Robert E. Burke

ORCID: 0000-0002-4760-8553
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About
Contact & Profiles
Research Areas
  • Nerve injury and regeneration
  • Neuroscience and Neuropharmacology Research
  • Parkinson's Disease Mechanisms and Treatments
  • Neurological disorders and treatments
  • Neurogenesis and neuroplasticity mechanisms
  • Nuclear Receptors and Signaling
  • Neuroscience and Neural Engineering
  • Botulinum Toxin and Related Neurological Disorders
  • Muscle activation and electromyography studies
  • Neural dynamics and brain function
  • Neonatal and fetal brain pathology
  • Genetic Neurodegenerative Diseases
  • American Constitutional Law and Politics
  • Mitochondrial Function and Pathology
  • Cell death mechanisms and regulation
  • Ion channel regulation and function
  • Autophagy in Disease and Therapy
  • Spinal Cord Injury Research
  • Hereditary Neurological Disorders
  • Vestibular and auditory disorders
  • Transcranial Magnetic Stimulation Studies
  • Receptor Mechanisms and Signaling
  • Endoplasmic Reticulum Stress and Disease
  • Pain Mechanisms and Treatments
  • Neurogenetic and Muscular Disorders Research

University of Florida
2025

HonorHealth
2022-2023

National Institutes of Health
2000-2022

National Institute of Neurological Disorders and Stroke
1999-2022

University of Pennsylvania
2020

Columbia University
2009-2018

Columbia University Irving Medical Center
2005-2018

Columbia College
1986-2016

Royal College of Physicians
1985-2016

Montefiore Health System
2015

For quantitative assessment of the primary torsion dystonias, a rating scale is proposed that has two sections—a Movement Scale, based on examination, and Disability patient9s statements about seven activities daily living. We assessed validity Scale by comparing scores with ranking patients according to dystonia severity ratings Scale. In addition, we inter-and intra-rater reliability independent scorings four examiners same performed at different times. found was valid reliable indicator dystonia.

10.1212/wnl.35.1.73 article EN Neurology 1985-01-01

Despite tremendous growth in recent years our knowledge of the molecular basis Parkinson disease (PD) and pathways cell injury death, we remain without therapies that forestall progression. Although there are many possible explanations for this lack success, one is experimental therapeutics to date have not adequately focused on an important component process, axon degeneration. It remains unknown what neuronal compartment, either soma or axon, involved at onset, although some proposed it...

10.1002/ana.21995 article EN Annals of Neurology 2010-05-26

The correlation among a variety of physiological properties and the histochemical characteristics muscle fibers belonging to single motor units in mixed mammalian is directly demonstrated. population making up cat gastrocnemius was classified into three nonoverlapping groups on basis combination parameters. each type exhibited distinctive profile, such that basic "fiber types" exactly matched physiologically defined groups. Within individual unit, were histochemically uniform.

10.1126/science.174.4010.709 article EN Science 1971-11-12

Mechanisms responsible for 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced dopamine (DA) neuronal death remain unknown and in mice it is even unclear whether does occur. In vitro studies suggest that 1-methyl-4-phenylpyridinium ion (MPP+), the active metabolite of MPTP, kills neurons by apoptosis. Herein, we investigated MPTP induces DA vivo mechanism C57/bl Mice received different doses administered four intraperitoneal injections every 2 hours were sacrificed at time points...

10.1016/1055-8330(95)90015-2 article EN cc-by-nc-nd Neurodegeneration 1995-09-01

It is not widely recognized that antipsychotic drugs can cause late-onset and persistent dystonia. This dystonia, which we call tardive to be distinguished from acute dystonic reactions, are transient, classic dyskinesia, a choreic disorder predominantly affects the oral region. We present 42 patients with The age of onset dystonia was 13 60 years. Symptoms began after 3 days 11 years therapy. Younger tended have more generalized In few patients, spontaneous remission occurred, but persisted...

10.1212/wnl.32.12.1335 article EN Neurology 1982-12-01

Parkinson's disease (PD) is most commonly a sporadic illness, and characterized by degeneration of substantia nigra dopamine (DA) neurons abnormal cytoplasmic aggregates α-synuclein. Rarely, PD may be caused missense mutations in MPTP, neurotoxin that inhibits mitochondrial complex I, prototype for an environmental cause because it produces pattern DA neurodegeneration closely resembles the neuropathology PD. Here we show α-synuclein null mice display striking resistance to MPTP-induced...

