Neudle.com: ataxia cerebellar

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abdominal distention

abdominal x-ray

abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

acanthocytosis

acetazolamide

acetylcholine

achilles tendon, enlarged

aciduria

acoustic nerve

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

Adies pupil

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

Africa

agenesis of aqueduct of Sylvius

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

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

alcoholism

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

AMPA receptor antibodies

amphiphysin antibodies

amphotericin B

amyloid plaques

amyotrophic lateral sclerosis

anatomy of

anemia

aneurysm

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

angiokeratoma

angiotensin-converting enzyme

aniridia

ankle reflex, absent

anorexia

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti mGluR1 encephalitis

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

antimetabolite

antioxidant

antithyroid antibodies

apraxia of eye movements

aqueduct of Sylvius, stenosis

Arnold Chiari malformation

arrhythmia, cardiac

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

aspartate aminotransferase

ataxia telangiectasia

ataxia, truncal, associated with ocular oscillations

ataxic gait

ataxic hemiparesis

ataxic-dystonia syndromes

ataxin

ataxin-2

atherosclerosis, premature

atonic bladder

ATP1A3 gene

atrial fibrillation

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia

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

bismuth

bitemporal visual field defect

bladder dysfunction

blindness

blood cultures

blood dyscrasias, neurologic findings with

brain biopsy, stereotaxic

brain scan

brainstem

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

brucellosis, nervous system involvement with

calcification, intracranial

calcification, periventricular

calcium channel dysfunction

cane

CAR syndrome

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carbon tetrachloride poisoning

carcinoembryonic antigen

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

cataplexy

cataracts

cataracts, congenital

cauda equina, enhancement

CD4 counts

celiac disease, adult

celiac disease, childhood

central core disease

central nervous system, infection of

central pontine myelinolysis

cephalosporins

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

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebral palsy

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

chemotherapy, CNS treatment and complications with

cherry red spot

chest pain

chest x-ray, abnormal

chickenpox

children

chlorambucil

chloride channel dysfunction

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Claude's syndrome

climate change

Clinical Pathologic Conference(C.P.C.)

clonus

clubbing of fingers

clubfoot as related to neurologic disease

coccidioidomycosis

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

collapsin response mediator protein 5 IgG

Collier's sign

coma

complications

concentration, impaired

concussion

cone-rod dystrophy

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

congestive heart failure

conjunctival biopsy

consanguinity

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

cough

counterimmunoelectrophoresis

Coxiella burnetti

CPAP

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

Cuba

cultured skin fibroblasts

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

Dandy Walker malformation

Dandy Walker malformation, adult

degenerative diseases of CNS

dementia, frontotemporal

dementia, posttraumatic

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

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

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

DPPX

DPPX, antibodies, encephalitis

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

drug induced neurologic disorders in children

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

dystonia, focal

ear, pain in

efficacy

ejection fraction, abnormal

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

embolism, vertebral-basilar artery

embryogenesis

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, parainfectious

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy

encephalopathy, delayed

encephalopathy, parainfectious

encephalopathy, progressive

encephalopathy, salmonella

endocarditis

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

endolymphatic sac tumors

epidemiology of neurology

episodic neurologic deficits

Epstein-Barr virus

Erdheim-Chester disease

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

facial pain, atypical

facial weakness

facial weakness, bilateral

falling

familial

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

finger nose finger test

fluorescene in situ hybridization

folic acid deficiency

foot deformity

foot drop

foot numbness

fourth ventricle, compression

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

ganglioglioma

gargoylism

gasoline sniffing

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

glucose tolerance test, abnormal

glue sniffing

glutamate dehydrogenase deficiency

glutamic acid

glutamic acid decarboxylase, antibody

granular osmiphilic material

granule cell

granulomatous disease

grasp reflex

gray matter

growth hormone

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

gynecomastia

Hallervorden Spatz disease

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

handwriting

Hartnup's disease

head injury

head injury, delayed deterioration following

head nodding

head tilt

headache

headache, awakened by

headache, awakening with

headache, bifrontal

headache, progressive

headache, severe

headache, sudden onset of

headache, worst of life

hearing loss

hearing loss, bilateral

hematoma, intracerebral

hematuria, gross

hematuria, microscopic

hemochromatosis, primary

hemorrhagic diathesis

hemosiderin

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herbs

herpes simplex virus

herpes virus

herpes virus infection

herpes zoster

herpes zoster, disseminated

heterophile antibody test

Hodgkin's disease, neurologic involvement with

Hoesch test

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)

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydroxyglutaric aciduria

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hyperreflexia

hypersomnia

hypertension

hypertension, cerebrovascular disease with

hypoglycorrhachia, causes of

hypogonadism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypopigmentation of skin

hypotension, systemic

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

iatrogenic neurologic disorders

imbalance

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

immunotherapy

impotence

impulsivity

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

incoordination

industrial neurologic disorders

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior vermian artery

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

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

JC virus cerebellar granule cell neuronopathy

JC virus encephalopathy

jittery baby

karyotyping

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

keratoconus

kernicterus

Kernig's sign

Korsakoff's psychosis

lactic dehydrogenase(LDH)

lacunar infarction, differential diagnosis of

lateral medullary syndrome

lateropulsion

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

lead poisoning

learning disability

learning disability, in children

leg numbness

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

leukopenia

level of consciousness, decreased

lipid storage disorder of CNS

listeria monocytogenes

liver function enzymes

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphopenia

lysosomal storage disease

malabsorption syndrome

malaria

malformation, CNS, congenital

malignancy screen

malignancy, occult

malignant hyperpyrexia

Marchiafava-Bignami disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

masked facies

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

meningismus

meningitis

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, TB

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

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

mitral valve lesion

mitral valve prolapse

mitral valve regurgitation

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, optic nerve

MRI, punctate pattern

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, vessel wall

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

mutism

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myxedema, neurologic manifestations of

