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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

aceruloplasminemia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

addiction, heroin

adult polyglucosan body disease

adverse drug reaction

alcohol intolerance

altered states of consciousness

alternating rapid movement

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

anemia, megaloblastic

ankle reflex, absent

antecedent illness

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

antiviral agents

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

azidodeoxythymidine

B 12 deficiency

Babinski sign in new born

bacterial infection

bacterial infection, CNS

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior modification

behavioral disorder

Bell's phenomenon

Bickerstaff's brainstem encephalitis

bladder dysfunction

brain biopsy, false negative

brainstem, atrophy

brainstem, infarction of

brainstem, lesion of

Brudzinski's sign

bulbar palsy, progressive

burning paresthesia

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

central nervous system, infection of

cerebellar atrophy, primary

cerebellar lesion

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrovascular accident

ceruloplasmin, serum

Chaddock's sign

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

choreoathetosis

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

comprehension, impaired

compression fracture

concentration, impaired

congenital bilateral perisylvian syndrome

congenital malformation

convergence, impaired

conversion reaction

copper deficiency

corneomandibular reflex

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy

C-reactive protein, elevated

critical care unit

crying, pathologic

cystatin C mutation

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

delay in diagnosis

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, focal

dystonia, treatment of

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

emergencies, neurologic

emergencies, neurosurgical

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis, brainstem

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

Erdheim-Chester disease

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

face, numbness of

facial weakness

facial weakness, bilateral

feeding disorder

ferritin, elevated

fine motor function, impaired

finger nose finger test

fingers, abnormal

Fisher's syndrome

flaccid paralysis

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

giant axonal neuropathy

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

glycogen storage disease

granular osmiphilic material

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

headache, positional

headache, recurrent

headache, severe

heel-knee-shin test

hematoma, epidural-spinal

hemiplegia, progressive

hexosaminidase-A

high arched feet

hip flexor weakness

history of neurology

Hoffmann's sign

homocysteine, serum

human immunodeficiency virus type 1

hypereosinophilic syndrome(HES)

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypomyelination

hypotension, systemic

hypothalamus, disturbance of

imbalance, postural

immunosuppression

inborn errors of metabolism

inclusion bodies

incontinence, fecal

initiative, lack of

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

interobserver agreement

intrinsic hand muscles, wasting of

iron, serum, low

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw jerk, abnormal

Krabbe's disease

lactic acidemia

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

laughing, pathologic

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lipid storage disorder of CNS

locked-in syndrome

loss of sympathy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

manganese intoxication

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, bacterial

meningitis, neutrophilic

meningitis, pneumococcal

mental retardation

mental retardation, familial

mental status, abnormal

methylmalonic acid, serum

methylmalonic acidemia

midbrain, lesion of

middle cerebellar peduncle, lesion

molecular genetics

Montreal cognitive assessment

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle weakness

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, post infectious

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy, chronic progressive

myelopathy, vacuolar

myeloradiculopathy

myoclonus, epilepsy

nausea and vomiting

neoplasm, primary of CNS

nerve conduction studies

nerve root hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, sensory

neuropsychiatry

next-generation sequencing

night blindness

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular motility, disorders of

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, total

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

orthostatic hypotension

osteomyelitis, spinal

pain, interscapular

palmomental response

palpebromandibular synkinesia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraplegia, in flexion

paraplegia, progressive

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, hemiparesis in

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive material in the brain

pathologic reflex

patient information and support

pediatric neurology

perivascular enhancement

pernicious anemia

Persistent postural-perceptual dizziness

personality change

pharyngeal sensation

photic sneeze reflex

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polyneuropathy, familial

pons, infarction of

pons, lesion of

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

postictal neurologic deficits

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, light reflex, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

reflex, cutaneous

release phenomena

repetition, impaired

respiratory failure

respiratory tract infection

retinal degeneration

retinal exudates

retinitis pigmentosa

reversible neurologic disorder

saccadic eye movements, abnormal

saddle anesthesia

sarcoidosis, CNS

sea-blue histiocytes

seizure, children

seizure, familial

seizure, hysterical

selective serotonin reuptake inhibitors

sensory loss, cutaneous

serologic testing

serotonin norepinephrine reuptake inhibitors

severe acute respiratory syndrome

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

spastic paraplegia, type 11

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spongy degeneration of brain

spontaneous remission

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

subarachnoid hemorrhage

substantia nigra

superior sagittal sinus thrombosis

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

tonic foot response

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

unconsciousness

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

vaccination, neurologic complications with

valsalva maneuver

ventricular enlargement

vertigo, episodic

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

walking, delayed

walking, difficulty with

watershed infarcts

weakness, generalized

weakness, progressive

weaning from respirator, failure to

white matter disease

wide based gait

x-linked mental retardation

x-ray, thoracic spine

Showing articles 600 to 650 of 733 << Previous Next >>

Chronic Progressive Myelopathy:Investigation with CSF Electrophoresis, Evoked Potentials, & CT Scan
Ann Neurol 6:419-424, Patty,D.W.,et al, 1979

