Accurate detection of cerebellar smooth pursuit eye movement abnormalities via mobile phone video and machine learning
暂无分享,去创建一个
Jeremy D. Schmahmann | Guillermo Sapiro | Hau-Tieng Wu | Anoopum S. Gupta | Zhuoqing Chang | Ziyu Chen | Christopher D. Stephen | Anoopum S. Gupta | G. Sapiro | J. Schmahmann | C. Stephen | Hau‐Tieng Wu | Ziyu Chen | Zhuoqing Chang
[1] Daniel R. Scoles,et al. Oligonucleotide therapeutics in neurodegenerative diseases , 2018, RNA biology.
[2] Katharina Reinecke,et al. Computer mouse use captures ataxia and parkinsonism, enabling accurate measurement and detection , 2019, Movement disorders : official journal of the Movement Disorder Society.
[3] Magdalena Ewa Król,et al. A novel machine learning analysis of eye-tracking data reveals suboptimal visual information extraction from facial stimuli in individuals with autism , 2019, Neuropsychologia.
[4] Hubert Kimmig,et al. Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17) , 2007, Neurology.
[5] Tatsuya Ueno,et al. Downbeat nystagmus as an initial clinical sign in spinocerebellar ataxia type 6 , 2017, Neurological Sciences.
[6] Paola Giunti,et al. Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study , 2015, The Lancet Neurology.
[7] Jeremy D. Schmahmann,et al. Eye Movement Abnormalities Are Ubiquitous in the Spinocerebellar Ataxias , 2019, The Cerebellum.
[8] P. Benson,et al. Simple Viewing Tests Can Detect Eye Movement Abnormalities That Distinguish Schizophrenia Cases from Controls with Exceptional Accuracy , 2012, Biological Psychiatry.
[9] Daniel R. Scoles,et al. Antisense oligonucleotide therapy for spinocerebellar ataxia type 2 , 2017, Nature.
[10] U. Ziemann,et al. Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2 , 2009, Clinical Neurophysiology.
[11] Kristin A Schuller,et al. Models of Care Delivery for Patients With Parkinson Disease Living in Rural Areas , 2017, Family & community health.
[12] Lance M. Optican,et al. Eye Movements in Parkinson’s Disease and Inherited Parkinsonian Syndromes , 2017, Front. Neurol..
[13] Christopher Gomez,et al. Clinical Evaluation of Eye Movements in Spinocerebellar Ataxias: A Prospective Multicenter Study , 2015, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.
[14] Elsdon Storey,et al. Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) , 2008, Journal of Neurology.
[15] John D. Mollon,et al. An oculomotor signature , 2013 .
[16] Paola Giunti,et al. Self‐rated health status in spinocerebellar ataxia—Results from a European multicenter study , 2010, Movement disorders : official journal of the Movement Disorder Society.
[17] Ursula Gather,et al. Fast and Robust Filtering of Time Series with Trends , 2002, COMPSTAT.
[18] Yi Wang,et al. ConceFT: concentration of frequency and time via a multitapered synchrosqueezed transform , 2015, Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.
[19] Peka Christova,et al. Impaired eye movements in presymptomatic spinocerebellar ataxia type 6. , 2008, Archives of neurology.
[20] Ruth E. Hogg,et al. Individual differences in human eye movements: An oculomotor signature? , 2017, Vision Research.
[21] Harry T. Orr,et al. Polyglutamine spinocerebellar ataxias — from genes to potential treatments , 2017, Nature Reviews Neuroscience.
[22] Lippincott Williams Wilkins,et al. Scale for the assessment and rating of ataxia: Development of a new clinical scale , 2006, Neurology.
[23] Teresa Kay,et al. Nystagmus as an early ocular alteration in Machado-Joseph disease (MJD/SCA3) , 2014, BMC Neurology.
[24] Ursula Gather,et al. Robust Preprocessing of Time Series with Trends , 2002, GI Jahrestagung.
[25] Michele Matarazzo,et al. Remote Monitoring of Treatment Response in Parkinson's Disease: The Habit of Typing on a Computer , 2019, Movement disorders : official journal of the Movement Disorder Society.
[26] Alexandra Durr,et al. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond , 2010, The Lancet Neurology.
[27] S. Soyal,et al. A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort , 2014, BMC Neurology.
[28] Tereza Soukupová,et al. Eye-Blink Detection Using Facial Landmarks , 2016 .
[29] T. Anderson,et al. Eye movements in patients with neurodegenerative disorders , 2013, Nature Reviews Neurology.
[30] Suchi Saria,et al. Using Smartphones and Machine Learning to Quantify Parkinson Disease Severity: The Mobile Parkinson Disease Score , 2018, JAMA neurology.
[31] Guillermo Sapiro,et al. Automatic emotion and attention analysis of young children at home: a ResearchKit autism feasibility study , 2018, npj Digital Medicine.
[32] S. Friend,et al. The mPower study, Parkinson disease mobile data collected using ResearchKit , 2016, Scientific Data.
[33] Jeremy D. Schmahmann,et al. Development of a brief ataxia rating scale (BARS) based on a modified form of the ICARS , 2009, Movement disorders : official journal of the Movement Disorder Society.