Search research articles
Contact Us
Filters
Showing results (261-270 of 351) with videos related to
Page
of 36
Sort By:
JIMD Reports
|
February 23, 2013
Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency
A A M Morris, S E Olpin, M J Bennett, et al.
Structure (London, England : 1993)
|
June 15, 1997
Steroid recognition and regulation of hormone action: crystal structure of testosterone and NADP+ bound to 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase
M J Bennett, R H Albert, J M Jez, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 5, 1982
Radioimmunoassay of thyroxine and 3,3',5'-triiodothyronine (reverse T3) in human amniotic fluid
E Cooper, A Anderson, M J Bennett, et al.
Anesthesiology
|
September 1, 1976
Interaction of anesthesia, beta-receptor blockade, and blood loss in dogs with induced myocardial infarction
C Prys-Roberts, J G Roberts, P Foëx, et al.
Molecular Genetics and Metabolism
|
June 30, 2000
A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene
G D Vladutiu, M J Bennett, D Smail, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Isolated biotin-resistant 3-methylcrotonyl CoA carboxylase deficiency presenting with life-threatening hypoglycaemia
K Bartlett, M J Bennett, R P Hill, et al.
Biomedical & Environmental Mass Spectrometry
|
August 1, 1990
Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometry
M J Bennett, D R Cryer, M Yudkoff, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Clinical Chemistry
|
February 1, 1992
When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
M J Bennett, A Bhala, S F Poirier, et al.
Steroids
|
January 1, 1997
Structure and function of 3 alpha-hydroxysteroid dehydrogenase
T M Penning, M J Bennett, S Smith-Hoog, et al.
Page
of 36
Search research articles
Search
Showing results (261-270 of 351) with videos related to
Sort By:
Page
of 36
JIMD Reports
|
February 23, 2013
Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency
A A M Morris, S E Olpin, M J Bennett, et al.
Structure (London, England : 1993)
|
June 15, 1997
Steroid recognition and regulation of hormone action: crystal structure of testosterone and NADP+ bound to 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase
M J Bennett, R H Albert, J M Jez, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 5, 1982
Radioimmunoassay of thyroxine and 3,3',5'-triiodothyronine (reverse T3) in human amniotic fluid
E Cooper, A Anderson, M J Bennett, et al.
Anesthesiology
|
September 1, 1976
Interaction of anesthesia, beta-receptor blockade, and blood loss in dogs with induced myocardial infarction
C Prys-Roberts, J G Roberts, P Foëx, et al.
Molecular Genetics and Metabolism
|
June 30, 2000
A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene
G D Vladutiu, M J Bennett, D Smail, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Isolated biotin-resistant 3-methylcrotonyl CoA carboxylase deficiency presenting with life-threatening hypoglycaemia
K Bartlett, M J Bennett, R P Hill, et al.
Biomedical & Environmental Mass Spectrometry
|
August 1, 1990
Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometry
M J Bennett, D R Cryer, M Yudkoff, et al.
Progress in Clinical and Biological Research
|
January 1, 1992
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation
E Schmidt-Sommerfeld, D Penn, M Duran, et al.
Clinical Chemistry
|
February 1, 1992
When do gut flora in the newborn produce 3-phenylpropionic acid? Implications for early diagnosis of medium-chain acyl-CoA dehydrogenase deficiency
M J Bennett, A Bhala, S F Poirier, et al.
Steroids
|
January 1, 1997
Structure and function of 3 alpha-hydroxysteroid dehydrogenase
T M Penning, M J Bennett, S Smith-Hoog, et al.
Page
of 36