Zobrazeno 1 - 10
of 162
pro vyhledávání: '"Catherine Chaussain"'
Autor:
Elis J. Lira dos Santos, Kenta Nakajima, Julien Po, Ayako Hanai, Volha Zhukouskaya, Martin Biosse Duplan, Agnès Linglart, Takashi Shimada, Catherine Chaussain, Claire Bardet
Publikováno v:
International Journal of Oral Science, Vol 15, Iss 1, Pp 1-10 (2023)
Abstract Elevated fibroblast growth factor 23 (FGF23) in X-linked hypophosphatemia (XLH) results in rickets and phosphate wasting, manifesting by severe bone and dental abnormalities. Burosumab, a FGF23-neutralizing antibody, an alternative to conven
Externí odkaz:
https://doaj.org/article/7315cc6e2b4443c8abd78d6f5c752a46
Autor:
Élisa Caussin, Frédéric Courson, Elisabeth Dursun, Yohann Brukarz, Daniel Dot, Catherine Chaussain, Jean‐Pierre Attal, Philippe François
Publikováno v:
Clinical Case Reports, Vol 12, Iss 3, Pp n/a-n/a (2024)
Key Clinical Message Treatment of patients with amelogenesis imperfecta extends over many years, from childhood to early adulthood. Their management at any age is complex and has to be adapted in relation to therapies validated in the general populat
Externí odkaz:
https://doaj.org/article/b834965f7c1c44b88aae938747b2ba2f
Autor:
Julia André, Volha V. Zhukouskaya, Anne-Sophie Lambert, Jean-Pierre Salles, Brigitte Mignot, Claire Bardet, Catherine Chaussain, Anya Rothenbuhler, Agnès Linglart
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background/aim Despite optimal conventional treatment (oral phosphate supplements and active vitamin D analogs), about 40–50% of children with well-controlled X-linked hypophosphatemia (XLH) show linear growth failure, making them less lik
Externí odkaz:
https://doaj.org/article/f6c19042ac8f44099d6965eb56139ed8
Autor:
Elodie Fiot, Bertille Alauze, Bruno Donadille, Dinane Samara-Boustani, Muriel Houang, Gianpaolo De Filippo, Anne Bachelot, Clemence Delcour, Constance Beyler, Emilie Bois, Emmanuelle Bourrat, Emmanuel Bui Quoc, Nathalie Bourcigaux, Catherine Chaussain, Ariel Cohen, Martine Cohen-Solal, Sabrina Da Costa, Claire Dossier, Stephane Ederhy, Monique Elmaleh, Laurence Iserin, Hélène Lengliné, Armelle Poujol-Robert, Dominique Roulot, Jerome Viala, Frederique Albarel, Elise Bismuth, Valérie Bernard, Claire Bouvattier, Aude Brac, Patricia Bretones, Nathalie Chabbert-Buffet, Philippe Chanson, Regis Coutant, Marguerite de Warren, Béatrice Demaret, Lise Duranteau, Florence Eustache, Lydie Gautheret, Georges Gelwane, Claire Gourbesville, Mickaël Grynberg, Karinne Gueniche, Carina Jorgensen, Veronique Kerlan, Charlotte Lebrun, Christine Lefevre, Françoise Lorenzini, Sylvie Manouvrier, Catherine Pienkowski, Rachel Reynaud, Yves Reznik, Jean-Pierre Siffroi, Anne-Claude Tabet, Maithé Tauber, Vanessa Vautier, Igor Tauveron, Sebastien Wambre, Delphine Zenaty, Irène Netchine, Michel Polak, Philippe Touraine, Jean-Claude Carel, Sophie Christin-Maitre, Juliane Léger
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss S1, Pp 1-39 (2022)
Abstract Turner syndrome (TS; ORPHA 881) is a rare condition in which all or part of one X chromosome is absent from some or all cells. It affects approximately one in every 1/2500 liveborn girls. The most frequently observed karyotypes are 45,X (40
Externí odkaz:
https://doaj.org/article/47d7e0d1bd19414b82a3ff48728cebb1
Implantation of engineered human microvasculature to study human infectious diseases in mouse models
Autor:
