Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Members of the BBD"'
Autor:
Mohammadamin Najirad, Mang Shin Ma, Frank Rauch, Vernon Reid Sutton, Brendan Lee, Jean-Marc Retrouvey, Members of the BBD, Shahrokh Esfandiari
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background Osteogenesis imperfecta (OI) affects dental and craniofacial development and may therefore impair Oral Health-Related Quality of Life (OHRQoL). However, little is known about OHRQoL in children and adolescents with OI. The aim of
Externí odkaz:
https://doaj.org/article/7757f1aa9be44808b7ed5357d4994963
Autor:
Jaskaran S Bains, Erin M Carter, Kate P Citron, Adele L Boskey, Jay R Shapiro, Robert D Steiner, Peter A Smith, Michael B Bober, Tracy Hart, David Cuthbertson, Jeff Krischer, Peter H Byers, Melanie Pepin, Michaela Durigova, Francis H Glorieux, Frank Rauch, Joseph M Sliepka, V Reid Sutton, Brendan Lee, Members of the BBD Consortium, Sandesh CS Nagamani, Cathleen L Raggio
Publikováno v:
JBMR Plus, Vol 3, Iss 5, Pp n/a-n/a (2019)
Abstract Osteogenesis imperfecta (OI) is characterized by low bone mass and bone fragility. Using data from a large cohort of individuals with OI from the Osteogenesis Imperfecta Foundation's linked clinical research centers, we examined the associat
Externí odkaz:
https://doaj.org/article/6e4fbae8bcd74f8eb57849a4170f4b1a
Autor:
null Chaya N. Murali, null Brady Slater, null Salma Musaad, null David Cuthbertson, null Dianne Nguyen, null Alicia Turner, null Mahshid Azamian, null Laura Tosi, null Frank Rauch, null V. Reid Sutton, null Brendan Lee, null Sandesh C. S. Nagamani, null Members of the BBD Consortium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acfea5a13801f09b6d6eb5e927bd2eff
https://doi.org/10.1111/cge.13939/v2/response1
https://doi.org/10.1111/cge.13939/v2/response1
Autor:
Najirad, Mohammadamin, Ma, Mang Shin, Rauch, Frank, Sutton, Vernon Reid, Lee, Brendan, Retrouvey, Jean-Marc, Esfandiari, Shahrokh, Members of the BBD
Publikováno v:
Orphanet Journal of Rare Diseases; 10/25/2018, Vol. 13 Issue 1, pN.PAG-N.PAG, 1p