Encyclopedia of Movement Disorders
- 1st Edition
- Editors: Katie Kompoliti, Leonard Verhagen
- Language: English
The Encyclopedia of Movement Disorders is a comprehensive reference work on movement disorders, encompassing a wide variety of topics in neurology, neurosurgery, psychiatr… Read more
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The Encyclopedia of Movement Disorders is a comprehensive reference work on movement disorders, encompassing a wide variety of topics in neurology, neurosurgery, psychiatry and pharmacology. This compilation will feature more than 300 focused entries, including sections on different disease states, pathophysiology, epidemiology, genetics, clinical presentation, diagnostic tools, as well as discussions on relevant basic science topics. This Encyclopedia is an essential addition to any collection, written to be accessible for both the clinical and non-clinical reader. Academic clinicians, translational researchers and basic scientists are brought together to connect experimental findings made in the laboratory to the clinical features, pathophysiology and treatment of movement disorders. The Encyclopedia targets a broad readership, ranging from students to general physicians, basic scientists and Movement Disorder specialists. Published both in print and via Elsevier’s online platform of Science Direct, this Encyclopedia will have the enhanced option of integrating traditional print with online multimedia.
- Connects experimental findings made in the laboratory to the clinical features, pathophysiology, and treatment of movement disorders
- Encompasses a wide variety of topics in neurology neurosurgery, psychiatry, and pharmacology
- Written for a broad readership ranging from students to general physicians, basic scientists, and movement disorder specialists
Clinicians, researchers, post-doctoral fellows, medical residents and medical school students with an interest in the current research and approaches for the diagnosis and treatment of Movement Disorders. It will be an essential addition to any collection, written to be accessible for both the clinical and non-clinical reader
Serotonin and Tryptophan
Akathisia
Akinetic-Rigid Syndrome
Alien limb
Alpha-2 Adrenergic Agonists in Tic Disorders
The amyotrophic lateral sclerosis/Parkinsonism-dementia complex of three Pacific isolates. New understandings from Guam
Aluminum
Using animal models to understand Tourette Syndrome
ANTICHOLINERGICS
Asterixis
Athetosis
Autonomic dysfunction
Basal Ganglia
Bradykinesia
Corticobasal Degeneration
Complex tics
CYANIDES
Diffusion Tensor Imaging in Parkinson’s Disease
Drug-induced movement disorders
Drug-induced myoclonus
Drug-induced parkinsonism
Drug-induced tremor
Dyskinesias
ELECTROENCEPHALOGRAPHY (EEG)
Encephalitis lethargica and Postencephalitic parkinsonism
Epilepsia partialis continua
Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)
Gait Disturbances in Parkinsonism
Hallucinations and movement disorders
Hemiatrophy Hemiparkinsonism
Hemiballismus
Hoehn and Yahr Staging Scale
Hydrocarbons
Jumpy Stumps and Phantom Dyskinesias
Juvenile myoclonic epilepsy
Kinesia paradoxica
Lance-Adams Syndrome
Manganese
Mercury
Myoclonus
Myoclonus, animal models
Brainstem Reticular Myoclonus
Cortical Myoclonus
Epileptic Myoclonus
Palatal Myoclonus
Propriospinal Myoclonus
Spinal Segmental Myoclonus
Myoclonus-Dystonia/Essential myoclonus
