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accomodation, abnormal

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

adverse drug reaction

alien hand syndrome

Alzheimer's disease

amyotrophic lateral sclerosis

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

anticholinergic drugs

antiviral agents

aphasia, classification of

aphasia, progressive, primary

ataxia, cerebellar

ataxia, frontal

ataxia, hereditary

ataxia, progressive

autoimmune disease

bacterial infection

bacterial infection, CNS

basal ganglia, degeneration

behavior modification

behavioral disorder

Bell's phenomenon

blinking, reduced

brainstem, lesion of

calcium antagonist

carbon monoxide poisoning

CAT scan, abnormal

CAT scan, angiography

cerebellar atrophy, primary

cerebellar degeneration

cerebellum, disease of

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, young adult

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

concentration, impaired

contractures, joint

convergence, impaired

conversion reaction

corpus callosum

corpus callosum, lesion of

cortical-basal ganglionic degeneration

Coxiella burnetti

crying, pathologic

cryopyrin-associated periodic syndrome

cystatin C mutation

degenerative diseases of CNS

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

developmental retardation

diagnostic criteria

differential diagnosis

digital subtraction angiography

disability, neurological

disconnection syndrome

dopamine agonist

drug induced neurologic disorders

dysdiadochokinesia

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

encephalitis, brainstem

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy, delayed

episodic disorders

Erdheim-Chester disease

eye movement, disorders of

fever, recurrent

finger nose finger test

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait, festinating

gaze palsy, vertical

genetic neurologic disorders

genetic testing

hallucination, visual

head circumference

headache, awakened by

headache, awakening with

headache, bifrontal

headache, occipital

headache, recurrent

headache, severe

highly active antiretroviral therapy

hip flexor weakness

human immunodeficiency virus type 1

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hypertrophic intracranial pachymeningitis

hypometric saccades

hypomyelination

imbalance, postural

immune reconstitution inflammatory syndrome

immunosuppression

immunosuppressive agents

incontinence, fecal

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw jerk, abnormal

kinesia paradoxica

lacunar infarction

laughing, pathologic

leg weakness, bilateral

Legionnaires'disease

marche a petits pas

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, neurologic aspects and complications of

mental status, abnormal

middle cerebellar peduncle, lesion

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI, angiography

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal intensity of basal ganglia

MRI, nodular enhancement

multimodal neuroimaging

multiple system atrophy

nausea and vomiting

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuropathy, demyelinating

next-generation sequencing

nystagmus, gaze-evoked

nystagmus, upbeating on upgaze

ocular motility, disorders of

old age, neurology of

opportunistic infection, CNS

optic atrophy, bilateral

paraparesis, spastic

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

PAS positive material in the brain

pathologic reflex

patient information and support

Pelizaeus Merzbacher

perivascular enhancement

Persistent postural-perceptual dizziness

personality change

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymerase chain reaction, false negative

pons, lesion of

posterior leukoencephalopathy syndrome

precipitating factors

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pupil, light reflex, abnormal

reflex, cutaneous

release phenomena

respiratory tract infection

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rickettsial organism

selective serotonin reuptake inhibitors

sensorineural hearing loss

serologic testing

serotonin norepinephrine reuptake inhibitors

shunt procedure, ventricular

shunt procedure, ventricular-complications of

single photon emission computed tomography

skin, lesions in neurologic disorders

skull bone, thickening

slow virus infection of CNS

speech disorder

splenium of corpus callosum

spongy degeneration of brain

startle myoclonus

startle reaction

steroid therapy, CNS treatment and complications with

stooped posture

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

temporal lobe, atrophy

thrombocytopenia

tongue, fasciculations of

transient neurologic deficit

treatment of neurologic disorder

tremor, resting

upgaze, paralysis of

urinary incontinence

vasospasm, cerebral

ventriculostomy

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual impairment

voice, abnormality of

walking, difficulty with

weakness, generalized

white matter disease

wide based gait

Showing articles 650 to 700 of 1434 << Previous Next >>

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

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

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,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

Ataxic Hemiparesis,Critical Appraisal of a Lacunar Syndrome
Stroke 29:2549-2555, Gorman,M. J.,et al, 1998

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

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

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

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

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

Evaluation of Five Primitive Reflexes in 240 Young Adults
Neurol 51:322, Brown,D.L.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Neuropsychological Consequences of Posteroventral Pallidotomy for the Treatment of Parkinson's Disease
Neurol 51:207-215, Trepanier,L.L.,et al, 1998

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

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

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

Stereotactic pallidotomy for Trtm of Parkinson's Disease, Efficacy & Adverse Effects at 6 Mo in 26 Pts
Neurol 50:434-438, Shannon,K.M.,et al, 1998

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

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

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,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

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

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

Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
Arch Neurol 55:33-37, Murata,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

A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
JNNP 64:306-313, Talbot,P.R.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,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

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

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

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

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

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,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

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

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

Showing articles 650 to 700 of 1434 << Previous Next >>