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U Wendel

Showing results (141-150 of 186) with videos related to

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Clinical Chemistry|May 1, 1995
Standardized method for high-resolution 1H-NMR of cerebrospinal fluidR A Wevers, U Engelke, U Wendel, et al.
AJR. American Journal of Roentgenology|July 20, 2001
MR imaging of bone marrow in glycogen storage disease type IB in children and young adultsA Scherer, V Engelbrecht, G Neises, et al.
Neurology|March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiencyK Hyland, I Smith, T Bottiglieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1996
Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onsetR Gold, U Bogdahn, L Kappos, et al.
European Journal of Pediatrics|April 1, 1986
Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)I Lombeck, U Wendel, J Versieck, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorderH Przyrembel, U Wendel, K Becker, et al.
Lancet (London, England)|March 23, 1991
Colony-stimulating factors for neutropenia in glycogen storage disease IbH Schroten, U Wendel, S Burdach, et al.
Journal of Bioenergetics and Biomembranes|April 1, 1996
Importance of mitochondrial transmembrane processes in human mitochondriopathiesM Huizing, V DePinto, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine diseaseU Langenbeck, U Wendel, A Mench-Hoinowski, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 8, 1975
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studiesH Przyrembel, D Bachmann, I Lombeck, et al.
Pageof 19

Showing results (141-150 of 186) with videos related to

Sort By:
Pageof 19
Clinical Chemistry|May 1, 1995
Standardized method for high-resolution 1H-NMR of cerebrospinal fluidR A Wevers, U Engelke, U Wendel, et al.
AJR. American Journal of Roentgenology|July 20, 2001
MR imaging of bone marrow in glycogen storage disease type IB in children and young adultsA Scherer, V Engelbrecht, G Neises, et al.
Neurology|March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiencyK Hyland, I Smith, T Bottiglieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1996
Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onsetR Gold, U Bogdahn, L Kappos, et al.
European Journal of Pediatrics|April 1, 1986
Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)I Lombeck, U Wendel, J Versieck, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorderH Przyrembel, U Wendel, K Becker, et al.
Lancet (London, England)|March 23, 1991
Colony-stimulating factors for neutropenia in glycogen storage disease IbH Schroten, U Wendel, S Burdach, et al.
Journal of Bioenergetics and Biomembranes|April 1, 1996
Importance of mitochondrial transmembrane processes in human mitochondriopathiesM Huizing, V DePinto, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine diseaseU Langenbeck, U Wendel, A Mench-Hoinowski, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 8, 1975
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studiesH Przyrembel, D Bachmann, I Lombeck, et al.
Pageof 19