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F K Trefz

Showing results (51-60 of 70) with videos related to

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European Journal of Pediatrics|February 9, 1999
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997P Burgard, H J Bremer, P Bührdel, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1992
[Maternal phenylketonuria. Problems in detecting and risk educating identified females]H J Salize, B Fünders-Bücker, U Knorrek, et al.
Human Genetics|September 1, 1992
Haplotype distribution and mutations at the PAH locus in CroatiaI Barić, D Mardesić, G Gjurić, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1993
Genotype-phenotype correlations in phenylketonuriaF K Trefz, P Burgard, T König, et al.
The Journal of Pediatrics|December 1, 1992
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Outcome of tyrosinaemia type IIIC J Ellaway, E Holme, S Standing, et al.
Journal of Inherited Metabolic Disease|May 15, 2007
Effects of cholesterol and simvastatin treatment in patients with Smith-Lemli-Opitz syndrome (SLOS)D Haas, S F Garbade, C Vohwinkel, 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.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]F K Trefz, G F Hoffmann, E Mayatepek, et al.
Biochemistry|April 19, 1988
Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase geneU Lichter-Konecki, D S Konecki, A G DiLella, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
European Journal of Pediatrics|February 9, 1999
Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997P Burgard, H J Bremer, P Bührdel, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1992
[Maternal phenylketonuria. Problems in detecting and risk educating identified females]H J Salize, B Fünders-Bücker, U Knorrek, et al.
Human Genetics|September 1, 1992
Haplotype distribution and mutations at the PAH locus in CroatiaI Barić, D Mardesić, G Gjurić, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 30, 1993
Genotype-phenotype correlations in phenylketonuriaF K Trefz, P Burgard, T König, et al.
The Journal of Pediatrics|December 1, 1992
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.
Journal of Inherited Metabolic Disease|March 28, 2002
Outcome of tyrosinaemia type IIIC J Ellaway, E Holme, S Standing, et al.
Journal of Inherited Metabolic Disease|May 15, 2007
Effects of cholesterol and simvastatin treatment in patients with Smith-Lemli-Opitz syndrome (SLOS)D Haas, S F Garbade, C Vohwinkel, 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.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]F K Trefz, G F Hoffmann, E Mayatepek, et al.
Biochemistry|April 19, 1988
Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase geneU Lichter-Konecki, D S Konecki, A G DiLella, et al.
Pageof 7