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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
October 1, 1984
[Scintigraphic diagnosis of multiple pheochromocytomas in childhood with 131I-m-benzylguanidine]
S Koletzko, F Ritzl, U Wendel, et al.
Journal of Inherited Metabolic Disease
|
October 2, 2003
Renal excretion of galactose and galactitol in patients with classical galactosaemia, obligate heterozygous parents and healthy subjects
P Schadewaldt, S Killius, L Kamalanathan, et al.
Journal of Inherited Metabolic Disease
|
January 14, 1998
Cerebral metabolic changes in biotinidase deficiency
M Schürmann, V Engelbrecht, K Lohmeier, et al.
European Journal of Pediatrics
|
January 17, 1978
Beta cell nesidioblastosis
K Becker, U Wendel, H Przyrembel, et al.
European Journal of Pediatrics
|
November 1, 1995
Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain
U Wendel, W Ruitenbeek, H A Bentlage, et al.
Human Mutation
|
August 3, 2000
Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients
R Santer, J Rischewski, G Block, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease
M B Krawinkel, H D Oldigs, R Santer, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2000
Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spots
U Spiekerkötter, B Schwahn, H Korall, et al.
Biofactors (Oxford, England)
|
May 6, 1998
Disturbances in mitochondrial transport systems leading to encephalomyopathies
F Trijbels, M Huizing, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 30, 1973
Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblasts
U Wendel, W Wöhler, H W Goedde, et al.
Page
of 19
Search research articles
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Showing results (121-130 of 186) with videos related to
Sort By:
Page
of 19
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
October 1, 1984
[Scintigraphic diagnosis of multiple pheochromocytomas in childhood with 131I-m-benzylguanidine]
S Koletzko, F Ritzl, U Wendel, et al.
Journal of Inherited Metabolic Disease
|
October 2, 2003
Renal excretion of galactose and galactitol in patients with classical galactosaemia, obligate heterozygous parents and healthy subjects
P Schadewaldt, S Killius, L Kamalanathan, et al.
Journal of Inherited Metabolic Disease
|
January 14, 1998
Cerebral metabolic changes in biotinidase deficiency
M Schürmann, V Engelbrecht, K Lohmeier, et al.
European Journal of Pediatrics
|
January 17, 1978
Beta cell nesidioblastosis
K Becker, U Wendel, H Przyrembel, et al.
European Journal of Pediatrics
|
November 1, 1995
Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain
U Wendel, W Ruitenbeek, H A Bentlage, et al.
Human Mutation
|
August 3, 2000
Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients
R Santer, J Rischewski, G Block, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease
M B Krawinkel, H D Oldigs, R Santer, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2000
Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spots
U Spiekerkötter, B Schwahn, H Korall, et al.
Biofactors (Oxford, England)
|
May 6, 1998
Disturbances in mitochondrial transport systems leading to encephalomyopathies
F Trijbels, M Huizing, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
May 30, 1973
Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblasts
U Wendel, W Wöhler, H W Goedde, et al.
Page
of 19