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F K Trefz

Showing results (61-70 of 70) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1991
Macrocephaly: an important indication for organic acid analysisG F Hoffmann, F K Trefz, P G Barth, et al.
The New England Journal of Medicine|May 2, 1991
Molecular basis of phenotypic heterogeneity in phenylketonuriaY Okano, R C Eisensmith, F Güttler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1991
Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detectionG F Hoffmann, L Sweetman, H J Bremer, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.
Annals of Neurology|November 1, 1991
Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeC A Stanley, S DeLeeuw, P M Coates, et al.
Lancet (London, England)|December 10, 1994
Maternal mild hyperphenylalaninaemia: an international survey of offspring outcomeH L Levy, S E Waisbren, D Lobbregt, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Glutaric aciduria type III: a distinctive non-disease?I Knerr, J Zschocke, U Trautmann, et al.
Molecular Genetics and Metabolism|February 21, 2021
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countriesR A F Evers, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism|October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 casesA MacDonald, K Ahring, M F Almeida, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Journal of Inherited Metabolic Disease|January 1, 1991
Macrocephaly: an important indication for organic acid analysisG F Hoffmann, F K Trefz, P G Barth, et al.
The New England Journal of Medicine|May 2, 1991
Molecular basis of phenotypic heterogeneity in phenylketonuriaY Okano, R C Eisensmith, F Güttler, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1991
Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detectionG F Hoffmann, L Sweetman, H J Bremer, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.
Annals of Neurology|November 1, 1991
Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeC A Stanley, S DeLeeuw, P M Coates, et al.
Lancet (London, England)|December 10, 1994
Maternal mild hyperphenylalaninaemia: an international survey of offspring outcomeH L Levy, S E Waisbren, D Lobbregt, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Glutaric aciduria type III: a distinctive non-disease?I Knerr, J Zschocke, U Trautmann, et al.
Molecular Genetics and Metabolism|February 21, 2021
Defining tetrahydrobiopterin responsiveness in phenylketonuria: Survey results from 38 countriesR A F Evers, A M J van Wegberg, K Ahring, et al.
Molecular Genetics and Metabolism|October 27, 2015
The challenges of managing coexistent disorders with phenylketonuria: 30 casesA MacDonald, K Ahring, M F Almeida, et al.
Pageof 7