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pro vyhledávání: '"John H. Warner"'
Baseline multimodal information predicts future motor impairment in premanifest Huntington's disease
Autor:
Eduardo Castro, Pablo Polosecki, Irina Rish, Dorian Pustina, John H. Warner, Andrew Wood, Cristina Sampaio, Guillermo A. Cecchi
Publikováno v:
NeuroImage: Clinical, Vol 19, Iss , Pp 443-453 (2018)
In Huntington's disease (HD), accurate estimates of expected future motor impairments are key for clinical trials. Individual prognosis is only partially explained by genetics. However, studies so far have focused on predicting the time to clinical d
Externí odkaz:
https://doaj.org/article/909389c205d04a9b9f58108aa89c616f
Autor:
John H, Warner, Jeffrey D, Long, James A, Mills, Douglas R, Langbehn, Jennifer, Ware, Amrita, Mohan, Cristina, Sampaio
Publikováno v:
Journal of Huntington's Disease. 11:153-171
Background: Huntington’s disease (HD) is an autosomal dominant, neurological disease caused by an expanded CAG repeat near the N-terminus of the huntingtin (HTT) gene. A leading theory concerning the etiology of HD is that both onset and progressio
Autor:
Maitrei Kohli, Dorian Pustina, John H Warner, Daniel C Alexander, Rachael I Scahill, Sarah J Tabrizi, Peter A Wijeratne
Publikováno v:
E: Imaging.
Publikováno v:
The Journal of Clinical Pharmacology. 60:1051-1060
Development of effective therapeutics that slow Huntington's disease progression is a research priority that requires an understanding of natural disease progression. We applied a population-modeling approach to describe the progression of 2 routinel
Autor:
P. A. Wijeratne, John H. Warner, Dorian Pustina, Rachael I. Scahill, Daniel C. Alexander, Sarah J. Tabrizi, Maitrei Kohli
Publikováno v:
F: Clinical studies: case reports, observational studies and trials.
Autor:
Cristina Sampaio, Amrita Mohan, Edward J. Wild, John H. Warner, Beth Ann Griffin, Claude Messan Setodji, Monica Busse, Marika Booth
Publikováno v:
Parkinsonism Relat Disord
Introduction\ud Despite being genetically inherited, it is unclear how non-genetic factors (e.g., substance use, employment) might contribute to the progression and severity of Huntington's disease (HD).\ud \ud Methods\ud We used propensity score (PS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4295b41f7e97924a82460a4fa9add383
Autor:
Monica Busse-Morris, Marika Booth, John H. Warner, Edward J. Wild, Beth Ann Griffin, Amrita Mohan, Claude Messan Setodji
Publikováno v:
Clinical studies.
Background Although Huntington’s disease (HD) is a genetically inherited disorder, it is not clear how non-genetic factors such as environment and behavior may contribute to progression. Aims We used a causal inference approach to run simulated pse
Baseline multimodal information predicts future motor impairment in premanifest Huntington's disease
Autor:
Dorian Pustina, Eduardo Castro, Andrew Wood, John H. Warner, Guillermo A. Cecchi, Pablo Polosecki, Irina Rish, Cristina Sampaio
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 19, Iss, Pp 443-453 (2018)
NeuroImage: Clinical, Vol 19, Iss, Pp 443-453 (2018)
In Huntington's disease (HD), accurate estimates of expected future motor impairments are key for clinical trials. Individual prognosis is only partially explained by genetics. However, studies so far have focused on predicting the time to clinical d
Autor:
Douglas R. Langbehn, Won Chan Lee, John H. Warner, Mitch DeKoven, Karen E. Anderson, J Giuliano, Victoria Divino
Publikováno v:
Journal of Huntington's Disease. 3:355-363
BACKGROUND Huntington's disease (HD) is a progressive neurodegenerative disease that spans distinct disease stages over 15-20 years. Various interventions are available which may allow patients to live outside of a nursing home for a longer time. How
Autor:
John H. Warner, Allan J. Tobin, Blair R. Leavitt, Chris Becker, Howard Schulman, Raymund A.C. Roos, Sarah J. Tabrizi, Cristina Sampaio, Alexandra Durr, Beth Borowsky
Publikováno v:
Neurology, 80(21), 1934-1941
Objective: To evaluate plasma 8-hydroxy-deoxy-guanosine (8OHdG) levels as a potential biomarker of premanifest and early Huntington disease (HD). Methods: Personnel from 2 independent laboratories quantified 8OHdG in blinded longitudinal plasma sampl