Neudle.com: idiopathic cerebellar ataxia

Differential
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abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

abscess, intracerebral

acanthocytosis

acetylcholine

achilles tendon, enlarged

acoustic nerve

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acute ataxia of childhood

acute cerebellar ataxia

Addison's disease

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

Africa

agenesis of aqueduct of Sylvius

alcohol, neurologic complications with

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

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alkalosis

alkalosis, respiratory

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

AMPA receptor antibodies

amphiphysin antibodies

aneurysm, vertebral basilar system

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS, benign focal

angiography, cerebral

angiography, vertebral artery

angiokeratoma

angiotensin-converting enzyme

aniridia

ankle reflex, absent

anorexia

anti GQ1b IgG antibody

anti GT1aIgG antibody

anti Hu antibody

anti mGluR1 encephalitis

antibiotics, neurologic complications with

anticardiolipin antibodies

anticholinesterase

antiganglioside antibodies

antimetabolite

antineutrophil cytoplasmic autoantibodies

antioxidant

antithyroid antibodies

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arterial dissection, vertebral

ataxia telangiectasia

ataxia, truncal, associated with ocular oscillations

ataxic gait

ataxic-dystonia syndromes

ataxin

ataxin-2

atherosclerosis, premature

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

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

Bickerstaff's brainstem encephalitis

bilirubin encephalopathy

biologic markers

bismuth

bitemporal visual field defect

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

Borrelia burgdorferi infection

brain biopsy, stereotaxic

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma

brainstem, glioma, adult

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

cane

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 nervous system, infection of

central retinal artery occlusion

cephalosporins

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

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 hemangioma

cerebellar hypoplasia

cerebellar infarction

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

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

chest pain

chest x-ray, abnormal

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

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

coma

complications

concentration, impaired

concussion

confusion

congenital infection, CNS

conjunctival biopsy

conjunctivitis

consanguinity

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cough

counterimmunoelectrophoresis

CPAP

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

Crigler-Najjar disease, type I

cryptococcal meningitis

Cuba

cultured skin fibroblasts

Cushing's syndrome

cyst

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

degenerative diseases of CNS

dementia, frontotemporal

dementia, posttraumatic

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental disability

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

diet

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

dizziness

down-beat nystagmus

DPPX

DPPX, antibodies, encephalitis

drooling

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

ear, pain in

edema, periorbital

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, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy

encephalopathy, parainfectious

epidemiology of neurology

epinephrine

Epstein-Barr virus

Erdheim-Chester disease

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

falling

familial

familial hemiplegic migraine

familial periodic ataxia

fine motor function, impaired

finger nose finger test

Fisher's syndrome, atypical

flaccid paralysis

fluorescene in situ hybridization

folic acid deficiency

foot deformity

foot drop

foot numbness

fourth ventricle, enlargement 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

gargoylism

gasoline sniffing

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

globus pallidus, lesion of

glucose tolerance test, abnormal

glue sniffing

glutamic acid decarboxylase, antibody

granular osmiphilic material

granulomatous disease

grasp reflex

growth hormone

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

halo sign

hammertoes

hand flapping

Hand-Schuller-Christian disease

head turning, neurologic complications with

headache

headache, elderly

headache, progressive

headache, severe

hearing loss

hearing loss, bilateral

hematuria, microscopic

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

hemosiderin

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

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

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)

Hurler's syndrome

hydranencephally

hydrocephalus

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hypertrophic intracranial pachymeningitis

hyperventilation

hypocalcemia

hypocalcemia, causes of

hypodontia

hypofibrinogenemia

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypoparathyroidism, idiopathic

hypophonia

hypophosphatemia

hypopigmentation of skin

hypotension, systemic

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

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

incoordination

industrial neurologic disorders

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza A virus

insomnia

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kayser-Fleischer ring

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

keratoconus

kernicterus

Korsakoff's psychosis

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

laryngismus stridulus

lateral medullary syndrome

lateral rectus palsy

lateropulsion

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

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

leukopenia

level of consciousness, decreased

life expectancy

limbic encephalitis

limbic system

lipid storage disorder of CNS

listeria monocytogenes

liver function enzymes

liver transplantation

long bone lesion

low back pain

lumbosacral radiculopathy

Lyme disease

lymphadenopathy

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lymphopenia

lysosomal storage disease

malabsorption syndrome

malaria

malformation, CNS, congenital

Marinesco-Sjogren syndrome

mediastinum, mass of

medulla oblongata, infarction 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, toxoplasma

meningoencephalopathy

mental retardation

mental status, abnormal

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylhydrazine derivatives

metronidazole

microcephaly

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

midbrain, infarction of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

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 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

mucopolysaccharidoses

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, causes of

muscle weakness, proximal

mutism

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

myelinolysis, extrapontine

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myoedema

myoglobinuria

myopathy

myopathy, mitochondrial

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

negative

neonatal infection, viral

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

nephrotic syndrome

nerve conduction studies

neuraminidase deficiency

neuritis

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

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

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neurootology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, recurrent

