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abdominal cramps

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

acute disseminated encephalomyelitis

adenylate kinase 5 autoantibodies

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agranulocytosis

Alexanders disease

alpha glucosidase

alpha-fetoprotein

altered states of consciousness

alternating rapid movement

alveolar hypoventilation

Alzheimer's disease

amnesia, anterograde

amnestic syndrome

AMPA receptor antibodies

amphiphysin antibodies

amyotrophic lateral sclerosis, differential diagnosis

anesthesia, general

anesthesia, local

angina pectoris

angiotensin-converting enzyme

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti Hu antibody

anti La antibody

anti MAG antibodies

anti Ri antibody

anti Ro antibody

anti signal recognition particle antibody

anti Tr antibodies

anti Yo antibody

antiamphiphysin

antibodies to voltage-gated calcium channels

anticoagulant, treatment

antiendomysial antibodies

antiganglioside antibodies

antineurofascin antibodies

antiphospholipid antibodies

antiphospholipid antibody syndrome

antiretinal antibodies

anti-sulfatide antibodies

antithyroid antibodies

antiviral agents

aphasia, progressive, primary

apnea, primary central

apraxia of eye movements

area postrema syndrome

arm swing, reduced

arrhythmia, cardiac

arteritis, temporal

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

attention deficit disorder with hyperactivity

autoimmune autonomic ganglionopathy

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

autoimmune GFAP astrocytopathy

automatic behavior

automobile accidents

autonomic dysfunction

autonomic neuropathy

axonal degeneration

axonal spheroid

B 12 deficiency

ballismus, bilateral

Barkhof MR criteria for MS

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

Bickerstaff's brainstem encephalitis

bilateral periventricular nodular heterotopia

biologic markers

bladder dysfunction

blindness, sudden

bone marrow biopsy

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brain natriuretic peptide

brain transplantation

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

bulbar dysfunction

bulbar palsy, childhood

bulbar palsy, progressive

burning feet, differential diagnosis of

burning paresthesia

campylobacter infection

Canavan's disease

cancer, unknown origin

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of pancreas

carcinoma of testis

carcinoma of unknown origin

carcinoma of uterus

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cauda equina, enhancement

celiac disease, adult

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral cortical encephaliis

cerebral edema, vasogenic

cerebral folate deficiency syndrome

cerebral infarction

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal bands, absent

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, mimics

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

cesarean section

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chloride channel dysfunction

chorea, autoimmune

choreoathetosis

chromosomal abnormality

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

cogwheel rigidty

cold hands sign

collapsin response mediator protein 5 IgG

color vision, impaired

coma, medically induced

concentration, impaired

confusional state, acute

congenital malformation

congestive heart failure

conjunctival biopsy

conjunctival injection

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

conversion reaction

Coombs test, positive

cornea, opacity of

corneal dystrophy

corneal reflex, abnormal

corneal ulceration

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical ribbon sign

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyclophosphamide

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, autoimmune

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, treatment of

demyelinating disease

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability, neurological

disease modifying agents

distal muscle atrophy

distal muscle weakness

dopamine agonist

dopaminergic neurons

down-beat nystagmus

DPPX, antibodies

DPPX, antibodies, encephalitis

dropped head syndrome

drug induced neurologic disorders

dura, thickened

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dysostosis multiplex

dysthyroid ocularmyopathy

dystonia, focal

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram, decremental response

electromyogram, fasciculation potentials

electromyogram, incremental response

electron microscopy

electronystagmography

electroretinograph

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, episodic

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, recurrent

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy, Hashimoto's

endocarditis, marantic

enzyme treatment

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

esophageal manometry

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exercise-related muscle strength increase

exome sequencing

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

Fabry's disease

face, numbness of

facial appearance, abnormal

facial weakness, bilateral

faciobrachial dystonic seizure

failure to thrive

Farber's disease

feeding disorder

fine motor function, impaired

fingerprint bodies

Fisher's syndrome

Fisher's syndrome, atypical

flaccid paralysis

flu-like illness

folic acid deficiency

fourth ventricle, floor

Fragile-X associated tremor/ataxia-syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

