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Differential
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abscess, intracerebral

acetylcholinesterase

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

aminoacidopathies

amyloid beta protein

amyloid imaging

anesthesia, general

angiofibroma, facial

angiomyolipomas

ankle reflex, absent

anterior horn cell disease

antibiotic prophylaxis

anticholinesterase

aortic valve, bicuspid

aortic valve, insufficiency

aortic valve, lesion of

aortic valve, stenosis

aphasia, children

aphasia, progressive

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apolipoprotein E

apraxia, constructional

apraxia, speech

arrhythmia, cardiac

arterial dissection, aorta

arteriovenous malformation

arteriovenous malformation, pulmonary

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

atrial enlargement

atrial fibrillation

attention deficit disorder with hyperactivity

auditory and vestibular pathways

auditory evoked brainstem potentials

autistic behavior

automatic implantable cardioverter-defibrillator

automobile accidents

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

behavioral disorder

Benedict's solution test

bicaudate index

biologic markers

biotinidase deficiency

bladder dysfunction

bone marrow transplantation

brachial plexus

brachial plexus neuropathy

burning paresthesia

calcification, heart

calcification, intracranial

calcification, muscle

calcium oxalate crystals

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

caudate nucleus

caudate nucleus, atrophy

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, subcortical

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral palsy, work up

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cesarean section

Charcot-Marie-Tooth

cherry red spot

chest x-ray, abnormal

cholesterol, HDL

choreoathetosis

chromosomal abnormality

cirrhosis, infancy

cisterna magna, enlarged

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

compression neuropathy

compression neuropathy, recurrent

conduction block

confidentiality

congenital heart disease

congenital myasthenic syndromes

congestive heart failure

contraindications

controversies in neurology

cornea, abnormal

cornea, opacity of

corneal dystrophy

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

cortical blindness

cortical infarction

cost effectiveness

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, subcortical

demyelinating disease

denervation of muscle

dermatoglyphics

descending paralysis

developmental abnormality of brain

developmental evaluation

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

dilated aortic root

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

disability rating scale, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dysplasia of C.N.S.

