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J Rey
F Rey

Showing results (31-40 of 820) with videos related to

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Pediatric Research|November 1, 1972
Intraluminal and mucosal starch digestion in congenital deficiency of intestinal sucrase and isomaltase activitiesS Auricchio, F Ciccimarra, L Moauro, et al.
Pediatric Research|May 1, 1974
Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variantsF Rey, C Pellié, M Sivy, et al.
Molecular Genetics and Metabolism|September 10, 1999
The mutant genotype is the main determinant of the metabolic phenotype in phenylalanine hydroxylase deficiencyP Bénit, F Rey, F Blandin-Savoja, et al.
Archives Francaises De Pediatrie|May 1, 1973
[Idiopathic disorder of intestinal fat transport (Anderson's disease). A further case]J Rey, J Jos, F Rey, et al.
Archives Francaises De Pediatrie|November 1, 1979
["Transitory" phenylketonuria. A permanent deficit]F Rey, R J Leeming, H C Curtius, et al.
American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Lancet (London, England)|August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuriaS Lyonnet, C Caillaud, F Rey, et al.
Archives Francaises De Pediatrie|August 1, 1977
[Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase]F Rey, J P Harpey, R J Leeming, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Partial deficiency of tetrahydrobiopterin]F Rey, J M Saudubray, R J Leeming, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
Pageof 82

Showing results (31-40 of 820) with videos related to

Sort By:
Pageof 82
Pediatric Research|November 1, 1972
Intraluminal and mucosal starch digestion in congenital deficiency of intestinal sucrase and isomaltase activitiesS Auricchio, F Ciccimarra, L Moauro, et al.
Pediatric Research|May 1, 1974
Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variantsF Rey, C Pellié, M Sivy, et al.
Molecular Genetics and Metabolism|September 10, 1999
The mutant genotype is the main determinant of the metabolic phenotype in phenylalanine hydroxylase deficiencyP Bénit, F Rey, F Blandin-Savoja, et al.
Archives Francaises De Pediatrie|May 1, 1973
[Idiopathic disorder of intestinal fat transport (Anderson's disease). A further case]J Rey, J Jos, F Rey, et al.
Archives Francaises De Pediatrie|November 1, 1979
["Transitory" phenylketonuria. A permanent deficit]F Rey, R J Leeming, H C Curtius, et al.
American Journal of Human Genetics|April 1, 1989
Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiencyS Lyonnet, C Caillaud, F Rey, et al.
Lancet (London, England)|August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuriaS Lyonnet, C Caillaud, F Rey, et al.
Archives Francaises De Pediatrie|August 1, 1977
[Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase]F Rey, J P Harpey, R J Leeming, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Partial deficiency of tetrahydrobiopterin]F Rey, J M Saudubray, R J Leeming, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
Pageof 82