fundus, abnormality of

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gangliosidosis GM1

gangliosidosis GM2

gastroenteritis

gastrointestinal disease, neurologic complications

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glare, light-induced

gliadin antibodies

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

glycine receptor antibodies

glycogen storage disease

GM1 ganglioside antibodies

granular osmiphilic material

granulomatosis with polyangiitis

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, olfactory

hallucination, visual

head circumference

head injury, mild

headache, episodic

health insurance

hearing loss, bilateral

heat intolerance

heavy metal intoxication

heel-knee-shin test

hemimyoclonic jerks

hemorrhagic diathesis

heparin, low-molecular-weight

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

hexosaminidase-A

hexosaminidase-A and B

high arched feet

hippocampal atrophy

hippocampus, hyperintense

HMGcoA reductase inhibitors

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

hot cross bun sign

H-reflex testing

H-sign, spinal cord

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

hypergammaglobulinemia

hyperthyroidism

hypomelanosis of Ito

hypomyelination

hyponatremia with cerebral disorders

hypopigmentation of skin

hypotension, systemic

hypothalamus, damage to

hypothalamus, lesion of

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

IgG4-related disease

imbalance, postural

immunodeficiency

immunofluorescence

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infantile neuronal degeneration

infection, recurrent

initiative, lack of

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intrauterine infection

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw claudication

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Krabbe's disease

kyphoscoliosis, neurologic causes of

labor, complicated

lactic acidemia

language disorder in adults

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa, drug interactions with and side effects of

leg spasms, painful

leg weakness, bilateral

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness

level of consciousness, decreased

libido, decreased

life expectancy

limbic encephalitis

limbic-predominant age-related TDP-43 encephalopathy

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

locus ceruleus, lesion of

loss of sympathy

lupus anticoagulant

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphocyte fingerprint profiles

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnesium sulfate

malformation, CNS, congenital

malignancy screen

malignancy, occult

marche a petits pas

Marcus Gunn pupil

masseter muscle wasting

McDonald criteria for MS

medial longitudinal fasciculus(MLF)

mediastinum, mass of

medulla oblongata

medulla oblongata, lesion of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningoencephalitis

meningoencephalomyelitis

mental retardation

mental status, abnormal

mesial temporal lobe

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

mGlu R5 antibodies

microangiopathy, brain

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mild cognitive impairment

Mini Mental Status Examination

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

Montreal cognitive assessment

Morvan's fibrillary chorea

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, contrast enhanced, cloud-like

MRI, cortical enhancement

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, hypointense signal foci on

MRI, lumbosacral plexus

MRI, optic nerve

MRI, paramagnetic effect

MRI, ring sign, open

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

multiple organ failure

multiple sclerosis

multiple sclerosis, diagnostic criteria

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle stiffness

muscle strength, testing

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, late-onset

myasthenia gravis, neonatal

myasthenia gravis, paraneoplastic

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenic crisis

myasthenic syndrome

myelination of nervous system

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, recurrent

myeloneuropathy

myelopathy, chronic progressive

myocardial infarction

myoclonic jerks

myoclonus, epilepsy

myoclonus, segmental

myopathy, drug-induced

myopathy, mitochondrial

myopathy, necrotizing, autoimmune

nasal bridge, wide

nausea and vomiting

nephrotic syndrome

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

nerve root hypertrophy

neuraminidase deficiency

neurexin-3 alpha antibodies

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neuroinfectious diseases

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, multiple

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuromyelitis optica (Devic's disease), screening

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, asymmetric

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

NMDA antagonists

node of Ranvier

nodopathy, autoimmune

noncommunicative

nucleus basalis of Meynert

numbness, ascending

numbness, extremity

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

obsessive-compulsive disorder

obstetric complications

ocular motility, disorders of

oculocephalic reflex

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

optic chiasm, lesion of

optic disc edema

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, decompression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis, alternating

optic neuritis, bilateral

optic neuritis, recurrent

optic neuropathy

optic neuropathy, ischemic

optical coherence tomography

orthostatic hypotension

overlap syndrome

pachymeningitis, cranial

pain, abdominal

pain, neuropathic

palatal myoclonus

palmomental response

paralysis, acute

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraproteinemia

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, pathogenesis of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal neurologic deficits

