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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 transplantation
M 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 ferrochelatase
J 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 man
E A Jones, R Shrager, J R Bloomer, et al.
Gut
|
February 1, 1980
Benign recurrent intrahepatic cholestasis: studies of bilirubin kinetics, bile acids, and cholangiography
J A Summerfield, J Scott, M Berman, et al.
The Journal of Pediatrics
|
January 1, 1991
Hematin therapy for the neurologic crisis of tyrosinemia
J M Rank, A Pascual-Leone, W Payne, et al.
British Journal of Haematology
|
August 1, 1990
Hematin therapy in late onset congenital erythropoietic porphyria
J 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 failure
B 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 porphyria
C 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 rejection
D C Snover, D K Freese, H L Sharp, et al.
Gastroenterology
|
July 1, 1989
Liver transplantation in a patient with protoporphyria
J R Bloomer, M K Weimer, I C Bossenmaier, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 102) with videos related to
Sort By:
Page
of 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 transplantation
M 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 ferrochelatase
J 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 man
E A Jones, R Shrager, J R Bloomer, et al.
Gut
|
February 1, 1980
Benign recurrent intrahepatic cholestasis: studies of bilirubin kinetics, bile acids, and cholangiography
J A Summerfield, J Scott, M Berman, et al.
The Journal of Pediatrics
|
January 1, 1991
Hematin therapy for the neurologic crisis of tyrosinemia
J M Rank, A Pascual-Leone, W Payne, et al.
British Journal of Haematology
|
August 1, 1990
Hematin therapy in late onset congenital erythropoietic porphyria
J 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 failure
B 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 porphyria
C 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 rejection
D C Snover, D K Freese, H L Sharp, et al.
Gastroenterology
|
July 1, 1989
Liver transplantation in a patient with protoporphyria
J R Bloomer, M K Weimer, I C Bossenmaier, et al.
Page
of 11