Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Sciauvaud A"'
Autor:
Zatyka, Malgorzata, Rosenstock, Tatiana R., Sun, Congxin, Palhegyi, Adina M., Hughes, Georgina W., Lara-Reyna, Samuel, Astuti, Dewi, di Maio, Alessandro, Sciauvaud, Axel, Korsgen, Miriam E., Stanulovic, Vesna, Kocak, Gamze, Rak, Malgorzata, Pourtoy-Brasselet, Sandra, Winter, Katherine, Varga, Thiago, Jarrige, Margot, Polvèche, Hélène, Correia, Joao, Frickel, Eva-Maria, Hoogenkamp, Maarten, Ward, Douglas G., Aubry, Laetitia, Barrett, Timothy, Sarkar, Sovan
Publikováno v:
In Stem Cell Reports 9 May 2023 18(5):1090-1106
Autor:
Pourtoy-Brasselet, Sandra, Sciauvaud, Axel, Boza-Moran, Maria-Gabriela, Cailleret, Michel, Jarrige, Margot, Polvèche, Hélène, Polentes, Jérôme, Chevet, Eric, Martinat, Cécile, Peschanski, Marc, Aubry, Laetitia
Publikováno v:
In The American Journal of Human Genetics 4 November 2021 108(11):2171-2185
Autor:
Malgorzata Zatyka, Tatiana R. Rosenstock, Congxin Sun, Adina M. Palhegyi, Georgina W. Hughes, Samuel Lara-Reyna, Dewi Astuti, Alessandro di Maio, Axel Sciauvaud, Miriam E. Korsgen, Vesna Stanulovic, Gamze Kocak, Malgorzata Rak, Sandra Pourtoy-Brasselet, Katherine Winter, Thiago Varga, Margot Jarrige, Hélène Polvèche, Joao Correia, Eva-Maria Frickel, Maarten Hoogenkamp, Douglas G. Ward, Laetitia Aubry, Timothy Barrett, Sovan Sarkar
Publikováno v:
Stem Cell Reports. 18:1090-1106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eea67dac5d3e62e6cee12045d3442df
https://doi.org/10.1016/j.stemcr.2023.04.002
https://doi.org/10.1016/j.stemcr.2023.04.002
Autor:
Jérôme Polentes, Hélène Polvèche, Cécile Martinat, Axel Sciauvaud, Maria-Gabriela Boza-Moran, Laetitia Aubry, Marc Peschanski, Margot Jarrige, Sandra Pourtoy-Brasselet, Michel Cailleret, Eric Chevet
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, 2021, 108 (11), pp.2171-2185. ⟨10.1016/j.ajhg.2021.10.001⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (11), pp.2171-2185. ⟨10.1016/j.ajhg.2021.10.001⟩
Am J Hum Genet
American Journal of Human Genetics, 2021, 108 (11), pp.2171-2185. ⟨10.1016/j.ajhg.2021.10.001⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2021, 108 (11), pp.2171-2185. ⟨10.1016/j.ajhg.2021.10.001⟩
Am J Hum Genet
International audience; Recent studies indicate that neurodegenerative processes that appear during childhood and adolescence in individuals with Wolfram syndrome (WS) occur in addition to early brain development alteration, which is clinically silen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48846496992065aec0d0d30ad68bd9b0
https://doi.org/10.1016/j.ajhg.2021.10.001
https://doi.org/10.1016/j.ajhg.2021.10.001
Transmission of infectious diseases from internationally adopted children to their adoptive families
Autor:
Sciauvaud, J., Rigal, E., Pascal, J., Nourrisson, C., Poirier, P., Poirier, V., Vidal, M., Mrozek, N., Laurichesse, H., Beytout, J., Labbe, A., Lesens, O.
Publikováno v:
In Clinical Microbiology and Infection August 2014 20(8):746-751
Autor:
Sciauvaud, Axel
Publikováno v:
Physiologie [q-bio.TO]. Université Paris-Saclay, 2022. Français. ⟨NNT : 2022UPASQ034⟩
Wolfram syndrome type 1 (WS1) is a rare autosomal recessive neurodegenerative disorder characterized by a combination of devastating clinical symptoms, namely: diabetes insipidus (DI), insulin-dependent diabetes mellitus (DM), optic atrophy (OA) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::741182edc46dc03740415b286600ff1a
https://theses.hal.science/tel-03917165
https://theses.hal.science/tel-03917165
Autor:
Pascal, Julie, Décombas-Marion, Marion, Poirier, Véronique, Lautrette, Alexandre, Rigal, Emilie, Sciauvaud, Julie, Pereira, Bruno, Labbe, André, Lesens, Olivier
Publikováno v:
Disaster Medicine & Public Health Preparedness; Aug2018, Vol. 12 Issue 4, p450-454, 5p
Akademický článek
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Autor:
Charlotte Texier, Jean Beytout, André Labbé, Céline Nourrisson, Julie Sciauvaud, Violaine Corbin, Julie Pascal, Olivier Lesens, Emilie Rigal, Véronique Poirier
Publikováno v:
European journal of dermatology : EJD. 26(4)
Internationally adopted children often present diseases contracted in the country of origin. Skin diseases are common in new arrivals, and diagnosis may prove challenging for GPs or even dermatologists if they are inexperienced in the extensive geogr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::473a7fe46a6c71db31ef5578f7880c91
https://pubmed.ncbi.nlm.nih.gov/27436771
https://pubmed.ncbi.nlm.nih.gov/27436771
Transmission of infectious diseases from internationally adopted children to their adoptive families
Autor:
J. Pascal, J. Sciauvaud, M. Vidal, A. Labbe, V. Poirier, N. Mrozek, Céline Nourrisson, Jean Beytout, Olivier Lesens, E. Rigal, Philippe Poirier, Henri Laurichesse
Publikováno v:
Clinical Microbiology and Infection
Clinical Microbiology and Infection, Elsevier for the European Society of Clinical Microbiology and Infectious Diseases, 2014, 20 (8), pp.24261464. ⟨10.1111/1469-0691.12454⟩
Clinical Microbiology and Infection, 2014, 20 (8), pp.24261464. ⟨10.1111/1469-0691.12454⟩
Clinical Microbiology and Infection, Elsevier for the European Society of Clinical Microbiology and Infectious Diseases, 2014, 20 (8), pp.24261464. ⟨10.1111/1469-0691.12454⟩
Clinical Microbiology and Infection, 2014, 20 (8), pp.24261464. ⟨10.1111/1469-0691.12454⟩
Internationally adopted children may suffer from different pathologies, including infectious diseases contracted in the country of origin. We evaluated the frequency of infectious diseases that may disseminate from adoptees to adoptive families on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::269a95fc2300ba37b03140c9e777a423
https://pubmed.ncbi.nlm.nih.gov/24261464
https://pubmed.ncbi.nlm.nih.gov/24261464