paroxysmal neurologic disorder

PAS positive material in the brain

pathologic reflex

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric neurology

penguin silhouette sign

periaqueductal lesion

perineuritis, optic

perioral numbness

peripheral blood smear

peripheral nerve, lesion of

perivascular enhancement

peroxisomal disease

personality change

photosensitivity, eye

pigmentary retinopathy

platelet inhibiting drugs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polyneuropathy, carcinomatous

polyradiculoneuropathy

Pompe's disease of glycogen storage

pontocerebellar atrophy

positional head-hanging test

posterior leukoencephalopathy syndrome

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proptosis, unilateral

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis, acute

psychosis, childhood

psychotic behavior

ptosis, bilateral

pulmonary infection

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

pupil, light reflex of

pupil, light reflex, abnormal

pupil, light reflex, reversed

pure autonomic failure

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

ragged-red fibers

rapidly progressing neurologic illness

Raynaud's phenomenon

refractive errors

Refsum's disease

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal vein thrombosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

retinal arteriole attenuation

retinal degeneration

retinitis pigmentosa

reversal of sleep wake cycle

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rhomboencephalopathy

rigidity, axial

rippling muscle disease

saccadic eye movements, abnormal

salivation, excessive

Sandhoff's disease

scalp tenderness

Schmidt syndrome

scoliosis, neurologic association with

scotoma, central

scotoma, paracentral-homonymous

sea-blue histiocytes

sedimentation rate, elevated

segmental demyelination

seizure, adult onset

seizure, children

seizure, drug resistance

seizure, familial

seizure, intractable

seizure, intractable, treatment of

seizure, laughing as manifestation

seizure, psychomotor-temporal lobe

seizure, treatment of

seizure, unknown origin

semantic dementia

sensorineural hearing loss

sensory loss, asymmetric

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serum alanine aminotransferase

serum tumor markers

sex reassignment surgery

sick sinus syndrome

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal cord degeneration

spinal cord, cervical

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenium of corpus callosum

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

staphylococcal protein A column therapy

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

survival motor neuron gene

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

TDP-43 proteinopathy

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratoma, ovarian

testicular germinoma

testicular teratoma

thalamus, lesion of

thalamus, lesion of-bilateral

third ventricle, wall

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thyroglobulin antibodies

thyroid function tests

thyroid peroxidase antibodies

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

treatment, empirical

tremor, cerebellar

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

trichopoliodystrophy

trinucleotide repeats

tuberous sclerosis

tumefactive lesion

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

upright-tilt test

urinary incontinence

urinary retention

urinary sulfatidase excretion

urine test for metabolic disorders

Usher's syndrome

varicella zoster virus

ventricular enlargement

vestibular function, tests of

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

visual symptoms

visuospatial disturbance

voice, abnormality of

vomiting, intractable

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

water channel antibodies

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

whole body imaging

whole genome sequencing

wide based gait

Wolfram syndrome

word-finding difficulty

Showing articles 3500 to 3550 of 4785 << Previous Next >>

Relationship of Hearing Impairment to Dementia and Cognitive Dysfunction in Older Adults
JAMA 261:1916-1919, Uhlmann,R.F.,et al, 1989

Vestibular Testing in Comatose Patients
Arch Neurol 46:561-563, Buettner,U.W.&Zee,D.S., 1989

Prevention of Falls Among the Elderly
NEJM 320:1055-1059, Tinetti,M.E.&Speechley,M., 1989

Frequency, Etiology, and Prevention of Stroke in Patients with Systemic Lupus Erythematosus
Stroke 20:583-591, Futrell,N.&Millikan,C., 1989

Hypergeusia as the Presenting Symptom of a Posterior Fossa Lesion
JNNP 52:804-805, Noda,S.,et al, 1989

The Effect of Radiation of Carotid Arteries, A Review Article
Arch Neurol 46:449-455, Murros,K.E.&Toole,J.F., 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Neurobrucellosis:Clinical Characteristics, Diagnosis, and Outcome
Neurol 39:498-501, AlDeeb,S.M.,et al, 1989

Delayed Neurologic Display in Murine Typhus, Report of Two Cases
Arch Int Med 149:949-951, Samra,Y.,et al, 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Infectious and Toxic Syndromes from Fish and Shellfish Consumption, A Review
Arch Int Med 149:1735-1740, Estaugh,J.&Shepherd,S., 1989

