Neudle.com: dystonia delayed onset

Neurology Specific Literature Search

Differential
(Click to cross reference)

adolescent medicine

advances in neurology

adverse drug reaction

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amphiphysin antibodies

anti GQ1b IgG antibody

anticholinergic drugs

arylsulfatase A

ataxia, cerebellar

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bent spine syndrome

botulinum toxin

Brueghel's syndrome

carbon monoxide poisoning

cardiac arrest and resuscitation

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

caudate nucleus, atrophy

cerebellar degeneration

cerebral cortical atrophy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, infancy and childhood

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

conversion reaction

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

dementia, presenile

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

disease modifying agents

dopa responsive dystonia

dopamine agonist

dopamine depleting agents

DPPX, antibodies

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalopathy, neonatal

encephalopathy, post anoxic

executive dysfunction

exome sequencing

eye movement, disorders of

facial nerve palsy

forceps delivery

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

Hodgkin's disease

Huntington's chorea

Huntington's disease, children

hypoglycorrhachia

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

immunologic disease

inborn errors of metabolism

inclusion bodies, intranuclear

infantile hemiplegia

intellectual deficit

intellectual deterioration

internal cerebral vein

islet cell tumor

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

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lumbar puncture

lysosomal storage disease

memory, impairment of

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

migraine, children

mitochondrial disease

monoclonal antibodies

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, paramagnetic effect

muscle weakness

muscular dystrophy

myasthenia gravis

myopathy, metabolic

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic signs

neuronal intranuclear inclusion disease

Niemann-Pick disease

nitroproprionic acid

NMDA antagonists

nystagmus, monocular

obsessive-compulsive disorder

oculogyric crisis

old age, neurology of

ophelia syndrome

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

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

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

phenothiazine, dyskinesia associated with

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychotic behavior

putamen, lesion of

putamen, lesion of, bilateral

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

reserpine treatment in movement disorder

retinal degeneration

retinitis pigmentosa

salivation, excessive

seizure, adult onset

seizure, children

seizure, laughing as manifestation

seizure, neonatal

seizure, unknown origin

sensorineural hearing loss

serologic testing

serologic testing, false negative

sleep pathology and physiology

speech disorder

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

sugarcane, mildewed

swallow evaluation

tardive akathisia

tardive dyskinesia

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

tetrahydrobiopterin

thalamus, infarction of

thalamus, lesion of-bilateral

tonic foot response

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

toxic encephalopathy

toxins, nervous system

treatment of neurologic disorder

tremor, postural

tremor, resting

tremor, thalamic

tricyclic antidepressant

trinucleotide repeats

urinary sulfatidase excretion

walking, difficulty with

weakness, progressive

white matter disease

whole genome sequencing

wide based gait

Showing articles 950 to 1000 of 1853 << Previous Next >>

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

A Blinding Headache
Lancet 350:182, Embil,J.J.,et al, 1997

Maternal Infection and Cerebral Palsy in Infants of Normal Birth Weight
JAMA 278:207-211, 2471997., Grether,J.K.&Nelson,K.B., 1997

Clinicopath Conf
Placental Vascular Thrombosis Due to Listeria Infection, Cerebral Embolism and Infarction, Case 15-1, 97EJM 336:1439-1446,1997., 1997

Clinical Utility of Diffusion-Weighted Magnetic Resonance Imaging in the Assessment of Ischemic Stroke
Ann Neurol 41:574-580, 5651997., Letsep,H.L.,et al, 1997

Why Would You Remove Half a Brain? Outcome of 58 Children after Hemispherectomy-Johns Hopkins 1968-96
Pediatrics 100:163-171, Vining,E.P.G.,et al, 1997

Risk Factors for Status Epilepticus in Children with Symptomatic Epilepsy
Neurol 49:533-537, Novak,G.,et al, 1997

Etiology and Early Prognosis of Newly Diagnosed Partial Seizures in Adults
Neurol 49:753-757, Van Paesschen,W.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Stroke Associated with Cardiac Surgery, Determinants, Timing, & Stroke Subtypes
Arch Neurol 54:83-87, Libman,R.B.,et al, 1997

Ibuprofen or Acetaminophen for Acute Treatment of Migraine in Children:A Double-Blind Study
Neurol 48:103-107, Hamalainen,M.L.,et al, 1997

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Therapeutic Dilemma of Inclusion Body Myositis
Neurol 48:567-568, Barohn,R.J., 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
Neurol 48:376-380, Louis,E.D.,et al, 1997

