Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mélanie Bué"'
Autor:
Véronique Abadie, Valeria Dipasquale, Mélanie Bué-Chevalier, Frédéric Gottrand, Amandine Rubio, Valérie Le Ru-Raguénès, D. Guimber, Audrey Van Malleghem, Katia Lecoeur, Aline Genevois-Peres, Haude Clouzeau, Sophie Dubedout, Sophie Baeckeroot, Marc Bellaiche, Irène Loras-Duclaux, Laila Rivard, Gaëlle Malécot-Le Meur, Audrey Lecoufle, Véronique Leblanc
Publikováno v:
European journal of clinical nutrition. 76(4)
Enteral nutrition (EN) allows adequate nutritional intake in children for whom oral intake is impossible, insufficient or unsafe. With maturation and health improvements, most children ameliorate oral skills and become able to eat orally, therefore w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ad253ef267069e219ca8dd7cf89aea2
https://pubmed.ncbi.nlm.nih.gov/34462558
https://pubmed.ncbi.nlm.nih.gov/34462558
Autor:
Christelle Pons, Juliette Ropars, Mélanie Bué, Sylvain Brochard, Laetitia Houx, Dominique Guyader, Jean-Sébastien Bourseul, Philippe Le Moine, Isabelle Manesse, Amandine Dubois
Publikováno v:
Annals of Physical and Rehabilitation Medicine
Annals of Physical and Rehabilitation Medicine, Elsevier Masson, 2016, 59 (5-6), pp.314-319. ⟨10.1016/j.rehab.2016.04.009⟩
Annals of Physical and Rehabilitation Medicine, 2016, 59 (5-6), pp.314-319. ⟨10.1016/j.rehab.2016.04.009⟩
Annals of Physical and Rehabilitation Medicine, Elsevier Masson, 2016, 59 (5-6), pp.314-319. ⟨10.1016/j.rehab.2016.04.009⟩
Annals of Physical and Rehabilitation Medicine, 2016, 59 (5-6), pp.314-319. ⟨10.1016/j.rehab.2016.04.009⟩
Background Pain is one of the symptoms reported most by children with motor disabilities particularly during daily living activities in institutions and during rehabilitation. Despite the care and consideration of professionals, a wide range of motor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a56a5d996b8823242d5a4c209c7d1b9
https://hal.univ-rennes2.fr/hal-01883766
https://hal.univ-rennes2.fr/hal-01883766
Autor:
Bernd H. Belohradsky, Miriam Hoernes, Sophie Cypowyj, Janine Reichenbach, Saleh Al-Muhsen, Magali Audry, Joachim Roesler, Amos Etzioni, Francisco Espinosa Rosales, Matías Oleastro, Luyan Liu, Tatiana Kochetkov, Viktor P. Chernyshov, Olivier Lortholary, Cécile Masson, Julie Toubiana, Stéphane Blanche, Caroline Thumerelle, Reinhard Seger, Dan Engelhard, Beáta Tóth, Yuval Itan, Lizbeth Blancas-Galicia, Patrick Nitschke, Gizi Wildbaum, Ludmyla Chernyshova, Avinash Abhyankar, Jérome Flatot, Ellen D. Renner, Ileana Maria Madrigal Beas, Xiao-Fei Kong, Maya Chrabieh, Antoine Toulon, Capucine Picard, Masao Kobayashi, László Maródi, J. Hiller, Alexandra Y. Kreins, Christine Bodemer, Julie Sawalle-Belohradsky, Alexandre Bolze, Claudia Traidl-Hoffmann, Stéphanie Boisson-Dupuis, Jean-Laurent Casanova, Anastasia Bondarenko, Alain Fischer, Emmanuelle Jouanguy, Laurent Abel, Theresia Kusuma, Nathan Karin, Rosa María Cortés Grimaldo, Pierre-Régis Burgel, Alessandro Borghesi, Annette Jansson, Anne Puel, Mélanie Bué, Jacinta Bustamante, Kilian Eyerich, Mélanie Migaud, Carlos Torres Lozano, Stefanie Eyerich, Barbara Drexel, Sara Sebnem Kilic, Klaus Magdorf, Satoshi Okada, Vera Gulácsy
Publikováno v:
The Journal of Experimental Medicine
J. Exp. Med. 208, 1635-1648 (2011)
J. Exp. Med. 208, 1635-1648 (2011)
Whole-exome sequencing reveals activating STAT1 mutations in some patients with autosomal dominant chronic mucocutaneous candidiasis disease.
Chronic mucocutaneous candidiasis disease (CMCD) may be caused by autosomal dominant (AD) IL-17F defici
Chronic mucocutaneous candidiasis disease (CMCD) may be caused by autosomal dominant (AD) IL-17F defici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f22afce4bf3f7b792989039cf399f52
http://europepmc.org/articles/PMC3149226
http://europepmc.org/articles/PMC3149226
Autor:
Melanie Buehler, Sonja T. Jesse, Heike Kueck, Bastian Lange, Patricia Koenig, Wendy K. Jo, Albert Osterhaus, Andreas Beineke
Publikováno v:
BMC Veterinary Research, Vol 16, Iss 1, Pp 1-6 (2020)
Abstract Background Rabbit hemorrhagic disease virus (RHDV, Lagovirus europeus GI.1) induces a contagious and highly lethal hemorrhagic disease in rabbits. In 2010 a new genotype of lagovirus (GI.2), emerged in Europe, infecting wild and domestic pop
Externí odkaz:
https://doaj.org/article/1964f6a64cd34ec18eb6811429d134e6