Neudle.com: ataxia cerebellar

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Differential
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abdominal distention

abdominal x-ray

abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

achilles tendon, enlarged

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

agranulocytosis

alcohol intolerance

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

Alexanders disease

Alexanders disease, adult onset

alien hand syndrome

alkylating agents

alpha-fetoprotein

alpha-synuclein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

amnesia, concussion

AMPA receptor antibodies

amphiphysin antibodies

amyloid plaques

amyotrophic lateral sclerosis

aneurysm, asymptomatic

aneurysm, children

aneurysm, fusiform

aneurysm, intracranial

aneurysm, vertebral basilar system

Angelman syndrome

angiitis, granulomatous of CNS

angiitis, isolated of CNS, benign focal

angiography, cerebral

angiography, posterior fossa

angiotensin-converting enzyme

ankle reflex, absent

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti Hu antibody

anti La antibody

anti MAG antibodies

anti mGluR1 encephalitis

anti Ri antibody

anti Ro antibody

anti Tr antibodies

anti Yo antibody

antiamphiphysin

antiarrhythmic drugs

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

Arnold Chiari malformation

arrhythmia, cardiac

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

arteritis, temporal

aspartate aminotransferase

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxia, truncal, associated with ocular oscillations

ataxic hemiparesis

ataxic-dystonia syndromes

atherosclerosis, premature

atrial fibrillation

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

Ayurvedic medicine

B 12 deficiency

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Bergmann's gliosis

Bickerstaff's brainstem encephalitis

bilirubin encephalopathy

biologic markers

bitemporal visual field defect

bladder dysfunction

blood dyscrasias, neurologic findings with

blue tongue virus

bone marrow biopsy

border zone infarct

brachial neuritis

BRAF protooncogene

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, dysfunction, eye movement disorders with

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hematoma

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar dysfunction

burning paresthesia

calcification, intracranial

calcification, periventricular

calcium channel dysfunction

carbamazepine, toxicity

carbon monoxide poisoning

carbon tetrachloride poisoning

carcinoembryonic antigen

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of testis

carcinoma of uterus

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

celiac disease, childhood

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar calcification

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar edema

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, etiology

cerebrovascular accident, prognosis in

cerebrovascular accident, surgical treatment of

cerebrovascular accident, vascular territory involved

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

Chamberlane's line

Charcot-Marie-Tooth

chasing the dragon

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

chest x-ray, abnormal

chloride channel dysfunction

chorea, familial

choreoathetosis

chorioretinitis

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

ciguatera poisoning

cisterna magna, enlarged

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

coccidioidomycosis

Cockayne's syndrome

coenzyme Q10 deficiency

Cogan's syndrome

cognition, slowed

cognitive delay

cogwheel rigidty

collapsin response mediator protein 5 IgG

concentration, impaired

cone-rod dystrophy

congenital infection, CNS

congenital infection, viral

congenital malformation

congestive heart failure

conjunctival biopsy

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

cornea, abnormal

corneal reflex, abnormal

corneal reflex, depressed

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

counterimmunoelectrophoresis

Coxiella burnetti

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

Crigler-Najjar disease, type I

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, peritumoral

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cyst, parenchymal

cyst, porencephalic

cyst, subcortical

cystatin C mutation

cytosine arabinoside

Dandy Walker malformation

Dandy Walker malformation, adult

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, posttraumatic

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dietary supplement

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability, neurological

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

DPPX, antibodies, encephalitis

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

drug induced neurologic disorders in children

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

dystonia, focal

ejection fraction, abnormal

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

electroretinograph

embolism, septic

embolism, systemic

embolism, vertebral-basilar artery

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, parainfectious

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy, delayed

encephalopathy, parainfectious

encephalopathy, progressive

encephalopathy, salmonella

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

endolymphatic sac tumors

epicanthal folds

epidemiology of neurology

episodic neurologic deficits

Epstein-Barr virus

Erdheim-Chester disease

erectile dysfunction

erythema migrans

ethics in neurology

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial pain, atypical

facial weakness

facial weakness, bilateral

familial hemiplegic migraine

familial periodic ataxia

family planning

feeding disorder

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fisher's syndrome

fluorescene in situ hybridization

folic acid deficiency

fourth ventricle, compression

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gasoline sniffing

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant cell arteritis

Gillespie syndrome

gliadin antibodies

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of

glucose tolerance test, abnormal

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

gram negative rod

gram positive rod

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

Hartnup's disease

head injury, delayed deterioration following

headache, awakened by

headache, awakening with

headache, bifrontal

headache, progressive

headache, severe

headache, sudden onset of

headache, worst of life

hearing loss, bilateral

heel-knee-shin test

hemangioblastoma

hematoma, intracerebral

hematuria, gross

hematuria, microscopic

hemisensory loss

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes simplex virus

herpes virus infection

herpes zoster, disseminated

heterophile antibody test

high arched feet

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

hot cross bun sign

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 2

human T-lymphotropic virus type I(HTLV-I)

