Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elisabeth Celestin"'
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:
Agnès Linglart, Delphine Chambolle, Martin Biosse Duplan, Lisa Friedlander, Caroline Nguyen, Catherine Chaussain, Elisabeth Celestin
Publikováno v:
Endocrine Connections, Vol 11, Iss 1, Pp 1-12 (2022)
Background. 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 any
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::997e12a6204703d66d1431890a664c57
https://doi.org/10.21203/rs.3.rs-450002/v2
https://doi.org/10.21203/rs.3.rs-450002/v2
Autor:
Martin Biosse Duplan, Delphine Chambolle, Agnès Linglart, Caroline Nguyen, Lisa Friedlander, Catherine Chaussain, Elisabeth Celestin
Background. X-linked hypophosphatemia (XLH) is a rare, hereditary, progressive, and lifelong phosphate wasting disorder characterized by pathological elevations in fibroblast growth factor (FGF) 23 serum concentration and activity. In the oral cavity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eda6335bca7458543b1fdf0ad6791823
https://doi.org/10.21203/rs.3.rs-450002/v1
https://doi.org/10.21203/rs.3.rs-450002/v1
Autor:
Anne-Sophie Lambert, Perrine Charles, Agnès Linglart, Nadia Bahi-Buisson, Anya Rothenbuhler, Elisabeth Celestin
Publikováno v:
Bone Abstracts.
Autor:
Lotfi Miladi, Perrine Charles, Agnès Linglart, Emmanuel Durand, Isabelle Fontaine, Elisabeth Celestin, Nadia Bahi-Buisson, Anya Rothenbuhler, Anne-Sophie Lambert, Philippe Wicart, Sylvie Brailly-Tabard, Séverine Trabado
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186941 (2017)
PLoS ONE
PLoS ONE
Background Classic Rett Syndrome (RS) is a disabling condition mainly caused by MECP2 mutations. Girls with RS are at risk of developing bone fragility and fractures at a young age which results in pain and may seriously impair quality of life. Objec
Autor:
Anne-Sophie Lambert, Anya Rothenbuhler, Perrine Charles, Sylvie Brailly-Tabard, Séverine Trabado, Elisabeth Célestin, Emmanuel Durand, Isabelle Fontaine, Lotfi Miladi, Philippe Wicart, Nadia Bahi-Buisson, Agnès Linglart
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186941 (2017)
Classic Rett Syndrome (RS) is a disabling condition mainly caused by MECP2 mutations. Girls with RS are at risk of developing bone fragility and fractures at a young age which results in pain and may seriously impair quality of life.To retrospectivel
Externí odkaz:
https://doaj.org/article/fda0bfe6504547169618796b229aa24d