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Autor:
M. Kujas
Publikováno v:
Morphologie. 102:133-134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93b27ed783285bc08df6f6a43116d6c0
https://doi.org/10.1016/j.morpho.2018.07.001
https://doi.org/10.1016/j.morpho.2018.07.001
Autor:
M. Kujas
Publikováno v:
EMC - Endocrinologie - Nutrition. 4:1-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::373bc44a0d92ba570984b9b9d79f9a90
https://doi.org/10.1016/s1155-1941(07)46571-4
https://doi.org/10.1016/s1155-1941(07)46571-4
Autor:
M. Kujas
Publikováno v:
EMC - Gynécologie. 2:1-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c34ba823ff3cb0a512286e1fbc37749
https://doi.org/10.1016/s0246-1064(07)44331-6
https://doi.org/10.1016/s0246-1064(07)44331-6
Autor:
M. Kujas
Publikováno v:
EMC - Ginecología-Obstetricia. 43:1-10
Los datos aportados por la biologia molecular y la genomica en los ultimos 25 anos han esclarecido en parte los fenomenos implicados no solo en la embriogenesis en general, sino tambien en lo que se refiere a los organos concretos que proceden de un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2885af683b97228ccdc68a0c93ab9499
https://doi.org/10.1016/s1283-081x(07)70824-x
https://doi.org/10.1016/s1283-081x(07)70824-x
Autor:
Albert Louvel, M. Kujas, S. Ouzounian, Xavier Bertagna, Frédérique Tissier, Paul Legmann, H. Gouya
Publikováno v:
La Presse Médicale. 34:511-515
Resume Introduction Le syndrome de Cushing a une tres faible incidence (1 a 10 cas/million/an), et les cas familiaux sont encore plus exceptionnels. Nous rapportons 2 situations inedites d’associations de differentes causes de syndrome de Cushing.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::debf94e3ca5fb441b8aaaeba9f7cc9eb
https://doi.org/10.1016/s0755-4982(05)83961-2
https://doi.org/10.1016/s0755-4982(05)83961-2
Publikováno v:
Scopus-Elsevier
¶ Objective and Importance. Cerebellar pilocytic astrocytomas are common benign tumours of childhood and mostly easy to treat because of their location and conformation. Nevertheless, unpredictable recurrence as well as the lack of features to predi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7df40565e4004a14d05a5a1c9a5a9cbf
https://doi.org/10.1007/s007010050044
https://doi.org/10.1007/s007010050044
Autor:
I. Brito, M. Kujas, M. Mokhtari, Elodie Manié, Yannick Marie, Olivier Delattre, Ahmed Idbaih, Virginie Raynal, Khê Hoang-Xuan, J.-Y. Delattre, Alain Aurias, Marc Sanson, G. Pierron, Carlo Lucchesi, Emmanuel Barillot
Publikováno v:
Revue Neurologique. 163:21-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8211e391ecd662c4fdb6edc4f894af86
https://doi.org/10.1016/s0035-3787(07)90373-2
https://doi.org/10.1016/s0035-3787(07)90373-2
Publikováno v:
Human Molecular Genetics. 4:915-920
The neurofibromatosis 1 gene seems to play essential roles at several different stages of life. During embryogenesis, it is involved in cardiac development while in the adult, neurofibromin (the corresponding protein) is mainly expressed in the nervo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0ea682e013a1671b5b05bc23cd65ed
https://doi.org/10.1093/hmg/4.5.915
https://doi.org/10.1093/hmg/4.5.915
Autor:
Liu, Longqi1 (AUTHOR), Shi, Liang1 (AUTHOR) jstshiliang@126.com, Su, Yibing1 (AUTHOR), Wang, Keda1 (AUTHOR), Wang, Hanbin1 (AUTHOR)
Publikováno v:
BMC Musculoskeletal Disorders. 8/1/2024, Vol. 25 Issue 1, p1-7. 7p.