echocardiogram, contrast

echocardiogram, transesophageal

echocardiogram, transthoracic

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electron microscopy

embolism, paradoxical

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

endocarditis, acute bacterial

endocarditis, infectious

endocarditis, prophylaxis

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

epistaxis, recurrent

ethics in neurology

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

Fabry's disease

face, elongated

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

feeding disorder

ferric chloride test

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

fistula, arterio-venous, pulmonary

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

F-wave response

gangliosidosis GM2

gastrointestinal bleeding

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

granular osmiphilic material

headache, recurrent

hearing problems in children

heel-knee-shin test

hemianopia, homonymous

hemianopia, transient

hemiparesis, transient

hepatic failure

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

hexosaminidase-A

high arched feet

hormone replacement

H-reflex testing

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hyperinsulinism

hypertrophic cardiomyopathy

hypopigmentation of skin

hypotonia, causes of

hypotonia, infants

ileus, paralytic

inborn errors of metabolism

inclusion bodies

infantile hemiplegia

infantile spasm

inflexibility, mental

informed consent

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intrauterine infection

intrinsic hand muscles, wasting of

joint hypermobility

karyotyping, cerebrospinal fluid

klippel feil syndrome

Kluver-Bucy syndrome

lactic acidemia

lacunar infarction

language disorder in adults

language disorders in children

L-dopa, drug interactions with and side effects of

learning disability

learning disability, in children

leg weakness, bilateral

leucine-rich repeat kinase 2 gene

leukocyte enzyme abnormality

leukoencephalopathy

lid closure, weakness of

lipid storage disorder of CNS

locus ceruleus, lesion of

lymphangiomyomatosis

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular, cerebral

malignant hyperpyrexia

manic-depressive

maple syrup urine disease

McLeod syndrome

median neuropathy

memory, impairment of

meningioma, familial

meningioma, multiple

meningitis, carcinomatous

mental retardation

mental retardation, familial

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

microangiopathy, brain

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

midline defect in children

migratory lesion pattern

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

molecular genetics

mononeuropathy multiplex

mononeuropathy, children

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya, adult

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, focal

muscle atrophy, progressive

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myelin protein zero gene

myelomeningocele

myeloneuropathy

myopathy, quadriceps

myotonia dystrophica

nasal bridge, wide

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-familial occurrence

nephrocalcinosis

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

neural tube defect

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular junction

neuronal migration disorder

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

newborn, evaluation of

next-generation sequencing

night blindness

nigrostriatal pathway

Noonan Syndrome

numbness, extremity

occipital lobe, infarction

ophthalmoplegia

orthostatic hypotension

ovarian insufficiency

oxalosis, primary

pacemaker, cardiac-transvenous

pain, increased response

palatopharyngeal incompetence

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paresthesias, feet

paresthesias, lower extremity

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, familial

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

patient information and support

pectus carinatum

pectus excavatum

personality change

phenylketonuria

photosensitivity, skin

Pittsburgh Compound B

platelet inhibiting drugs

polyglucosan body

polyglucosan body disease

polymerase chain reaction

positional head-hanging test

posterior cerebral artery territory infarction

posterior cortical atrophy

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis, childhood

psychosocial aspects

ptosis, bilateral

puberty, delayed

pulmonary disease

pupil, dilated and fixed, bilateral

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

ragged-red fibers

reading disorder, acquired

release phenomena

respiratory failure

retinal hamartoma

reversible neurologic disorder

rhabdomyosarcoma of heart

risk-benefit assessment

saccadic eye movements, abnormal

Sandhoff's disease

scoliosis, neurologic association with

seizure, advice to parents and teachers regarding

seizure, familial

seizure, psychosocial aspects of

seizure, treatment of

self-mutilation

sensorineural hearing loss

sensory loss, truncal

sensory nerve action potentials

serologic testing

shoulder, numbness

shoulder-girdle wasting

simultanagnosia

single photon emission computed tomography

skin, lesions in neurologic disorders

slit lamp examination

small vessel disease

somatosensory evoked potentials

Southern immunoblot test

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenium of corpus callosum

spongy degeneration of brain

spontaneous muscle activity

spontaneous remission

stereotyped behavior

stimulant drugs

stimulation, deep brain

stress, emotional

strokelike episodes

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

suprascapular neuropathy

sweating, abnormality of

systemic illness

tandem gait, ataxic

Tangier's disease

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

thrombocytopenia

tomaculous neuropathy

tongue, fasciculations of

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, thalamic stimulation for suppression of

trinucleotide repeats

tuberous sclerosis

tuberous sclerosis, screening for

ulnar neuropathy

ultrasonography

ultrasonography, nerve

urinary incontinence

urine test for metabolic disorders

very long chain fatty acids

vibratory sensation, abnormal

visual field defect

visual impairment

visuospatial disturbance

vitamin E deficiency

voice, abnormality of

Von Hippel Lindau

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

whistle, inability to

white matter disease

whole genome sequencing

wide based gait

winging of scapula

Wolff-Parkinson-White syndrome

word-finding difficulty

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Showing articles 1050 to 1100 of 2135 << Previous Next >>

Normal-Pressure Hydrocephalus:Evaluation with Cerebrospinal Fluid Flow Measurements at MR Imaging
Radiology 198:523-529, Bradley,W.G.,et al, 1996

Assessment of Brain SPECT:Report of the Therapeutics and Technology Assessment Subcommittee of the AAN
Neurol 46:278-285, , 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Multifocal Motor Neuropathy with Conduction Block and Campylobacter Jejuni
Neurol 46:562-563, White,J.R.,et al, 1996

Recurrent Right Hemiplegia Associated with Progressive Ipsilateral Carotid Artery Stenosis
Stroke 27:753-755, Chollet,F.,et al, 1996

Atherosclerotic Disease of the Aortic Arch as a Risk Factor for Recurrent Ischemic Stroke
NEJM 334:1216-1221, Amarenco,P.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Mitral Valve Strands in Patients with Focal Cerebral Ischemia
Stroke 27:1183-1186, Tice,F.D.,et al, 1996

Evidence for Genetic Basis of Multiple Sclerosis
Lancet 347:1728-1730, Sadovnick,A.D.,et al, 1996

Presynaptic Dopaminergic Deficits in Lesch-Nyhan Disease
NEJM 334:1568-1572, 16021996., Ernst,M.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Neuroimaging in Chronic Fatigue Syndrome
JNNP 60:471-473, Cope,H.&David,A.S., 1996

Transesophageal Echocardiography in Patients with Focal Cerebral Ischemia of Unknown Cause
Stroke 27:691-694, Rauh,G.,et al, 1996

Routine Transesophageal Echocardiograhy for Cerebral Ischemia
Arch Int Med 156:1719-1723, Warner,M.F.&Kingson,I.M., 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Chronic Inflammatory Demyelinating Polyradiculoneuropathy:Unusual Clinical Features and Therapeutic Responses
Neurol 46:1206-1212, Midroni,G.&Dyck,P.J., 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Cerebellar Induced Aphasia: Case Report of Cerebellar Induced Prefrontal Aphasic Language Phenomena Supported by SPECT Findings
J Neurol Sciences 144:34-43, Mari�n,P.,et al, 1996

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Non-Progressive Familial Idiopathic Intracranial Calcification:A Family Report
JNNP 59:432-434, Callender,J.S., 1995

Cardiac Myxomas
NEJM 333:1610-1617, Reynen,K., 1995

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Decreased SPECT[123I]B-CIT Striatal Uptake Correlates with Symptom Severity in Parkinson's Disease
Ann Neurol 38:589-598, Seibyl,J.P.,et al, 1995

Effect of Intensive Diabetes Treatment on Nerve Conduction
Diabetes Control and Complication Trial (DCCT) Reserach Group, Ann Neurol 38:869-88095., , 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Transcranial Doppler Ultrason & TEE in Invest Pulm AVM in Pts with Hereditary Hemorrhagic Telangiectasis with Stroke
Stroke 26:1941-1944, Yeung,M.,et al, 1995

Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Selection of Patients for Transesophageal Echocardiography after Stroke and Systemic Embolic Events:Role of TTE
Stroke 26:1820-1824, Leung,D.Y.,et al, 1995

Comparison of Ictal SPECT and Interictal PET in the Presurgical Evaluation of Temporal Lobe Epielspy
Ann Neurol 37:738-745, Ho,S.S.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Clinical Significance of Fetal Choroid Plexus Cysts
Lancet 346:724-729, Gupta,J.K.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

Showing articles 1050 to 1100 of 2135 << Previous Next >>