Neudle.com: idiopathic generalized dystonia

Differential
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abscess, intracerebral

abscess, intracranial

abscess, sphenoid sinus

advances in neurology

adverse drug reaction

algorithm

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

AMPA receptor antibodies

amyloidosis

amyotrophic lateral sclerosis

anemia

ankle edema

anti GQ1b IgG antibody

anticholinergic drugs

apraxia of eye movements

areflexia

artane

arthralgia

arthrogryposis multiplex

ascites

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, truncal

ataxic-dystonia syndromes

athetosis

athetosis, causes of

atlanto-axial subluxation

ATP1A3 gene

attention deficit disorder with hyperactivity

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic neuropathy

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

calcification, intracranial

camptocormia

carbamazepine

carcinoembryonic antigen

carcinoma

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

cataracts

catecholamine

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral cortical atrophy

cerebral hypoperfusion

cerebral ischemia

cerebral palsy

cerebral palsy, associated problems with

cerebral vasculature, calcification

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 11

chromosome 14

chromosome 9

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

deferiprone

degenerative diseases of CNS

delay in diagnosis

dementia

dental procedure, neurologic complications with

depression

dermatomyositis

developmental milestones, loss of

developmental retardation

differential diagnosis

dopa responsive dystonia

dopamine

drooling

drop attacks

drug induced neurologic disorders

dural sinus thrombosis

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystonia, axial

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, symptomatic

dystonia, treatment of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalopathy

encephalopathy, progressive

endarterectomy, carotid

enzyme, defect

episodic neurologic deficits

equinovarus

esophageal varices

exome sequencing

eye movement, disorders of

facial expression abnormality

facial movement disorder

fine motor function, impaired

foot deformity

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

galactorrhea

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, stimulation

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

granuloma, pulmonary

grasp reflex

growth retardation

Guillain Barre syndrome

heparin, subcutaneous

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hydrocephalus, normal pressure

hypoparathyroidism, idiopathic

hyporeflexia

hyposmia

hypotonia

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies, intranuclear

intellectual deficit

intellectual deterioration

intracranial hypertension, benign

intracranial pressure, increased

iron, brain

jugular foramen syndrome

Kayser-Fleischer ring

klippel feil syndrome

L-dopa

leg spasms

leg spasms, painful

leg weakness, bilateral

leucine rich glioma inactivated 1 antibodies

liver function enzymes

lymphoma

masked facies

mastoiditis

memory, impairment of

meningismus

meningitis

meningitis, carcinomatous

meningitis, fungal

meningitis, syphilitic

meningitis, TB

mental retardation

mental status, abnormal

monoclonal antibodies

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, treatment of

MRI

MRI pattern

MRI, abnormal

MRI, eye of tiger sign

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

multiple sclerosis

multiple system atrophy

Munchausen syndrome

muscle diseases, characteristics of

muscle pain

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myelitis, transverse, idiopathic

myelitis, transverse, prognosis

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, thyroid disease causing

neurocutaneous disease

neuroendocrinology

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic signs

neuronal intranuclear inclusion disease

next-generation sequencing

NMDA antagonists

norepinephrine

numb clumsy hands syndrome

nystagmus

nystagmus, monocular

obsessive-compulsive disorder

ocular motility, disorders of

otitis, neurologic complications with

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal hemiplegia

paroxysmal neurologic deficits

parsidol

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

penicillamine

personality change

phenylketonuria

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

primary familial brain calcification

PRKN gene

progeria

prognosis

progressive neurologic disorder

prolactin, elevated

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychosis

pupil, abnormality in neurologic disorders

pupil, tonic

quadriparesis

quality of life

radiation hypersensitivity

radiculopathy

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reversible neurologic disorder

sedimentation rate, elevated

seizure

sensorineural hearing loss

sensory level

sensory tricks

serologic testing

serologic testing, false negative

seronegative

sexual dysfunction in neurologic disease

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

stimulation, deep brain, bilateral

striatal encephalitis

striopallidodentate calcifications, familial idiopathic

substantia nigra

symmetric brain lesions

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

thrombophlebitis, prophylaxis

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, postural

trientine dihydrochloride

trigeminal neuralgia

tripping

tyrosine hydroxylase deficiency

unconsciousness

unconsciousness, transient

walking, difficulty with

Werdnig-Hoffman disease

Showing articles 1000 to 1050 of 2642 << Previous Next >>

Dissections of the Internal Carotid Artery:Three-Dimensional Time-of-Flight MR Angiography and MR Imaging Features
AJR 173:139-143, Bousson,V.,et al, 1999

