Neudle.com: idiopathic cerebellar ataxia

Differential
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abdominal x-ray

abducens nerve paralysis

abortion, spontaneous

abscess, intracerebral

acanthocytosis

acetylcholine

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

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, granulomatous of CNS

angiitis, isolated of CNS, benign focal

angiokeratoma

angiotensin-converting enzyme

aniridia

ankle reflex, absent

anorexia

anti GQ1b IgG antibody

anti Hu antibody

anti mGluR1 encephalitis

antibiotics, neurologic complications with

anticholinesterase

antimetabolite

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 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

bilirubin encephalopathy

biologic markers

bismuth

bitemporal visual field defect

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

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

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

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

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, prognosis in

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

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

consanguinity

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cough

counterimmunoelectrophoresis

CPAP

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

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

dilantin

diplopia

disorientation

distal muscle atrophy

dizziness

down-beat nystagmus

DPPX

DPPX, antibodies, encephalitis

drooling

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

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

enzyme, defect

eosinophilia

ependymoma

epidemiology of neurology

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

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, etiology of

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

headache, progressive

headache, severe

hearing loss

hearing loss, bilateral

hematuria, microscopic

hemochromatosis, primary

hemorrhagic diathesis

hemosiderin

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

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)

hyperactivity

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hypoglycorrhachia, causes of

hypogonadism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

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

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

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

keratoconus

kernicterus

Korsakoff's psychosis

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

lateral medullary syndrome

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

level of consciousness, decreased

life expectancy

limbic encephalitis

limbic system

lipid storage disorder of CNS

listeria monocytogenes

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

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

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, demyelinating

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

obesity

ocular flutter

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculomasticatory myorhythmia

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic nerve, enhancement

optic neuritis

optic neuropathy

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteoblastic lesions, causes of

osteoporosis

otitis, neurologic complications with

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parathyroid adenoma

paresthesias

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

parvovirus

PAS positive

PAS positive material in the brain

past pointing

pathologic reflex

pathology

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

penicillin

pericarditis

peripheral nerve, lesion of

pigmentary retinopathy

pinealoma

piperazine

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

pneumonia

POLG1 gene

poliomyelitis-like illness

POLR3B

polydactyly

polymerase chain reaction

polymyositis

polyneuropathy

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

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

punch-drunk syndrome

Purkinje cell

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriplegia

radiation hypersensitivity

radiculitis

radiculopathy

Ramsay Hunt syndrome

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

sedimentation rate, elevated

seizure

seizure, intractable

seizure, laughing as manifestation

seizure, psychomotor-temporal lobe

seminoma

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 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

somnolence

spastic ataxia

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

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

thalamus, lesion of-bilateral

tongue, protrusion of

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transglutaminase antibodies

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethyltin

trinucleotide repeats

varicella zoster virus

varicella zoster virus, encephalitis

vasculitides

Vemurafenib

vertebral artery

vertebral artery disease

vertebral artery occlusion

vertebral artery stenosis

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

vitamin supplementation

vitiligo

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, progressive

weight loss

Wernekinck commissure syndrome

West Nile fever

Western immunoblot test

Showing articles 100 to 150 of 3612 << Previous Next >>

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

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

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

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

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

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

Legionella Infection
emedicine.com, Mobeen,R., 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

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

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

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

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

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

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

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

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

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

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

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

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

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

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

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,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

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 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

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

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 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

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,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

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

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 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

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