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acetylcholine receptor antibody

Addison's disease

adrenergic blocker

advances in neurology

adverse drug reaction

airway obstruction

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alpha adrenergic blocker

alternating rapid movement

Alzheimer's disease

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anemia, hemolytic

aneurysm, intracranial

ankle reflex, absent

ankle, swelling of

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

aorta, atherosclerosis

Arnold Chiari malformation

arylsulfatase A

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic-dystonia syndromes

athetosis, causes of

auditory evoked brainstem potentials

auditory evoked potentials

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavioral disorder

Behcet's syndrome

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

biologic markers

blinking, reduced

blood dyscrasias, neurologic findings with

bone marrow suppression

botulinum toxin

botulinum toxin, complications of

brain transplantation

brainstem, lesion of

Brueghel's syndrome

calcification, intracranial

calcium antagonist

carbon monoxide poisoning

carbonic anhydrase inhibitor

carcinoma of pancreas

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral infarction, hemorrhagic

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

ceruloplasmin, serum

Charcot-Marie-Tooth

chelation therapy

cherry red spot

cherry red spot-myoclonus syndrome

chorea, causes of

choreoathetosis

chromosomal abnormality

cingulate island sign

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

coat-hanger pain

cogwheel rigidty

complicated migraine

copper metabolism, abnormal

cornea, abnormal

coronary artery bypass

corpus callosum, lesion of

corpus callosum, thinning

Cushing's syndrome

cyst, parenchymal

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetic coma, diagnosis and treatment

differential diagnosis

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

dopamine receptor, D2

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, laryngeal

dystonia, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

electroencephalogram, abnormalities of

electrolyte imbalance

electron microscopy

electronystagmography

emotional lability

encephalitis, Japanese

encephalitis, viral

epidemiology of neurology

erectile dysfunction

esophageal varices

evoked potentials

exome sequencing

eye movement, disorders of

Fabry's disease

facial expression abnormality

failed medical management

failure to thrive

familial hemiplegic migraine

fine motor function, impaired

finger nose finger test

fingerprint bodies

fracture, long bone

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, lesion of

frontal lobe, pathologic signs of

gait, festinating

gamma knife therapy

gaze fixation, distractable

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

granular osmiphilic material

Hallervorden Spatz disease

heavy metal intoxication

heel-knee-shin test

hemochromatosis

hemochromatosis, primary

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), late onset

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

Huntington's chorea

hyperadrenalism

hyperbilirubinemia

hyperparathyroidism

hyperthyroidism

hypoalbuminemia

hypometric saccades

hypomyelination

hypoparathyroidism

hypotension, neurologic causes of

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

jaw contractures

Kayser-Fleischer ring

kinesia paradoxica

kyphoscoliosis, neurologic causes of

lactic acidemia

laminectomy, lumbar

L-dopa, drug interactions with and side effects of

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body disease, diffuse

lipid storage disorder of CNS

liver function enzymes

liver transplantation

locus ceruleus, lesion of

lymphoma involving CNS

lysosomal storage disease

marche a petits pas

Marinesco-Sjogren syndrome

memory, impairment of

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mitochondrial disease

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, face of giant panda sign on

