Mya C. Schiess

ORCID: 0000-0001-9348-2587
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About
Contact & Profiles
Research Areas
  • Parkinson's Disease Mechanisms and Treatments
  • Neurological disorders and treatments
  • Botulinum Toxin and Related Neurological Disorders
  • Advanced Neuroimaging Techniques and Applications
  • Genetic Neurodegenerative Diseases
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Functional Brain Connectivity Studies
  • Nuclear Receptors and Signaling
  • Alzheimer's disease research and treatments
  • Olfactory and Sensory Function Studies
  • Advanced MRI Techniques and Applications
  • Mesenchymal stem cell research
  • Stroke Rehabilitation and Recovery
  • Nerve injury and regeneration
  • Cerebral Palsy and Movement Disorders
  • Neurological and metabolic disorders
  • Neurogenesis and neuroplasticity mechanisms
  • Restless Legs Syndrome Research
  • Neuroscience and Neuropharmacology Research
  • Neuropeptides and Animal Physiology
  • Neurological diseases and metabolism
  • Ion channel regulation and function
  • Dementia and Cognitive Impairment Research
  • Memory and Neural Mechanisms
  • Neuroscience and Neural Engineering

The University of Texas Health Science Center at Houston
2016-2025

Institute for Neurodegenerative Disorders
2023

Neurology, Inc
2020

The University of Texas at Austin
2004-2015

Texas Medical Center
2008

Memorial Hermann
2006

The University of Texas Medical Branch at Galveston
1988-1999

The University of Texas Southwestern Medical Center
1987

UConn Health
1982

Brent Bluett Daniel M. Togasaki Dragos Mihaila Marian L. Evatt Michael Rezak and 95 more Samay Jain Michael A. Schwarzschild Alberto Ascherio Cindy Casaceli Gary C. Curhan Rebecca C. Fitzgerald Cornelia Kamp Codrin Lungu Eric A. Macklin Kenneth Marek Dariush Mozaffarian David Oakes Alice Rudolph Ira Shoulson Aleksandar Videnović B.L. Scott Lisa Gauger Jason Aldred Melissa Bixby Jill Ciccarello Steven A. Gunzler Claire Henchcliffe Matthew Brodsky Kellie Keith Robert A. Hauser Christopher G. Goetz Mark S. LeDoux Vanessa K. Hinson Rajeev Kumar Alberto J. Espay Joohi Jimenez‐Shahed Christine Hunter Chadwick W. Christine Aaron Daley Maureen A. Leehey Joy Antonelle de Marcaida Joseph H. Friedman Albert Y. Hung Grace Bwala Irene Litvan David K. Simon Tanya Simuni Cynthia Poon Mya C. Schiess Kelvin L. Chou Ariane Park Danish Bhatti Carolyn Peterson Susan R. Criswell Liana S. Rosenthal Jennifer Durphy Holly A. Shill Shyamal H. Mehta Anwar Ahmed Andres Deik John Y. Fang Natividad Stover Lin Zhang Richard B. Dewey Ashley Gerald James T. Boyd Emily Houston Valerie Suski Sherri Mosovsky Leslie Cloud Binit Shah Marie Saint‐Hilaire Raymond James S. Elizabeth Zauber Stephen G. Reich David Shprecher Rajesh Pahwa April Langhammer Kathrin LaFaver Peter A. LeWitt Patricia L. Kaminski John L. Goudreau Doozie Russell David Houghton Ashley LaRoche Karen Thomas Martha McGraw Zoltan Mari Carmen Serrano Karen Blindauer Marcie Rabin Roger Kurlan John C. Morgan Michael J. Soileau Melissa Ainslie Iván Bódis-Wollner Ruth B. Schneider Cheryl Waters Amber Servi Ratel Christopher A. Beck

Urate elevation, despite associations with crystallopathic, cardiovascular, and metabolic disorders, has been pursued as a potential disease-modifying strategy for Parkinson disease (PD) based on convergent biological, epidemiological, clinical data.To determine whether sustained urate-elevating treatment the urate precursor inosine slows early PD progression.Randomized, double-blind, placebo-controlled, phase 3 trial of oral in PD. A total 587 individuals consented, 298 not yet requiring...

10.1001/jama.2021.10207 article EN JAMA 2021-09-14

Background and purpose The intestinal microbiome plays a primary role in the pathogenesis of neurodegenerative disorders may provide an opportunity for disease modification. We performed pilot clinical study looking at safety fecal microbiota transplantation (FMT), its effect on microbiome, improvement symptoms Parkinson's disease. Methods This was randomized, double-blind placebo-controlled study, wherein orally administered lyophilized FMT product or matching placebo given to 12 subjects...

10.3389/fneur.2023.1104759 article EN cc-by Frontiers in Neurology 2023-03-02

Abstract The neurodegenerative synucleinopathies, including Parkinson’s disease and dementia with Lewy bodies, are characterized by a typically lengthy prodromal period of progressive subclinical motor non-motor manifestations. Among these, idiopathic REM sleep behaviour disorder is powerful early predictor eventual phenoconversion, therefore represents critical opportunity to intervene neuroprotective therapy. To inform the design randomized trials, it essential study natural progression...

