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abdominal distention

abdominal x-ray

abducens nerve paralysis

abscess, intracerebral

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

advances in neurology

adverse drug reaction

alcohol intolerance

alcohol, neurologic complications with

alkylating agents

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amnesia, concussion

AMPA receptor antibodies

amphiphysin antibodies

amyloid plaques

aneurysm, asymptomatic

aneurysm, intracranial

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiography, cerebral

angiography, posterior fossa

angiotensin-converting enzyme

anti GQ1b IgG antibody

anti Hu antibody

anti MAG antibodies

anti Ri antibody

anti Yo antibody

antiamphiphysin

antibiotics, neurologic complications with

anticonvulsants

anticonvulsants, effectiveness

apraxia of eye movements

Arnold Chiari malformation

arterial dissection

arterial dissection, intracranial

arterial dissection, ruptured

arterial dissection, vertebral

aspartate aminotransferase

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

bilirubin encephalopathy

biologic markers

bitemporal visual field defect

blood dyscrasias, neurologic findings with

bone marrow biopsy

brachial neuritis

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma in children

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar dysfunction

burning paresthesia

calcification, intracranial

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of testis

carcinoma of uterus

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

celiac disease, adult

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar edema

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral infarction, hemorrhagic

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, prognosis in

cerebrovascular accident, surgical treatment of

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

Charcot-Marie-Tooth

chasing the dragon

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choreoathetosis

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coccidioidomycosis

Cockayne's syndrome

coenzyme Q10 deficiency

collapsin response mediator protein 5 IgG

concentration, impaired

congenital infection, CNS

conjunctival biopsy

contactin associated protein like 2 antibodies

cornea, abnormal

counterimmunoelectrophoresis

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Crigler-Najjar disease, type I

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, epidermoid of CNS

cytosine arabinoside

deep gray nuclei

degenerative diseases of CNS

dementia, familial

dementia, posttraumatic

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

disability, neurological

distal muscle atrophy

down-beat nystagmus

down-beat nystagmus, primary position of gaze

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

drug induced neurologic disorders in children

dysdiadochokinesia

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

embolism, septic

embolism, systemic

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, parainfectious

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy, delayed

encephalopathy, parainfectious

encephalopathy, progressive

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

epidemiology of neurology

Epstein-Barr virus

erythema migrans

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

finger nose finger test

fingerprint bodies

Fisher's syndrome

folic acid deficiency

fourth ventricle, compression

Friedreich's ataxia

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gasoline sniffing

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

Gillespie syndrome

glioblastoma multiforme(astrocytoma Gr.III)

gliomatosis cerebri

glutamic acid decarboxylase, antibody

gram negative rod

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, variant forms of

Hallgren's syndrome

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

Hartnup's disease

headache, severe

headache, sudden onset of

headache, worst of life

heel-knee-shin test

hematoma, intracerebral

hematuria, microscopic

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes zoster, disseminated

heterophile antibody test

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

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

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

Hurler's syndrome

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperinsulinism

hyperosmolality

hyperparathyroidism

hyperphosphatasia

hyperpigmentation of skin

hypertension, cerebrovascular disease with

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypoproteinemia

hypoprothrombinemia

hypothalamus, disturbance of

iatrogenic neurologic disorders

immediate recall

immune-mediated pathogenesis

immunization, neurologic complications with

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

immunosuppression

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deficit

intellectual deterioration

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, clot evacuation

intrathecal chemotherapy

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Korsakoff's psychosis

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, toxic

level of consciousness, decreased

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

liver function enzymes

locked-in syndrome

lymphadenopathy

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphoma involving CNS

macular degeneration

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

marche a petits pas

Marcus Gunn pupil

Marinesco-Sjogren syndrome

mediastinum, mass of

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

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, toxoplasma

meningoencephalitis

meningoencephalitis, mumps

meningoencephalitis, toxoplasma

meningoencephalomyelitis

meningoencephalopathy

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

methylhydrazine derivatives

midbrain, infarction of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

mitral valve regurgitation

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal intensity of basal ganglia

