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adolescent medicine

adverse drug reaction

akinesia of eyelid function

alexia without agraphia

alien hand syndrome

alpha-fetoprotein

Alzheimer's disease

anticholinergic drugs

anticholinesterase

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

arm swing, reduced

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

ataxic-dystonia syndromes

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bent spine syndrome

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

botulinum toxin

brainstem, dysfunction

brainstem, lesion of

bulbar dysfunction

calcification, intracranial

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, false negative

CAT scan, muscle

caudate nucleus, atrophy

central hypoventilation

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar pontine angle

cerebellar pontine angle tumor

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral palsy, associated problems with

cerebral peduncle

cerebrovascular accident

ceruloplasmin, serum

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

cold intolerance

conjugate gaze, forced

conversion reaction

cortical-basal ganglionic degeneration

cranial nerve palsies

creatine phosphokinase(CPK)elevated

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, presenile

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

diurnal variation

dopa responsive dystonia

down-beat nystagmus

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, painful

dystonia, post traumatic

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

emotional lability

encephalitis, autoimmune

episodic disorders

episodic neurologic deficits

esophageal varices

ethics in neurology

executive dysfunction

exercise-induced neurologic dysfunction

exome sequencing

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial expression abnormality

fine motor function, impaired

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

gangliosidosis GM1

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

health insurance

hemianopia, homonymous

hemifacial spasm

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

heralding manifestation

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hypoalbuminemia

hypometric saccades

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunodeficiency

immunosuppression

inclusion bodies, intranuclear

incontinence, fecal

intellectual deficit

intellectual deterioration

intracranial pressure, increased

Jakob-Creutzfeldt disease

jaw jerk, abnormal

Kayser-Fleischer ring

laughing, pathologic

leg spasms, painful

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

life expectancy

lipid storage disorder of CNS

liver function enzymes

lysosomal storage disease

manganese intoxication

memory, defect of recent

memory, impairment of

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

midbrain, atrophy

midbrain, infarction of

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle hypertrophy

muscle spasm, face

muscle weakness

muscular dystrophy

myasthenia gravis

myelopathy, chronic progressive

myoclonic jerks

myopathy, metabolic

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neurocutaneous disease

neuroendocrinology

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuroophthalmology

Niemann-Pick disease

numb clumsy hands syndrome

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

old age, neurology of

ophthalmoplegia

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polycythemia, secondary

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postural abnormality

precipitating factors

pregnancy, neurologic complications in

primary episodic ataxia

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychotic behavior

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

release phenomena

respirations in CNS disease

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rigidity, axial

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

seizure, laughing as manifestation

sensorineural hearing loss

sensory loss, cortical

sequencing difficulty

shoulder, elevation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

stem cell transplantation

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

substantia nigra

swallow evaluation

symmetric brain lesions

tardive dystonia

tetrahydrobiopterin

thalamus, infarction of

thrombocytopenia

tonic foot response

treatment of neurologic disorder

treatment, empirical

tremor, intention

tremor, postural

tricyclic antidepressant

trientine dihydrochloride

trinucleotide repeats

upgaze, paralysis of

urinary incontinence

urinary sulfatidase excretion

vision, blurred

visual evoked response

visual field defect

visual symptoms

visuospatial disturbance

vocal cord paralysis

walking, difficulty with

weakness, progressive

Whipple's disease

white matter disease

whole genome sequencing

wide based gait

Showing articles 600 to 650 of 1219 << Previous Next >>

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Globus Pallidus Deep Brain Stimulation for Generalized Dystonia:Clinical and PET Investigation
Neurol 53:871-874, Kumar,R.,et al, 1999

Catalepsy After Stroke
Neurol 53:1132-1135, Saposnik,G.,et al, 1999

Acute Dystonia Induced by Drug Treatment
BMJ 319:623-626, vanHarten,P.N.,et al, 1999

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

Optimality Score for the Neurologic Examination of the Infant at 12 and 18 Months of Age
J Pediatr 135:153-161,140, Haataja,L.,et al, 1999

A Man with Progressive Weakness in His Legs
Lancet 354:830, van der Meulen,M.F.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

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

A Case-Controlled MRI/MRA Study of Neurovascular Contact in Hemifacial Spasm
Neurol 53:2132-2139, Ho,S.L.,et al, 1999

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Hemifacial Spasm:Clinical Findings and Treatment
Muscle & Nerve 21:1740-1747, Wang,A & Jankovic,J, 1998

Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

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

Review of 23 Patients Affected by the Stiff Man Syndrome:Clinical Subdivision into Stiff Trunk (man) Syndrome,Stiff Limb Syndrome,and Progressive Encephalopmyelitis with Rigidity
JNNP 65:633-640, Barker,R.A.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

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Aggressive Approach in the Treatment of Acute Lead Encephalopathy with an Extraordinarily High Concentration of Lead
Arch Pediatr Adolesc Med 152:1100-1104, Gordon,R.A.,et al, 1998

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

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

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

Acute Vestibular Syndrome
NEJM 339:680-685, Hotson,J.R.&Baloh,R.W., 1998

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

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

Long Term Results of Botulinum Toxin Type A (Dysport) in the Treatment of Hemifacial Spasm:A Report of 175 Cases
JNNP 64:751-757, Jitpimolmard,S.,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

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

An Open-Label Trial of Gabapentin Treatment of Paroxysmal Symptoms in Multiple Sclerosis Patients
Neurol 51:609-611, Solaro,C.,et al, 1998

Tardive Dyskinesia:Diagnosis, Pathogenesis, and Management
The Neurologist 4:180-187, Trugman,J.M., 1998

Long-Term Effect of Botulinum Toxin in Impairment and Functional Health in Cervical Dystonia
Neurol 50:1461-1463, Brans,J.W.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

Relationship Between Balance & Abnormalities in Cerebral MRI in Older Adults
Arch Neurol 55:73-79, Tell,G.S.,et al, 1998

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

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

Pallidotomy for Generalized Dystonia
Movement Disorders 13:693-698, Ondo,W.G.,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

Neurofibromatosis:An Unusual Cause of Cervical Myopathy
J Spine Cord Med 21:148-150, Barber,D.B.,et al, 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

Patterns of Sensory Dysfunction in Lateral Medullary Infarction, Clinical-MRI Correlation
Neurol 49:1557-1563, Kim,J.S.,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

Cocaine-Associated Dystonic Reaction
Am J Emerg Med 15:513-516, Fines,R.E.,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

Showing articles 600 to 650 of 1219 << Previous Next >>