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, intermittent

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculomasticatory myorhythmia

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opisthotonus

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic nerve, enhancement

optic neuritis

optic neuropathy

optic neuropathy, ischemic

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteoblastic lesions, causes of

osteoporosis

otitis, neurologic complications with

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraplegia

parasitic infection, CNS

parathyroid adenoma

paresthesias

paresthesias, feet

parietal lobe, lesion of

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

parvovirus

PAS positive

PAS positive material in the brain

past pointing

pathologic reflex

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

peripheral nerve, lesion of

peripheral pulse, absent

pigmentary retinopathy

pinealoma

piperazine

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

pneumonia

POLG1 gene

poliomyelitis-like illness

POLR3B

polyclonal gammopathy

polydactyly

polymerase chain reaction

polymyositis

polyneuritis

polyneuritis, acute sensory

polyneuropathy

polyneuropathy, acute sensory

polyneuropathy, chronic idiopathic

polyneuropathy, chronic idiopathic, ataxic

polyneuropathy, chronic relapsing

polyradiculoneuropathy

pons, atrophy

pons, lesion of

pontine glioma

pontocerebellar atrophy

Poretti-Boltshauser syndrome

positional head-hanging test

post infectious cerebellar ataxia

posterior column disease

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

postinfectious

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

preclinical

prevention of neurologic disorders

primary aldosteronism

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

propranolol

proprioception, abnormal

proptosis

protein 14-3-3, cerebrospinal fluid

pruritus

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

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

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, tonic

Purkinje cell

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

radial pulse, unilateral decrease of

radiation hypersensitivity

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

reticulum cell sarcoma

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

rubella syndrome

rubella virus

Sabin-Feldman dye test

saccadic eye movements, abnormal

safety

salivation, excessive

sedimentation rate, elevated

seizure

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, psychomotor-temporal lobe

seminoma

sensorineural hearing loss

sensory loss

sensory loss, crossed pattern

sensory loss, leg

sensory polyneuropathy

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serum glutamic oxaloacetic transaminase

short stature

shrimp sign

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

slurred speech

smiling

snout reflex

sodium channel dysfunction

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

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

spirochete infection

splenium of corpus callosum

splenomegaly

splinter hemorrhages

spongy degeneration of brain

sports medicine, neurology of

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

stridor

striopallidodentate calcifications, familial idiopathic

stuttering

subconjunctival hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, acute

superior cerebellar artery infarction

superior cerebellar artery syndrome

symmetric brain lesions

teeth, number of in infants

teeth, wide-spaced

telangiectases

temporal artery, biopsy

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

tetany, normocalcemic

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, protrusion of

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethyltin

trinucleotide repeats

varicella zoster virus

varicella zoster virus, encephalitis

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

vertebral-basilar insufficiency

vertigo

vestibular areflexia

vestibulopathy

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual obscurations, transient

vitamin deficiency

vitamin E

vitamin E deficiency

vitamin supplementation

vitiligo

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

von Bonsdorff's sign

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, generalized

weakness, progressive

weight loss

Wernekinck commissure syndrome

West Nile fever

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

whole genome sequencing

Showing articles 500 to 550 of 3658 << Previous Next >>

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

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

Lyme Neuroborreliosis Presenting as the Syndrome of Inappropriate Antidiutetic Hormone Secretion
MedGenMed 8:71, Perkins, M.P.,et al, 2006

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

Vertebrobasilar Disease
NEJM 352:2618-2626, Savitz,S.I.&Caplan,L.R., 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

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

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

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

Central Nervous System Manifestations of Mycoplasma Pneumoniae Infections
J Infection 51:343-354, Tsiodras, S.,et al, 2005

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 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

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Five New Cases of a Recently Described Leukoencephalopathy with High Brain Lactate
Neurol 63:688-692, Linnankivi,T.,et al, 2004

Treatment-Induced Leukoencephalopathy in Primary CNS Lymphoma,A Clinical and Autopsy Study
Neurol 62:451-456, Lai,R.,et al, 2004

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

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

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

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

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Clinical Manifestations of Sarin Nerve Gas Exposure
JAMA 290:659-662, Lee,E.C., 2003

Biochemical And Clinical Aspects of Methotrexate Neurotoxicity
Chemotherapy 49:92-104, Vezmar,S.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

Neurologic Manifestations of Vitamin B12 Deficiency
NEJM 348:2208, Scherer,K., 2003

Prevalence of Antigliadin Antibodies in Ataxia Patients
Neurol 60:1674-1675,1566, Abele,M.,et al, 2003

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

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

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

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

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

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

Clinical and Neuroradiologic Features of Acute Disseminated Encephalomyelitis in Children
Neurol 56:1308-1312,1257, Hynson,J.L.,et al, 2001

Monoataxia of Upper Extremity in Motor Cortical Infarction
Neurol 56:1418-1419, Noda,K.,et al, 2001

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

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000

Rhombencephalitis Caused by West Nile Fever Virus
Neurol 55:153, Nichter,C.A. et al, 2000

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

Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
NEJM 342:957-965, , 2000

Nitrous Oxide Anesthesia-Associated Myelopathy
ArchNeurol 57:380-382, Marie,R.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. 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

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

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