Pain and the Guillain-Barre Syndrome in Children Under 6 Years
J Pediatr 134:773-776, Nguyen,D.K.,et al, 1999

Focal, Steroid Responsive Myositis Causing Dropped Head Syndrome
Muscle & Nerve 22:769-771, Biran,I.,et al, 1999

Intraarterial Thrombolysis for Treatment of Acute Stroke:Experience in 26 Patients with Long-Term Follow-Up
AJNR 20:1291-1299, 1194, Jahan,R.,et al, 1999

Ptosis, Blepharospasm, and Apraxia of Eyelid Opening Secondary to Putaminal Hemorrhage
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Intravenous Immunoglobulin Treatment in Neurologic Disorders
Arch Neurol 56:1025-1027,1032, Sorensen,P.S., 1999

Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
Arch Neurol 56:1028-1032, Karussis,D.&Abramsky,O., 1999

Tracheostomy, In Guillain- Barre Syndrome
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Prognostic Factors of Guillain-Barre Syndrome After Intravenous Immunoglobulin or Plasma Exchange?
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Brain Biopsy in Primary Angiitis of the Central Nervous System
Neurol 53:858-860, Alrawi,A.,et al, 1999

Neurologic Complications Associated with Hepatitis C Virus Infection
Neurol 53:861-864, Tembl,J.I.,et al, 1999

Acute Dystonia Induced by Drug Treatment
BMJ 319:623-626, vanHarten,P.N.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Serum Vitamin A Concentration is Elevated in Idiopathic Intracranial Hypertension
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Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
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Bilateral Intracranial Vertebral Artery Disease in the New England Medical Center Posterior Circulation Registry
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Isolated Intracranial Hypertension as the Only Sign of Cerebral Venous Thrombosis
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Mechanisms and Clinical Features of Posterior Border-Zone Infarcts
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Preliminary Experience Using Contrast-Enhanced MR Angiography to Assess Vertebral Artery Structure for the Follow-up of Suspected Dissection
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A Sartorial Challenge
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Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Multiple Sclerosis, Side Effects of Interferon Beta Therapy and Their Management
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Beneficial Effect of Siphoning in Treatment of Adult Hydrocephalus
Arch Neurol 56:1224-1229,1199, Bergsneider,M.,et al, 1999

SIADH as the First Symptom of Guillain-Barre Syndrome
Neurol 53:1365, Hofmann,O.,et al, 1999

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999

Recurrent Orbital Myositis,Report of a Familial Incidence
Arch Neurol 56:1407-1409, Maurer,I.&Zierz,S., 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

A Case-Controlled MRI/MRA Study of Neurovascular Contact in Hemifacial Spasm
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Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
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Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
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Polyarteritis Nodosa Presenting as Temporal Arteritis in a 9-Year-Old Child
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Clinicopath Conf,Wegener's Granulomatosis with Pachymeningeal Granulomatous Inflammation, Case 9-1999
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Thrombotic Thrombocytopenic Purpura:Brain CT and MRI Findings in 12 Patients
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Rapidly Progressive Dementia
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Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Outcome in Severe Pediatric Guillain-Barre Syndrome after Immunotherapy or Supportive Care
Neurol 52:1494-1497, Graf,W.D.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Thrombotic Thrombocytopenic Purpura Associated with Ticlopidine Use,A Report of 3 Cases and Review of the Literature
Arch Int Med 159:311-314, Chen,D.K.,et al,, 1999

Hypertrophic Cranial Pachymeningitis and Lymphocytic Hypophysitis in Sjogren's Syndrome
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Paroxysmal Dyskinesias in Patients with HIV Infection
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Control of Primary Angiitis of the CNS Associated with Cerebral Amyloid Angiopathy by Cyclophosphamide Alone
Neurol 52:660-662, Fountain,N.B.&Lopes,B.S., 1999

Isolated Angiitis of the Central Nervous System:Lack of Inflammation after Long-Term Treatment
Neurol 52:196-199, Reimer,G.,et al, 1999

Effectiveness of Anticholinergics and Neuroleptic Dose Reduction on Neuroleptic-Induced Pleurothotonus (the Pisa Syndrome)
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Antiepileptics and Blood Dyscrasias: A Cohort Study
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Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
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Minimal Number of Plasma Exchanges Needed to Reduce Immunoglobulin in Guillain-Barre Syndrome
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Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
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Malignancy and Sensory Neuropathy of Unexplained Cause
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Small-Fiber Sensory Neuropathies:Clinical Course and Neuropathology of Idiopathic Cases
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The Predictive Value of Early CT and Angiography for Fatal Hemispheric Swelling in Acute Stroke
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Showing articles 1000 to 1050 of 2642 << Previous Next >>