Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Liesbeth, De Waele"'
Autor:
Ines Vandekerckhove, Eirini Papageorgiou, Britta Hanssen, Nathalie De Beukelaer, Marleen Van den Hauwe, Nathalie Goemans, Anja Van Campenhout, Liesbeth De Waele, Friedl De Groote, Kaat Desloovere
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Classifying gait patterns into homogeneous groups could enhance communication among healthcare providers, clinical decision making and clinical trial designs in boys with Duchenne muscular dystrophy (DMD). Sutherland’s classification has b
Externí odkaz:
https://doaj.org/article/f06d92ca69d34d43ad91a35164e69b0a
Autor:
Sam Geuens, Jeroen Van Dessel, Rosanne Govaarts, Nadine A. Ikelaar, Onno C. Meijer, Hermien E. Kan, Erik H. Niks, Nathalie Goemans, Jurgen Lemiere, Nathalie Doorenweerd, Liesbeth De Waele
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 12, Pp 2324-2333 (2023)
Abstract Objective Duchenne muscular dystrophy (DMD) is a neuromuscular disorder in which many patients also have neurobehavioral problems. Corticosteroids, the primary pharmacological treatment for DMD, have been shown to affect brain morphology in
Externí odkaz:
https://doaj.org/article/add3ba9314e94a10b739bcd5d963f0ee
Autor:
Leen Lagae, Marijke Proesmans, Marleen Van den Hauwe, François Vermeulen, Liesbeth De Waele, Mieke Boon
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Respiratory complications are common in spinal muscular atrophy (SMA) and significantly contribute to morbidity and mortality in these patients. Generalized respiratory and bulbar muscle weakness translates into diverse and complex clinical consequen
Externí odkaz:
https://doaj.org/article/e1ffaebddd764cd3a33492d66d1ef839
Autor:
Petrus J. de Vries, Tosca-Marie Heunis, Stephanie Vanclooster, Nola Chambers, Stacey Bissell, Anna W. Byars, Jennifer Flinn, Tanjala T. Gipson, Agnies M. van Eeghen, Robert Waltereit, Jamie K. Capal, Sebastián Cukier, Peter E. Davis, Catherine Smith, J. Chris Kingswood, Eva Schoeters, Shoba Srivastava, Megumi Takei, Sugnet Gardner-Lubbe, Aubrey J. Kumm, Darcy A. Krueger, Mustafa Sahin, Liesbeth De Waele, Anna C. Jansen
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-20 (2023)
Abstract Background Tuberous sclerosis complex (TSC) is associated with a wide range of physical manifestations for which international clinical recommendations for diagnosis and management have been established. TSC is, however, also associated with
Externí odkaz:
https://doaj.org/article/0f33b55db38e479d9f389a096963c78f
Autor:
Stephanie Vanclooster, Stacey Bissell, Agnies M. van Eeghen, Nola Chambers, Liesbeth De Waele, Anna W. Byars, Jamie K. Capal, Sebastián Cukier, Peter Davis, Jennifer Flinn, Sugnet Gardner-Lubbe, Tanjala Gipson, Tosca-Marie Heunis, Dena Hook, J. Christopher Kingswood, Darcy A. Krueger, Aubrey J. Kumm, Mustafa Sahin, Eva Schoeters, Catherine Smith, Shoba Srivastava, Megumi Takei, Robert Waltereit, Anna C. Jansen, Petrus J. de Vries
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 14, Iss 1, Pp 1-23 (2022)
Abstract Background Tuberous sclerosis complex (TSC)–associated neuropsychiatric disorders (TAND) is an umbrella term for the behavioural, psychiatric, intellectual, academic, neuropsychological and psychosocial manifestations of TSC. Although TAND
Externí odkaz:
https://doaj.org/article/5465835e27fa45c8abe959798b7d6f7e
Autor:
Petrus J. de Vries, Loren Leclezio, Sugnet Gardner-Lubbe, Darcy Krueger, Mustafa Sahin, Steven Sparagana, Liesbeth De Waele, Anna Jansen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Tuberous Sclerosis Complex (TSC), a multi-system genetic disorder, is associated with a wide range of TSC-Associated Neuropsychiatric Disorders (TAND). Individuals have apparently unique TAND profiles, challenging diagnosis, psych
Externí odkaz:
https://doaj.org/article/e8fba2272c7745f6abf4fdd10494af2e
Autor:
Laura Yedigaryan, Ester Martínez-Sarrà, Giorgia Giacomazzi, Nefele Giarratana, Bernard K. van der Veer, Alessio Rotini, Silvia Querceto, Hanne Grosemans, Álvaro Cortés-Calabuig, Sara Salucci, Michela Battistelli, Elisabetta Falcieri, Rik Gijsbers, Mattia Quattrocelli, Kian Peng Koh, Liesbeth De Waele, Gunnar M. Buyse, Rita Derua, Maurilio Sampaolesi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Skeletal muscle holds an intrinsic capability of growth and regeneration both in physiological conditions and in case of injury. Chronic muscle illnesses, generally caused by genetic and acquired factors, lead to deconditioning of the skeletal muscle
Externí odkaz:
https://doaj.org/article/75771e6b6f9f4141abd91f02144e00b8
Autor:
Ineke Verreydt, Ines Vandekerckhove, Elze Stoop, Nicky Peeters, Vanessa van Tittelboom, Patricia Van de Walle, Marleen Van den Hauwe, Nathalie Goemans, Liesbeth De Waele, Anja Van Campenhout, Britta Hanssen, Kaat Desloovere
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
The aim of this study was to determine the clinimetric properties, i.e., reliability, validity and responsiveness of an instrumented strength assessment in typically developing (TD) children and children with cerebral palsy (CP) and Duchenne muscular
Externí odkaz:
https://doaj.org/article/47546a32a87e408ea5bffb7075f2b7a1
Autor:
Ines Vandekerckhove, Marleen Van den Hauwe, Nathalie De Beukelaer, Elze Stoop, Marije Goudriaan, Margaux Delporte, Geert Molenberghs, Anja Van Campenhout, Liesbeth De Waele, Nathalie Goemans, Friedl De Groote, Kaat Desloovere
Publikováno v:
Frontiers in Human Neuroscience, Vol 16 (2022)
Prolonging ambulation is an important treatment goal in children with Duchenne muscular dystrophy (DMD). Three-dimensional gait analysis (3DGA) could provide sensitive parameters to study the efficacy of clinical trials aiming to preserve ambulation.
Externí odkaz:
https://doaj.org/article/35976de1279b4a55af4da9e290d93e03
Autor:
Mélanie Annoussamy, Andreea M. Seferian, Aurore Daron, Yann Péréon, Claude Cances, Carole Vuillerot, Liesbeth De Waele, Vincent Laugel, Ulrike Schara, Teresa Gidaro, Charlotte Lilien, Jean‐Yves Hogrel, Pierre Carlier, Emmanuel Fournier, Linda Lowes, Ksenija Gorni, Myriam Ly‐Le Moal, Nicole Hellbach, Timothy Seabrook, Christian Czech, Ricardo Hermosilla, Laurent Servais, the NatHis‐SMA study group
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 2, Pp 359-373 (2021)
Abstract Objective To characterize the natural history of spinal muscular atrophy (SMA) over 24 months using innovative measures such as wearable devices, and to provide evidence for the sensitivity of these measures to determine their suitability as
Externí odkaz:
https://doaj.org/article/5662815653b845ccaffc6ca741781c22