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U Wendel

Showing results (161-170 of 186) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1995
Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathologyJ Mourmans, J Bakkeren, J de Jong, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 1, 2006
Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient miceU Spiekerkoetter, J Ruiter, C Tokunaga, et al.
Ceskoslovenska Pediatrie|April 1, 1987
[Metabolic study of the classic form of leucinosis during exchange transfusion therapy]J Zeman, J Hyánek, H Houstková, et al.
Human Mutation|June 22, 2000
Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutationsM E Rubio-Gozalbo, K P Dijkman, L P van den Heuvel, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 18, 2001
Proton MR spectroscopy of the lumbar spine in patients with glycogen storage disease type IbA Scherer, H J Wittsack, V Engelbrecht, et al.
Journal of Inherited Metabolic Disease|July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patientsA Dursun, M Henneke, K Ozgül, et al.
European Journal of Pediatrics|November 1, 1988
Prevalence of coeliac disease in diabetic children and adolescents. A multicentre studyS Koletzko, A Bürgin-Wolff, B Koletzko, et al.
Human Genetics|March 1, 1989
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish populationU Lichter-Konecki, M Schlotter, C Yaylak, et al.
The Journal of Pediatrics|November 1, 1991
Granulocyte and granulocyte-macrophage colony-stimulating factors for treatment of neutropenia in glycogen storage disease type IbH Schroten, J Roesler, T Breidenbach, et al.
European Journal of Clinical Investigation|March 18, 2004
Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stressU Spiekerkoetter, C Tokunaga, U Wendel, et al.
Pageof 19

Showing results (161-170 of 186) with videos related to

Sort By:
Pageof 19
Journal of Inherited Metabolic Disease|January 1, 1995
Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathologyJ Mourmans, J Bakkeren, J de Jong, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 1, 2006
Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient miceU Spiekerkoetter, J Ruiter, C Tokunaga, et al.
Ceskoslovenska Pediatrie|April 1, 1987
[Metabolic study of the classic form of leucinosis during exchange transfusion therapy]J Zeman, J Hyánek, H Houstková, et al.
Human Mutation|June 22, 2000
Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutationsM E Rubio-Gozalbo, K P Dijkman, L P van den Heuvel, et al.
Journal of Magnetic Resonance Imaging : JMRI|December 18, 2001
Proton MR spectroscopy of the lumbar spine in patients with glycogen storage disease type IbA Scherer, H J Wittsack, V Engelbrecht, et al.
Journal of Inherited Metabolic Disease|July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patientsA Dursun, M Henneke, K Ozgül, et al.
European Journal of Pediatrics|November 1, 1988
Prevalence of coeliac disease in diabetic children and adolescents. A multicentre studyS Koletzko, A Bürgin-Wolff, B Koletzko, et al.
Human Genetics|March 1, 1989
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish populationU Lichter-Konecki, M Schlotter, C Yaylak, et al.
The Journal of Pediatrics|November 1, 1991
Granulocyte and granulocyte-macrophage colony-stimulating factors for treatment of neutropenia in glycogen storage disease type IbH Schroten, J Roesler, T Breidenbach, et al.
European Journal of Clinical Investigation|March 18, 2004
Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stressU Spiekerkoetter, C Tokunaga, U Wendel, et al.
Pageof 19