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Developmental Medicine and Child Neurology
|
August 1, 1988
Molybdenum co-factor deficiency: an easily missed inborn error of metabolism
A Aukett, M J Bennett, G P Hosking
The American Journal of Psychiatry
|
April 1, 1979
Adult mental health services in a health maintenance organization
S H Budman, J Feldman, M J Bennett
Biochemical Society Transactions
|
May 18, 2000
Perfused heart studies to investigate lipid metabolism
R D Evans, M J Bennett, D Hauton
Critical Reviews in Clinical Laboratory Sciences
|
March 29, 2000
Inborn errors of mitochondrial fatty acid oxidation
M J Bennett, P Rinaldo, A W Strauss
Molecular Genetics and Metabolism
|
September 26, 2000
Liver disease in pregnancy and fetal fatty acid oxidation defects
J A Ibdah, Z Yang, M J Bennett
The Journal of Pediatrics
|
September 1, 1994
Excretion of dicarboxylic acids in preterm infants fed medium- or long-chain triglycerides
S Baumgart, G R Pereira, M J Bennett
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
October 29, 1983
Induction of labour in pregnancy complicated by heart disease
R W Rush, T Mabin, M J Bennett
Biochimica Et Biophysica Acta
|
September 22, 2001
Utilisation of triacylglycerol and non-esterified fatty acid by the working rat heart: myocardial lipid substrate preference
D Hauton, M J Bennett, R D Evans
Medical Laboratory Sciences
|
April 1, 1984
A simple HPLC method for the determination of urate in serum and urine using 8-chlorotheophylline as internal standard
M J Bennett, B P Patchett, E Worthy
American Journal of Medical Genetics
|
June 5, 1995
Mitochondrial damage results in a reversible increase in lysosomal storage material in lymphoblasts from patients with juvenile neuronal ceroid-lipofuscinosis (Batten Disease)
R L Boriack, E Cortinas, M J Bennett
Page
of 36
Search research articles
Search
Showing results (101-110 of 351) with videos related to
Sort By:
Page
of 36
Developmental Medicine and Child Neurology
|
August 1, 1988
Molybdenum co-factor deficiency: an easily missed inborn error of metabolism
A Aukett, M J Bennett, G P Hosking
The American Journal of Psychiatry
|
April 1, 1979
Adult mental health services in a health maintenance organization
S H Budman, J Feldman, M J Bennett
Biochemical Society Transactions
|
May 18, 2000
Perfused heart studies to investigate lipid metabolism
R D Evans, M J Bennett, D Hauton
Critical Reviews in Clinical Laboratory Sciences
|
March 29, 2000
Inborn errors of mitochondrial fatty acid oxidation
M J Bennett, P Rinaldo, A W Strauss
Molecular Genetics and Metabolism
|
September 26, 2000
Liver disease in pregnancy and fetal fatty acid oxidation defects
J A Ibdah, Z Yang, M J Bennett
The Journal of Pediatrics
|
September 1, 1994
Excretion of dicarboxylic acids in preterm infants fed medium- or long-chain triglycerides
S Baumgart, G R Pereira, M J Bennett
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
October 29, 1983
Induction of labour in pregnancy complicated by heart disease
R W Rush, T Mabin, M J Bennett
Biochimica Et Biophysica Acta
|
September 22, 2001
Utilisation of triacylglycerol and non-esterified fatty acid by the working rat heart: myocardial lipid substrate preference
D Hauton, M J Bennett, R D Evans
Medical Laboratory Sciences
|
April 1, 1984
A simple HPLC method for the determination of urate in serum and urine using 8-chlorotheophylline as internal standard
M J Bennett, B P Patchett, E Worthy
American Journal of Medical Genetics
|
June 5, 1995
Mitochondrial damage results in a reversible increase in lysosomal storage material in lymphoblasts from patients with juvenile neuronal ceroid-lipofuscinosis (Batten Disease)
R L Boriack, E Cortinas, M J Bennett
Page
of 36