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K Bartholomé

Showing results (1-10 of 43) with videos related to

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Human Genetics|October 2, 1979
Genetics and biochemistry of the phenylketonuria-present stateK Bartholomé
Die Naturwissenschaften|October 1, 1980
[Molecular basis for the heterogeneity of phenylketonuria]K Bartholomé
Acta Paediatrica Scandinavica|November 1, 1983
Deficiency of tyrosine hydroxylase or tryptophan hydroxylase: a possible cause of two hypothetical metabolic diseasesK Bartholomé
Advances in Pharmacology (San Diego, Calif.)|November 5, 1997
Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystoniaK Bartholomé, B Lüdecke
Journal of Inherited Metabolic Disease|January 1, 1982
Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylaseK Bartholomé, A Dresel
Neuropediatrics|February 1, 1990
Biochemical and neurophysiological investigations in two forms of Segawa's diseaseW Görke, K Bartholomé
Human Genetics|June 1, 1995
Frequent sequence variant in the human tyrosine hydroxylase geneB Lüdecke, K Bartholomé
Lancet (London, England)|October 16, 1976
Immunological detection of phenylalanine hydroxylase in phenylketonuriaK Bartholomé, E Ertel
Monatsschrift Fur Kinderheilkunde|May 1, 1976
[Determination of phenylalanine hydroxylase in patients with phenylketonuria and hyperphenylalaninemia]K Bartholomé, P Lutz
Lancet (London, England)|November 22, 1975
Letter: L-dopa and 5-hydroxytryptophan therapy in phenylketonuria with normal phenylalanine-hydroxylase activityK Bartholomé, D J Byrd
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Human Genetics|October 2, 1979
Genetics and biochemistry of the phenylketonuria-present stateK Bartholomé
Die Naturwissenschaften|October 1, 1980
[Molecular basis for the heterogeneity of phenylketonuria]K Bartholomé
Acta Paediatrica Scandinavica|November 1, 1983
Deficiency of tyrosine hydroxylase or tryptophan hydroxylase: a possible cause of two hypothetical metabolic diseasesK Bartholomé
Advances in Pharmacology (San Diego, Calif.)|November 5, 1997
Mutations in the tyrosine hydroxylase gene cause various forms of L-dopa-responsive dystoniaK Bartholomé, B Lüdecke
Journal of Inherited Metabolic Disease|January 1, 1982
Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylaseK Bartholomé, A Dresel
Neuropediatrics|February 1, 1990
Biochemical and neurophysiological investigations in two forms of Segawa's diseaseW Görke, K Bartholomé
Human Genetics|June 1, 1995
Frequent sequence variant in the human tyrosine hydroxylase geneB Lüdecke, K Bartholomé
Lancet (London, England)|October 16, 1976
Immunological detection of phenylalanine hydroxylase in phenylketonuriaK Bartholomé, E Ertel
Monatsschrift Fur Kinderheilkunde|May 1, 1976
[Determination of phenylalanine hydroxylase in patients with phenylketonuria and hyperphenylalaninemia]K Bartholomé, P Lutz
Lancet (London, England)|November 22, 1975
Letter: L-dopa and 5-hydroxytryptophan therapy in phenylketonuria with normal phenylalanine-hydroxylase activityK Bartholomé, D J Byrd
Pageof 5