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Lancet (London, England)
|
February 2, 1991
Frequency of the G985 MCAD mutation in the general population
A I Blakemore, H Singleton, R J Pollitt, 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.
American Journal of Medical Genetics
|
April 1, 1990
Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings
S Przedborski, A Ferster, S Goldman, et al.
Psychopharmacology
|
September 1, 1979
Urinary dicarboxylic acids in patients receiving lithium or rubidium salts
S E Hill, F A Jenner, C R Lee, et al.
British Journal of Pharmacology
|
September 1, 1972
The effect of lithium salts on the urinary excretion of -oxoglutarate in man
P A Bond, F A Jenner, C R Lee, et al.
Journal of Inherited Metabolic Disease
|
December 16, 2000
Fumarate hydratase deficiency: increased fumaric acid in amniotic fluid of two affected pregnancies
N J Manning, S E Olpin, R J Pollitt, et al.
Pediatric Research
|
April 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
S Jackson, K Bartlett, J Land, et al.
Archives of Disease in Childhood
|
September 1, 1995
Trichothiodystrophy with sideroblastic anaemia and developmental delay
S A Lynch, D de Berker, A R Lehmann, et al.
Journal of Inherited Metabolic Disease
|
November 6, 2008
Qualitative urinary organic acid analysis: methodological approaches and performance
V Peters, S F Garbade, C D Langhans, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Problems in the detection of fatty acid oxidation defects: experience of a quality assurance programme for qualitative urinary organic acid analysis
M Downing, J C Allen, J R Bonham, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 133) with videos related to
Sort By:
Page
of 14
Lancet (London, England)
|
February 2, 1991
Frequency of the G985 MCAD mutation in the general population
A I Blakemore, H Singleton, R J Pollitt, 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.
American Journal of Medical Genetics
|
April 1, 1990
Trichothiodystrophy, mental retardation, short stature, ataxia, and gonadal dysfunction in three Moroccan siblings
S Przedborski, A Ferster, S Goldman, et al.
Psychopharmacology
|
September 1, 1979
Urinary dicarboxylic acids in patients receiving lithium or rubidium salts
S E Hill, F A Jenner, C R Lee, et al.
British Journal of Pharmacology
|
September 1, 1972
The effect of lithium salts on the urinary excretion of -oxoglutarate in man
P A Bond, F A Jenner, C R Lee, et al.
Journal of Inherited Metabolic Disease
|
December 16, 2000
Fumarate hydratase deficiency: increased fumaric acid in amniotic fluid of two affected pregnancies
N J Manning, S E Olpin, R J Pollitt, et al.
Pediatric Research
|
April 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
S Jackson, K Bartlett, J Land, et al.
Archives of Disease in Childhood
|
September 1, 1995
Trichothiodystrophy with sideroblastic anaemia and developmental delay
S A Lynch, D de Berker, A R Lehmann, et al.
Journal of Inherited Metabolic Disease
|
November 6, 2008
Qualitative urinary organic acid analysis: methodological approaches and performance
V Peters, S F Garbade, C D Langhans, et al.
Journal of Inherited Metabolic Disease
|
June 29, 1999
Problems in the detection of fatty acid oxidation defects: experience of a quality assurance programme for qualitative urinary organic acid analysis
M Downing, J C Allen, J R Bonham, et al.
Page
of 14