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accomodation, abnormal

acral sensory symptoms

advances in neurology

adverse drug reaction

alien hand syndrome

alveolar hypoventilation

AMPA receptor antibodies

anesthesia, general

Angelman syndrome

antiarrhythmic drugs

anticholinergic drugs

apraxia, constructional

arm swing, reduced

arrhythmia, cardiac

arteritis, temporal

arylsulfatase B

ataxia, truncal

atheromatous branch disease, intracranial

atrophy, muscle

autoimmune basal ganglia encephalitis

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavior, combative

behavioral disorder

behavioral disorder, acute

benign essential tremor

beta adrenergic blocker

blinking, reduced

bone marrow transplantation

botulinum toxin

brainstem, dysfunction

brainstem, hematoma

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

bulbar dysfunction

calcification, intracranial

carcinoma of lung

carcinoma of ovary

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, pelvis

cavernous hemangioma

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral hypoperfusion

cerebral infarction

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

ceruloplasmin, serum

Cheiro-oral syndrome

chest x-ray, abnormal

cholesterol, HDL

choreoathetosis

choreoathetosis, paroxysmal

chorioretinitis

chromosomal abnormality

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coat-hanger pain

Cockayne's syndrome

cogwheel rigidty

collapsin response mediator protein 5 IgG

complicated migraine

confusional state, acute

contractures, joint

convergence, impaired

cornea, opacity of

corneal reflex, abnormal

corneal reflex, absent

cortical hemorrhage

cortical infarction

cortical infarction, small

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

dementia, familial

denervation of muscle

dentate nuclei, lesion of

developmental retardation

dexterity, impaired

differential diagnosis

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

doll's head maneuver

dopa responsive dystonia

dopamine agonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dysostosis multiplex

