Neudle.com: "dystonia delayed onset"

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advances in neurology

adverse drug reaction

akathisia

algorithm

AMPA receptor antibodies

amphiphysin antibodies

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anti IgLON5

anticholinergic drugs

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

carbon monoxide poisoning

cardiac arrest

cardiac arrest and resuscitation

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

caudate nucleus, atrophy

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, infancy and childhood

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonazepam

clozapine

cognition

collapsin response mediator protein 5 IgG

coma

complications

conversion reaction

creatine phosphokinase(CPK)elevated

cyanide poison

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

developmental milestones, loss of

developmental retardation

diagnostic criteria

diet

differential diagnosis

dopa responsive dystonia

dopamine agonist

dopamine depleting agents

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dysphagia

dystonia

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

DYT1 mutation

efficacy

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalopathy

encephalopathy, neonatal

encephalopathy, post anoxic

enzyme, defect

eye movement, disorders of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gene

gene mutation

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hepatolenticular degeneration(Wilson's disease)

Hodgkin's disease

Huntington's chorea

Huntington's disease, children

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

infantile hemiplegia

insomnia

intellectual deficit

intellectual deterioration

internal cerebral vein

L-dopa, delayed treatment in Parkinsonism

L-dopa, drug interactions with and side effects of

left handedness

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

lysosomal storage disease

mellaril

memory

memory, impairment of

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

mitochondrial disease

monoclonal antibodies

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, negative

MRI, paramagnetic effect

neuroleptic, atypical

neurologic disease, diagnoses of

obsessive-compulsive disorder

oculogyric crisis

old age, neurology of

paraspinal muscle weakness

parkin gene

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, on-off phenomena in

Parkinson disease, prognosis of

Parkinson disease, rapid onset

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

phenothiazine

phenothiazine, dyskinesia associated with

pigmentary retinopathy

Pisa syndrome

pleocytosis of cerebrospinal fluid

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

prognosis

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

pull test

putamen, lesion of

putamen, lesion of, bilateral

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

rapid onset dystonia parkinsonism

remote effect of cancer on the nervous system

reserpine treatment in movement disorder

seizure, unknown origin

sensory tricks

serologic testing

serologic testing, false negative

seronegative

sinemet

sleep pathology and physiology

spasticity

speech disorder

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

tetrabenazine

tetrahydrobiopterin

thalamus, infarction of

thalamus, lesion of-bilateral

tonic foot response

torticollis

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

toxic encephalopathy

toxins, nervous system

treatment of neurologic disorder

tricyclic antidepressant

trinucleotide repeats

urinary sulfatidase excretion

weakness, progressive

Showing articles 0 to 50 of 1813 Next >>

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Long-Term Effects of Pallidal Deep Brain Stimulation in Tradive Dystonia
Neurol 73:53-58, Gruber,D.,et al, 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Post-Streptococcal Autoimmune Disorders of the Central Nervous System
Curr Opin Neurol 16:359-365, Snider,L. &Swedo,S., 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Drug-Induced Pisa Syndrome (Pleurothotomus)
CNS Drugs 10:166-174, Suzuki, T. & Matsuzaka, H., 2002

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Tardive Dyskinesia:Diagnosis, Pathogenesis, and Management
The Neurologist 4:180-187, Trugman,J.M., 1998

Thalamic Tremor:Case Reports and Implications of the Tremor-Generating Mechanism
Neurol 46:75-79, Miwa,H.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Improvement of Both Tardive Dystonia and Akathisia after Botulism Toxin Injection
Neurol 46:844-845, Shulman,L.M.,et al, 1996

Delayed Dystonia with Striatal CT Lucencies Induced by a Mycotoxin (3-Nitropropionic Acid)
Neurol 45:2178-2183, He,F.,et al, 1995

Oral and Genital Tardive Pain Syndromes
Neurol 44:2115-2119, Ford,B.,et al, 1994

Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993

Comparison of Striatal 18F-dopa Uptake in Adult-Onset Dystonia-Parkinsonism, Parkinson's & Dopa-Responsive Dystonia
Neurol 43:1563-1568, Turjanski,N.,et al, 1993

Delayed Cyanide Induced Dystonia
JNNP 55:198-199, Valenzuela,R.,et al, 1992

Young-Onset Parkinson's Disease:A Clinical Review
Neurol 41:168-173, Golbe,L.I., 1991

Early Development of Levodopa-Induced Dyskinesias and Response Fluctuations in Young-Onset Parkinson's Disease
Neurol 41:202-205, Kostic,V., 1991

Delayed-Onset Dystonia Due to Perinatal or Early Childhood Asphyxia
Neurol 41:216-222, Saint Hilaire,M.H.,et al, 1991

Early-Onset Dementia & Extrapyramidal Disease:Clinicopath Variant of Gerstmann-Straussler-Scheinker or Alzheimer's Disease?
JNNP 53:932-934, Hart,J.Jr.&Gordon,B., 1990

Progressive Dystonia Following Resuscitation From Cardiac Arrest
Neurol 40:1458-1461, Boylan,K.B.,et al, 1990

Tardive Oculogyric Crises
Neurol 39:1434-1437, FitzGerald,P.M.&Jankovic,J., 1989

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Tetrabenazine Therapy of Dystonia, Chorea, Tics, & Other Dyskinesias
Neurol 38:391-394, Jankovic,J.&Orman,J., 1988

Dystonia in Parkinson's Disease:Clinical & Pharmacological Features
Ann Neurol 23:73-78, Poewe,W.H.,et al, 1988

Forms of Dystonia in Patients with Parkinson's Disease
Neurol 37:1009-1011, Kidron,D.&Melamed,E., 1987

Parkinsonism Following Dystonia in Three Patients
Movement Disorders 1:151-157, Katchen,M.&Duvoisin,R.C., 1986

Dystonia-Parkinson Syndrome:Differential Effects of Levodopa and Dopamine Agonists
Clin Neuropharmacol 9:298-302, Klawans,H.L.&Paleologos,N., 1986

Dystonia in Untreated Parkinsonism
Clin Neuropharmacol 9:293-297, LeWitt,P.A.,et al, 1986

Progressive Dyskinesia Due to Internal Cerebral Vein Thrombosis
Neurol 32:769-772, Solomon,G.E.,et al, 1982

Delayed-onset Posthemiplegic Dystonia:CT Demonstration of Basal Ganglia Pathology
Neurol 32:1033-1035, Grimes,J.D.,et al, 1982

Tardive Dystonia:Late-onset & Persistent Dystonia Caused by Antipsychotic Drugs
Neurol 32:1335-1346, Burke,R.E.,et al, 1982

Benign Paroxysmal Torticollis in Infancy
Arch Dis Child 56:956-959, Deonna,T.,et al, 1981

Delayed-onset Dystonia in Patients with"Static"Encephalopathy
JNNP 43:789-797, Burke,R.E.,et al, 1980

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Tenecteplase for Stroke - Opening the Window?
NEJM 390:760-761, Leifer,D.,, 2024

Showing articles 0 to 50 of 1813 Next >>