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W Endres

Showing results (71-80 of 112) with videos related to

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European Journal of Pediatrics|April 1, 1991
Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuriaH Böhles, K Ullrich, W Endres, et al.
The Arabidopsis Book|February 4, 2012
The Functions of RNA-Dependent RNA Polymerases in ArabidopsisMatthew R Willmann, Matthew W Endres, Rebecca T Cook, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1987
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylaseY S Shin, H P Niedermeier, W Endres, et al.
Helvetica Paediatrica Acta|January 1, 1982
Atypical phenylketonuria due to biopterin deficiency. Early treatment with tetrahydrobiopterin and neurotransmitter precursors, trials of monotherapyW Endres, A Niederwieser, H C Curtius, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paperN Blau, L Kierat, C W Heizmann, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotypeA Ponzone, N Blau, O Guardamagna, et al.
Clinical Genetics|October 1, 1986
First trimester diagnosis of Pompe's disease (glycogenosis type II) with normal outcome: assay of acid alpha-glucosidase in chorionic villous biopsy using antibodiesA Grubisic, Y S Shin, W Meyer, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotesY S Shin, H Steigüber, P Klemm, et al.
Klinische Wochenschrift|October 1, 1987
Priapism in Fabry's disease during testosterone treatmentW Endres, Y S Shin, M Rieth, et al.
Helvetica Paediatrica Acta|January 1, 1981
A case of fatal hereditary fructose intolerance. Misleading information of formula compositionA von Ruecker, W Endres, Y S Shin, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
European Journal of Pediatrics|April 1, 1991
Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuriaH Böhles, K Ullrich, W Endres, et al.
The Arabidopsis Book|February 4, 2012
The Functions of RNA-Dependent RNA Polymerases in ArabidopsisMatthew R Willmann, Matthew W Endres, Rebecca T Cook, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1987
Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylaseY S Shin, H P Niedermeier, W Endres, et al.
Helvetica Paediatrica Acta|January 1, 1982
Atypical phenylketonuria due to biopterin deficiency. Early treatment with tetrahydrobiopterin and neurotransmitter precursors, trials of monotherapyW Endres, A Niederwieser, H C Curtius, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Screening for tetrahydrobiopterin deficiency in newborns using dried urine on filter paperN Blau, L Kierat, C W Heizmann, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotypeA Ponzone, N Blau, O Guardamagna, et al.
Clinical Genetics|October 1, 1986
First trimester diagnosis of Pompe's disease (glycogenosis type II) with normal outcome: assay of acid alpha-glucosidase in chorionic villous biopsy using antibodiesA Grubisic, Y S Shin, W Meyer, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotesY S Shin, H Steigüber, P Klemm, et al.
Klinische Wochenschrift|October 1, 1987
Priapism in Fabry's disease during testosterone treatmentW Endres, Y S Shin, M Rieth, et al.
Helvetica Paediatrica Acta|January 1, 1981
A case of fatal hereditary fructose intolerance. Misleading information of formula compositionA von Ruecker, W Endres, Y S Shin, et al.
Pageof 12