Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Droz, Dominique"'
Publikováno v:
In Actualités pharmaceutiques October 2018 57(579):35-40
Publikováno v:
In American Journal of Kidney Diseases December 2002 40(6):1179-1184
Autor:
Karras, Alexandre, Noël, Laure-Hélène, Droz, Dominique, Delansorne, Dominique, Saint-André, Jean-Paul, Aucouturier, Pierre, Alyanakian, Marie-Alexandra, Grünfeld, Jean-Pierre, Lesavre, Philippe
Publikováno v:
In American Journal of Kidney Diseases November 2002 40(5):1091-1096
Autor:
Valleix, Sophie, Drunat, Séverine, Philit, Jean-Baptiste, Adoue, Daniel, Piette, Jean-Charles, Droz, Dominique, MacGregor, Brigitte, Canet, Denis, Delpech, Marc, Grateau, Gilles *
Publikováno v:
In Kidney International March 2002 61(3):907-912
Akademický článek
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Autor:
Clauss François, Manière Marie-Cécile, Reibel Amélie, Droz Dominique, Alembik Yves, Mornet Etienne, Bloch-Zupan Agnès
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 4, Iss 1, p 6 (2009)
Abstract Background Hypophosphatasia (HP) is a rare inherited disorder characterized by a wide spectrum of defects in mineralized tissues and caused by deficiency in the tissue non-specific alkaline phosphatase gene (ALPL). The symptoms are highly va
Externí odkaz:
https://doaj.org/article/f1c5fc8462394283a839104260d68b79
Publikováno v:
In American Journal of Kidney Diseases June 2001 37(6):1324-1329
Autor:
Prasad, Megana K., Geoffroy, Véronique, Vicaire, Serge, Jost, Bernard, Dumas, Michael, Le Gras, Stéphanie, Switala, Marzena, Gasse, Barbara, Laugel-Haushalter, Virginie, Paschaki, Marie, Leheup, Bruno, Droz, Dominique, Dalstein, Amelie, Loing, Adeline, Grollemund, Bruno, Muller-Bolla, Michèle, Lopez-Cazaux, Serena, Minoux, Maryline, Jung, Sophie, Obry, Frédéric, Vogt, Vincent, Davideau, Jean-Luc, Davit-Béal, Tiphaine, Kaiser, Anne-Sophie, Moog, Ute, Richard, Béatrice, Morrier, Jean-Jacques, Duprez, Jean-Pierre, Odent, Sylvie, Bailleul-Forestier, Isabelle, Rousset, Monique Marie, Merametdijan, Laure, Toutain, Annick, Joseph, Clara, Giuliano, Fabienne, Dahlet, Jean-Christophe, Courval, Aymeric, Alloussi, Mustapha El, Laouina, Samir, Soskin, Sylvie, Guffon, Nathalie, Dieux, Anne, Doray, Bérénice, Feierabend, Stephanie, Ginglinger, Emmanuelle, Fournier, Benjamin, De la Dure Molla, Muriel, Alembik, Yves, Tardieu, Corinne, Clauss, François, Berdal, Ariane, Stoetzel, Corinne, Manière, Marie Cécile, Dollfus, Hélène, Bloch-Zupan, Agnès
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2016, 53 (2), pp.98-110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, 2016, 53 (2), pp.98--110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, 2016, 53 (2), pp.98--110. 〈10.1136/jmedgenet-2015-103302〉
Journal of Medical Genetics, 2016, 53 (2), pp.98-110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, BMJ Publishing Group, 2016, 53 (2), pp.98--110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, BMJ Publishing Group, 2016, 53 (2), pp.98-110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, 2016, 53 (2), pp.98--110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, 2016, 53 (2), pp.98--110. 〈10.1136/jmedgenet-2015-103302〉
Journal of Medical Genetics, 2016, 53 (2), pp.98-110. ⟨10.1136/jmedgenet-2015-103302⟩
Journal of Medical Genetics, BMJ Publishing Group, 2016, 53 (2), pp.98--110. ⟨10.1136/jmedgenet-2015-103302⟩
BACKGROUND: Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or as part of a genetic syndrome. Due to the vast number of genes implicated in these disorders, establishing a molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::577bc8584971b1992ef43c06e09ac9c7
https://hal.archives-ouvertes.fr/hal-02517086
https://hal.archives-ouvertes.fr/hal-02517086
Akademický článek
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Autor:
Verine, Jérôme, Mourad, Nathalie, Desseaux, Kristell, Vanhille, Philippe, Noël, Laure-Hélène, Beaufils, Hélène, Grateau, Gilles, Janin, Anne, Droz, Dominique
Publikováno v:
Human Pathology
Human Pathology, WB Saunders, 2007, 38 (12), pp.1798-809. 〈10.1016/j.humpath.2007.04.013〉
Human Pathology, WB Saunders, 2007, 38 (12), pp.1798-809. ⟨10.1016/j.humpath.2007.04.013⟩
Human Pathology, WB Saunders, 2007, 38 (12), pp.1798-809. 〈10.1016/j.humpath.2007.04.013〉
Human Pathology, WB Saunders, 2007, 38 (12), pp.1798-809. ⟨10.1016/j.humpath.2007.04.013⟩
International audience; We retrospectively reviewed the clinicopathological features of a series of 68 renal AA amyloidosis observations collected between 1990 and 2005. The amyloidogenic disease was a chronic infection (40.8%), a chronic inflammatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::396898a0f4e8754e9450d0f36b9e6072
http://www.hal.inserm.fr/inserm-00152433/file/verine.pdf
http://www.hal.inserm.fr/inserm-00152433/file/verine.pdf