Neuroimaging, Parkinson’s Disease
Neuroleptics
Nicotine
PANDAS
Parkinson, James
Parkinson’s disease: definition, diagnosis, and management
THE GENETICS OF PARKINSON’S DISEASE
Paroxysmal movement disorders
Parkinson’s Disease Quesionniare-39 (PDQ-39)
Pesticides
Psychosis in parkinsonism
Rating scales in movement disorders
Rigidity
Schwab and England Activities of Daily Living Scale
Senile chorea
Simple tics
Spasm
SPECT imaging in Movement Disorders
Striatal hand
Striatonigral degeneration
Tardive syndromes
Transplantation
Tremor
Cortical Tremor
Tremor, essential (syndromes)
Essential Tremor, Genetics
Tremor, Holmes
Primary orthostatic tremor
Palatal Tremor
Postural Tremor
Rest Tremor
UNIFIED PARKINSON’S DISEASE RATING SCALE (UPDRS) AND THE MOVEMENT-DISORDER SOCIETY SPONSORED-UNIFIED PARKINSON’S DISEASE RATING SCALE (MDS-UPDRS)
Vascular parkinsonism
Accelerometry
Actigraphy
Animal models for dystonia
Benign Paroxysmal Torticollis of Infancy
Blephorospasm
Botulinum toxin
Fahn-Marsden Rating Scale
Cervical dystonia
Concentric needle EMG
Acute drug-induced dystonia
Dystonia
Secondary Dystonia
Dystonia, task-specific
Dystonia, traumatic
Dystonic storm
DYT1
Paroxysmal kinesiogenic dyskinesia (PKD) (DYT10)
DYT11, DYT15 – MYOCLONUS-DYSTONIA
DYT12 – RAPID ONSET DYSTONIA PARKINSONISM
DYT13 (cranio-cervical-brachial)
DYT2-AUTOSOMAL RECESSIVE GENERALIZED DYSTONIA
LUBAG OR X-LINKED DYSTONIA-PARKINSONISM: A REVIEW OF PHENOTYPE AND GENOTYPE
DYT4 AUTOSOMAL DOMINANT TYPE DYSTONIA OR WHISPERING DYSPHONIA
DYT5
DYT6- Mixed Phenotype Primary Dystonia
DYT7-AUTOSOMAL DOMINANT FOCAL DYSTONIA
Paroxysmal non-kinesiogenic dyskinesia (PNKD) (DYT8)
Paroxysmal dyskinesia with spasticity (DYT9)
Eye-of-the-Tiger Sign
Geste antagonistique
Hallervorden-Spatz syndrome (PKAN)
Hemifacial spasm
Meige’s syndrome
Dystonia in Amish-Mennonite and Mennonite Families
Neuroferritinopathy
Periodic Limb Movements
Generalized Primary Torsion Dystonia
Ramisectomy
REM-behavior disorder
Restless legs syndrome
Sleep attacks
Spasmodic Dysphonia: Focal Laryngeal Dystonia
Torsin A
TWSTRS
Writer's cramp
Acetylcholine
Cholinesterase inhibitors in Parkinson’s disease
Alzheimer's Disease and Parkinsonism
Animal models of multiple system atrophy, spinocerebellar ataxias
Aprataxin
UPPER LIMB APRAXIAS
Ataxia
Ataxia (familial cerebellar) with muscle CoQ10 deficiency
Ataxia with isolated vitamin E deficiency
Ataxia-Telangiectasia
ATM gene
Bradyphrenia
Cayman ataxia
CJD
Variant Creutzfeldt-Jakob disease
Cognitive assessments and Parkinson’s Disease
Cortical Sensory Dysfunction and the Parietal Lobe
Dementia with Lewy Bodies
Dementia, movement disorders
Executive dysfunction
FRIEDREICH’S ATAXIA AND VARIANTS
Frontotemporal dementia-parkinsonism
Glucocerebrosidase gene mutations and parkinsonism
Gluten ataxia
ICARS – International Cooperative Ataxia Rating Scale
Idebenone and Friedreich Ataxia
Kuru
MMSE - Mini-Mental State Examination
NARP
Olivopontocerebellar atrophy
Paraneoplastic movement disorders
Refsum Disease- a disorder of peroxisomal alpha-oxidation
RNA interference
Roussy-Levy disease
Sacsin
Spinocerebellar ataxia type 19, 20, 21, 22, 23, 26 (SCA19, 20, 21, 22, 23, 26)
Spinocerebellar ataxias genetics
Spinocerebellar Ataxia Type 1
SPINOCEREBELLAR ATAXIA TYPE 10 (SCA10)
Spinocerebellar ataxia type 11 (SCA11)
Spinocerebellar Ataxia Type 12
Spinocerebellar ataxia types 13, 14, 15 and 16
