Zobrazeno 1 - 3
of 3
pro vyhledávání: '"MESH: Postmortem Changes"'
Publikováno v:
Deutsche Zeitschrift für die Gesamte Gerichtliche Medizin
Deutsche Zeitschrift für die Gesamte Gerichtliche Medizin, 2007, 121 (6), pp.469-75. ⟨10.1007/s00414-007-0197-z⟩
Deutsche Zeitschrift für die Gesamte Gerichtliche Medizin, 2007, 121 (6), pp.469-75. ⟨10.1007/s00414-007-0197-z⟩
International audience; The aim of this work was to estimate the accuracy of craniofacial reconstruction (CFR), from a series of 25 controlled cases. Three protocols of blind CFRs (exhibiting an increasing complexity from A to C) were assessed in thi
Autor:
Frédéric Treguer, Remi Baruteau, Raphaël P. Martins, Philippe Mabo, Alban-Elouen Baruteau, Ryad Joomye, Jean-Claude Daubert, Julien Baruteau, Michel Roussey
Publikováno v:
European Journal of Pediatrics
European Journal of Pediatrics, Springer Verlag, 2009, 168 (7), pp.771-7. ⟨10.1007/s00431-009-0951-y⟩
European Journal of Pediatrics, 2009, 168 (7), pp.771-7. ⟨10.1007/s00431-009-0951-y⟩
European Journal of Pediatrics, Springer Verlag, 2009, 168 (7), pp.771-7. ⟨10.1007/s00431-009-0951-y⟩
European Journal of Pediatrics, 2009, 168 (7), pp.771-7. ⟨10.1007/s00431-009-0951-y⟩
International audience; INTRODUCTION: Congenital long-QT syndrome (LQTS) is a sporadic or familial inherited arrhythmia. It can lead to sudden death by ventricular fibrillation which occurs at any age but particularly during infancy. Recent studies o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c85170520ca0f4131b0dff28c6b4cda0
https://hal.archives-ouvertes.fr/hal-00911293
https://hal.archives-ouvertes.fr/hal-00911293
Publikováno v:
Neurobiol Aging
Neurobiol Aging, 2007, 28 (4), pp.568-78. ⟨10.1016/j.neurobiolaging.2006.02.010⟩
Neurobiol Aging, 2007, 28 (4), pp.568-78. ⟨10.1016/j.neurobiolaging.2006.02.010⟩
International audience; Glutamatergic pathways play a key role in the functional organization of neuronal circuits involved in Parkinson disease (PD). Recently, three vesicular glutamate transporters (VGLUT1-3) were identified. VGLUT1 and VGLUT2 are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ae6093a42e4a66ddb59594dcb814fc9
https://www.hal.inserm.fr/inserm-00154872
https://www.hal.inserm.fr/inserm-00154872