphyria. Studies with purified ferrochelataseJ R Bloomer, H D Hill, K O Morton, et al.
The Journal of Clinical Investigation|September 1, 1972
Quantitative studies of the delivery of hepatic-synthesized bilirubin to plasma utilizing -aminolevulinic acid-4- 14 C and bilirubin- 3 H in manE A Jones, R Shrager, J R Bloomer, et al.
Gut|February 1, 1980
Benign recurrent intrahepatic cholestasis: studies of bilirubin kinetics, bile acids, and cholangiographyJ A Summerfield, J Scott, M Berman, et al.
The Journal of Pediatrics|January 1, 1991
Hematin therapy for the neurologic crisis of tyrosinemiaJ M Rank, A Pascual-Leone, W Payne, et al.
British Journal of Haematology|August 1, 1990
Hematin therapy in late onset congenital erythropoietic porphyriaJ M Rank, J G Straka, M K Weimer, et al.
Digestive Diseases (Basel, Switzerland)|November 1, 1995
Review of support systems used in the management of fulminant hepatic failureB M McGuire, T D Sielaff, S L Nyberg, et al.
JAMA|January 2, 1987
Red blood cell porphobilinogen deaminase in the evaluation of acute intermittent porphyriaC A Pierach, M K Weimer, R A Cardinal, et al.
The American Journal of Surgical Pathology|January 1, 1987
Liver allograft rejection. An analysis of the use of biopsy in determining outcome of rejectionD C Snover, D K Freese, H L Sharp, et al.
Gastroenterology|July 1, 1989
Liver transplantation in a patient with protoporphyriaJ R Bloomer, M K Weimer, I C Bossenmaier, et al.
Pageof 11