Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Ellen Van der Plas"'
Autor:
Nicholas Trapp, Benjamin Pace, Brandan Penaluna, Victoria Muller Ewald, Linder Wendt, Jacob Miller, Anthony Purgianto, Ellen van der Plas, Krystal Parker, Aaron Boes
Publikováno v:
Brain Stimulation, Vol 16, Iss 1, Pp 233- (2023)
Externí odkaz:
https://doaj.org/article/79a5954967be4748b7beb5f4b6641804
Publikováno v:
Frontiers in Psychology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/191fe2c9860b4f558d94f5723ba704e2
Autor:
Timothy R. Koscik, Ellen van der Plas, Laurie Gutmann, Sarah A. Cumming, Darren G. Monckton, Vincent Magnotta, Richard K. Shields, Peggy C. Nopoulos
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Deficits in white matter (WM) integrity and motor symptoms are among the most robust and reproducible features of myotonic dystrophy type 1 (DM1). In the present study, we investigate whether WM integrity, obtained from diffusion-weighted MR
Externí odkaz:
https://doaj.org/article/0e5a87339ef14fe0b3a871680f6a4da9
Autor:
Hend M. Al-Kaylani, Bradley T. Loeffler, Sarah L. Mott, Melissa Curry, Sneha Phadke, Ellen van der Plas
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
IntroductionYounger age at diagnosis is a risk factor for poor health-related quality of life (HRQOL) in long-term breast cancer survivors. However, few studies have specifically addressed HRQOL in young adults with breast cancer (i.e., diagnosed pri
Externí odkaz:
https://doaj.org/article/24e20302ef4b4457b17bd5fba16cca30
Autor:
Ellen van der Plas, Jeffrey D. Long, Timothy R. Koscik, Vincent Magnotta, Darren G. Monckton, Sarah A. Cumming, Amy C. Gottschalk, Marco Hefti, Laurie Gutmann, Peggy C. Nopoulos
Publikováno v:
Frontiers in Neurology, Vol 12 (2022)
IntroductionThe present study had four aims. First, neuronal injury markers, including neurofilament light (NF-L), total tau, glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase (UCH-L1), were compared between individuals with a
Externí odkaz:
https://doaj.org/article/009018d5ab65499fb8768c4ab0e95700
Autor:
Jacob N. Miller, Alison Kruger, David J. Moser, Laurie Gutmann, Ellen van der Plas, Timothy R. Koscik, Sarah A. Cumming, Darren G. Monckton, Peggy C. Nopoulos
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Myotonic dystrophy type 1 is the most common form of muscular dystrophy in adults, and is primarily characterized by muscle weakness and myotonia, yet some of the most disabling symptoms of the disease are cognitive and behavioral. Here we evaluated
Externí odkaz:
https://doaj.org/article/e471c06bf36444afb72579129c838841
Autor:
Ellen van der Plas, T. Leigh Spencer Noakes, Darci T. Butcher, Rosanna Weksberg, Laura Galin-Corini, Elizabeth A. Wanstall, Patrick Te, Laura Hopf, Sharon Guger, Brenda J. Spiegler, Johann Hitzler, Russell J. Schachar, Shinya Ito, Brian J. Nieman
Publikováno v:
NeuroImage: Clinical, Vol 28, Iss , Pp 102428- (2020)
Introduction: Cure rates for pediatric acute lymphoblastic leukemia (ALL) have reached an all-time high (>90%); however, neurocognitive difficulties continue to affect quality of life in at least a subset of survivors. There are relatively few quanti
Externí odkaz:
https://doaj.org/article/c35aaa3954814a38952ea53818eb85ba
Autor:
Sabine A. S. Langie, Matthieu Moisse, Katarzyna Szarc vel Szic, Ellen Van Der Plas, Gudrun Koppen, Sofie De Prins, Tijs Louwies, Vera Nelen, Guy Van Camp, Diether Lambrechts, Greet Schoeters, Wim Vanden Berghe, Patrick De Boever
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-13 (2018)
Abstract Background The prevalence of respiratory allergy in children is increasing. Epigenetic DNA methylation changes are plausible underlying molecular mechanisms. Results Saliva samples collected in substudies of two longitudinal birth cohorts in
Externí odkaz:
https://doaj.org/article/d0acd1b24e9c4b7786cd66612c06e094
Autor:
Kathleen E. Langbehn, Ashley M. Cochran, Ellen van der Plas, Amy L. Conrad, Eric Epping, Erin Martin, Patricia Espe-Pfeifer, Peg Nopoulos
Publikováno v:
Brain Sciences, Vol 10, Iss 8, p 543 (2020)
Reports of behavioral disturbance in Juvenile-Onset Huntington’s Disease (JOHD) have been based primarily on qualitative caregiver reports or retrospective medical record reviews. This study aims to quantify differences in behavior in patients with
Externí odkaz:
https://doaj.org/article/1ed36338ee694bb0986e56057e3681e4
Autor:
Jordan L. Schultz, Douglas R. Langbehn, Hend M. Al‐Kaylani, Ellen van der Plas, Timothy R. Koscik, Eric A. Epping, Patricia B. Espe‐Pfeifer, Erin P. Martin, David J. Moser, Vincent A. Magnotta, Peggy C. Nopoulos
Publikováno v:
Movement Disorders. 38:113-122
Juvenile-onset Huntington's disease (JOHD) is a rare form of Huntington's disease (HD) characterized by symptom onset before the age of 21 years. Observational data in this cohort is lacking.Quantify measures of disease progression for use in clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::733e07925a6bc2e302629f96e90985fa
https://doi.org/10.1002/mds.29251
https://doi.org/10.1002/mds.29251