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abdominal distention

abdominal protrusion

abducens nerve paralysis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adolescent medicine

adverse drug reaction

airway obstruction

alpha-fetoprotein

alpha-synuclein

Alzheimer's disease

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

angiography, cerebral

anti Tr antibodies

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antiphospholipid antibodies

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

Argyll Robertson pupil

arteritic anterior ischemic optic neuropathy

arteritis, temporal

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

autoimmune cerebellar ataxia

autoimmune disease

autonomic cardiovascular reflexes

autonomic dysfunction

autonomic dysfunction, acute

autonomic dysfunction, evaluation of

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

B 12 deficiency

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Behcet's syndrome

benign essential tremor

biologic markers

bladder dysfunction

blinking, reduced

bradykinesia, facial

BRAF protooncogene

brainstem, atrophy

brainstem, lesion of

calcification, intracranial

carcinoembryonic antigen

cardiac surgery, neurologic complications with

carotid artery occlusion, intracranial

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, venography

cauda equina, lesion of

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

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 lesion

cerebellar vermis

cerebellum, disease of

cerebral arteries

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, young adult

choreoathetosis

chromosomal abnormality

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cogwheel rigidty

cold hands sign

collateral circulation

contractures, joint

controversies in neurology

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cotton-wool spots

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniectomy, decompressive

creatine phosphokinase(CPK)elevated

critical care unit

cryopyrin-associated periodic syndrome

deep gray nuclei

degenerative diseases of CNS

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, thalamic

dementia, treatment of

demyelinating disease

dermatitis herpetiformis

developmental retardation

diabetes insipidus

diabetes mellitus

differential diagnosis

difficulty climbing stairs

distal muscle weakness

dopamine receptor

dopamine receptor, D2

down-beat nystagmus

dural sinus thrombosis

dysdiadochokinesia

edema, periorbital

electroencephalogram, abnormalities of

emergencies, ocular

emotional lability

encephalitis, autoimmune

encephalitis, focal

encephalomalacia

endovascular therapy

epidemiology of neurology

episodic disorders

Erdheim-Chester disease

erectile dysfunction

erythema migrans

evidence-based research

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial weakness

Factor V Leiden

fatal familial insomnia

fever, recurrent

fibrinolytic agents

fibrinolytic agents, intra-venous local infusion

fine motor function, impaired

fingers, abnormal

fluorescein angiography

foot drop, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal bossing

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic linkage

genetic neurologic disorders

genetic testing

genital ulcerations

giant cell arteritis

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

gluten sensitivity

gluten-free diet

growth retardation

Guillain Barre syndrome, differential diagnosis of

hallucination, visual

head circumference

headache, intermittent

headache, severe

heralding manifestation

Horner's syndrome

Horner's syndrome, childhood

hot cross bun sign

Huntington's chorea

hypertrophic intracranial pachymeningitis

hypotension, systemic

iatrogenic neurologic disorders

IgG4-related disease

imbalance, postural

immunodeficiency

immunologic disease

immunosuppression

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

incontinence, fecal

infraorbital nerve

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal medication

Jakob-Creutzfeldt disease

keratoconjunctivitis

lacrimal gland enlargement

leg weakness, bilateral

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

life expectancy

limbic encephalitis

long bone lesion

lymphoma involving CNS

lymphoma, primary of CNS

malignant papulosis

marche a petits pas

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, aseptic

meningitis, chronic

mental retardation

mental status, abnormal

methylmalonic aciduria

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal gammopathy

mononeuritis multiplex

morning glory sign

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya, adult

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, mass effect on

MRI, spinal cord

MRI, venography

multiple organ failure

multiple sclerosis

multiple system atrophy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenic syndrome

myelopathy, necrotizing

myoclonic jerks

myoclonus, stimulus sensitive

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

nausea and vomiting

neurocutaneous disease

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuromyelitis optica (Devic's disease)