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

myasthenia gravis

myoclonic jerks

myoclonus, epilepsy

myoclonus, essential

nausea and vomiting

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neuroaxonal leukodystrophy

neuroendocrinology

neurofibromatosis 1

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neuropathy, sensory

neuropsychiatry

nigrostriatal pathway

nutritional deficiency

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

old age, neurology of

organ transplantation

orthostatic hypotension

osmotic demyelination syndrome

pain, abdominal

palatal myoclonus

paraparesis, spastic

parenteral alimentation

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

Pelizaeus Merzbacher

pernicious anemia

personality change

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

poison, neurologic problems with

pons, lesion of

positional head-hanging test

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

progressive neurologic disorder

progressive supranuclear palsy

prothrombin time, prolonged

pseudobulbar palsy

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, cause of

psychosocial aspects

pulmonary function tests

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quality of life

radiation therapy, stereotactic

reading disorder, acquired

reflex sympathetic dystrophy

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

respirations in CNS disease

respiratory failure

retinal degeneration

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

risus sardonicus

Rosenthal fibers

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

seizure, children

seizure, differential diagnosis of

seizure, psychomotor-temporal lobe

serum alanine aminotransferase

shoulder, pain in

single photon emission computed tomography

skin, darkening of

sleep pathology and physiology

slit lamp examination

Smell Identification Test

SNCA duplication

somatosensory evoked potentials

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 12

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

status epilepticus

stereotaxic surgery

stimulation, deep brain

stimulation, thalamic

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

tardive dyskinesia

tardive dystonia

teeth, abnormal

teeth, number of in infants

tetrathiomolybdate

thalamic tumors

thalamic tumors, bilateral

thalamotuberal artery

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombus, mural

thymus and neuromuscular function

tongue, fasciculations of

tongue, protrusion of

tonic foot response

torticollis, post traumatic

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, orthostatic

tremor, physiologic

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

tremor, writing

trientine dihydrochloride

trinucleotide repeats

ultrasonography

ultrasonography, head

ultrasonography, high-intensity focused

urine test for metabolic disorders

ventricular enlargement

vertigo, migraine causing

vibratory sensation, abnormal

viral infection

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

voice, abnormality of

Von Hippel Lindau

walking, difficulty with

Wernicke's encephalopathy

white matter disease

wide based gait

X-linked bulbospinal neuronopathy

Showing articles 200 to 250 of 2480 << Previous Next >>

Late Onset of Wilson's Disease
Arch Neurol 38:729-730, Czlonkowska,A.,et al, 1981

Computed Tomography in Wilson Disease
Neurol 31:107-110, Harik,S.I.,et al, 1981

Benign Familial Tremor Treated with Primidone
BMJ 282:178-180, O'Brien,M.D.,et al, 1981

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Metoprolol in Essential Tremor
Arch Neurol 37:596-597, Newman,R.R.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
Ann Neurol 8:329-332, Zifkin,B.,et al, 1980

Computed Tomography in Wilson Disease:Report of 2 Cases
Ann Neurol 5:102-103, Ropper,A.H.,et al, 1979

Computerized Cranial Tomography in Wilson Disease
Neurol 29:866-868, Nelson,R.F.,et al, 1979

Metopropol For Essential Tremor
NEJM 301:331, Britt,C.W.Jr.,et al, 1979

Treatment Of Essential Tremor With Metopropol
NEJM 301:1005, Ljung,O., 1979

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

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

Cholelithiasis and Wilson Disease
J Pediatr 2:210-213, Rosenfield,N.,et al, 1978

The Ophthalmologic Manifestations of Wilson's Disease
Mayo Clinic Proc 42:409-416, Wiebers,D.O.,et al, 1977

Familial Essential Myoclonus
Brain 93:131-138, Korten,J.J.,et al, 1977

Penicillamine-associated Myasthenia Gravis, Antiacetylcholine Receptor & Antistriational Antibodies
Am J Med 63:689, Masters,C.L.,et al, 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Central Pontine Myelinolysis
Quart J Med 45:373, Tomlinson,B.E.,et al, 1976

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

Pregnancy in Penicillamine Treated PNts with Wilson's Disease
NEJM 293:1300, Scheinberg,I.H.,et al, 1975

Non-Beta Blocking Action of Propranolol
NEJM 293:988, Koch-Weser,J., 1975

Efficacy of Chronic Propranolol Therapy in Action Tremors of the Familial, Senile or Essential Varieties
NEJM 290:984, Winkler,G.,et al, 1974

Neurologic Changes in Liver Disease
Brain Dysfunction in Metabolic Disorders, ed. by F. Plum, Res. Publ. Assn. Nerv. Ment. Dis. , Vol. 5, , New York:RaVictor, M., 1974

Treatment of Essential Tremor with Propranolol
Lancet 205, Jan1973., , 1973

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

Differential Diagnosis of Tremors
Med Clin North Am 56:1363, Fahn,S., 1972

Benign Essential Tremor
Lancet 471, 1972 Sept., , 1972

Diseases of the Extrapyramidal System
Disease-a-month-Jan 1970., Klawans,H.,et al, 1970

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Treatment of Hepatolenticular Degeneration (Wilson's Disease)
Am J Gastro 52:121, After 1966., Spellberg,M., 1966

Metabolic Defects Associated with Mental Retardation
Am J Dis Child 104:401, Garell,D., 1962

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

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

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,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

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

Showing articles 200 to 250 of 2480 << Previous Next >>