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Hurler's syndrome

hydranencephally

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydroxyglutaric aciduria

hydroxytryptophan L-5(L-5 HTP)

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperinsulinism

hyperosmolality

hyperparathyroidism

hyperphosphatasia

hyperpigmentation of skin

hypertension, cerebrovascular disease with

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hypotension, systemic

hypothalamus, damage to

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

imbalance, postural

immediate recall

immune reconstitution inflammatory syndrome

immune-mediated pathogenesis

immunization, neurologic complications with

immunocompetent

immunodeficiency

immunofluorescent exam of CSF cells

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

industrial neurologic disorders

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior vermian artery

influenza A virus

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, small

intracranial hypotension

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw claudication

JC virus cerebellar granule cell neuronopathy

JC virus encephalopathy

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Korsakoff's psychosis

Krabbe's disease

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction, differential diagnosis of

lateral medullary syndrome

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukodystrophy, 4H

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

liver function enzymes

locked-in syndrome

long bone lesion

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma involving CNS

lysosomal storage disease

macroglobulinemia

macular degeneration

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

malignant hyperpyrexia

mammillary bodies

marche a petits pas

Marchiafava-Bignami disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

mediastinum, mass of

medulla oblongata

medulla oblongata, infarction of

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, cysticercosis

meningitis, echinococcal

meningitis, elderly

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, mumps

meningoencephalitis, toxoplasma

meningoencephalomyelitis

meningoencephalopathy

meningovascular syphilis

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylhydrazine derivatives

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, children

migraine, hemiplegic

Minamata disease

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

mitral valve lesion

mitral valve prolapse

mitral valve regurgitation

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy multiplex

monoparesis, focal

motor neuron disease

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, optic nerve

MRI, punctate pattern

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, vessel wall

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myelitis, transverse

myelopathy, chronic progressive

myoclonic jerks

myoclonus, epilepsy

myoclonus, stimulus sensitive

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

neonatal infection, viral

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nephrotic syndrome

nerve conduction studies

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic signs

neurologic symptoms

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

NMDA antagonists

nodular infarction

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, monocular

nystagmus, pendular

nystagmus, periodic

nystagmus, periodic alternating

nystagmus, positional

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculodentodigital dysplasia

oculogyric crisis

oculomasticatory myorhythmia

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic disc edema

optic nerve, enhancement

optic neuropathy

optic neuropathy, bilateral

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

osmotic demyelination syndrome

osteoblastic lesions, causes of

otitis, neurologic complications with

ovarian dysgenesis

ovary, enlarged

Paget's disease

pain, abdominal

palatal myoclonus

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parathyroid adenoma

parietal lobe, lesion of

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

pathologic reflex

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

periaqueductal lesion

periodic paralysis

peripheral nerve, lesion of

Perrault syndrome

personality change

pheochromocytoma

pigmentary retinopathy

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

polyradiculoneuropathy

pons, lesion of

pontine hemorrhage

pontocerebellar atrophy

Poretti-Boltshauser syndrome

positional head-hanging test

post infectious cerebellar ataxia

posterior cerebral artery

posterior column disease

posterior fossa

posterior fossa, lesion of

posterior fossa, mass of

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

prion protein gene

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

puberty, delayed

pulmonary embolism

pulmonary infection

pulmonary infiltrates

punch-drunk syndrome

pupil, abnormality in neurologic disorders

pure motor hemiplegia

pure sensory stroke

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation induced neoplasm

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

reflex, brainstem

Refsum's disease

release phenomena

remote effect of cancer on the nervous system

renal cell carcinoma

respiratory failure

respiratory tract infection

reticular activating system

reticulum cell sarcoma

retina, abnormal

retinal degeneration

retinal detachment

retinal hemangioma