Sophia Schönherr-Hellec, Eirini Chatzopoulou, Jean-Philippe Barnier, Yoann Atlas, Sébastien Dupichaud, Thomas Guilbert, Yves Dupraz, Julie Meyer, Catherine Chaussain, Caroline Gorin, Xavier Nassif, Stephane Germain, Laurent Muller, Mathieu Coureuil
Publikováno v:
iScience, Vol 26, Iss 4, Pp 106286- (2023)
Summary: Animal models for studying human pathogens are crucially lacking. We describe the implantation in mice of engineered human mature microvasculature consisting of endothelial and perivascular cells embedded in collagen hydrogel that allows inv
Externí odkaz:
https://doaj.org/article/42dd2748dbfa4182b28a846f68f9536c
Autor:
Eloïse Giabicani, Aurélie Pham, Céline Sélénou, Marie-Laure Sobrier, Caroline Andrique, Julie Lesieur, Agnès Linglart, Anne Poliard, Catherine Chaussain, Irène Netchine
Publikováno v:
International Journal of Oral Science, Vol 14, Iss 1, Pp 1-8 (2022)
Abstract Parental imprinting is an epigenetic process leading to monoallelic expression of certain genes depending on their parental origin. Imprinting diseases are characterized by growth and metabolic issues starting from birth to adulthood. They a
Externí odkaz:
https://doaj.org/article/9a988a1be4c44aa7ba3015d2d49b8cff
Autor:
Caroline Nguyen, Elisabeth Celestin, Delphine Chambolle, Agnès Linglart, Martin Biosse Duplan, Catherine Chaussain, Lisa Friedlander
Publikováno v:
Endocrine Connections, Vol 11, Iss 1, Pp 1-12 (2022)
Introduction: X-linked hypophosphatemia (XLH) is a rare, hereditary, and lifelong phosphate-wasting disorder characterized by rickets in childhood and impaired teeth mineralization. In the oral cavity, spontaneous abscesses can often occur without an
Externí odkaz:
https://doaj.org/article/c4602f9543b94322adf787d77203d836
Autor:
Adeline Le Cabec, Thomas Colard, Damien Charabidze, Catherine Chaussain, Gabriele Di Carlo, Sabine Gaudzinski-Windheuser, Jean-Jacques Hublin, Rita T. Melis, Laura Pioli, Fernando Ramirez-Rozzi, Margherita Mussi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Childhood is an ontogenetic stage unique to the modern human life history pattern. It enables the still dependent infants to achieve an extended rapid brain growth, slow somatic maturation, while benefitting from provisioning, transitional f
Externí odkaz:
https://doaj.org/article/ceb7899eacea44e9958125f27ca86fe4
Autor:
Margaux Gadion, Agathe Hervé, Julia Herrou, Anya Rothenbuhler, Violaine Smail‐Faugeron, Frédéric Courson, Agnès Linglart, Catherine Chaussain, Martin Biosse Duplan
Publikováno v:
JBMR Plus, Vol 6, Iss 11, Pp n/a-n/a (2022)
ABSTRACT X‐linked hypophosphatemia (XLH) is a rare genetic disorder that disrupts skeletal and dental mineralization. In addition to rickets in children, XLH patients also have frequent spontaneous dental abscesses that increase the risk of tooth l
Externí odkaz:
https://doaj.org/article/ba5b9067e91d46b9823e2e97a6806941
Autor:
Virginie Bourdin, Philippe Charlier, Stéphane Crevat, Lotfi Slimani, Catherine Chaussain, Mélodie Kielbasa, Olivier Pible, Jean Armengaud
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 3011 (2023)
Scientific examination of the heart of Blessed Pauline Jaricot—a French missionary figure—was carried out in 2022. As tandem mass spectrometry proteotyping has proven to be valuable to obtain the broad taxonomic repertoire of a given sample witho
Externí odkaz:
https://doaj.org/article/49b1ea5829684509808b4f98907375d9