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H C Curtius

Showing results (71-80 of 89) with videos related to

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Helvetica Paediatrica Acta|February 1, 1978
In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonuricsH C Curtius, M J Zagalak, K Baerlocher, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Suspected pterin-4a-carbinolamine dehydratase deficiency: hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterinC Adler, S Ghisla, I Rebrin, et al.
Lancet (London, England)|March 19, 1983
Successful treatment of depression with tetrahydrobiopterinH C Curtius, A Niederwieser, R A Levine, et al.
European Journal of Biochemistry|November 1, 1996
Location of the active site and proposed catalytic mechanism of pterin-4a-carbinolamine dehydrataseS Köster, G Stier, R Ficner, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Partial deficiency of tetrahydrobiopterin]F Rey, J M Saudubray, R J Leeming, et al.
The Journal of Biological Chemistry|March 5, 1990
7-Substituted pterins. A new class of mammalian pteridinesH C Curtius, A Matasovic, G Schoedon, et al.
European Journal of Pediatrics|August 1, 1986
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuriaA Niederwieser, H Shintaku, T Hasler, et al.
European Journal of Pediatrics|May 1, 1987
"Peripheral" tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosityA Niederwieser, H Shintaku, W Leimbacher, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 16, 1979
Atypical phenylketonuria due to tetrahydrobiopterin deficiency. Diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterinH C Curtius, A Niederwieser, M Viscontini, et al.
Lancet (London, England)|January 20, 1979
Atypical phenylketonuria caused by 7, 8-dihydrobiopterin synthetase deficiencyA Niederwieser, H C Curtius, O Bettoni, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Helvetica Paediatrica Acta|February 1, 1978
In vivo studies of the phenylalanine-4-hydroxylase system in hyperphenylalaninemics and phenylketonuricsH C Curtius, M J Zagalak, K Baerlocher, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Suspected pterin-4a-carbinolamine dehydratase deficiency: hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterinC Adler, S Ghisla, I Rebrin, et al.
Lancet (London, England)|March 19, 1983
Successful treatment of depression with tetrahydrobiopterinH C Curtius, A Niederwieser, R A Levine, et al.
European Journal of Biochemistry|November 1, 1996
Location of the active site and proposed catalytic mechanism of pterin-4a-carbinolamine dehydrataseS Köster, G Stier, R Ficner, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Partial deficiency of tetrahydrobiopterin]F Rey, J M Saudubray, R J Leeming, et al.
The Journal of Biological Chemistry|March 5, 1990
7-Substituted pterins. A new class of mammalian pteridinesH C Curtius, A Matasovic, G Schoedon, et al.
European Journal of Pediatrics|August 1, 1986
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuriaA Niederwieser, H Shintaku, T Hasler, et al.
European Journal of Pediatrics|May 1, 1987
"Peripheral" tetrahydrobiopterin deficiency with hyperphenylalaninaemia due to incomplete 6-pyruvoyl tetrahydropterin synthase deficiency or heterozygosityA Niederwieser, H Shintaku, W Leimbacher, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 16, 1979
Atypical phenylketonuria due to tetrahydrobiopterin deficiency. Diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterinH C Curtius, A Niederwieser, M Viscontini, et al.
Lancet (London, England)|January 20, 1979
Atypical phenylketonuria caused by 7, 8-dihydrobiopterin synthetase deficiencyA Niederwieser, H C Curtius, O Bettoni, et al.
Pageof 9