retinitis pigmentosa

retroperitoneal fibrosis

retroperitoneal mass

Rett's syndrome

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rhomboencephalopathy

rickettsial organism

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

Sabin-Feldman dye test

saccadic eye movements, abnormal

sagging of the brain

sarcoidosis, CNS

scalp tenderness

sclerosis, bone

sedimentation rate, elevated

seizure, children

seizure, drug-induced

seizure, familial

seizure, febrile

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

seizure, treatment of

sensorimotor stroke

sensorineural hearing loss

sensory loss, crossed pattern

sensory loss, leg

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

shell fish poisoning

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

somatosensory evoked potentials

spastic paraplegia, type 7

spatial orientation

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 14

spinocerebellar ataxia type 17

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

splenium of corpus callosum

spongy degeneration of brain

sports medicine, neurology of

square wave jerks

standing difficulty

staphylococcal protein A column therapy

startle myoclonus

startle reaction

status epilepticus

stem cell rescue

stem cell transplantation

stereotaxic surgery

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

subconjunctival hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, acute

superior cerebellar artery infarction

superior cerebellar artery syndrome

superior cerebellar peduncle

symmetric brain lesions

synucleinopathy

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temporal artery, biopsy

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratogenesis, viral

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third ventricle, wall

thrombocytopenia

tick-borne encephalitis

tongue, enlarged

tongue, protrusion of

tonsillar herniation of cerebellum

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

tremor, treatment of

tremor, writing

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

ultrasonography

unconsciousness

upgaze, paralysis of

upside-down vision

upward deviation of eyes

urinary gonadotropin

urinary incontinence

urinary retention

urinary urgency

Usher's syndrome

varicella zoster virus

varicella zoster virus, encephalitis

vasogenic edema

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo, episodic

vertigo, positional

vestibular areflexia

vibratory sensation

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Wernekinck commissure syndrome

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

Whipple's disease

white matter disease

white matter disease, periventricular

wide based gait

Wolfram syndrome

xanthoma, eyelid

X-linked bulbospinal neuronopathy

zoster sine herpete

Showing articles 1000 to 1050 of 1804 << Previous Next >>

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Vertigo
Lancet 352:1841-1846, Baloh,R.W., 1998

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Predicting Neurologic Deterioration in Patients with Cerebellar Hematomas
Neurol 511:1364-1369, St. Louis,E.K.,et al, 1998

Dilemma of Discontin of Anticoag Therapy for Pts with Intracran Hem & Mech Heart Valves
Neurosurg 42:769-773, Eelco,F.M.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

Acute Vestibular Syndrome
NEJM 339:680-685, Hotson,J.R.&Baloh,R.W., 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

Intracranial Hemorrhage: Diagnosis and Emergency
Neuro Clin 16:373-390, Stieg,P.E.&Kase,C.S., 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Thrombolysis-Related Intracranial Hemorrhage, Analysis of 224 Cases from GUSTO-1 Trial with Clin Correl
Stroke 29:563-569, Gebel,J.M.,et al, 1998

Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
Arch Neurol 55:33-37, Murata,Y.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Delayed Cerebellar Disease and Death After Accidental Exposure to Dimethylmercury
NEJM 338:1672-1676, 16921998., Nierenberg,D.W.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Cerebellum in Attention-Deficit Hyperactivity Disorder
Neurol 50:1087-1093, Berquin,P.C.,et al, 1998

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Metabolic Abnormalities in Development Dyslexia Detected by 1H Magnetic Resonance Spectroscopy
Lancet 351:1849-1852, Rae,C.,et al, 1998

Recovery Following Lateral Medullary Infarction
Neurol 50:1418-1422, Nelles,G.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Patterns of Lateral Medullary Infarction, Vascular Lesion-MR Imaging Correl of 34 Cases
Stroke 29:645-652, Kim,J.S.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Features of MRI Diffusion Weighted Image in Early Stage of Lateral Medullary Infarction Presenting Wallenberg Syndrome
Rinsho Shinkeigaku 38:157-160, Hirose,Y., 1998

Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
JNNP 65:233-240, Sue,C.M.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
Mov Dis 12:342-353, Singer,C.,et al, 1997

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Patterns of Sensory Dysfunction in Lateral Medullary Infarction, Clinical-MRI Correlation
Neurol 49:1557-1563, Kim,J.S.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

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

Tremor Caused by Trimethoprim-Sulfamethoxazole in a Patient with AIDS
Neurol 48:537-538, VanGerpen,J.A., 1997

MR of Childhood Metachromatic Leukodystrophy
AJNR 18:733-738, Kim,T.S.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Showing articles 1000 to 1050 of 1804 << Previous Next >>