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European Journal of Pediatrics|August 1, 1993
Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading testA Ponzone, O Guardamagna, M Spada, et al.Pediatric Research|February 1, 1993
Catalytic activity of tetrahydrobiopterin in dihydropteridine reductase deficiency and indications for treatmentA Ponzone, O Guardamagna, I Dianzani, et al.Pediatric Research|November 1, 1991
Tetrahydrobiopterin loading test in hyperphenylalaninemiaA Ponzone, O Guardamagna, S Ferraris, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|July 16, 1993
Hyperphenylalaninemia and pterin metabolism in serum and erythrocytesA Ponzone, O Guardamagna, M Spada, et al.Pediatrie|January 1, 1987
[Trial of indirect screening of tetrahydrobiopterin deficiency]S Ferraris, O Guardamagna, G Bracco, et al.The Turkish Journal of Pediatrics|January 1, 1996
Tetrahydrobiopterin and inherited hyperphenylalaninemiasN Blau, B Thony, M Spada, et al.Neurology|August 26, 2009
Dopamine agonists in 6-pyruvoyl tetrahydropterin synthase deficiencyF Porta, A Mussa, D Concolino, et al.Archives of Disease in Childhood|February 1, 1988
Two mutations of dihydropteridine reductase deficiencyA Ponzone, O Guardamagna, S Ferraris, et al.Journal of Medical Genetics|March 1, 1993
Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutationI Dianzani, C Camaschella, G Saglio, et al.Journal of Inherited Metabolic Disease|July 13, 2004
A novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome detected by neonatal screening for galactosaemiaA Peduto, M Spada, A Alluto, et al.Pageof 39