Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Jean Rey"'
Autor:
Samy Cadranel, Peter J. Milla, A S McNeish, Michael J. Lentze, Deirdre Kelly, Birgitta Strandvik, Salvatore Auricchio, Jacques Schmitz, J K Visakorpi, Jean Rey, Jan A.J.M. Taminiau
Publikováno v:
Journal of pediatric gastroenterology and nutrition, 66, S20-S28. Lippincott Williams and Wilkins
Thirty-six founding members from Europe were present in 1968, when the European Society of Paediatric Gastroenterology (ESGA) had its first meeting in Paris. The aim was to create a forum for presentations and discussions of research activities in pa
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 66
The first Committee on Nutrition (CoN) was founded in 1974. Two years later nutrition (N) was added to the society's name, which then became ESPGAN. The Committee systematised compositional and quality criteria for breast milk substitutes and food fo
Autor:
Peter J. Milla, Jean Rey, A S McNeish, Samy Cadranel, Raanan Shamir, Birgitta Strandvik, Jacques Schmitz, Stefano Guandalini, Berthold Koletzko, Michael J. Lentze, Salvatore Auricchio, J K Visakorpi, Riccardo Troncone, Deirdre Kelly
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 66
Since the conception of an idea of a few paediatric gastroenterologists in Europe to create a society for Paediatric Gastroenterology in 1967, and its foundation in 1968, half a century has passed. The European Society for Paediatric Gastroenterology
Autor:
Concetta Meli, Georg F. Hoffmann, Françoise Rey, Alberto Ponzone, Kurt Ullrich, Luc Michiels, Per Guldberg, Irma Dianzani, Enrica Riva, Baudouin François, H. Schmidt, Johannes Zschocke, Valentino Romano, Flemming Güttler, Peter Burgard, Jean Rey
Publikováno v:
The American Journal of Human Genetics. 63:71-79
SummaryPhenylketonuria (PKU) and mild hyperphenylalaninemia (MHP) are allelic disorders caused by mutations in the gene encoding phenylalanine hydroxylase (PAH). Previous studies have suggested that the highly variable metabolic phenotypes of PAH def
Autor:
Arnold Munnich, Françoise Rey, Jadwiga Jaruzelska, Jean Rey, Véronique Abadie, P. Millasseau, M. Berthelon, Stanislas Lyonnet
Publikováno v:
Human Molecular Genetics. 2:31-34
Taking advantage of the 'illegitimate' transcription of the phenylalanine hydroxylase (PAH) gene, we have been able to analyse the PAH cDNA sequence of hyperphenylalaninemic children in circulating lymphocytes. Using this approach, we have also ident
Autor:
Hubert Journel, Pierre Guibaud, Josué Feingold, Philippe Labrune, Philippe Tron, Jean Rey, Arnold Munnich, Marie-Louise Briard, Catherine Caillaud, Françoise Rey, Henri Plauchu, N Maurin, Jean-Louis Nivelon, D. Melle, M. Berthelon, Jean Frézal, Jean-Pierre Farriaux, Jean-Marie Saudubray, Stanislas Lyonnet, Bernard Le Marec
Publikováno v:
Human Genetics. 86:355-358
A total of 252 chromosomes from 126 patients with phenylalanine hydroxylase (PAH) deficiencies were analyzed for both mutant genotypes and restriction fragment length polymorphism (RFLP) haplotypes at the PAH locus. The mutant genes studied originate
Autor:
A Rubino, G. Schöch, P J Aggett, R. Tormo, Ferdinand Haschke, Jean Rey, K Launiala, W Heine, Olle Hernell, J Senterre
Publikováno v:
Acta Paediatrica. 79:1001-1005
Comment on the composition of soy protein based infant and follow-up formulas. ESPGAN Committee on Nutrition.
Autor:
Mariane de Montalembert, Jean-Jacques Lefrère, Martine Mariotti, Philippe Rouger, Jean Rey, Robert Girot, Charles Salmon
Publikováno v:
Vox Sanguinis. 59:218-221
The risk of infection with human immunodeficiency virus (HIV) by transfusion is not totally eliminated, since contaminated blood given before seroconversion to HIV is not detected on the actual biological screening. We used the polymerase chain react