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Journal of Inherited Metabolic Disease
|
January 1, 1984
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally
M J Bennett, D A Curnock, P C Engel, et al.
Clinical Chemistry
|
June 28, 2001
Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain l-3-hydroxyacyl-CoA dehydrogenase: a useful diagnostic aid
P M Jones, M Moffitt, D Joseph, et al.
European Journal of Pediatrics
|
May 20, 1999
N-acetylaspartylglutamate in Canavan disease: an adverse effector?
A P Burlina, V Ferrari, P Divry, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Pyruvate carboxylase deficiency in twins
M A Pollock, M Cumberbatch, M J Bennett, et al.
Prenatal Diagnosis
|
February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency
M J Bennett, F Allison, G W Lowther, et al.
The Journal of Clinical Investigation
|
June 8, 2001
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
J A Ibdah, H Paul, Y Zhao, et al.
Steroids
|
September 1, 1996
Mammalian 3 alpha-hydroxysteroid dehydrogenases
T M Penning, J E Pawlowski, B P Schlegel, et al.
The New England Journal of Medicine
|
December 10, 1998
A defect in the transport of long-chain fatty acids associated with acute liver failure
A A Odaib, B L Shneider, M J Bennett, et al.
Steroids
|
May 1, 1997
"Mammalian 3 alpha-hydroxysteroid dehydrogenases"
T M Penning, J E Pawlowski, B P Schlegel, et al.
International Journal of Group Psychotherapy
|
January 1, 1987
Preliminary findings on a new instrument to measure cohesion in group psychotherapy
S H Budman, A Demby, M Feldstein, et al.
Page
of 36
Search research articles
Search
Showing results (311-320 of 351) with videos related to
Sort By:
Page
of 36
Journal of Inherited Metabolic Disease
|
January 1, 1984
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally
M J Bennett, D A Curnock, P C Engel, et al.
Clinical Chemistry
|
June 28, 2001
Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain l-3-hydroxyacyl-CoA dehydrogenase: a useful diagnostic aid
P M Jones, M Moffitt, D Joseph, et al.
European Journal of Pediatrics
|
May 20, 1999
N-acetylaspartylglutamate in Canavan disease: an adverse effector?
A P Burlina, V Ferrari, P Divry, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Pyruvate carboxylase deficiency in twins
M A Pollock, M Cumberbatch, M J Bennett, et al.
Prenatal Diagnosis
|
February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency
M J Bennett, F Allison, G W Lowther, et al.
The Journal of Clinical Investigation
|
June 8, 2001
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
J A Ibdah, H Paul, Y Zhao, et al.
Steroids
|
September 1, 1996
Mammalian 3 alpha-hydroxysteroid dehydrogenases
T M Penning, J E Pawlowski, B P Schlegel, et al.
The New England Journal of Medicine
|
December 10, 1998
A defect in the transport of long-chain fatty acids associated with acute liver failure
A A Odaib, B L Shneider, M J Bennett, et al.
Steroids
|
May 1, 1997
"Mammalian 3 alpha-hydroxysteroid dehydrogenases"
T M Penning, J E Pawlowski, B P Schlegel, et al.
International Journal of Group Psychotherapy
|
January 1, 1987
Preliminary findings on a new instrument to measure cohesion in group psychotherapy
S H Budman, A Demby, M Feldstein, et al.
Page
of 36