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

neuritis

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

neuronopathy, sensory

neuroophthalmology

neurootology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

next-generation sequencing

nutritional deficiency

nystagmus

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

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

opsoclonus-myoclonus syndrome

optic nerve, enhancement

optic neuritis

optic neuropathy

optic neuropathy, bilateral

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteoblastic lesions, causes of

osteoporosis

otitis, neurologic complications with

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

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

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

parvovirus

PAS positive

PAS positive material in the brain

past pointing

pathologic reflex

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

pelvic mass

penicillin

periaqueductal lesion

pericarditis

periodic paralysis

peripheral nerve, lesion of

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

pneumonia

POEMS syndrome

poison, mercury

poison, neurologic problems with

POLG1 gene

poliomyelitis-like illness

POLR3B

polydactyly

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyradiculoneuropathy

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

postinfectious

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

precipitating factors

preclinical

pregnancy, neurologic complications in

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

propranolol

proprioception, abnormal

proptosis

protein 14-3-3, cerebrospinal fluid

pruritus

pseudoaneurysm

pseudobulbar palsy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

punch-drunk syndrome

pupil, abnormality in neurologic disorders

pure motor hemiplegia

pure sensory stroke

Purkinje cell

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

Q fever

quadriparesis

quadriplegia

radiation hypersensitivity

radiation induced neoplasm

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

real-time quaking-induced conversion

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

respiratory failure

respiratory tract infection

restiform body

reticular activating system

reticulum cell sarcoma

retroperitoneal fibrosis

retroperitoneal mass

retropulsion

Rett's syndrome

reversible neurologic disorder

review article

RFC1 gene

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

rubella syndrome

rubella virus

Sabin-Feldman dye test

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

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

seminoma

sensorimotor stroke

sensorineural hearing loss

sensory loss

sensory loss, crossed pattern

sensory loss, leg

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

shell fish poisoning

short stature

shrimp sign

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

sinemet

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

slurred speech

smiling

snout reflex

sodium channel dysfunction

somatosensory evoked potentials

somnolence

spastic ataxia

spastic paraplegia, type 7

spasticity

spatial orientation

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

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

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

staphylococcal protein A column therapy

stem cell transplantation

stereotaxic surgery

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

strabismus

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stridor

striopallidodentate calcifications, familial idiopathic

stuttering

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

sweating

symmetric brain lesions

syndactyly

synucleinopathy

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syringomyelia

systemic illness

systemic lupus erythematosus

teeth, number of in infants

teeth, wide-spaced

telangiectases

temporal artery, biopsy

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

third nerve palsy

third ventricle, wall

tick-borne encephalitis

tongue, protrusion of

tonsillar herniation of cerebellum

topiramate

torticollis

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

trazodone

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethyltin

trinucleotide repeats

upward deviation of eyes

varicella zoster virus

varicella zoster virus, encephalitis

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual cortex

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin deficiency

vitamin E

vitamin E deficiency

vitamin supplementation

vitiligo

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking frame

walking, delayed

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

weight loss

Wernekinck commissure syndrome

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

X-linked bulbospinal neuronopathy

zoster sine herpete

Showing articles 150 to 200 of 1804 << Previous Next >>

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Upside Down Reversal of Vision Due to an Isolated Acute Cerebellar Ischemic Infarction
J Neurol 253:953-954, Hern�ndez,A.H.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Cerebellar Ataxia and Central Nervous System Whipple Disease
Arch Neurol 62:618-620, Matthews,B.R.,et al, 2005

Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
Neurol 64:1461-1464, Wolf,N.I.,et al, 2005

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

Autoantibodies in Postinfectious Acute Cerebellar Ataxia
Neurol 65:1114-1116, Uchibori,A.,et al, 2005

Acute Cerebellar Ataxia Due to Sjogren Syndrome
Neurol 62:2332-2333, Wong,S.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Acute Bilateral Inferior Cerebellar Infarction in a Patient With Neurosyphillis
Arch Neurol 61:953-956, Umashankar,G.,et al, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
Arch Neurol 61:35-38, Lu,C.,et al, 2004

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003

Symmetric Deep Cerebellar Lesions After Smoking Heroin
Arch Neurol 60:1605-1606, Ropper,A.H. &Blair,R., 2003

Cerebellar Ataxia and Coenzyme Q10 Deficiency
Neurol 60:1206-1208, Lamperti,C.,et al, 2003

Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
Medicine 82:216-223, Rojas-Marcos,I.,et al, 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
JNNP 74:998-999, Antonini,G.,et al, 2003

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
NEJM 346:68-69, Woodruff,B.K.,et al, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Legionella Infection
emedicine.com, Mobeen,R., 2002

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
Ann Neurol 49:540-543, Bushara,K.O.,et al, 2001

Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Vertigo and Gait Ataxia Without Usual Signs of Lateral Medullary Infarction: A Clinical Variant Related to Rostral-dorsolateral Lesions
Cerebrovasc Dis 10:471-474, Kim,J.S., 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Superficial Siderosis of the Central Nervous System,A Late Complication of Cerebellar Tumors
Neurol 52:163-169, Anderson,N.E.,et al, 1999

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

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Showing articles 150 to 200 of 1804 << Previous Next >>