Encyclopedia of Movement Disorders, Three-Volume Set book cover

Encyclopedia of Movement Disorders, Three-Volume Set

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.

Audience

The encyclopedia targets a broad readership, including 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.

Hardbound, 1632 Pages

Published: February 2010

Imprint: Academic Press

ISBN: 978-0-12-374101-1

Contents

  • 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

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