Spinocerebellar ataxia type 17 (SCA17)
Spinocerebellar ataxia type 2
SCA-3 (Spinocerebellar ataxia 3 / Machado-Joseph disease)
Spinocerebellar Ataxia Type 4
SCA-5 (Spinocerebellar ataxia 5)
Spinocerebellar Ataxia Type 6
SCA-7 (spinocerebellar ataxia with macular dystrophy)
SCA 8
Senataxin
Tauopathies
Tocopherol Transfer Protein and Ataxia with Vitamin E Deficiency
Transmissible spongiform encephalopathy
Whipple's Disease
CJD
Alpha synuclein
Animal models for essential tremor
Animal models for Parkinson's disease
Caenorhabditis elegans
Caspases and Neuronal Cell Death
Climbing behavior
Complex I deficiency
Confocal microscopy
Cylinder test (Paw reach test)
Cystatin B
Dopaminergic Agonists in Parkinson’s Disease
Dopamine depletors
Dopamine receptors
Dopamine Transporter: Aging and Parkinson’s disease
DROSOPHILA MODELS OF PARKINSON DISEASE
SPINOCEREBELLAR ATAXIA 27 (SCA27) IS ASSOCIATED WITH A MISSENSE MUTATION IN THE FGF14 GENE
Foot print analysis (rat)
GABA and movement disorders
GDNF (including nurturin)
Gene microarrays
Glial cell activation in PD
Glial cytoplasmic inclusions
Hand-reach task
Harmaline tremor model
Immunophilin Ligands
Inflammation and PD
Junctophilin
Kainic Acid Model of Dystonia
Leaner mouse
Lick-force rhythm test
Mitochondrial dysfunction
MPTP
Neurofibrillary tangles
Neuroleptic-induced nonhuman primate models of EPS and TD
Nitric oxide
Locus Coeruleus and Norepinephrine
Object retrieval-detour task
Opioid system
Press-while-licking task
The proteasome system in Movement Disorders
Rotation, drug-induced
Staircase (skilled reaching) test
Stepping (forelimb akinesia) test
Stereology
Substantia Nigra
Subthalamic nucleus
Synucleinopathies
Tail-pinch stimulus
Tottering Mouse- a definition
Western blot
Abetalipoproteinemia (ABL)
Movement Disorders Caused by CNS Stimulants
Aromatic amino acid decarboxylase deficiency
Atrophin-1
Beam walking test
Belly Dancer’s Dyskinesia
Benzodiazepines in the Treatment of Movement Disorders
Beta-blockers
Carbon Monoxide Poisoning
Cerebrotendinous xanthomatosis
Co-enzyme Q10 and neurodegenerative diseases
COMT Inhibitors in the Treatment of Parkinson’s Disease
Somatoform Disorders
Dopa-decarboxylase Inhibitors
The Small Molecule Neurotransmitter – Dopamine
Dysarthria
Dysphagia
Abnormal eye movements in movement disorders
Eyelid opening apraxia
Factitious disorders
Fumarase deficiency
Gaucher's Disease
GLABELLAR REFLEX
GM1 type 3 gangliosidosis
GM2 gangliosidosis
Hypophonia
Kayser-Fleischer
Kernicterus
Lafora disease
Leigh syndrome
Levodopa
Magnetoencephalography (MEG)
Malingering
Marinesco-Sj¿gren syndrome
MERRF
Mitochondrial encephalopathies
INTRODUCTION
Myokymia
Niemann-Pick Type C
Obsessive-Compulsive Disorder
Oculomasticatory myorhythmia
Opsoclonus-Myoclonus Syndrome
Painful Limbs Moving Extremities (PLME)
Pallido-nigro-luysian Degeneration
PARK2 (parkin)
PARK5 (UCH-L1)
PARK7 (DJ1)
Pelizaeus-Merzbacher disease
Primidone
Propionic acidemia
Pseudobulbar symptoms
Psychogenic movement disorders
Rabbit syndrome
Rett syndrome
Sialidosis
Oral dyskinesia
Subacute Sclerosing Panencephalitis
Supranuclear eye movement control
Tics
Tourette syndrome
Unverricht-Lundborg's disease
Weaver mouse
Yale Global Tic Severity Scale (YGTSS)
3-nitropropionic acid: a mitochondrial toxin leading to striatal degeneration
Applause sign
Chorea-acanthocytosis
Chorea
Chorea gravidarum
Postpump Chorea
Dentatorubropallidoluysian Atrophy
