Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ingunn Westerheim"'
Autor:
Taco van Welzenis, Ingunn Westerheim, Tracy Hart, Lena Lande Wekre, Oliver Semler, Frank Rauch, Laetitia Dewavrin, Ruby Dadzie, Samantha Prince, Cathleen Raggio
Publikováno v:
BMC Public Health, Vol 24, Iss 1, Pp 1-13 (2024)
Abstract Background The IMPACT Survey explored the humanistic, clinical, and economic burden of osteogenesis imperfecta (OI) on individuals with OI, their families, caregivers, and wider society. Two previous publications report research methodology,
Externí odkaz:
https://doaj.org/article/31c02d520bf7407a8593b63822256d35
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Introduction Osteogenesis imperfecta (OI) is a heritable skeletal disorder and comprises various subtypes that differ in clinical presentation, with Type I considered the least severe and Types III/IV the most severe forms. The study aim was
Externí odkaz:
https://doaj.org/article/fe01cdb171b845b9a21fb28a9b45f2b2
Autor:
Tracy Hart, Ingunn Westerheim, Taco van Welzenis, Oliver Semler, Cathleen Raggio, Frank Rauch, Ruby Dadzie, Samantha Prince, Lena Lande Wekre
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background The IMPACT survey aimed to elucidate the humanistic, clinical and economic burden of osteogenesis imperfecta (OI) on individuals with OI, their families, caregivers and wider society. Research methodology, demographics and initial
Externí odkaz:
https://doaj.org/article/f204f1f580a4442fae9c7ea6a36b7ad3
Autor:
Ingunn Westerheim, Tracy Hart, Taco van Welzenis, Lena Lande Wekre, Oliver Semler, Cathleen Raggio, Michael B. Bober, Maria Rapoport, Samantha Prince, Frank Rauch
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-21 (2024)
Abstract Background Osteogenesis imperfecta (OI) is a rare, heritable connective tissue disorder associated with a variety of symptoms, that affect individuals’ quality of life (QoL) and can be associated with increased healthcare resource use. Whi
Externí odkaz:
https://doaj.org/article/48bbeb81bbf247809910592e5df103b2
Autor:
Maria Rapoport, Michael B. Bober, Cathleen Raggio, Lena Lande Wekre, Frank Rauch, Ingunn Westerheim, Tracy Hart, Taco van Welzenis, Arun Mistry, James Clancy, Lucy Booth, Samantha Prince, Oliver Semler
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-26 (2023)
Abstract Background Osteogenesis imperfecta (OI) is a rare heritable connective tissue disorder primarily characterised by skeletal deformity and fragility, and an array of secondary features. The purpose of this review was to capture and quantify th
Externí odkaz:
https://doaj.org/article/dd1eed6b9a474a42b1a3956f3fd01095
Autor:
Debra Smyth, Monica Hytiris, Coreen Kelday, Ciara McDonnell, Christine Burren, Adrian Gardner, Lisa Mills, Susan Parekh, Oliver Semler, Angela Stewart, Ingunn Westerheim, Muhammad Kassim Javaid, Patricia Osborne, S. Faisal Ahmed
Publikováno v:
Frontiers in Public Health, Vol 10 (2023)
BackgroundResearch on the effects of the COVID-19 pandemic on people with rare diseases is limited. Few studies compare healthcare throughout the progression of the ongoing pandemic.AimsTo assess the impact of the pandemic on individuals with osteoge
Externí odkaz:
https://doaj.org/article/5e25f3659191436a8bde0da47058f050
Autor:
Muhammad Kassim Javaid, Marina Mordenti, Manila Boarini, Luca Sangiorgi, ERN BOND Working Group, Ingunn Westerheim, Inês Alves, Rebecca Tvedt Skarberg, Natasha M. Appelman-Dijkstra, Corinna Grasemann
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Understanding the natural history of rare bone and mineral conditions is essential for improving clinical practice and the development of new diagnostics and therapeutics. Recruitment and long-term participation in registries are
Externí odkaz:
https://doaj.org/article/164bf1ebabe745438f86281f9fc1a1cd