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American Industrial Hygiene Association Journal
|
February 1, 1977
A professional crisis
J W Hammond
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 28, 1973
Polyacrylamide gel electrophoresis as a method for differentiation and quantitation of serum enzymes hydrolysing phosphate monoesters
M Potter, J W Hammond
Journal of Inherited Metabolic Disease
|
January 1, 1996
Neonatal multiple acyl-CoA dehydrogenase deficiency: essentially absent fatty acid oxidation activity in proband but normal activity in parental cultured skin fibroblasts
W C Ip, J W Hammond, B Wilcken
Ecology and Evolution
|
December 3, 2019
Preaching to the choir or composing new verses? Toward a writerly climate literacy in introductory undergraduate biology
Meghan A Duffy, J W Hammond, Susan J Cheng
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 24, 1990
gamma-Glutamylglutamine identified in plasma and cerebrospinal fluid from hyperammonaemic patients
J W Hammond, M Potter, R Truscott, et al.
Biomedical Chromatography : BMC
|
February 1, 1986
Measurement of urinary cystine and cysteinyl-penicillamine in patients with cystinuria
D C Sampson, P M Stewart, J W Hammond
Journal of Inherited Metabolic Disease
|
January 1, 1995
Siblings with gamma-glutamyltransferase deficiency
J W Hammond, M Potter, B Wilcken, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Reduced glutathione, gamma-glutamylcysteine, cysteine and gamma-glutamylglutamine in gamma-glutamyltransferase deficiency
J W Hammond, M Potter, K G Sim, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Benign persistent orotic aciduria and the possibility of misdiagnosis of ornithine carbamoyltransferase deficiency
K H Carpenter, M Potter, J W Hammond, et al.
The Journal of Pediatrics
|
March 1, 1976
Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemia
L J Sheffield, D M Danks, J W Hammond, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
American Industrial Hygiene Association Journal
|
February 1, 1977
A professional crisis
J W Hammond
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 28, 1973
Polyacrylamide gel electrophoresis as a method for differentiation and quantitation of serum enzymes hydrolysing phosphate monoesters
M Potter, J W Hammond
Journal of Inherited Metabolic Disease
|
January 1, 1996
Neonatal multiple acyl-CoA dehydrogenase deficiency: essentially absent fatty acid oxidation activity in proband but normal activity in parental cultured skin fibroblasts
W C Ip, J W Hammond, B Wilcken
Ecology and Evolution
|
December 3, 2019
Preaching to the choir or composing new verses? Toward a writerly climate literacy in introductory undergraduate biology
Meghan A Duffy, J W Hammond, Susan J Cheng
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 24, 1990
gamma-Glutamylglutamine identified in plasma and cerebrospinal fluid from hyperammonaemic patients
J W Hammond, M Potter, R Truscott, et al.
Biomedical Chromatography : BMC
|
February 1, 1986
Measurement of urinary cystine and cysteinyl-penicillamine in patients with cystinuria
D C Sampson, P M Stewart, J W Hammond
Journal of Inherited Metabolic Disease
|
January 1, 1995
Siblings with gamma-glutamyltransferase deficiency
J W Hammond, M Potter, B Wilcken, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Reduced glutathione, gamma-glutamylcysteine, cysteine and gamma-glutamylglutamine in gamma-glutamyltransferase deficiency
J W Hammond, M Potter, K G Sim, et al.
Journal of Inherited Metabolic Disease
|
July 1, 1997
Benign persistent orotic aciduria and the possibility of misdiagnosis of ornithine carbamoyltransferase deficiency
K H Carpenter, M Potter, J W Hammond, et al.
The Journal of Pediatrics
|
March 1, 1976
Massive pulmonary hemorrhage as a presenting feature in congenital hyperammonemia
L J Sheffield, D M Danks, J W Hammond, et al.
Page
of 2