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, amyloid

neuropathy, peripheral

non-arteritic antererior ischemic optic neuropathy

nutritional deficiency

ocular motility, disorders of

old age, neurology of

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, total

optic atrophy, bilateral

optic disc edema

optic disc ischemia

optic nerve, blood supply of

optic nerve, infarction of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

optic neuropathy, ischemic, posterior

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral ulcerations

orbit, inflammation in

orbit, lesions of

orbit, pseudotumor of

orbit, tomograms of

orthostatic hypotension

orthostatic hypotension, idiopathic

Paget's disease

pain, abdominal

paraparesis, spastic

parasympathetic nervous system

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, rapid progression

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, critically ill

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prethrombotic state

prevention of neurologic disorders

progressive neurologic disorder

progressive supranuclear palsy

protein C deficiency

protein S deficiency

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

puberty, delayed

pupil, abnormality in neurologic disorders

pure autonomic failure

purple glove syndrome

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

radiation hypersensitivity

ragged-red fibers

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

respirations in CNS disease

respiratory failure

respiratory tract infection

retina, abnormal

retinal hemorrhages

retinal ischemia

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retroperitoneal mass

reversible neurologic disorder

rigidity, axial

Riley-Day syndrome

sclerosis, bone

sedimentation rate, elevated

sensorineural hearing loss

sensory loss, leg

serologic testing

sexual behavior, disorder of

sexual dysfunction in neurologic disease

Shy-Drager syndrome

single photon emission computed tomography

skin, lesions in neurologic disorders

skull bone, thickening

spinal cord, injury of

spinal cord, injury, sexual dysfunction in

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spirochete infection

stem cell transplantation

steroid therapy, CNS treatment and complications with

striatonigral degeneration

subdural effusion

subdural hygroma

superior sagittal sinus thrombosis

sympathetic nervous system

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

systemic lupus erythematosus, neuro-opthal.complications with

tandem gait, ataxic

thalamus, lesion of

third nerve palsy

tissue plasminogen activator, intravenous

Tolosa Hunt syndrome

treatment of neurologic disorder

tremor, cerebellar

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

trochlear nerve palsy

upgaze, paralysis of

urinary incontinence

vascular endothelial growth factor

vestibular areflexia

vibratory sensation, abnormal

visual acuity, decreased, monocular

visual field defect

visual field defect, altitudinal

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

vitamin deficiency

walking, difficulty with

walking, difficulty with in dark

Wallerian degeneration

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Whipple's disease

white matter disease

wide based gait

word-finding difficulty

Showing articles 50 to 100 of 2483 << Previous Next >>

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Survival of Patients with Pathologically Proven Multiple System Atrophy:A Meta-Analysis
Neurol 48:384-393, Ben-Shlomo,Y.,et al, 1997

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

Distinction of Idiopathic Parkinson's Dis from Multi-Syst Atrophy by Stim of Growth-Hormone Release w Clonidine
Lancet 349:1877-1881, Kimber,J.R.,et al, 1997

Consensus Statement on the Definition of Orthostatic Hypotension, Pure Autonomic Failure, and Multiple System Atrophy
Neurol 46:1470, Schatz,I.J.,et al, 1996

Long-term Prognosis in Cerebral Venous Thrombosis:Follow-up of 77 Patients
Stroke 27:243-246, Preter,M.,et al, 1996

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

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

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

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
Arch Neurol 52:179-185, Perani,D.,et al, 1995

Different of Multi Syst Atrophy from Idiopathic Parkinson's Disease Using Proton MR Spectroscopy
Ann Neurol 37:204-210, Davie,C.A.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

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

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
Brain 115:1875-1888, Chen,R.,et al, 1992

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

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

Abnormal Respiration and Sudden Death During Sleep in Multiple System Atrophy with Autonomic Failure
Neurol 40:677-679, Munschauer,F.E.,et al, 1990

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Critical Illness Polyneuropathy:A Complication of Sepsis and Multiple Organ Failure
Brain 110:819-842, Zochodne,D.W.,et al, 1987

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Bladder Dysfunction in Progressive Autonomic Failure
BMJ 293:223-224, Kirby,R.S.&Bannister,R., 1986

Tobacco Intolerance in Multiple System Atrophy
Neurol 36:986-988, Johnsen,J.A.,et al, 1986

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Encephalitis with Myoclonus in Whipple's Disease
JNNP 32:338, Stoupel,N.,et al, 1969

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Bobble-Head Doll Syndrome in a Child
Neurol 104: e213694, Chityala,A.,et al, 2025

Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
Neurol 104: e213682, Hayakawa,I.,et al, 2025

Neuroimaging Spectrum of Erdheim-Chester Disease:An Image-Based Review
AJNR 46:1300-1308, Rai,P.,et al, 2025

A 27-Year-Old Man with Progressive Bilateral Vision Loss Resistant to Steroid Therapy
Neurol 105: e213897, Zhang,W.,et al, 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

Risdiplam in Presymptomatic Spinal Muscular Atrophy
NEJM 393:671-682, Finkel,R.S.,et al, 2025

Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
Neurol 105:e214124, Gerrao,C.,et al, 2025

A Woman with Subacute Progression of Distal Upper Extremity Weakness
Neurol 105:e214212, Zhao,A.J.,et al, 2025

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

A 66-Year-Old Female Patient with Rapidly Progressive Memory Changes
Neurol 105:e214211, Fokas,J.A.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Automated Detection of Normal Pressure Hydrocephalus Using CT Imaging for Calculating the Ventricle-to-Subarachnoid Volume Ratio
AJNR 46:141-146, Knittel,J.J.,et al, 2025

Automated Idiopathic Normal Pressure Hydrocephalus Diagnosis via Artificial Intelligence-Based 3D T1 MRI Volumetric Analysis
AJNR 46:33-40, Lee,J.,et al, 2025

Showing articles 50 to 100 of 2483 << Previous Next >>