Huntington’s disease-like 2
Huntington’s Disease: Genetics
George Huntington (1850-1916) and hereditary chorea
Huntington's disease
Choreiform disorders
Juvenile parkinsonism
Monoamine Oxidase Type B Inhibitors
McLeod syndrome
Milkmaid's grip
Motor impersistence
Neuroacanthocytosis syndromes
Neuroprotection in movement disorders
Pseudoathetosis
Quinolinic acid
Antidepressants
Serotonin syndrome
Lupus Chorea
St. Vitus dance
Stiff person syndrome and variants
Sydenham's chorea
Trinucleotide repeat disorders
Westphal variant
Wilson’s disease
Approximate entropy
Basal ganglia, functional organization
Binswanger's subcortical arteriosclerotic encephalopathy
Braak classification
Blood oxygenation level dependent (BOLD)
Bruxism
Camptocormia
Cannabinoids
CAPIT, CAPSIT
Cock-walk
Complex regional pain syndrome
Deep brain stimulation
Depression and parkinsonism
Direct pathway
Electromyography (EMG)
Event-Related Potentials: Slow Potentials
Freezing of Gait
Gait ignition failure
Paratonia (Gegenhalten)
HARP syndrome
Movement Disorders in HIV infection
Hot-Cross Bun Sign (MRI and MSA)
H-reflex
Hyperekplexia
Indirect pathway
Interspike Interval
Jumping Frenchmen of Maine
Latah
Lesch-Nyhan Disease
Melanin
Metachromatic leukodystrophy
Micrographia
Motor evoked potential
Motor fluctuations
Motor unit
Motor unit synchronization
Movement time
Multiple system atrophy
Myorhythmia
Myriachit
Neuronal ceroid lipofuscinosis
Neural networks
Normal pressure hydrocephalus
Biology of NR4A subfamily
Paired pulse TMS
Pallidotomy for Parkinson's disease
Alpha-synuclein
PARK6 (PINK1)
PARK8 (LRRK2, Dardarin)
Paroxysmal exertion-induced dyskinesia
PARK3
PET Imaging in Movement Disorders
Pisa syndrome
PRIMARY PROGRESSIVE FREEZING GAIT: CURRENT VIEW
Progressive supranuclear palsy
Punding (PD)
Reaction time
Motor Output Variability
rhizotomy
rTMS
Shy-Drager Syndrome
Single pulse TMS
Spastic paraparesis
Surgery for movement disorders, overview, including history
Thalamotomy
Theta burst TMS
Intra-Individual Variability in Movement
Recessive hereditary methemoglobinemia type II
SARA (Scale for the Assessment and Rating of Ataxia)
FARS (Friedreich's ataxia Rating Scale)
Prof. Samuel Alexander Kinnier Wilson: his impact on the concepts of Extrapyramidal Syndromes and Movement Disorders
Parkinson Hyperpyrexia Syndrome
Dopamine Dysregulation Syndrome
Alexander Disease
Tardive dystonia
THE GENETICS OF PARKINSONISM
Animal models of dyskinesias
Oxidative Stress and Movement Disorders
Stem Cells
- Edition: 1
- Published:
- Language: English
KK
Katie Kompoliti
Dr. Kompoliti was born in Greece and completed her early education there, including Medical School. She graduated from the University of Patras, college of Medicine in 1988. She came to the United States in 1989, where she completed the rest of her medical education. She first trained in internal medicine (1990-1992) at St Francis Hospital, Evanston, IL. Following that she pursued her interest in neuroscience by completing a residency in Neurology at Northwestern University, Chicago, IL (1992-1995). After the completion of her residency she held a fellowship in Movement Disorders at Rush University Medical Center, Chicago, IL (1995-1997). She became Assistant Professor of Neurology in 1998 and Associate Professor in 2004. She is board certified in Neurology (1997-present) and is a member of the American Academy of Neurology, the