Neudle.com: cerebellar atrophy primary

Differential
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abdominal contractions

abdominal distention

abducens nerve paralysis

abortion, spontaneous

acetylcholine

acoustic nerve

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adverse drug reaction

agenesis of aqueduct of Sylvius

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic polyneuropathy

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

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amenorrhea

amnesia

amphiphysin antibodies

amphotericin B

amyloid plaques

amyotrophic lateral sclerosis

anatomy of

anemia

aneurysm

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiography, cerebral

angiotensin-converting enzyme

aniridia

ankle edema

ankle reflex, absent

ankylosing spondylitis

anorexia

anterior inferior cerebellar artery

anterior inferior cerebellar artery occlusion

anterior inferior cerebellar artery syndrome

anti Hu antibody

anti Ma

anti mGluR1 encephalitis

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants, untoward effects of

antimetabolite

antithyroid antibodies

antiviral agents

aphasia

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

arenavirus

Arnold Chiari malformation

arterial dissection, aorta

ataxia telangiectasia

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

Babinski sign

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bilirubin encephalopathy

biologic markers

bitemporal visual field defect

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

brain biopsy, stereotaxic

brainstem, glioma, adult

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brazil

Brown Sequard syndrome

calcification, intracranial

calcification, intraventricular

calcification, periventricular

calcium channel dysfunction

cane

CAR syndrome

carcinoembryonic antigen

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, indications for

CAT scan, pelvis

cataracts

cataracts, congenital

cauda equina, enhancement

cavernous sinus, syndrome

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central pontine myelinolysis

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 degeneration

cerebellar disease, eye movement disorder in

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle tumor

cerebellar tonsils

cerebellar vermis

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral folate deficiency syndrome

cerebral palsy

cerebral vasculature

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, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, prevention of

cerebrovascular disease, infant and childhood

cervical rib

Chamberlane's line

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

cigarette smoking

cisterna magna

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

cogwheel rigidty

collapsin response mediator protein 5 IgG

coma

compression neuropathy

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital ocular motor apraxia

conjunctival biopsy

consanguinity

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, thinning

cough

CPAP

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst

cyst, epidermoid of CNS

cyst, porencephalic

cysticercosis

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

deafness

deep gray nuclei

degenerative diseases of CNS

dementia, frontotemporal

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

diet

differential diagnosis

digits, abnormal

dilantin

dilantin, factors influencing metabolism of

dilantin, serum level

dilantin, toxicity

diplopia

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

disulfiram

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

DPPX

DPPX, antibodies, encephalitis

drooling

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

ear, abnormal

echolalia

ectatic basilar artery

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

endocarditis, subacute bacterial

enzyme, defect

eosinophilia

ependymoma

epidemiology of neurology

evoked potentials

exome sequencing

exophthalmus

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 weakness

facial weakness, bilateral

falling

false negative

familial

familial hemiplegic migraine

familial periodic ataxia

fasciculation

fatigue

feeding disorder

fetal alcohol syndrome

fever

fine motor function, impaired

finger nose finger test

fingerprint bodies

fish

flavivirus

fluorescene in situ hybridization

folic acid deficiency

foot deformity

foot drop

foot numbness

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 brain sagging syndrome

frontotemporal dementia, behavioral variant

fundus, abnormality of

gadolinium

gait disorder

gait, spastic

gammaglobulin therapy, intravenous

ganglionitis

gangliosidosis GM2

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, horizontal

gene

gene mutation

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

Gillespie syndrome

gliadin antibodies

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

granular osmiphilic material

granule cell

granulomatous disease

grasping

gray matter

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gynecomastia

Hallervorden Spatz disease

hallucination

hallucination, auditory

hammertoes

Hand-Schuller-Christian disease

hearing loss, sudden, unilateral

heatstroke

heel-knee-shin test

hemianopia

hemianopia, transient

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatitis

hepatomegaly

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

hot cross bun sign

human immunodeficiency virus type 1

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

hydranencephally

hydrocephalus

hydrocephalus, congenital

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hypoglycorrhachia, causes of