10.1093/brain/awad072 article EN Brain 2023-03-07

Rapid eye movement sleep behavior disorder (RBD) is a condition closely associated with Parkinson disease (PD). RBD disturbance that frequently manifests early in the development of PD, likely reflecting disruption normal functioning anatomical areas affected by neurodegenerative processes. Although specific neuropathological aspects shared and PD have yet to be fully documented, further characterization critical discovering reliable biomarkers predict onset. In current study, we tested...

10.5665/sleep.3222 article EN SLEEP 2013-11-26

The integrity of frontal systems responsible for voluntary control and their interaction with subcortical regions involved in reflexive responses were studied patients Parkinson's disease (PD). Previous studies have shown that PD impaired executive function, including deficits attention, motor planning decision making.Executive function was measured through eye movements: (stimulus driven) prosaccades (internally guided) antisaccades. Patients advanced idiopathic PD, off on optimal levodopa...

10.1136/jnnp.2006.099754 article EN Journal of Neurology Neurosurgery & Psychiatry 2006-12-19

α-synuclein is thought to play a key role in Parkinson's disease (PD) because it the major protein Lewy bodies, and its gene mutations, duplication, triplication are associated with early-onset PD. There conflicting reports as whether serum plasma concentrations of anti-α-synuclein antibodies differ between PD control subjects. The objectives this study were compare levels individuals typical (n = 14), atypical Parkinson syndromes 11), idiopathic rapid eye movement sleep behavior disorder...

10.1371/journal.pone.0052285 article EN cc-by PLoS ONE 2012-12-17

ABSTRACT Background Direct targeting of the dentato‐rubro‐thalamic tract is efficacious in DBS for tremor suppression. Objectives We sought to compare outcomes and optimal stimulation parameters control using technique directly those who underwent indirect ventral intermediate nucleus thalamus. Methods Twenty consecutive essential patients obtained preoperative diffusion MRIs, where was individually drawn used target thalamus during surgery. These were compared an earlier cohort 20 surgery...

10.1002/mds.27463 article EN Movement Disorders 2018-09-05

ABSTRACT Background Neuroinflammation plays a key role in PD pathogenesis, and allogeneic bone marrow–derived mesenchymal stem cells can be used as an immunomodulatory therapy. Objective The objective of this study was to prove the safety tolerability intravenous patients. Methods This 12‐month single‐center open‐label dose‐escalation phase 1 20 subjects with mild/moderate assigned single infusion 4 doses: 1, 3, 6, or 10 × 6 cells/kg, evaluated 12, 24, 52 weeks postinfusion. Primary outcome...

10.1002/mds.28582 article EN Movement Disorders 2021-03-27

OBJECTIVE Patients with Parkinson disease (PD) who undergo subthalamic nucleus (STN) deep brain stimulation (DBS) often develop a deterioration in speech performance, but there is no clear consensus on the specific effects seen or mechanism involved and little description of impact DBS conversational speech. Furthermore, has been fiber tract connectivity analysis to identify structures potentially modulated by cause such deficits. The main objective this study was quantify spontaneous...

10.3171/2016.5.jns16243 article EN Journal of neurosurgery 2016-09-01

The Trail Making Test (TMT) is one of the most frequently administered neuropsychological instruments, having been used in evaluation cognitive dysfunction for over 50 years. Despite measure's extensive clinical use and proliferation research, no comprehensive review adult TMT normative literature available. This report examines available reports provides a summary sample characteristics. Significant variability between studies precludes metanorms. Clinically, these findings indicate that...

10.1207/s15324826an0502_2 article EN Applied Neuropsychology 1998-06-01

<h3>Objective:</h3> To examine the cognitive sequelae of unilateral posteroventral pallidotomy. <h3>Design:</h3> Single-group pretest and posttest methodologic assessment with baseline evaluation performed 1 to 2 days prior surgery follow-up conducted 3 months after <h3>Setting:</h3> Movement disorder clinic at a university medical center. <h3>Patients:</h3> Fourteen patients (age range, 43-82 years) Parkinson disease (average duration, 7.4 years). <h3>Intervention:</h3> Unilateral...

10.1001/archneur.1997.00550200015004 article EN Archives of Neurology 1997-08-01

Motor classifications of Parkinson's Disease (PD) have been widely used. This paper aims to update a subtype classification using the MDS-UPDRS-III and determine if cerebrospinal neurotransmitter profiles (HVA 5-HIAA) differ between these subtypes in cohort from Progression Marker Initiative (PPMI).UPDRS MDS-UPDRS scores were collected for 20 PD patients. Akinetic-rigid (AR), Tremor-dominant (TD), Mixed (MX) calculated formula derived UPDRS, new ratio was developed subtyping patients with...

10.1016/j.prdoa.2023.100187 article EN cc-by-nc-nd Clinical Parkinsonism & Related Disorders 2023-01-01

Forty central amygdala neurons labelled with 2% Neurobiotin were categorized according to their distinctive bioelectrical membrane properties and classified physiologically by hyperpolarized resting potential (−74 mV), short duration medium afterhyperpolarization (239.2 ms), non-accommodating response as Type A (63%; N = 25/40), or B (37%; 15/40) depolarized (-66 long slow-afterhyperpolarization (1.8 s), accommodation response. Visualized within subnuclei of the amygdala,...

10.1002/(sici)1097-4547(19991201)58:5<663::aid-jnr7>3.0.co;2-a article EN Journal of Neuroscience Research 1999-11-12
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