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Lancet (London, England)
|
July 31, 1976
Inheritance in protoporphyria. Comparison of haem synthetase activity in skin fibroblasts with clinical features
J R Bloomer, H L Bonkowsky, P S Ebert, et al.
Current Problems in Dermatology
|
January 1, 1991
Heme synthesis in protoporphyria
J R Bloomer, H D Hill, A M Kools, et al.
Gastroenterology
|
September 1, 1983
Enzymatic formation of zinc-protoporphyrin by rat liver and its potential effect on hepatic heme metabolism
J R Bloomer, R J Reuter, K O Morton, et al.
JAMA
|
October 11, 1971
Interpretation of plasma bilirubin levels based on studies with radioactive bilirubin
J R Bloomer, P D Berk, R B Howe, et al.
The American Journal of Medicine
|
June 1, 1975
Hepatic disease in erythropoietic protoporphyria
J R Bloomer, M J Phillips, D L Davidson, et al.
American Journal of Human Genetics
|
March 1, 1982
Bovine protoporphyria: documentation of autosomal recessive inheritance and comparison with the human disease through measurement of heme synthase activity
J R Bloomer, K O Morton, R J Reuter, 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 disease
M M Jenkins, R D LeBoeuf, G R Ruth, et al.
The Journal of Laboratory and Clinical Medicine
|
March 1, 1970
Preparation and properties of specifically labeled radiochemically stable 3H-bilirubin
R B Howe, P D Berk, J R Bloomer, et al.
The American Journal of Medicine
|
September 1, 1970
Constitutional hepatic dysfunction (Gilbert's syndrome). A new definition based on kinetic studies with unconjugated radiobilirubin
P D Berk, J R Bloomer, R B Howe, et al.
American Journal of Veterinary Research
|
July 1, 1990
Comparison of bile porphyrin concentrations in cattle and human beings with protoporphyria
J R Bloomer, J G Straka, H Hill, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 102) with videos related to
Sort By:
Page
of 11
Lancet (London, England)
|
July 31, 1976
Inheritance in protoporphyria. Comparison of haem synthetase activity in skin fibroblasts with clinical features
J R Bloomer, H L Bonkowsky, P S Ebert, et al.
Current Problems in Dermatology
|
January 1, 1991
Heme synthesis in protoporphyria
J R Bloomer, H D Hill, A M Kools, et al.
Gastroenterology
|
September 1, 1983
Enzymatic formation of zinc-protoporphyrin by rat liver and its potential effect on hepatic heme metabolism
J R Bloomer, R J Reuter, K O Morton, et al.
JAMA
|
October 11, 1971
Interpretation of plasma bilirubin levels based on studies with radioactive bilirubin
J R Bloomer, P D Berk, R B Howe, et al.
The American Journal of Medicine
|
June 1, 1975
Hepatic disease in erythropoietic protoporphyria
J R Bloomer, M J Phillips, D L Davidson, et al.
American Journal of Human Genetics
|
March 1, 1982
Bovine protoporphyria: documentation of autosomal recessive inheritance and comparison with the human disease through measurement of heme synthase activity
J R Bloomer, K O Morton, R J Reuter, 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 disease
M M Jenkins, R D LeBoeuf, G R Ruth, et al.
The Journal of Laboratory and Clinical Medicine
|
March 1, 1970
Preparation and properties of specifically labeled radiochemically stable 3H-bilirubin
R B Howe, P D Berk, J R Bloomer, et al.
The American Journal of Medicine
|
September 1, 1970
Constitutional hepatic dysfunction (Gilbert's syndrome). A new definition based on kinetic studies with unconjugated radiobilirubin
P D Berk, J R Bloomer, R B Howe, et al.
American Journal of Veterinary Research
|
July 1, 1990
Comparison of bile porphyrin concentrations in cattle and human beings with protoporphyria
J R Bloomer, J G Straka, H Hill, et al.
Page
of 11