Drawing-Induced Seizures
Arch Neurol 36:515-516, Brenner,R.P.,et al, 1979

Eating Epilepsy Associated with a Deep Forebrain Glioma
Jr, Neurol 6:271-2731979., Robertson,W.C., 1979

Conversion of Photosensitive to Scotosensitive Epilepsy:Report of a Case
Neurol 29:1550-1554, Panayiotopoulos,C.P., 1979

EEG Activation & Mathematical Calculation
Neurol 29:1499-1503, Wiebers,D.O.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Landry-Guillain-Barre Synd with Abnor Pupils & Normal Eye Movements:A Case Report
Neurol 29:1033, Williams,D.,et al, 1979

Primary Aberrant Oculomotor Regeneration due to Intracranial Aneurysm
Arch Neurol 36:570-571, Cox,T.A.,et al, 1979

Functional Paralysis of Horizontal Gaze
Neurol 29:82-85, Troost,B.T.,et al, 1979

Meige Disease:Striatal Dopaminergic Preponderance
Neurol 29:1126-1130, Tolosa,E.S.,et al, 1979

Quality of Survival after Out-of-hospital Cardiac Arrest:Predictive Value of Early Neurologic Evaluation
Neurol 29:56-60, Earnest,M.P.,et al, 1979

Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
Ann Neurol 5:118-120, Melgaard,B.,et al, 1979

Blepharospasm:Successful Treatment with Clonazepam
Ann Neurol 5:401-402, Merikangas,J.R.,et al, 1979

Interobserver Agreement in Assessment of Ocular Signs in Coma
JNNP 42:1163-1168, van den Berge,J.H.,et al, 1979

Visceral Stimuli Inducing Epilepsy
(letter) , NEJM 298:16678., Jacome,D.E., 1978

Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
Ann Neurol 3:253, Bird,T.D.,et al, 1978

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

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

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

Polyneuropathy in Waldenstrom's Macroglobulinemia
Arch Neurol 35:423, Julien,J.,et al, 1978

Forced Downward Ocular Deviation
Arch Neurol 35:456, Simon,R.P., 1978

Gaze-evoked Blepharoclonus
Ann Neurol 3:243, Keane,J.R., 1978

Neuropathy Following Abuse of Nitrous Oxide
. et al, Neurol 28:504978., Layzer,R.B., 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Epileptic Discharges Triggered by Eye Convergence
Neurol 28:589, Vignaendra,V.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Pineal Tumors
Arch Neurol 35:736-740, Donat,J.F.,et al, 1978

Human Pneumatic Tourniquet Paralysis
Neurol 28:787-793, Bolton,C.F.,et al, 1978

Successful Treatment of Primary Reading Epilepsy with Clonazepam
Ann Neurol 4:155-156, Login,I.S.,et al, 1978

Pseudocaloric Nystagmus
Arch Neurol 35:93, Becker,G.D.,et al, 1978

Hot Water Epilepsy
Can J Neurol Sci 5:247-251, Szymonowicz,W.,et al, 1978

Pseudopalsy of the Abducens Nerve, In Neuro-Ophthalmology Update
(Ed) , 1977, P. 64-72., Smith,J.L., 1977

A Syndrome of Early Recognition of Occult Hydrocephalus & Cerebral Atrophy
Quart J Med 183:365, Botez,M.I.,et al, 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Total Gaze Paresis in Amitriptyline Overdose
Neurol 27:695, Miadinich,E.K.,et al, 1977

Subclinical Eye Movement Disorders in Patients with Multiple Sclerosis
Neurol 27:614, Solingen,L.D.,et al, 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Bone Scanning & Diagnosis of Reflex Sympathetic Dystrophy Secondary to Herniated Lumbar Disks
Neurol 27:791, Carlson,D.H.,et al, 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

Stapedius Reflex Decay in Myastentia Gravis
Arch Neurol 34:496, Warren,W.R.,et al, 1977

Methyl Bromide Intoxication:Neurologic Features, Including Simulation of Reye Syndrome
Neurol 27:959, Shield,L.K.,et al, 1977

Thalamic Hemorrhage:A Computed Yomographic-clinical Correlation
Neurol 27:217, Walshe,T.M.,et al, 1977

Reversible Subacute Peripheral Neuropathy Induced by Phenytoin
Arch Neurol 34:189, Dobkin,B.H., 1977

Less Usual Forms of Epilepsy
BMJ p. 127, 15 January 1977., , 1977

Life or Death of the Brain After Cardiac Arrest
Neurol 27:805, Allen,N., 1977

Clinical Pathological Conference
Multiple Myeloma with Paraneoplastic Motor Neuropathy & Cauda-equina Compression, Case Record 31-197, , NE97:266,1977., 1977

An unusual Cause of Apparent Epilepsy:ECG & EEG Findings in a Case of Jervell Lange-Neilson Syndrome
JNNP 40:1102, Selby,P.J.,et al, 1977

Showing articles 600 to 650 of 733 << Previous Next >>