10.1073/pnas.172514599 article EN Proceedings of the National Academy of Sciences 2002-10-10
Michael Böhm Kazuomi Kario David E. Kandzari Felix Mahfoud Michael A. Weber and 95 more Roland E. Schmieder Konstantinos Tsioufis Stuart J. Pocock D. Konstantinidis James W. Choi Cara East David P. Lee Adrian Ma Sebastian Ewen Debbie L. Cohen Robert Wilensky Chandan Devireddy Janice P. Lea Axel Schmid Joachim Weil Tolga Agdirlioglu Denise Reedus Brian Jefferson David Reyes‐Leiva Richard D’Souza Andrew S.P. Sharp Faisal Sharif Martin Fahy Vanessa DeBruin Sidney A. Cohen Sandeep Brar Raymond R. Townsend Ertan Akarca Suhail Allaqaband E. Andrikou Jiro Aoki Ahran Arnold Herbert D. Aronow Masahiko Asami William Bachinsky John Barton Kyle Bass Bryan Batson Chris Bell Barry Bertolet Yvonne Bewarder Karl Bihlmaier Christian Binner Jason Bloom Benjamin Blossom Somjot Brar Angela L. Brown Robert E. Burke Martin Burke Michael Butler William J. Calhoun James Campbell Steve Carroll Neil Chapman Craig A. Chasen Shi-Chi Cheng Beth Chia Nishit Choksi Jordana B. Cohen Niall Connolly Johanna Contreras Ronan Cusack George Dangas Shukri David Justin E. Davies Juliane Dederer Matthew G. Denker Udo Desch Matthaios Didangelos Thomas Dienemann Kyriakos Dimitriadis Jean-François Dorval John Estess Sarah Fan Karl Fengler Lee Ferguson Marat Fudim Valentı́n Fuster Fidel Garcia Santiago Garcia Alex Garton C. Gessler Magdi Ghali Bharat Gummadi Amit Gupta Antonio Gutiérrez Peggy Hardesty Phillip Hartung Walter Herbert Haught Yonghong Haun Sara Hays Wolfgang Helmreich D.C. Hill Ingrid Hopper Yu Horiuchi

10.1016/s0140-6736(20)30554-7 article EN The Lancet 2020-03-29

A method to characterize dynamical interdependence among nonlinear systems is derived based on mutual prediction. Systems with correlation will show prediction when standard analysis linear cross might fail. Mutual also provides information the directionality of coupling between systems. Furthermore, existence bidirectional in unidirectionally coupled implies generalized synchrony. Numerical examples studied include three classes systems: identical parameters, nonidentical and stochastic...

10.1103/physreve.54.6708 article EN Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics 1996-12-01

Dopaminergic (DA) neurons of substantia nigra in the midbrain control voluntary movement, and their degeneration is cause Parkinson's disease. The complete set genes required to specifically determine development DA subgroups not known yet. We report here that mice lacking bicoid -related homeoprotein Pitx3 fail develop nigra. Other mesencephalic ventral tegmental area retrorubral field are unaltered dopamine expression histological organization. These data suggest Pitx3-dependent gene for...

10.1073/pnas.0230529100 article EN Proceedings of the National Academy of Sciences 2003-03-24

1. Muscle fibres belonging to single motor units of identified type were studied in frozen sections cat medial and lateral gastrocnemius muscles. Reconstruction the distribution individual showed that territories all three physiological types present quite extensive. Within its territory, unit distributed more or less uniformly without localized collections. The density suggests that, gastrocnemius, a given region muscle may be shared by as many fifty different units.2. Direct determination...

10.1113/jphysiol.1973.sp010370 article EN The Journal of Physiology 1973-11-01

Abstract There is increasing evidence that neuron death in neurodegenerative diseases, such as Parkinson's disease, due to the activation of programmed cell death. However, upstream mediators remain largely unknown. One approach identification perform gene expression analysis disease models. Such analyses, performed tissue culture models induced by neurotoxins, have identified up‐regulation CHOP/GADD153, a transcription factor implicated apoptosis endoplasmic reticulum stress or oxidative...

10.1111/j.1471-4159.2005.03428.x article EN Journal of Neurochemistry 2005-08-31

The 6-hydroxydopamine (6-OHDA) model of nigral injury in rats has been use as a standard animal parkinsonism for many years. While earlier studies established the time course loss catecholamine histofluorescence or tyrosine hydroxylase immunostaining cell bodies and terminals, these alterations phenotypic expression do not define morphologic degeneration. We have therefore used silver impregnation method to characterize morphology degeneration neurons nigrostriatal system. Abundant neuronal...

10.1006/neur.1995.0016 article EN cc-by-nc-nd Neurodegeneration 1995-06-01

We studied trihexyphenidyl in the treatment of torsion dystonia a prospective, double-blind crossover protocol. Thirty-one patients completed Twenty-two (71%) had clinically significant response. After mean follow-up 2.4 years, 68% continued to take trihexyphenidyl, and 42% show considerable or dramatic benefit. The 30-mg dose used was generally well tolerated. High-dosage therapy is effective management dystonia.

10.1212/wnl.36.2.160 article EN Neurology 1986-02-01
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