Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Elise Kostrzewa"'
Autor:
Nicolas Grenier, Marie-Sylvie Doutre, Elise Kostrzewa, Arnaud Saint-Lézer, Jean-François Viallard
Publikováno v:
Joint Bone Spine. 78:524-526
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects medium- and small-sized arteries. We report the case of a 32-year-old female with PAN in which renal involvement was revealed by a secondary hyperaldosteronism. Hypokaliemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37297eddd5aa3bcdd9a54cf9285849c8
https://doi.org/10.1016/j.jbspin.2011.03.012
https://doi.org/10.1016/j.jbspin.2011.03.012
Autor:
Elise Kostrzewa, Arnaud Saint-Lézer, Jean-François Viallard, Marie-Sylvie Doutre, Nicolas Grenier
Publikováno v:
Revue du Rhumatisme. 78:479-481
Resume La periarterite noueuse (PAN) est une vascularite necrosante systemique atteignant les arteres de moyen et de petit calibre. Nous rapportons l’observation d’une femme âgee de 32 ans ayant une PAN au cours de laquelle l’atteinte renale f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f16fc3bcc153f69ae8653149b0e851
https://doi.org/10.1016/j.rhum.2011.05.015
https://doi.org/10.1016/j.rhum.2011.05.015
Autor:
Laurent Arnaud, Stéphane Barete, Jean Donadieu, Antoine Néel, Valérie Taly, Baptiste Hervier, Julien Haroche, Karine Cury, Zahir Amoura, Jean-François Emile, Jean-Marie Michot, Maud Bézier, Camille Roubille, Aude Rigolet, Véronique Meignin, Eric Hachulla, Bruno Graffin, Laurence Marie, Olivier Hermine, Marie Conrad, Elise Kostrzewa, Frédéric Charlotte, François Lifermann, Thierry Carmoi, Carles Villabona
Publikováno v:
Blood
Blood, American Society of Hematology, 2014, 124 (7), pp.1119-1126. ⟨10.1182/blood-2013-12-543793⟩
Blood, 2014, 124 (7), pp.1119-1126. ⟨10.1182/blood-2013-12-543793⟩
Blood, American Society of Hematology, 2014, 124 (7), pp.1119-1126. ⟨10.1182/blood-2013-12-543793⟩
Blood, 2014, 124 (7), pp.1119-1126. ⟨10.1182/blood-2013-12-543793⟩
Comment in "A common progenitor cell in LCH and ECD. [Blood. 2014]"; International audience; Histiocytoses are a group of heterogeneous diseases that mostly comprise Langerhans cell histiocytosis (LCH) and non-LCH. The association of LCH with non-LCH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4d1d15cc27f9743d813d25f98a848b7
https://www.hal.inserm.fr/inserm-02299580
https://www.hal.inserm.fr/inserm-02299580
Autor:
Fanny, Morice-Picard, Elise, Kostrzewa, Claude, Wolf, Pascale, Benlian, Alain, Taïeb, Didier, Lacombe
Publikováno v:
Archives of dermatology. 147(9)
X-linked dominant chondrodysplasia punctata, also known as Conradi-Hünermann-Happle syndrome, is a rare skeletal dysplasia characterized by short stature, craniofacial defects, cataracts, ichthyosis, coarse hair, and alopecia. Conradi-Hünermann-Hap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc250ecc866d968b1bd33d26a585024f
https://pubmed.ncbi.nlm.nih.gov/21931048
https://pubmed.ncbi.nlm.nih.gov/21931048
Autor:
Elise Kostrzewa, Didier Lacombe, Alain Taïeb, Fanny Morice-Picard, Claude Wolf, Pascale Benlian
Publikováno v:
Archives of Dermatology. 147:1073
Background X-linked dominant chondrodysplasia punctata, also known as Conradi-H unermann-Happle syndrome, is a rare skeletal dysplasia characterized by short stature, craniofacial defects, cataracts, ichthyosis, coarse hair, and alopecia. Conradi-H u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2609777fa60936026c42397a7292c12d
https://doi.org/10.1001/archdermatol.2011.230
https://doi.org/10.1001/archdermatol.2011.230