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

multiple sclerosis

multiple system atrophy

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma pneumoniae

mycotic aneurysm

myelinolysis, extrapontine

myelitis, transverse

myelopathy, chronic progressive

myoclonic jerks

myoclonus, epilepsy

myoclonus, stimulus sensitive

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nephrotic syndrome

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

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, demyelinating

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

nitrogen mustard

NMDA antagonists

nystagmus, hereditary

nystagmus, monocular

nystagmus, periodic

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

optic disc edema

optic neuropathy

optic neuropathy, bilateral

orthostatic hypotension

osmotic demyelination syndrome

otitis, neurologic complications with

ovary, enlarged

pain, abdominal

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, spastic

parathyroid adenoma

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinsonism syndrome

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathologic reflex

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

Pelizaeus Merzbacher

peripheral nerve, lesion of

personality change

pheochromocytoma

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poliomyelitis-like illness

polymerase chain reaction

polyradiculoneuropathy

pons, lesion of

post infectious cerebellar ataxia

posterior column disease

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

primary aldosteronism

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

ptosis, bilateral

pulmonary embolism

pulmonary infection

pulmonary infiltrates

punch-drunk syndrome

pupil, abnormality in neurologic disorders

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reflex, brainstem

Refsum's disease

release phenomena

remote effect of cancer on the nervous system

respiratory failure

respiratory tract infection

reticular activating system

retina, abnormal

retinal degeneration

retinal detachment

retinitis pigmentosa

reversible neurologic disorder

rhomboencephalopathy

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sarcoidosis, CNS

scalp tenderness

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, photosensitive

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

staphylococcal protein A column therapy

startle myoclonus

startle reaction

status epilepticus

stem cell rescue

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subarachnoid hemorrhage

subarachnoid hemorrhage, recurrent

subconjunctival hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, acute

superior cerebellar artery infarction

superior cerebellar peduncle

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

teratoma, ovarian

third nerve palsy

thrombocytopenia

tick-borne encephalitis

tongue, enlarged

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

unconsciousness

upgaze, paralysis of

upward deviation of eyes

urinary retention

Usher's syndrome

varicella zoster virus

varicella zoster virus, encephalitis

vertebral-basilar insufficiency

vertigo, episodic

vertigo, positional

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss, progressive

visual loss, slow

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

Von Hippel Lindau

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

West Nile fever

Western immunoblot test

white matter disease

wide based gait

Wolfram syndrome

Showing articles 450 to 500 of 7718 << Previous Next >>

Management of Cerebellar Infarction With Mass Effect
The Neurologist 6:172-176, Koh, M. et al, 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

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

The Intensive Care Management of Acute Ischemic Stroke
The Neurologist 5:313-325, Deibert,E.&Diringer,M.N., 1999

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

Clinicopath Conf,Multifocal Inflammatory Leukoencephalopathy Related to Combination Chemo with Fluorouracil/levamisole
NEJM 341:512-519, Case 24-1999, 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

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

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

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

Acute Cerebellitis Caused by Coxiella Burnetii
Ann Neurol 45:124-127, Sawaishi,Y.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,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

Myelopathy Caused by Nitrous Oxide Toxicity
AJNR 19:894-896, 9941998., Pema,P.J.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,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

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Vertigo
Lancet 352:1841-1846, Baloh,R.W., 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Thrombolysis-Related Intracranial Hemorrhage, Analysis of 224 Cases from GUSTO-1 Trial with Clin Correl
Stroke 29:563-569, Gebel,J.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

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

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

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

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

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

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

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Causes and Mechanisms of Cerebellar Infarction in Young Patients
Stroke 28:2400-2404, Barinagarrementeria,F.,et al, 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

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 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

Showing articles 450 to 500 of 7718 << Previous Next >>