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

acromicria

ACTH, ectopic syndrome of

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

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

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

anosmia

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

apnea

apnea, primary central

apraxia of eye movements

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

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 dominant leukodystrophy

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

biotin deficiency

biotinidase deficiency

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

carcinoma of pancreas

CAT scan, contrast enhanced

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, indications for

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 accident, women

cerebrovascular accident, young adult

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

complications

compression neuropathy

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital ocular motor apraxia

conjunctival biopsy

conjunctivitis

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, lesion of

corpus callosum, thinning

cough

CPAP

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst

cyst, epidermoid of CNS

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

deafness

deep gray nuclei

degenerative diseases of CNS

dementia, frontotemporal

dementia, presenile

dementia, reversible

dementia, treatment of

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

disease modifying agents

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

disulfiram

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

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

eating disorder

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, acute

encephalopathy, metabolic

encephalopathy, neonatal

endocarditis, subacute bacterial

enzyme, defect

eosinophilia

ependymoma

epidemiology of neurology

episodic neurologic deficits

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

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

fluorescein angiography

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

gaze palsy, supranuclear

genetic diagnosis, prenatal

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

glucagonoma

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 flapping

Hand-Schuller-Christian disease

hearing loss, bilateral

hearing loss, sudden, unilateral

hearing problems in children

hemianopia, transient

hemosiderosis of CNS, superficial

hepatic encephalopathy

heralding manifestation

highly active antiretroviral therapy

histochemistry

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease

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

hypopigmentation of skin

hyporeflexia

hyposmia

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

imbalance

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

inattention

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

Kearns-Sayre syndrome

kernicterus

Klumpke palsy

Korsakoff's psychosis

Leber's congenital amaurosis

Leber's hereditary optic neuropathy

leg numbness

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

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, aseptic

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

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

methotrexate

methyl benzene

methylhydrazine derivatives

microcephaly

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, hemorrhage

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, disappearing lesion on

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

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myoedema

myopathy

myopathy, alcoholic

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, metastatic to CNS-treatment of

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

neurofibrillary degeneration

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 examination, focal

neurologic signs

neurologic testing

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

obesity

occipital lobe, infarction

occipital lobe, lesion of

octreotide

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

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleurisy

pneumoencephalogram(PEG)

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pontocerebellar atrophy

Poretti-Boltshauser syndrome

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

Prader-Labhart-Willi syndrome

precipitating factors

premature infant

prenatal diagnosis by amniocentesis

prepontine cistern, effaced

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

proprioception, abnormal

psychiatric disorder

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

radiation necrosis

radiation therapy, CNS treatment and complications with

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

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

sagging of the brain

salivation, excessive

scotomata, scintillating

screening

sedimentation rate, elevated

semialdehyde dehydrogenase deficiency

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 cord, pathologic exam 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

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

stridor

stuttering

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

subarachnoid hemorrhage

subdural hematoma

subthalamic nucleus

suck, poor

superior cerebellar peduncle

syphilis, neurologic complications with

syringomyelia

systemic illness

systemic lupus erythematosus

teeth, number of in infants

teeth, wide-spaced

telangiectases

temper tantrums

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

transient neurologic deficit

treatment of neurologic disorder

trinucleotide repeats

trisomes

trisomy 9p

trochlear nerve

trochlear nerve palsy

urea-cycle enzymopathies

urinary gonadotropin

urinary incontinence

urinary urgency

urine test for metabolic disorders

uveitis

vasculitides

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

whole genome sequencing

x-linked mental retardation

Zika virus infection

Showing articles 100 to 150 of 7385 << Previous Next >>

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

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

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

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

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

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

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

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

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

The Brain in Infantile Autism:Posterior Fossa Structures are Abnormal
Neurol 44:214-223, Courchesne,E.,et al, 1994

Moderate Alcohol Consumption and Loss of Cerebellar Purkinje Cells
BMJ 308:1663-1667, Karhunen,P.J.,et al, 1994

Ataxia-Telangiectasia:MR and CT Findings
J Comput Assist Tomogr 18:724-727, Farina,L.,et al, 1994

Reversal of Subacute Paraneoplastic Cerebellar Syndrome with Intravenous Immunoglobulin
Neurol 44:1184-1185, Counsell,C.E.,et al, 1994

Cerebellar Atrophy in Patients with Long-Term Phenytoin Exposure and Epilepsy
Arch Neurol 51:767-771, Ney,G.C.,et al, 1994

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

MRI in Lightning Encephalopathy
Neurol 43:1437-1438, Cherington,M.,et al, 1993

Paraneoplastic Cerebellar Degener II, Clin & Immunologic Find in 21 Pts with Hodgkin's Disease
Neurol 42:1938-1943, Hammack,J.,et al, 1992

Paraneoplastic Cerebellar Degener I A Clinical Analysis of 55 Anti-Yo Antibody-Positive Pts
Neurol 42:1931-1937, Peterson,K.,et al, 1992

The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
Neurol 43:110-113, Tanabe,Y.,et al, 1992

Paraneoplastic Cerebellar Degener III, Cerebellar Degener, Cancer & Lambert-Eaton Myasthenic Synd
Neurol 42:1944-1950, Clouston,P.D.,et al, 1992

Cerebellar and Cerebral Abnormalities in Rett Syndrome:A Quantitative MR Analysis
AJR 159:177-183, Murakami,J.W.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Paraneoplastic Syndrome Manifesting as Chronic Cerebellar Ataxia in a Child with Hodgkin Disease
J Pediatr 120:275-277, Topeu,M.,et al, 1992

MR Imaging Features of Medulloblastoma
AJR 158:859-865, Meyers,S.P.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
Am J Med 91:434-436, Holmes,A.,et al, 1991

Neuroanatomy of Fragile X Syndrome:The Posterior Fossa
Ann Neurol 29:26-32, Reiss,A.L.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Magnetic Resonance Imaging Shows Specific Abnormalities in the MELAS Syndrome
Neurol 41:1043-1046, Matthews,P.M., 1991

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