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Journal of Inherited Metabolic Disease
|
December 31, 1998
N-acetylglutamate synthetase deficiency: favourable experience with carbamylglutamate
A A Morris, S W Richmond, S J Oddie, et al.
Archives of Disease in Childhood
|
August 1, 1996
Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease
A A Morris, A Thekekara, Z Wilks, et al.
Human Molecular Genetics
|
April 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12
A A Morris, R W Taylor, R N Lightowlers, et al.
Journal of Cardiovascular Pharmacology
|
September 1, 1979
Cardiotonic effects of anthopleurin-A, a polypeptide from a sea anemone
A Scriabine, C G Van Arman, G Morgan, et al.
The Journal of Pediatrics
|
April 17, 1998
A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype
A A Morris, S E Olpin, M Brivet, et al.
Archives of Disease in Childhood
|
April 20, 1999
Glutaric aciduria and suspected child abuse
A A Morris, G F Hoffmann, E R Naughten, et al.
Pediatric Research
|
September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiency
A A Morris, C V Lascelles, S E Olpin, et al.
Brain : a Journal of Neurology
|
April 1, 1995
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients
M J Jackson, J A Schaefer, M A Johnson, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
Acylcarnitine analysis in the investigation of myopathy
S J Moore, N E Haites, I Broom, et al.
International Journal of Legal Medicine
|
August 25, 1999
Expanding the forensic German mitochondrial DNA control region database: genetic diversity as a function of sample size and microgeography
H Pfeiffer, B Brinkmann, J Hühne, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 52) with videos related to
Sort By:
Page
of 6
Journal of Inherited Metabolic Disease
|
December 31, 1998
N-acetylglutamate synthetase deficiency: favourable experience with carbamylglutamate
A A Morris, S W Richmond, S J Oddie, et al.
Archives of Disease in Childhood
|
August 1, 1996
Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease
A A Morris, A Thekekara, Z Wilks, et al.
Human Molecular Genetics
|
April 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency caused by a deletion of exons 11 and 12
A A Morris, R W Taylor, R N Lightowlers, et al.
Journal of Cardiovascular Pharmacology
|
September 1, 1979
Cardiotonic effects of anthopleurin-A, a polypeptide from a sea anemone
A Scriabine, C G Van Arman, G Morgan, et al.
The Journal of Pediatrics
|
April 17, 1998
A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype
A A Morris, S E Olpin, M Brivet, et al.
Archives of Disease in Childhood
|
April 20, 1999
Glutaric aciduria and suspected child abuse
A A Morris, G F Hoffmann, E R Naughten, et al.
Pediatric Research
|
September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiency
A A Morris, C V Lascelles, S E Olpin, et al.
Brain : a Journal of Neurology
|
April 1, 1995
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients
M J Jackson, J A Schaefer, M A Johnson, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
Acylcarnitine analysis in the investigation of myopathy
S J Moore, N E Haites, I Broom, et al.
International Journal of Legal Medicine
|
August 25, 1999
Expanding the forensic German mitochondrial DNA control region database: genetic diversity as a function of sample size and microgeography
H Pfeiffer, B Brinkmann, J Hühne, et al.
Page
of 6