Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Caroline Marr"'
Autor:
Brigitte Mueller, Raoul Engelbert, Frances Baratta-Ziska, Bart Bartels, Nicole Blanc, Evelise Brizola, Paolo Fraschini, Claire Hill, Caroline Marr, Lisa Mills, Kathleen Montpetit, Verity Pacey, Miguel Rodriguez Molina, Marleen Schuuring, Chantal Verhille, Olga de Vries, Eric Hiu Kwong Yeung, Oliver Semler
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)
Abstract On the occasion of the 13th International Conference on Osteogenesis imperfecta in August 2017 an expert panel was convened to develop an international consensus paper regarding physical rehabilitation in children and adolescents with Osteog
Externí odkaz:
https://doaj.org/article/63a7f964372f474a8efedc7d4512fc2c
Publikováno v:
Journal of Multidisciplinary Healthcare
Journal of Multidisciplinary Healthcare, Vol Volume 10, Pp 145-155 (2017)
Journal of Multidisciplinary Healthcare, Vol Volume 10, Pp 145-155 (2017)
Osteogenesis imperfecta (OI) is a heterogeneous heritable connective tissue disorder characterized by low bone density. The type and severity of OI are variable. The primary manifestations are fractures, bone deformity, and bone pain, resulting in re
Autor:
Alison Seasman, Rebecca Jones, Davina Ford, Caroline Marr, Metabolic Bone Team, Clare Pickett
Publikováno v:
Bone Abstracts.
Autor:
Meena Balasubramanian, Metabolic Bone Team, Rebecca Jones, Caroline Marr, Paul Arundel, Nick Bishop, Alison Seasman
Publikováno v:
Bone Abstracts.
Publikováno v:
Bone Abstracts.
Publikováno v:
Bone Abstracts.
Autor:
Verity Pacey, Brigitte Mueller, Eric Hiu Kwong Yeung, Frances Baratta-Ziska, Nicole Blanc, Chantal Verhille, Bart Bartels, Miguel Rodriguez Molina, Kathleen Montpetit, Claire Hill, Paolo Fraschini, Olga de Vries, Caroline Marr, Evelise Brizola, Oliver Semler, Marleen Schuuring, Lisa Mills, Raoul H.H. Engelbert
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 13(1). BioMed Central
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)
Orphanet Journal of Rare Diseases, 13(158)
Orphanet journal of rare diseases, 13:158. BioMed Central
Orphanet Journal of Rare Diseases, 13(1). BioMed Central
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)
Orphanet Journal of Rare Diseases, 13(158)
Orphanet journal of rare diseases, 13:158. BioMed Central
On the occasion of the 13th International Conference on Osteogenesis imperfecta in August 2017 an expert panel was convened to develop an international consensus paper regarding physical rehabilitation in children and adolescents with Osteogenesis im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55091e651f15df6a9a7540dc8cec6703
https://lirias.kuleuven.be/handle/20.500.12942/703532
https://lirias.kuleuven.be/handle/20.500.12942/703532
Autor:
Caroline Marr
Publikováno v:
Bone Abstracts.
Autor:
Caroline Marr
Publikováno v:
Physiotherapy. 102:e209
Publikováno v:
npj Digital Medicine, Vol 3, Iss 1, Pp 1-5 (2020)
Abstract Over recent years, the adoption of connected technologies has grown dramatically, with potential for improving health care delivery, research, and patient experience. Yet, little has been documented about the prevalence and use of connected
Externí odkaz:
https://doaj.org/article/d302a71ada7d4260aa9bc550a7a5d606