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O Guardamagna

Showing results (11-20 of 36) with videos related to

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Lancet (London, England)|February 28, 1987
Screening for malignant phenylketonuriaA Ponzone, O Guardamagna, S Ferraris, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant proteinR G Cotton, I Jennings, G Bracco, et al.
European Journal of Pediatrics|January 1, 1987
Neurotransmitter therapy and diet in malignant phenylketonuriaA Ponzone, O Guardamagna, S Ferraris, et al.
Archives of Disease in Childhood|February 1, 1988
Two mutations of dihydropteridine reductase deficiencyA Ponzone, O Guardamagna, S Ferraris, et al.
Minerva Pediatrica|April 15, 1984
[X-linked ectodermal dysplasia. Presentation of 2 cases]M Landi, V Ricca, R Oggero, 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.
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.
Minerva Pediatrica|June 19, 2002
[Influence of diet on lipoprotein profile in familial combined hyperlipidemia affected children]C Bondone, E Rutto, M Giaccone, et al.
Pediatric Research|November 1, 1991
Tetrahydrobiopterin loading test in hyperphenylalaninemiaA Ponzone, O Guardamagna, S Ferraris, et al.
Minerva Pediatrica|February 1, 1983
[The clinical score for diagnosis of bronchiolitis in sucklings. Retrospective checking of 133 cases (1974-1981)]R Oggero, V Ricca, E Parisi, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Lancet (London, England)|February 28, 1987
Screening for malignant phenylketonuriaA Ponzone, O Guardamagna, S Ferraris, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant proteinR G Cotton, I Jennings, G Bracco, et al.
European Journal of Pediatrics|January 1, 1987
Neurotransmitter therapy and diet in malignant phenylketonuriaA Ponzone, O Guardamagna, S Ferraris, et al.
Archives of Disease in Childhood|February 1, 1988
Two mutations of dihydropteridine reductase deficiencyA Ponzone, O Guardamagna, S Ferraris, et al.
Minerva Pediatrica|April 15, 1984
[X-linked ectodermal dysplasia. Presentation of 2 cases]M Landi, V Ricca, R Oggero, 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.
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.
Minerva Pediatrica|June 19, 2002
[Influence of diet on lipoprotein profile in familial combined hyperlipidemia affected children]C Bondone, E Rutto, M Giaccone, et al.
Pediatric Research|November 1, 1991
Tetrahydrobiopterin loading test in hyperphenylalaninemiaA Ponzone, O Guardamagna, S Ferraris, et al.
Minerva Pediatrica|February 1, 1983
[The clinical score for diagnosis of bronchiolitis in sucklings. Retrospective checking of 133 cases (1974-1981)]R Oggero, V Ricca, E Parisi, et al.
Pageof 4