Zobrazeno 1 - 10
of 267
pro vyhledávání: '"Ponard, D"'
Publikováno v:
In Annales de dermatologie et de venereologie March 2015 142(3):163-169
Autor:
Desauw, C *, Hachulla, E, Boumbar, Y, Bouroz-Joly, J, Ponard, D, Arvieux, J, Dubucquoi, S, Fauchais, A.L, Hatron, P.Y, Devulder, B
Publikováno v:
In La Revue de médecine interne 2002 23(4):357-363
Publikováno v:
In La Revue de médecine interne 2002 23(6):533-541
Autor:
Dumestre-Perard, C1, Ponard, D1, Drouet, C1, Leroy, V2, Zarski, J-P2, Dutertre, N3, Colomb, M. G1
Publikováno v:
Clinical & Experimental Immunology. Jan2002, Vol. 127 Issue 1, p131-136. 6p.
Akademický článek
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Autor:
Bygum, Anette, Fagerberg, Christina, Ponard, D., Monnier, Nicole, Lunardi, Joel, Drouet, Christian
Publikováno v:
Allergy
Allergy, Wiley, 2011, 66 (1), pp.76-84. ⟨10.1111/j.1398-9995.2010.02456.x⟩
Allergy, 2011, 66 (1), pp.76-84. ⟨10.1111/j.1398-9995.2010.02456.x⟩
Bygum, A, Fagerberg, C R, Ponard, D, Monnier, N, Lunardi, J & Drouet, C 2011, ' Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency ', Allergy, vol. 66, no. 1, pp. 76-84 . https://doi.org/10.1111/j.1398-9995.2010.02456.x
Allergy, Wiley, 2011, 66 (1), pp.76-84. ⟨10.1111/j.1398-9995.2010.02456.x⟩
Allergy, 2011, 66 (1), pp.76-84. ⟨10.1111/j.1398-9995.2010.02456.x⟩
Bygum, A, Fagerberg, C R, Ponard, D, Monnier, N, Lunardi, J & Drouet, C 2011, ' Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency ', Allergy, vol. 66, no. 1, pp. 76-84 . https://doi.org/10.1111/j.1398-9995.2010.02456.x
International audience; BACKGROUND: Hereditary angioedema (HAE), type I and II, is an autosomal dominant disease with deficiency of functional C1 inhibitor protein causing episodic swellings of skin, mucosa and viscera. HAE is a genetically heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a0ec1d04acb4ec0e10d96575f964dd4a
https://www.hal.inserm.fr/inserm-00567441/document
https://www.hal.inserm.fr/inserm-00567441/document
Publikováno v:
The Pediatric Infectious Disease Journal. 10:615-618
Autor:
Bouillet, L., Boccon-Gibod, I., Bork, K., Anette Bygum, Caballero, T., Drout, C., Farkas, H., Longhurst, H., Massot, C., Nielsen, E. W., Ponard, D., Cicardi, M.
Publikováno v:
Bouillet, L, Boccon-Gibod, I, Bork, K, Bygum, A, Caballero, T, Drout, C, Farkas, H, Longhurst, H, Massot, C, Nielsen, E W, Ponard, D & Cicardi, M 2007, ' Disease expression in women with hereditary angioedema ', 5th C1 inhibitor Deficiency Workshop, Budapest, Hungary, 31/05/2007-03/06/2007 .
University of Southern Denmark
University of Southern Denmark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::000df7e047385089527d210fcbcb216f
https://portal.findresearcher.sdu.dk/da/publications/aaab0ea0-3910-11dd-a26c-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/aaab0ea0-3910-11dd-a26c-000ea68e967b
Autor:
Drout, C., Cicardi, M., Pappalardo, E., Monnier, N., Gaboriand, C., Ponard, D., Roche, O., Tordai, A., Bos-Wagenaar, I., Perricone, R., Anette Bygum, Bouillet, L., Farkas, H., Bork, K., Lunardi, J., Tosi, M., Lopez-Trascasa, M.
Publikováno v:
Drout, C, Cicardi, M, Pappalardo, E, Monnier, N, Gaboriand, C, Ponard, D, Roche, O, Tordai, A, Bos-Wagenaar, I, Perricone, R, Bygum, A, Bouillet, L, Farkas, H, Bork, K, Lunardi, J, Tosi, M & Lopez-Trascasa, M 2007, ' Mutations of the SERPING1 gene associated with hereditary angioedema in a european population, lessons for their relevance to the disease ', 5th C1 inhibitor Deficiency Workshop, Budapest, Hungary, 31/05/2007-03/06/2007 .
University of Southern Denmark
University of Southern Denmark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::beca13221e421da782fab25fffe416f8
https://portal.findresearcher.sdu.dk/da/publications/7d0691c0-3912-11dd-a26c-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/7d0691c0-3912-11dd-a26c-000ea68e967b
Akademický článek
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