Search research articles
Contact Us
Filters
Showing results (101-110 of 186) with videos related to
Page
of 19
Sort By:
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 8, 1975
Alpha-ketoadipic aciduria: degradation studies with fibroblasts,
U Wendel, H W Rüdiger, H Przyrembel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1992
Determination of (S)- and (R)-2-oxo-3-methylvaleric acid in plasma of patients with maple syrup urine disease
U Wendel, G Even, U Langenbeck, et al.
Molecular Genetics and Metabolism
|
April 28, 2004
Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease
S Schönberger, B Schweiger, B Schwahn, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 3, 1990
A new approach to the newborn screening for hyperphenylalaninemias: use of L-phenylalanine dehydrogenase and microtiter plates
U Wendel, M Koppelkamm, W Hummel, et al.
Pediatric Research
|
May 19, 1998
Assessment of whole body L-leucine oxidation by noninvasive L-[1-13C]leucine breath tests: a reappraisal in patients with maple syrup urine disease, obligate heterozygotes, and healthy subjects
P Schadewaldt, A Bodner, H Brösicke, et al.
Annals of Neurology
|
April 1, 1993
Maple syrup urine disease: metabolic decompensation monitored by proton magnetic resonance imaging and spectroscopy
S R Felber, W Sperl, A Chemelli, et al.
Lancet (London, England)
|
December 8, 1984
First-trimester (chorion biopsy) diagnosis of citrullinaemia and methylmalonicaciduria
W J Kleijer, R Thoomes, H Galjaard, et al.
Pediatric Radiology
|
January 1, 1995
Proton magnetic resonance spectroscopy reflects metabolic decompensation in maple syrup urine disease
W Heindel, H Kugel, U Wendel, et al.
European Journal of Pediatrics
|
April 1, 1991
Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria
H Böhles, K Ullrich, W Endres, et al.
Clinical Chemistry
|
May 5, 2000
Analysis of concentration and (13)C enrichment of D-galactose in human plasma
P Schadewaldt, H W Hammen, K Loganathan, et al.
Page
of 19
Search research articles
Search
Showing results (101-110 of 186) with videos related to
Sort By:
Page
of 19
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 8, 1975
Alpha-ketoadipic aciduria: degradation studies with fibroblasts,
U Wendel, H W Rüdiger, H Przyrembel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1992
Determination of (S)- and (R)-2-oxo-3-methylvaleric acid in plasma of patients with maple syrup urine disease
U Wendel, G Even, U Langenbeck, et al.
Molecular Genetics and Metabolism
|
April 28, 2004
Dysmyelination in the brain of adolescents and young adults with maple syrup urine disease
S Schönberger, B Schweiger, B Schwahn, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 3, 1990
A new approach to the newborn screening for hyperphenylalaninemias: use of L-phenylalanine dehydrogenase and microtiter plates
U Wendel, M Koppelkamm, W Hummel, et al.
Pediatric Research
|
May 19, 1998
Assessment of whole body L-leucine oxidation by noninvasive L-[1-13C]leucine breath tests: a reappraisal in patients with maple syrup urine disease, obligate heterozygotes, and healthy subjects
P Schadewaldt, A Bodner, H Brösicke, et al.
Annals of Neurology
|
April 1, 1993
Maple syrup urine disease: metabolic decompensation monitored by proton magnetic resonance imaging and spectroscopy
S R Felber, W Sperl, A Chemelli, et al.
Lancet (London, England)
|
December 8, 1984
First-trimester (chorion biopsy) diagnosis of citrullinaemia and methylmalonicaciduria
W J Kleijer, R Thoomes, H Galjaard, et al.
Pediatric Radiology
|
January 1, 1995
Proton magnetic resonance spectroscopy reflects metabolic decompensation in maple syrup urine disease
W Heindel, H Kugel, U Wendel, et al.
European Journal of Pediatrics
|
April 1, 1991
Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria
H Böhles, K Ullrich, W Endres, et al.
Clinical Chemistry
|
May 5, 2000
Analysis of concentration and (13)C enrichment of D-galactose in human plasma
P Schadewaldt, H W Hammen, K Loganathan, et al.
Page
of 19