American Neurological Association and the Movement Disorder Society. The author and coauthor of numerous publications, her clinical interests as a principal investigator have focused on several therapeutic areas of on-going research including studies to evaluate the safety and efficacy of new compounds to treat Parkinson’s disease, Tourette syndrome, and Psychogenic Movement Disorders. Special interests of Dr. Kompoliti’s include the gender differences in Parkinson’s disease and other movement disorders, studies to define the effect of neuroleptics on weight, risk for diabetes and dyslipidemia in patients with Tourette syndrome, and define the current status of use of Complementatry and Alternative Medicine in patients with Tourette syndrome. Finally, Dr. Kompoliti has been conducting studies to assess therapeutic interventions for patients with functional movement disorders. Dr. Kompoliti is a member of the National Medical Advisory Board of the Tourette Syndrome Association and has given numerous lectures and Grand rounds around the country to increase public awareness in Tourette Syndrome.
Affiliations and expertise
Movement Disorders Section, Neurological Sciences, Rush University Medical Center, Chicago, USALV
Leonard Verhagen
Leonard Verhagen Metman earned his medical degree from the University of Leiden in the Netherlands in 1983. He moved to the United States in 1985 to work in the Artificial Heart Program at the University of Utah with Dr. Willem J. Kolff (1985-1987). He first pursued his interest in the Neurosciences by joining the Division of Restorative Neurology and Human Neurobiology at Baylor College of Medicine in Houston, Texas with Dr. Milan R. Dimitrijevic (1987-1988). Following an internship at Waterbury Hospital Health Center in Connecticut (1988-1989), he completed his Neurology residency at Thomas Jefferson University Hospital in Philadelphia, Pennsylvania under Robert J. Schwartzman (1989-1992). He then accepted a fellowship at the National Institutes of Health, in the Experimental Therapeutics Branch of the National Institute of Neurological Disorders and Stroke in Bethesda, Maryland under Thomas N. Chase (1992-1994). Upon completion he remained at the NIH as Visiting Associate and later as Visiting Scientist until 1999 when he joined the Movement Disorder Section of the Department of Neurological Sciences at Rush University Medical Center in Chicago, Illinois, directed by Dr. Christopher G. Goetz. In 2002 Dr. Verhagen received his Ph.D. from the University of Leiden based on his studies of motor response complications in Parkinson's disease. Over the past 10 years at Rush, Dr. Verhagen has served as Assistant Professor (1999-2000) and Associate Professor (2001-current) of Neurological Sciences. In addition, he established the Rush Movement Disorder Surgery Program and serves as its Medical Director. His clinical research interests include the development of new medical and surgical therapies for patients with advanced movement disorders. Dr. Verhagen is board certified in psychiatry and neurology (1994-present) and is a member of the American Academy of Neurology, the American Neurological Association and the Movement Disorder Society.
Affiliations and expertise
Movement Disorders Section, Neurological Sciences, Rush University Medical Center, Chicago, USARead Encyclopedia of Movement Disorders on ScienceDirect