More severe phenotype of early‐onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A

Autor: Caroline Caetano da Silva, Manon Ricquebourg, Philippe Orcel, Stéphanie Fabre, Thomas Funck‐Brentano, Martine Cohen‐Solal, Corinne Collet

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)

Abstract Background Early‐onset osteoporosis (EOOP) is defined by low bone mineral density (BMD), which increases the risk of fracture. Although the prevalence of osteoporosis at a young age is unknown, low BMD is highly linked to genetic backgroun

Externí odkaz: https://doaj.org/article/c601e16d66eb4054988173adaf84ed6c

Accuracy of the HumaSensplus point-of-care uric acid meter using capillary blood obtained by fingertip puncture

Autor: Stéphanie Fabre, Pierre Clerson, Jean-Marie Launay, Jean-François Gautier, Tiphaine Vidal-Trecan, Jean-Pierre Riveline, Adam Platt, Anna Abrahamsson, Jeffrey N. Miner, Glen Hughes, Pascal Richette, Thomas Bardin

Publikováno v: Arthritis Research & Therapy, Vol 20, Iss 1, Pp 1-9 (2018)

Abstract Background The uric acid (UA) level in patients with gout is a key factor in disease management and is typically measured in the laboratory using plasma samples obtained after venous puncture. This study aimed to assess the reliability of im

Externí odkaz: https://doaj.org/article/65453793918441df89947ddab41763a4

Author response for 'Lrp5 p. Val667Met variant compromises bone mineral density and matrix properties in osteoporosis'

Autor: null Stéphanie Fabre, null Morgane Bourmaud, null Guillaume Mabilleau, null Ruben Goulet, null Aude Couturier, null Alexandre Dentel, null Serge Picaud, null Thomas Funck‐Brentano, null Corinne Collet, null Martine Cohen‐Solal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0307553203b2031e35070a1043a15bf7
https://doi.org/10.1002/jbm4.10741/v2/response1

Traitements séquentiels de l'ostéoporose

Autor: Stéphanie Fabre, Martine Cohen-Solal

Publikováno v: L'actualité Rhumatologique 2022 ISBN: 9782294778599

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4b9730fad251302d70fffdc1a1150c32
https://doi.org/10.1016/b978-2-294-77859-9.00013-x

More severe phenotype of early‐onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A

Autor: Stéphanie Fabre, Thomas Funck-Brentano, Manon Ricquebourg, Caroline Caetano da Silva, Philippe Orcel, Martine Cohen-Solal, Corinne Collet

Publikováno v: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Wiley Periodicals, Inc. 2021, ⟨10.1002/mgg3.1681⟩
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)

Background Early‐onset osteoporosis (EOOP) is defined by low bone mineral density (BMD), which increases the risk of fracture. Although the prevalence of osteoporosis at a young age is unknown, low BMD is highly linked to genetic background. Hetero

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51a5e82b7f31feb854485dfda829bb2b
https://doi.org/10.1002/mgg3.1681