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, laryngeal

dystonia, treatment of

eating disorder

electrocardiogram, abnormal

electroencephalogram, abnormalities of

emergencies, neurologic

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, viral

encephalomyelitis

endarterectomy, carotid

enterovirus infection of CNS

epidemiology of neurology

episodic neurologic deficits

erectile dysfunction

esophageal varices

extinction on double simultaneous stimulation

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial movement disorder

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

failure to thrive

feeding disorder

fine motor function, impaired

flaccid paralysis

fracture, long bone

fundus, abnormality of

gait, festinating

gamma amino butyric acid receptor antibody

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genital hypoplasia

gests antagoniste

growth hormone deficiency

growth retardation

hand-foot-mouth disease

hemifacial spasm

hemisensory loss

hemisensory syndrome

hemorrhage, thalamic

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

high arched palate

hyperpigmentation of skin

hypoalbuminemia

hypometric saccades

hypopigmentation of skin

hypotension, neurologic causes of

hypotonia, infants

ideomotor apraxia

imbalance, postural

infection, recurrent

intellectual deficit

intellectual deterioration

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, small

intrinsic hand muscles, wasting of

jaw contractures

Kayser-Fleischer ring

kinesia paradoxica

kyphoscoliosis, neurologic causes of

lacunar infarction

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

liver function enzymes

liver transplantation

lysosomal storage disease

marche a petits pas

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, carcinomatous

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

mesial temporal lobe

midbrain, atrophy

midbrain, infarction of

midbrain, lesion of

mixed connective tissue disease

molecular genetics

monoclonal antibodies

mononeuritis multiplex

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, treatment of

mucopolysaccharidoses

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscular dystrophy

muscular dystrophy, cardiovascular changes with

myelitis, transverse, recurrent

myoclonic jerks

myotonia dystrophica

nausea and vomiting

neoplasm, metastatic to CNS

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, sensory

neurexin-3 alpha antibodies

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuronal cell surface antigen

neuronopathy, sensory and motor

neuroophthalmology

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, toxic

NMDA antagonists

non-dominant hemisphere

nystagmus, rotary

one and a half syndrome

operculum syndrome

ophthalmoplegia

optic neuropathy

optic neuropathy, bilateral

oral ulcerations

orthostatic hypotension

paralysis, acute

paralysis, acute areflexic

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, diagnosis

Parkinson disease, drug induced

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

percussion induced muscle contraction

perioral numbness

personality change

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polymerase chain reaction

polymyalgia rheumatica

pons, infarction of

pons, lesion of

pontine hemorrhage

postural abnormality

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary edema

pure sensory stroke

Rabbit syndrome

rapid onset dystonia parkinsonism

Raynaud's phenomenon

remote effect of cancer on the nervous system

respiratory failure

retinal ischemia

ribonucleoprotein antibody

rigidity, axial

saccadic eye movements, abnormal

scoliosis, neurologic association with

sedimentation rate, elevated

sensorineural hearing loss

sensory loss, cortical

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sequencing difficulty

serologic testing

serologic testing, false negative

shoulder, numbness

shoulder, pain in

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

SNCA duplication

spastic dysphonia

speech disorder

speech disorder, non aphasic

spinal cord, compression of

spirochete infection

spontaneous muscle activity

stereotaxic surgery

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

swallow evaluation

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic lupus erythematosus

Tangier's disease

tardive dystonia

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratoma, ovarian

thalamus, infarction of

thalamus, lesion of

thrombocytopenia

tongue, enlarged

tongue, protrusion of

tonic foot response

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

treatment of neurologic disorder

treatment, empirical

tremor, intention

tremor, postural

tremor, resting

tremor, treatment of

trientine dihydrochloride

trigeminal nerve, abnormality of

trigeminal neuropathy, sensory

trinucleotide repeats

unconsciousness

unconsciousness, transient

urine test for metabolic disorders

Venereal Disease Research Laboratory test

vertigo, positional

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual symptoms

visuospatial disturbance

voice, abnormality of

weakness, generalized

white matter disease

white matter disease, subcortical

wide based gait

Showing articles 0 to 50 of 1434 Next >>

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

Clinicopathologic Conference, Ocular Syphilis
NEJM 380:1062-1071, Case 8-2019, 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Cheiro-Oral Syndrome Secondary to Thalamic Infarction
The Neurologist 19:22-25, Satpute, S.,et al, 2013

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Clinical Study of 99 Patients with Pure Sensory Stroke
J Neurol 252:156-162, Arboix, A.,et al, 2005

Pure Sensory Stroke Caused by a Cerebral Hemorrhage: Clinical-Radiologic Correlations in Seven Patients
AJNR 21:515-520, Shintani,S.,et al, 2000

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

Clinical-Radiologic Correlations in Pure Sensory Stroke
Neurol 51:297-302, Shintani,S., 1998

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

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Radiologic-Clinical Correlation:One-and-a-Half Syndrome Associated with Cheirooral Syndrome
AJNR 17:1482-1484, Shintani,S.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Restricted Acral Sensory Syndrome Following Minor Stroke
Stroke 25:2497-2502, Kim,J.S., 1994

Ophthalmoplegia, Hemiparesis and Cheiro-Oral Syndrome in Basilar Artery Migraine
Eur Neurol 33:185-187, Yasuda,Y.,et al, 1993

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Cheiro-Oral Syndrome Due to Lesions in the Corona Radiata
Stroke 23:599-601, Omae,T.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Essential Tremor:Clinical Correlates in 350 Patients
Neurol 41:234-238, Lou,J.&Jankovic,J., 1991

A Genetic Study of Idiopathic Focal Dystonias
Ann Neurol 29:320-324, Waddy,H.M.,et al, 1991

Opercular Cheiro-oral Syndrome
Arch Neurol 48:658-661, Bogousslavsky,J.,et al, 1991

Basilar Branch Pontine Infarction with Prominent Sensory Signs
Stroke 22:1129-1136, Helgason,C.M.&Wilbur,A.C., 1991

Therapeutic Uses Of Botulinum Toxin
NEJM 324:1186-1194, Jankovic,J.&Brin,M.F., 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Ipsilateral Extinction in the Hemineglect Syndrome
Arch Neurol 47:802-804, Feinberg,T.E.,et al, 1990

Cheiro-Oral Syndrome with Bilateral Oral Involvement:A Study of Pontine Lesions by High-Resolution MRI
JNNP 52:792-794, Matsumoto,S.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Cheiro-Oral Syndrome: Does It Have a Specific Localizing Value?
Eur Neurol 28:326-330, Holter,J.T. &Tijssen,C., 1988

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

About the Cheiro-Oral Syndrome
Neurol 37:1564-1565, Valzelli,L., 1987

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Showing articles 0 to 50 of 1434 Next >>