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International Journal of Endocrinology
|
September 10, 2011
Moderate weight reduction in an outpatient obesity intervention program significantly reduces insulin resistance and risk factors for cardiovascular disease in severely obese adolescents
J Grulich-Henn, S Lichtenstein, F Hörster, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Emergency treatment in glutaryl-CoA dehydrogenase deficiency
S Kölker, C R Greenberg, M Lindner, et al.
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur
|
February 21, 2012
How much chicken is food? Questioning the definition of food by analyzing amino acid composition of modern convenience products
M Hermanussen, U Gonder, D Stegemann, et al.
Journal of Chromatography
|
May 19, 1993
Use of a thick-film capillary column for the analysis of organic acids in body fluids
W Meier-Augenstein, G F Hoffmann, B Holmes, et al.
Klinische Padiatrie
|
January 1, 1993
[Development of brain atrophy, therapy and therapy monitoring in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency)]
B Lawrenz-Wolf, K P Herberg, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Comprehensive analysis of pyrimidine metabolism in 450 children with unspecific neurological symptoms using high-pressure liquid chromatography-electrospray ionization tandem mass spectrometry
C Schmidt, U Hofmann, D Kohlmüller, et al.
Journal of Inherited Metabolic Disease
|
April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism
S Kölker, S W Sauer, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Challenges for basic research in glutaryl-CoA dehydrogenase deficiency
S Kölker, K A Strauss, S I Goodman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Organic acids in cerebrospinal fluid and plasma of patients with L-2-hydroxyglutaric aciduria
G F Hoffmann, C Jakobs, B Holmes, et al.
Pediatric Research
|
December 5, 2000
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism
J Zschocke, J P Ruiter, J Brand, et al.
Page
of 22
Search research articles
Search
Showing results (111-120 of 214) with videos related to
Sort By:
Page
of 22
International Journal of Endocrinology
|
September 10, 2011
Moderate weight reduction in an outpatient obesity intervention program significantly reduces insulin resistance and risk factors for cardiovascular disease in severely obese adolescents
J Grulich-Henn, S Lichtenstein, F Hörster, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Emergency treatment in glutaryl-CoA dehydrogenase deficiency
S Kölker, C R Greenberg, M Lindner, et al.
Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur
|
February 21, 2012
How much chicken is food? Questioning the definition of food by analyzing amino acid composition of modern convenience products
M Hermanussen, U Gonder, D Stegemann, et al.
Journal of Chromatography
|
May 19, 1993
Use of a thick-film capillary column for the analysis of organic acids in body fluids
W Meier-Augenstein, G F Hoffmann, B Holmes, et al.
Klinische Padiatrie
|
January 1, 1993
[Development of brain atrophy, therapy and therapy monitoring in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency)]
B Lawrenz-Wolf, K P Herberg, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
January 26, 2006
Comprehensive analysis of pyrimidine metabolism in 450 children with unspecific neurological symptoms using high-pressure liquid chromatography-electrospray ionization tandem mass spectrometry
C Schmidt, U Hofmann, D Kohlmüller, et al.
Journal of Inherited Metabolic Disease
|
April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism
S Kölker, S W Sauer, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Challenges for basic research in glutaryl-CoA dehydrogenase deficiency
S Kölker, K A Strauss, S I Goodman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Organic acids in cerebrospinal fluid and plasma of patients with L-2-hydroxyglutaric aciduria
G F Hoffmann, C Jakobs, B Holmes, et al.
Pediatric Research
|
December 5, 2000
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism
J Zschocke, J P Ruiter, J Brand, et al.
Page
of 22