Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marjolein Verhoef"'
Autor:
Ralph J Sakkers, Kathleen Montpetit, Argerie Tsimicalis, Thomas Wirth, Marjolein Verhoef, Reginald Hamdy, Jean A Ouellet, Rene M Castelein, Chantal Damas, Guus J Janus, Wouter H Nijhuis, Leonardo Panzeri, Simona Paveri, Dagmar Mekking, Kelly Thorstad, Richard W Kruse
Publikováno v:
Acta Orthopaedica, Vol 92, Iss 5, Pp 608-614 (2021)
Background and purpose — Involvement of patient organizations is steadily increasing in guidelines for treatment of various diseases and conditions for better care from the patient’s viewpoint and better comparability of outcomes. For this reason
Externí odkaz:
https://doaj.org/article/bce3df7d98e54d798d7eb2d13fc1f625
Autor:
Wouter Nijhuis, Anton Franken, Kara Ayers, Chantal Damas, Lars Folkestad, Antonella Forlino, Paolo Fraschini, Claire Hill, Guus Janus, Richard Kruse, Lena Lande Wekre, Lieve Michiels, Kathleen Montpetit, Leonardo Panzeri, Valerie Porquet-Bordes, Frank Rauch, Ralph Sakkers, Jean-Pierre Salles, Oliver Semler, Jony Sun, Michael To, Laura Tosi, Yangyang Yao, Eric Hiu Kwong Yeung, Lidiia Zhytnik, Maria Carola Zillikens, Marjolein Verhoef
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-16 (2021)
Abstract Background Osteogenesis Imperfecta (OI) is a genetic disorder also known as ‘brittle bone disease’. The clinical manifestation of OI shows a wide variation. Therefore, care for patients with OI requires an interdisciplinary approach. The
Externí odkaz:
https://doaj.org/article/e4473b5c08aa4163ac055f6a82da002b
Publikováno v:
Children, Vol 9, Iss 2, p 268 (2022)
Fractures in patients with osteogenesis imperfecta (OI) are caused by a decreased strength of bone due to a decreased quality and quantity of bone matrix and architecture. Mutations in the collagen type 1 encoding genes cause the altered formation of
Externí odkaz:
https://doaj.org/article/ab26714fbf5b40afbeb272fb6a198dd9
Autor:
Camiel A. Wijngaarde, Leonard H. van den Berg, Rob C. Brink, Joyce Sombroek, W-Ludo van der Pol, René M. Castelein, Ruben P A van Eijk, Floor A.S. de Kort, Louise A.M. Otto, Fay-Lynn Asselman, Marjolein Verhoef, Renske I. Wadman, Bart Bartels, Marloes Stam, Inge Cuppen
Publikováno v:
Neurology. 93:e149-e158
ObjectiveTo investigate the natural course of scoliosis and to estimate lifetime probability of scoliosis surgery in spinal muscular atrophy (SMA).MethodsWe analyzed cross-sectional data from 283 patients from our population-based cohort study. Addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83285b3b2d77a2b9fc1d35eedafe049e
https://doi.org/10.1212/wnl.0000000000007742
https://doi.org/10.1212/wnl.0000000000007742
Autor:
Johanna M. A. Visser-Meily, W. Ludo van der Pol, Esther T. Kruitwagen-Van Reenen, Fay-Lynn Asselman, Carin D. Schröder, Maarten J Fischer, Marjolein Verhoef, Renske I. Wadman
Purpose: Patients with spinal muscular atrophy (SMA) suffer from slowly progressive weakness of axial, respiratory and proximal muscles, leading to restrictions in activity and participation. This study aims to investigate patients’ level of psycho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7594f8efff26d7ff12605f9af930cab
Autor:
Marjolein Verhoef, Hans A Barf, Marcel WM Post, Floris WA van Asbeck, Rob HJM Gooskens, Arie JH Prevo
Publikováno v:
Developmental Medicine & Child Neurology; Feb2006, Vol. 48 Issue 2, p114-119, 6p