Zobrazeno 1 - 10
of 89
pro vyhledávání: '"A. Mollet Boudjemline"'
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:
Vincent Gajdos, Sandrine Katsahian, Nicole Beydon, Véronique Abadie, Loïc de Pontual, Sophie Larrar, Ralph Epaud, Bertrand Chevallier, Sylvain Bailleux, Alix Mollet-Boudjemline, Jean Bouyer, Sylvie Chevret, Philippe Labrune
Publikováno v:
PLoS Medicine, Vol 7, Iss 9, p e1000345 (2010)
BackgroundAcute bronchiolitis treatment in children and infants is largely supportive, but chest physiotherapy is routinely performed in some countries. In France, national guidelines recommend a specific type of physiotherapy combining the increased
Externí odkaz:
https://doaj.org/article/0feadb2c91b24b0cb0d6981c4db08ec4
Autor:
Gajdos, Vincent, Petit, François, Trioche, Pascale, Mollet–Boudjemline, Alix, Chauveaud, Aurelia, Myara, Anne, Trivin, François, Francoual, Jeanne, Labrune, Philippe
Publikováno v:
In Gastroenterology 2006 131(3):921-924
Publikováno v:
Haematologica, Vol 92, Iss 7 (2007)
Externí odkaz:
https://doaj.org/article/ffd4602057bb4884a74a189f3544e74b
Autor:
Gajdos, V. *, L'Hélias, L. Foix, Mollet-Boudjemline, A., Perreaux, F., Trioche, P., Labrune, P.
Publikováno v:
In Archives de pédiatrie 2005 12(4):397-403
Autor:
Flechtner, I., Viaud, M., Bidet, M., Coeugniet, F., Mollet-Boudjemline, A., Labrune, P., de Lonlay, P., Thibaud, E., Polak, M.
Publikováno v:
In Archives de pédiatrie May 2013 20(5) Supplement 1:H79-H80
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
Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type Ib
Autor:
Philippe Labrune, Vincent Gajdos, Alix Mollet Boudjemline, Arnaud Isapof, François Petit, Jean-Bernard Witas
Publikováno v:
Journal of Inherited Metabolic Disease. 33:477-480
Patients with type I glycogen storage disease (GSD) have poor tolerance to fasting, sometimes less than 3 hours during infancy. Even though most patients are able, as they get older, to tolerate a longer fasting period, they are at permanent risk for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9da4dcae29cf69772423556409836e40
https://doi.org/10.1007/s10545-010-9243-y
https://doi.org/10.1007/s10545-010-9243-y
Autor:
Philippe Labrune, Isabelle Flechtner, Michel Polak, Maud Bidet, A. Mollet-Boudjemline, P. de Lonlay, Magali Viaud, Elisabeth Thibaud, F. Coeugniet
Publikováno v:
Annales d'Endocrinologie. 79:210
Introduction La galactosemie est une maladie hereditaire rare du metabolisme du galactose qui touche 1 nouveau-ne sur 30 000 naissances. Les complications a long terme sont : l’insuffisance ovarienne prematuree (IOP), des troubles de la cognition,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb840c33570e6653481a8c2767e42b5a
https://doi.org/10.1016/j.ando.2018.06.059
https://doi.org/10.1016/j.ando.2018.06.059