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Pediatric Research
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November 1, 1972
Intraluminal and mucosal starch digestion in congenital deficiency of intestinal sucrase and isomaltase activities
S 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 variants
F 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 deficiency
P 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 deficiency
S Lyonnet, C Caillaud, F Rey, et al.
Lancet (London, England)
|
August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuria
S 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 phenylketonuria
P Labrune, D Melle, F Rey, et al.
Page
of 82
Search research articles
Search
Showing results (31-40 of 820) with videos related to
Sort By:
Page
of 82
Pediatric Research
|
November 1, 1972
Intraluminal and mucosal starch digestion in congenital deficiency of intestinal sucrase and isomaltase activities
S 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 variants
F 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 deficiency
P 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 deficiency
S Lyonnet, C Caillaud, F Rey, et al.
Lancet (London, England)
|
August 27, 1988
Guthrie cards for detection of point mutations in phenylketonuria
S 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 phenylketonuria
P Labrune, D Melle, F Rey, et al.
Page
of 82