hypogonadism

hypogonadism, hypogonadotropic

hypokalemia

hypokalemic alkalosis

hypokalemic periodic paralysis

hypomyelination

hyponatremia

hypoparathyroidism

hypopigmentation of skin

hyposmia

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

immune reconstitution inflammatory syndrome

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

immunosuppression

immunotherapy

impotence

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

incoordination

inferior vermian artery

influenza A virus

intellectual deficit

intellectual deterioration

internal auditory artery

internal auditory artery, occlusion

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

interpeduncular cistern, compressed

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, multiple

intracranial pressure, increased

intrathecal chemotherapy

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Korsakoff's psychosis

Leber's congenital amaurosis

leg numbness

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

level of consciousness, decreased

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macrognathia

macular degeneration

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

marche a petits pas

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

mediastinum, mass of

medulloblastoma

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal gliomatosis

meningismus

meningitis

meningitis, actinomycotic

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, leukemic

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

methotrexate

methyl benzene

methylhydrazine derivatives

microcephaly

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, swollen

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, hemiplegic

Millard Gubler syndrome

mimics

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

molar tooth sign

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, FLAIR

MRI, high signal foci on

multiple system atrophy

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, paraneoplastic

myelopathy, carcinomatous

myelopathy, necrotizing

myopathy, mitochondrial

myopia

myxedema coma

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

negative

neonatal infection, viral

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial, children

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-intraventricular

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nephrotic syndrome

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular junction

neuromyelitis optica (Devic's disease)

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, motor

neuropathy, paraneoplastic

neuropathy, peripheral

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, direction fixed

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, pendular

nystagmus, peripheral

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, spontaneous

nystagmus, upbeating on upgaze

nystagmus, vertical

occipital lobe, infarction

occipital lobe, lesion of

ocular bobbing

ocular bobbing, atypical

ocular bobbing, monocular

ocular dysmetria

ocular flutter

ocular motility, disorders of

ocular myoclonus

ocular myorhythmia

old age, neurology of

oligophrenin 1

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic neuropathy, bilateral

optic neuropathy, nutritional

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

oscillopsia

osteoporosis

otitis, neurologic complications with

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parathyroid adenoma

paratrigeminal syndrome

paresthesias

parietal lobe, lesion of

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

parvovirus

PAS positive

PAS positive material in the brain

peripheral nerve, lesion of

photosensitivity, skin

physostigmine

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

POLG1 gene

poliomyelitis

POLR3B

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pontocerebellar atrophy

positional head-hanging test

posterior cerebral artery

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior fossa, mass of

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

postural abnormality

practice guidelines

precipitating factors

premature infant

prepontine cistern, effaced

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

proprioception, abnormal

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation hypersensitivity

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

remote effect of cancer on the nervous system

renal failure

respiratory depression

respiratory failure

reticulum cell sarcoma

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, children

seizure, withdrawal

sensorineural hearing loss

sensory loss

sensory loss, leg

serologic testing

serologic testing of cerebrospinal fluid

serum tumor markers

sheathing of retinal veins

short stature

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

sicca syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

slow virus infection of CNS

smiling

spastic ataxia

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord

spinal cord, injury of

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 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

splenium of corpus callosum

splenium of corpus callosum, displaced

splenomegaly

spongy degeneration of brain

staggering

staphylococcal protein A column therapy

startle myoclonus

status epilepticus

steatorrhea

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stridor

stuttering

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subdural hematoma

subthalamic nucleus

superior cerebellar peduncle

syndactyly

synucleinopathy

syphilis, neurologic complications with

teeth, number of in infants

teeth, wide-spaced

telangiectases

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

tongue, protrusion of

tonsillar herniation of cerebellum

tonsillectomy

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transglutaminase antibodies

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

vertebral-basilar insufficiency

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection

viral infection, CNS

viral infection, CNS, treatment of

viral isolation

virus, slow

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Walker-Warburg syndrome

walking frame

walking, difficulty with

walking, difficulty with in dark

Wallerian degeneration

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Weber's syndrome

weight loss

Wernicke's encephalopathy

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

x-linked mental retardation

Zika virus infection

Showing articles 50 to 100 of 7013 << Previous Next >>

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UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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JC Viral Infection-Related Cerebellar Degeneration as the First Manifestation of AIDS
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Auto-Immune Cerebellar Ataxia with Anti-GAD Antibodies Accompanied by De Novo Late-Onset Type 1 Diabetes Mellitus
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A 23-Year-Old Man With Seizures and Visual Deficit
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Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
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Anti-Ma and Anti-Ta Associated Paraneoplastic Neurological Syndromes: 22 Newly Diagnosed Patients and Review of Previous Cases
JNNP 79:767-773,742, Hoffmann,L.A.,et al, 2008

Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
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Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
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JC Virus Granule Cell Neuronopathy: A Novel Clinical Syndrome Distinct from Progressive Multifocal Leukoencephalopathy
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Oligophrenin 1 Mutations Frequently Cause X-Linked Mental Retardation with Cerebellar Hypoplasia
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Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

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

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
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

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

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
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Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
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Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

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

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 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

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,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

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Anti-Yo-Associated Paraneoplastic Cerebellar Degeneration in a Man with Adenocardinoma of Unknown Origin
Neurol 46:1486-1487, Krakauer,J.,et al, 1996

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