Zobrazeno 1 - 10
of 142
pro vyhledávání: '"M, Silvie"'
Autor:
Boë, J. M. Silvie.
Th.--Méd.--Montpellier, 1814?
Voyez tom. 3, Montpellier.
Voyez tom. 3, Montpellier.
Externí odkaz:
http://catalogue.bnf.fr/ark:/12148/cb36856725b
Autor:
C. Duverger, V. Souyri, C. Monteil, S. Fournier, F. Espinasse, M.C. Gramer, M. Lepainteur, D. Seytre, J.R. Zahar, S. Nerome, C. Ciotti, I. Garrigues, M.L. Delaby, N. Fortineau, S. Ouzani, M. Kecharem, J.C. Lucet, S. Kernéis, S. Géra, G. Bendjelloul, L. Vaillant, M. Vanderbrugghe, V. Goldstein, C. Loison, S. Borde, V. Moulin, C. Leboydre, V. Derouin, A. Casetta, L. Meyer, A. Akpabie, N. Kassis-Chikhani, A. Maurand, M. Silvie, J.W. Decousser, F. Fourreau, B. Hacquin, A. Tackin, A. Lomont, N. Sabourin, R. Amarsy, S. Roulleau, Y. Boufflers, N. Idri, P. Frange, P. Baune, J. Robert, N. Osinski, C. Tamames, J. Auraix, N. Forest, E. Pierson, C. Lawrence, C. Flament, G. Rolland, P. Mariani, K. Belhacel, B. Salauze, F. Barbut, S. Jolivet, N. Audrain, I. Simon, L. Turpin, M. Rouveau, M.T. Le Cam, C. Eble, W. Zebiche, V. Simha, C. Grudzien, M. Denis, E. Le-Roux, S. Angerand, C. Charpinet
Publikováno v:
The Journal of Hospital Infection
Autor:
M. Silvie, A. Lapeyrade, Virginie Laurier, J. Jauregi, F. Lorenzini, F. Labrousse, E. Bieth, Catherine Molinas, G. Demeer, D. Thuilleaux, Maithé Tauber, Muriel Coupaye, P. Copet, C. Poitou
Publikováno v:
Journal of Intellectual Disability Research. 59:411-421
Background Prader–Willi syndrome (PWS) is a developmental genetic disorder characterised by a variable expression of medical, cognitive and behavioural symptoms. In adulthood, the prevalence and severity of these symptoms determine the quality of l
Autor:
Bansal, Abhisheka1 (AUTHOR) abhisheka@jnu.ac.in, Sharma, Manish1 (AUTHOR), Choudhury, Himashree1 (AUTHOR)
Publikováno v:
Scientific Reports. 10/15/2024, Vol. 14 Issue 1, p1-14. 14p.
Autor:
V, Laurier, A, Lapeyrade, P, Copet, G, Demeer, M, Silvie, E, Bieth, M, Coupaye, C, Poitou, F, Lorenzini, F, Labrousse, C, Molinas, M, Tauber, D, Thuilleaux, J, Jauregi
Publikováno v:
Journal of intellectual disability research : JIDR. 59(5)
Prader-Willi syndrome (PWS) is a developmental genetic disorder characterised by a variable expression of medical, cognitive and behavioural symptoms. In adulthood, the prevalence and severity of these symptoms determine the quality of life of the af
Autor:
Moine, M. (AUTHOR), Canon, O. (AUTHOR), Chedhomme, F. X. (AUTHOR), Tesson, A. L. (AUTHOR), Bourquin, M. (AUTHOR), Vitale, G. (AUTHOR), Davidau, E. (AUTHOR), Sujol, G. (AUTHOR)
Publikováno v:
Journal de Pharmacie Clinique. Sep2024, Vol. 43 Issue 3, p131-138. 8p.
Autor:
Kou, Yong-Jie1,2 (AUTHOR) 17393145594@163.com, Gao, Jin1,2 (AUTHOR) jingao2022@163.com, Li, Rui2 (AUTHOR), Ma, Zhi-Ya1 (AUTHOR) mzy16635048046@126.com, Elsheikha, Hany M.3 (AUTHOR) hany.elsheikha@nottingham.ac.uk, Wu, Xiao-Jing1,2 (AUTHOR) wuxiaojing2017@163.com, Zheng, Xiao-Nan1 (AUTHOR) zhengxiaonan8889@126.com, Wang, Meng2,4 (AUTHOR) wangmeng02@caas.cn, Zhu, Xing-Quan1 (AUTHOR) wangmeng02@caas.cn
Publikováno v:
International Journal of Molecular Sciences. Jul2024, Vol. 25 Issue 14, p7834. 14p.
Publikováno v:
Pathologie-biologie. 45(9)
Since January 1, 1995, the supply, stockage, dispensing and traceability of Blood Derivative Medicinal Products (BDMP) are subject to pharmaceutical regulations. A review of 24 months' application at Necker-Enfants Malades Hospital is presented and a
Autor:
Abd El-Aziz, Fatma El-Zahraa A.1 fatma.abdelgalil1@science.aun.edu.eg, Dawood, Asmaa F. A.2,3, Refaie, Shereen M.3, Khan, Shahina3
Publikováno v:
Egyptian Academic Journal of Biological Sciences. D, Histology & Histochemistry. Dec2023, Vol. 15 Issue 2, p89-100. 12p.
Autor:
Maiqun Gu1, Jiaxin Tian1, Yulu Lou1, Jia Ran1, Mohamed, Amr2, Keyhani, Nemat O.3, Jaronski, Stefan4, Guangmin Wang1, Xuanyu Chen1, Lian-Sheng Zang1, Wei Zhang1 wzhang9@gzu.edu.cn
Publikováno v:
Entomologia Generalis. 2023, Vol. 43 Issue 6, p1211-1219. 9p.