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J Rey
F Rey

Showing results (21-30 of 820) with videos related to

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Annales De Medecine Interne|June 1, 1971
[Long term development of celiac disease in children. Effects of reintroducing gluten]J Rey, J Jos, F Rey, et al.
Human Molecular Genetics|April 1, 1994
Novel frame shift deletions of the phenylalanine hydroxylase gene in phenylketonuriaP Bénit, F Rey, D Melle, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy]F Rey, M Berthelon, A Munnich, et al.
Archives of Disease in Childhood|August 1, 1980
Biopterin defect in a normal-appearing child affected by a transient phenylketonuriaF Rey, R J Leeming, J A Blair, et al.
Archives Francaises De Pediatrie|February 1, 1974
[Organization of the brush border and the digestion-absorption concept. Recent data on the ultrastructure and physiology of the enterocyte]J Schmitz, J Jos, F Drillet, et al.
Human Mutation|January 1, 1994
Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuriaP Bénit, F Rey, D Melle, et al.
Archives Francaises De Pediatrie|October 1, 1980
[Perfusion study of intestinal sugar absorption after extensive intestinal resection (author's transl)]J Schmitz, F Rey, J L Bresson, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Dietetic therapy of phenylketonuria. New composition tables and exchange lists of fruits and vegetables expressed in volumetric measurements]M Du Fraysseix, F Rey, E Audran, et al.
Archives Francaises De Pediatrie|December 1, 1978
[Results after 5 years of early treated phenyketonuria. Correlations with the quality of dietetic control]F Rey, D Rapoport, M du Fraysseix, et al.
Acta Paediatrica Scandinavica|May 1, 1971
Studies on intestinal digestion of starch in children with congenital deficiency of sucrase and isomaltase activityS Auricchio, F Ciccimarra, J Jos, et al.
Pageof 82

Showing results (21-30 of 820) with videos related to

Sort By:
Pageof 82
Annales De Medecine Interne|June 1, 1971
[Long term development of celiac disease in children. Effects of reintroducing gluten]J Rey, J Jos, F Rey, et al.
Human Molecular Genetics|April 1, 1994
Novel frame shift deletions of the phenylalanine hydroxylase gene in phenylketonuriaP Bénit, F Rey, D Melle, et al.
Archives Francaises De Pediatrie|October 1, 1987
[Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy]F Rey, M Berthelon, A Munnich, et al.
Archives of Disease in Childhood|August 1, 1980
Biopterin defect in a normal-appearing child affected by a transient phenylketonuriaF Rey, R J Leeming, J A Blair, et al.
Archives Francaises De Pediatrie|February 1, 1974
[Organization of the brush border and the digestion-absorption concept. Recent data on the ultrastructure and physiology of the enterocyte]J Schmitz, J Jos, F Drillet, et al.
Human Mutation|January 1, 1994
Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuriaP Bénit, F Rey, D Melle, et al.
Archives Francaises De Pediatrie|October 1, 1980
[Perfusion study of intestinal sugar absorption after extensive intestinal resection (author's transl)]J Schmitz, F Rey, J L Bresson, et al.
Archives Francaises De Pediatrie|January 1, 1983
[Dietetic therapy of phenylketonuria. New composition tables and exchange lists of fruits and vegetables expressed in volumetric measurements]M Du Fraysseix, F Rey, E Audran, et al.
Archives Francaises De Pediatrie|December 1, 1978
[Results after 5 years of early treated phenyketonuria. Correlations with the quality of dietetic control]F Rey, D Rapoport, M du Fraysseix, et al.
Acta Paediatrica Scandinavica|May 1, 1971
Studies on intestinal digestion of starch in children with congenital deficiency of sucrase and isomaltase activityS Auricchio, F Ciccimarra, J Jos, et al.
Pageof 82