Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Goetz, Violette"'
Autor:
Goetz, Violette, Yang, David Dawei, Lacaille, Florence, Pelosi, Michele, Angoulvant, François, Brassier, Anais, Arnoux, Jean-Baptiste, Schiff, Manuel, Heilbronner, Claire, Salvador, Elodie, Debray, Dominique, Oualha, Mehdi, Renolleau, Sylvain, Girard, Muriel, de Lonlay, Pascale
Publikováno v:
In Molecular Genetics and Metabolism April 2022 135(4):320-326
Autor:
Maler, Victor1,2 (AUTHOR), Goetz, Violette1 (AUTHOR), Tardieu, Marine1 (AUTHOR), Khalil, Abderrahmane El1,2 (AUTHOR), Alili, Jean Meidi3 (AUTHOR), Meunier, Philippe3 (AUTHOR), Maillot, François1,4 (AUTHOR), Labarthe, François1,5 (AUTHOR) labarthe@univ-tours.fr
Publikováno v:
Orphanet Journal of Rare Diseases. 6/8/2023, Vol. 18 Issue 1, p1-7. 7p.
Autor:
Goetz, Violette1 (AUTHOR), Yang, David-Dawei2 (AUTHOR), Abid, Hanene3 (AUTHOR), Roux, Charles-Joris4 (AUTHOR), Levy, Raphael4 (AUTHOR), Kossorotoff, Manoelle1 (AUTHOR), Desguerre, Isabelle1 (AUTHOR), Angoulvant, François2,5 (AUTHOR) frafrancois.angoulvant@aphp.fr, Aubart, Mélodie1,6 (AUTHOR) melodie.aubart@aphp.fr
Publikováno v:
European Journal of Pediatrics. Jun2023, Vol. 182 Issue 6, p2615-2624. 10p. 1 Color Photograph, 1 Diagram, 1 Chart, 1 Graph.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Goetz, Violette, Yang, David Dawei, Lacaille, Florence, Pelosi, Michele, Angoulvant, François, Brassier, Anais, Arnoux, Jean-Baptiste, Schiff, Manuel, Heilbronner, Claire, Salvador, Elodie, Debray, Dominique, Oualha, Mehdi, Renolleau, Sylvain, Girard, Muriel, de Lonlay, Pascale
Publikováno v:
Molecular Genetics and Metabolism
Molecular Genetics and Metabolism, 2022, 135 (4), pp.320-326. ⟨10.1016/j.ymgme.2022.02.001⟩
Molecular Genetics and Metabolism, 2022, 135 (4), pp.320-326. ⟨10.1016/j.ymgme.2022.02.001⟩
International audience; ObjectivesReye Syndrome is an acute encephalopathy with increased liver enzymes and blood ammonia, without jaundice. The prevalence of an underlying inherited metabolic disorder (IMD) is unclear, nor the clinical or biological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40bbd4f7ca562a50b40429b5477e6ad0
https://pubmed.ncbi.nlm.nih.gov/35221207
https://pubmed.ncbi.nlm.nih.gov/35221207
Autor:
Civit, Antoine, Gueguen, Paul, Blasco, Helene, Benz-de-Bretagne, Isabelle, Lebredonchel, Élodie, Dingeo, Giulia, Jeanne, Médéric, Rouxel, Sophie, Tardieu, Marine, Raynor, Alexandre, Labarthe, François, Bruneel, Arnaud, Goetz, Violette
Publikováno v:
In Clinica Chimica Acta 1 November 2023 551