Low-Dose Clozapine Improves Dyskinesias in Parkinson's Disease
Neurol 48:658-662, Durif,F.,et al, 1997

Clinical Course of Untreated Tonic-Clonic Seizures in Childhood:Prospective, Hospital Based Study
BMJ 314:401-404, 3911997., vanDonselaar,C.A.,et al, 1997

Long-Term Psychosocial Outcome in Typical Absence Epilepsy
Arch Pediatr Adolesc Med 151:152, 1581997., Wirrell,E.C.,et al, 1997

Variables Associated with Hospital Arrival Time After Stroke
Stroke 28:537-542, Azzimondi,G.,et al, 1997

Seizures and Epilepsy in the Elderly
Arch Int Med 157:605-617, Thomas,R.J., 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Circadian Fluctuations in Onset of Subarachnoid Hemorrhage
Stroke 28:805-808, Vermeer,S.E.,et al, 1997

Stroke Patients'Knowledge of Stroke
Stroke 28:912-915, Williams,L.S.,et al, 1997

Tremor and Other Movement Disorders after Whiplash Type Injuries
JNNP 63:110-112, Ellis,S.J., 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Sumatriptan for Migraine Attacks in Children:A Randomized Placebo-Controlled Study
Neurol 48:1100-1103, Hamalainen,M.L.,et al, 1997

Seizures in Medically Complex Patients
Epilepsia 38:S55-S59, Boggs,J.G., 1997

Arterial Injuries in Transsphenoidal Surgery for Pituitary Adenoma:The Role of Angiography and Endovascular Treatment
ANJR 18:655-665, Raymond,J.,et al, 1997

If First AED Fails to Control Child's Epilepsy, What Are the Chances of Success with Next Drug
J Pediatr 131:821-824, 7941997., Camfield,P.R.,et al, 1997

Epilepsy in Childhood
BMJ 315:924-930, Neville,B.G.R., 1997

A Meta-Analytic Review of the Preventive Treatment of Recurrences of Febrile Seizures
J Pediatr 131:922-925, Rantala,H.,et al, 1997

Tongue Protrusion Dystonia:Treatment with Botulinum Toxin
South Med J 90:522-525, Charles,P.D.,et al, 1997

Treatment of First Tonic-Clonic Seizure Does Not Improve the Prognosis of Epilepsy
Neurol 49:991-998, Musicco,M.,et al, 1997

Movement Disorders Associated with the Serotonin Selective Reuptake Inhibitors
J Clin Psychiatry 57:449-454, Leo,R.J., 1996

Status Epilepticus in Children with Epilepsy:The Role of Antiepileptic Drug Levels in Prevention
Pediatrics 98:1119-1121, Maytal,J.,et al, 1996

Early Treatment of a Single Generalized Tonic-Clonic Seizure to Prevent Recurrence
Arch Neurol 53:1149-1152, Gilad,R.,et al, 1996

Post-Traumatic Movement Disorders in Survivors of Severe Head Injury
Neurol 47:1488-1492, Krauss,J.K.,et al, 1996

Neurocysticercosis:Report of Unusual Pediatric Cases
Pediatrics 98:974-977, Stamos,J.K.,et al, 1996

Precipitants of Brain Infarction:Roles of Preceding Infection/Inflammation & Recent Psychological Stress
Stroke 27:1999-2004, Macko,R.F.,et al, 1996

Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
Neurol 47:1578-1580, Nance,M.A.,et al, 1996

Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996

Factors Delaying Hospital Admission After Acute Stroke
Stroke 27:398-400, Fogelholm,R.,et al, 1996

Striatopallidal and Thalamic Dystonia, A Magnetic Resonance Imaging Anatomoclinical Study
Arch Neurol 53:241-250, Lehericy,S.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

High-Dose Corticotropin (ACTH) vs. Prednisone for Infantile Spasms:A Prospective, Randomized, Blinded Study
Pediatrics 97:375-379, Baram,T.Z.,et al, 1996

An Increased Frequency of Patent Foramen Ovale in Patients with Transient Global Amnesia
Arch Neurol 53:504-508, Klotzsch,C.,et al, 1996

Is Stroke Incidence Related to Season or Temperature
Lancet 347:934-936, Rothwell,P.M.,et al, 1996

Showing articles 950 to 1000 of 1853 << Previous Next >>