Nerve Conduction Study of Human Tetrodotoxication
Neurol 39:743-745, Oda,K.,et al, 1989

Cranial Nerve Deficit:A Clue to the Diagnosis of Ethylene Glycol Poisoning
Am J Med 87:91-92, Palmer,B.F.,et al, 1989

Hyperosmolar Coma:Cellular Dehydration and the Serum Sodium Concentration
Ann Int Med 110:855-857, Daugirdas,J.T.,et al, 1989

Lymphocytic Hypophysitis, Report of 3 New Cases and Review of the Literature
Medicine 66:240-256, Cosman,F.,et al, 1989

Cerebellopontine Angle Epidermoid Cysts:A Report on 30 Cases
JNNP 52:986-990, deSouza,C.E.,et al, 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989

Bilateral Loss of Vision in Bright Light
Stroke 20:554-558, Weibers,D.O.,et al, 1989

The Ethical Use of Human Fetal Tissue in Medicine
NEJM 320:1093-1096, Greely,H.T.,et al, 1989

The Politics of Transplantation of Human Fetal Tissue
NEJM 320:1079-1082, Annas,G.J.&Elias,S., 1989

Intracranial Injury after Moderate Head Trauma in Children
J Pediatr 115:346-350, Rosenthal,B.W.&Bergman,I., 1989

Traumatic Monocular Blindness and Associated Carotid Injuries
Pediatrics 84:128-134, King,M.A.,et al, 1989

Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
NEJM 320:1735-1740, Schindler,D.,et al, 1989

Neurologic Complications in Long-Standing Nephropathic Cystinosis
Arch Neurol 46:543-548, Fink,J.K.,et al, 1989

Subdural Hematoma after Normal CT
Neurol 39:985-987, Deitch,D.&Kirshner,H.S., 1989

Cortical Blindness Due to Osmotic Disruption of the Blood-Brain Barrier by Angiographic Contrast Material:CT and MRI Studies
Neurol 39:567-571, Lantos,G., 1989

Neuroleptic Malignant Syndrome, Review of Response to Therapy
Arch Int Med 149:1927-1931, Rosenberg,M.R.&Green,M., 1989

Tilting Towards a Diagnosis in Recurrent Unexplained Syncope
Lancet 1:658-660, Fitzpatrick,A.&Sutton,R., 1989

Multiple Forms of Epileptic Attacks Secondary to a Small Chronic Subdural Haematoma
BMJ 299:439-441, Jones,S.C.,et al, 1989

Intrachiasmal Hemorrhage:A Cause of Delayed Post-Traumatic Blindness
Neurol 39:863-865, Crowe,N.W.,et al, 1989

Duration of Impaired Consciousness in Relation to Side of Lesion After Severe Head Injury
Lancet 1:1001-1003, Levin,H.S.,et al, 1989

Clinical Indicators of Intracranial Lesion on Computed Tomographic Scan in Children with Parietal Skull Fracture
Am J Dis Child 143:194-196, Bonadio,W.A.,et al, 1989

Sudden Sensorineural Hearing Loss as a Presentation of HIV infection
J Laryngol Otol 103:1071-1072, Timon, C.I. & Walsh, M.A., 1989

Pentobarbital Therapy Does Not Improve Neurologic Outcome in Nearly Drowned, Flaccid-Comatose Children
Pediatrics 81:630-634, Nussbaum,E.&Maggi,J.C., 1988

Hysterical Conversion Reactions Mimicking Neurological Disease
Am J Dis Child 142:1203-1206, Bangash,I.H.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Peripheral Neuropathy in Essential Mixed Cryoglobulinemia
Arch Neurol 45:1210-1214, Carcia-Bragado,F.,et al, 1988

Sensory Form of Acute Polyneuritis
Neurol 38:1728-1731, Dawson,D.M.,et al, 1988

Diffuse Lewy Body Disease and Progressive Dementia
Neurol 38:1520-1528, Burkhardt,C.R.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Sensitivity and Specificity of Rinne Tuning Fork Test
BMJ 297:1381-1382, Browning,C.C.&Swan,I.R.C., 1988

Pituitary Apoplexy
BMJ 297:1526-1527, Lewin,I.G.,et al, 1988

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