Zobrazeno 1 - 10
of 52
pro vyhledávání: '"A. Hubert Buron"'
Autor:
Petit, F., Hubert-Buron, A., Mollet-Boudjemline, A., Sechepine, A., Milcent, K., Guyonnet, C., Labrune, P.
Publikováno v:
In Progres en Urologie March 2013 23(3):210-218
Publikováno v:
In EMC – Pediatría 2010 45(3):1-13
Autor:
Labrune, Philippe, Eberschweiler, Pascale Trioche, Boudjemline, Alix Mollet, Hubert-Buron, Aurélie, Petit, François, Gajdos, Vincent
Publikováno v:
In La Presse Médicale July 2008 37(7-8):1172-1177
Autor:
Hubert-Buron, Aurélie *, Leblond, Jonathan *, Jacquot, Arnaud *, Ducrotté, Philippe *, †, Déchelotte, Pierre *, †, Coëffier, Moïse *, †
Publikováno v:
In The Journal of Nutrition June 2006 136(6):1461-1465
Autor:
Leblond, Jonathan, Hubert-Buron, Aurélie, Bole-Feysot, Christine, Ducrotté, Philippe, Déchelotte, Pierre, Coëffier, Moïse
Publikováno v:
In Biochimie 2006 88(7):759-765
Autor:
Mylène Mabille, Philippe Labrune, Marie Brevet, Coralie Pelissou, Gilles Mithieux, Laurence Dubourg, Louis Lassalle, Ariane Perry, Monika Gjorgjieva, A. Stefanutti, Antonin Tortereau, Margaux Raffin, A. Duchampt, Fabienne Rajas, Aurélie Hubert-Buron
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2016, 25 (17), pp.3784-3797. ⟨10.1093/hmg/ddw224⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (17), pp.3784-3797. ⟨10.1093/hmg/ddw224⟩
Human Molecular Genetics, 2016, 25 (17), pp.3784-3797. ⟨10.1093/hmg/ddw224⟩
Human Molecular Genetics, Oxford University Press (OUP), 2016, 25 (17), pp.3784-3797. ⟨10.1093/hmg/ddw224⟩
International audience; Glycogen storage disease type I (GSDI) is a rare metabolic disease due to glucose-6 phosphatase deficiency, characterized by fasting hypoglycemia. Patients also develop chronic kidney disease whose mechanisms are poorly unders
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb400cc40b66301960bb938bdfa26c8f
https://doi.org/10.1093/hmg/ddw224
https://doi.org/10.1093/hmg/ddw224
Autor:
Labrune Philippe, Gajdos Vincent, Eberschweiler Pascale, Hubert-Buron Aurélie, Petit François, Vianey-Saban Christine, Boudjemline Alix, Piraud Monique, Froissart Roseline
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 27 (2011)
Abstract Glucose-6-phosphatase deficiency (G6P deficiency), or glycogen storage disease type I (GSDI), is a group of inherited metabolic diseases, including types Ia and Ib, characterized by poor tolerance to fasting, growth retardation and hepatomeg
Externí odkaz:
https://doaj.org/article/ae904d641239403fa1239c9511301326
Autor:
Philippe Labrune, K. Milcent, A. Hubert-Buron, A. Sechepine, F. Petit, A. Mollet-Boudjemline, C. Guyonnet
Publikováno v:
Progrès en Urologie. 23:210-218
Resume But Elaborer et valider aupres d’une population temoin une enquete sous forme d’auto-questionnaires en francais pour evaluer la sante sexuelle d’hommes et de femmes adultes presentant une maladie metabolique. Materiels et methodes Etude
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b8384f16701b1b9adb51b9300d88664
https://doi.org/10.1016/j.purol.2012.10.014
https://doi.org/10.1016/j.purol.2012.10.014
Publikováno v:
EMC - Pediatría. 45:1-13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efcb344fb904fdd441e8571149bd5a86
https://doi.org/10.1016/s1245-1789(10)70170-0
https://doi.org/10.1016/s1245-1789(10)70170-0
Autor:
François Petit, Philippe Labrune, Alix Mollet Boudjemline, Pascale Trioche Eberschweiler, Vincent Gajdos, Aurélie Hubert-Buron
Publikováno v:
La Presse Médicale. 37:1172-1177
Hepatic glycogen storage diseases are rare inherited conditions affecting glycogen metabolism. During the last twenty years, medical progress has allowed children who used to die before they reached the age of ten years to reach adulthood. It is impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2713979df0bb71c30025f41c74951f5f
https://doi.org/10.1016/j.lpm.2007.09.023
https://doi.org/10.1016/j.lpm.2007.09.023