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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 phenylketonuria
P 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 phenylketonuria
F 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 phenylketonuria
P 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 activity
S Auricchio, F Ciccimarra, J Jos, et al.
Page
of 82
Search research articles
Search
Showing results (21-30 of 820) with videos related to
Sort By:
Page
of 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 phenylketonuria
P 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 phenylketonuria
F 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 phenylketonuria
P 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 activity
S Auricchio, F Ciccimarra, J Jos, et al.
Page
of 82