Neudle.com: startle disease

Differential
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abdominal contractions

abdominal distention

abdominal reflex, absent

abdominal x-ray

abortion, spontaneous

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome-related complex

acrocyanosis

acute disseminated encephalomyelitis

acute respiratory distress syndrome

Addison's disease

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

Aicardi-Goutieres syndrome

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating hemiplegia

alternating rapid movement

alternating rapid movement, impaired

aluminum

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, heterogeneity of

Alzheimer's disease, prognosis of

Alzheimer's disease, treatment of

amenorrhea

ammonia

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid plaques

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

anemia, hemolytic

anemia, megaloblastic

anesthesia, general

anesthesia, spinal

aneurysm, intracranial

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anterior horn cell disease

anterior tibial muscle weakness

anti basal ganglia antibodies

anti GQ1b IgG antibody

antibiotics, neurologic complications with

antibodies to measles

anticholinergic drugs

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, untoward effects of

antidepressant

antioxidant

antiphospholipid antibodies

antithyroid antibodies

apraxia of eye movements

apraxia, constructional

apraxia, speech

aqueduct of Sylvius, stenosis

Arnold Chiari malformation

aspartate aminotransferase

ataxia, truncal, associated with ocular oscillations

ataxic gait

atherosclerosis, premature

athetosis

atlanto-axial subluxation

atrioventricular block

attention deficit disorder with hyperactivity

atypical

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic nervous system

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder, acute

Behcet's syndrome

benign essential tremor

benzodiazepine

beta adrenergic blocker

Bickerstaff's brainstem encephalitis

blood gases, arterial

blood transfusion

bone marrow biopsy

bone marrow transplantation

bone pain

boomerang sign

Borrelia miyamotoi infection

bovine spongiform encephalopathy

brain biopsy, false negative

brainstem, dysfunction

brainstem, infarction of

bulbar palsy, acute-causes of

bulbar palsy, progressive

burn injury

burning feet

burning feet, differential diagnosis of

burst suppression pattern, electroencephalogram

busulfan

cachexia

CAG repeats

calcification, intracranial

calcium antagonist

calcium antagonist, side effects of

camptocormia

campylobacter infection

cancer, unknown origin

cane

carbamazepine

carbamazepine, toxicity

carbidopa

carbon monoxide poisoning

carcinoma of pancreas

carcinoma of prostate

carcinoma of unknown origin

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

carotid angiogram

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, spine

cataracts

catatonia

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of, bilateral

ceftazidime

celiac disease, adult

central nervous system, infection of

central nervous system, infection, cancer patient

central pontine myelinolysis

cephaloridine

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellum

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gamma amino butyric acid

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, hydroxyindoleacetic acid, 5(5-HIAA)

cerebrospinal fluid, intraventricular

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical myelopathy

cervical spine

cervical spine abnormality

cervical spondylosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chilbran skin lesions

choreoathetosis, paroxysmal

chorioretinitis

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

cigarette smoking

cisternogram, radionuclide

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clomipramine

clonazepam

clonus

cobalamin C deficiency

collapsin response mediator protein 5 IgG

confusional state, acute

congenital deformities

congenital malformation

congenital malformation, non CNS

congestive heart failure

conjugate gaze, forced

consanguinity

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conversion reaction

copper deficiency

copper metabolism, abnormal

coronavirus

corpus callosum, atrophy of

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cough

COVID-19

coxsackievirus

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

C-reactive protein, elevated

Creutzfeldt-Jakob disease, genetic

critical care unit

crossed adductor reflex

cytomegalic inclusion disease

cytomegalovirus infection

deafness

deep gray nuclei

deep tendon reflexes

degenerative cervical myelopathy

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, thalamic

dementia, transmissible

dementia, treatment of

demyelinating disease

dental prostheses

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

denture cream

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis

dialysis dementia

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

dilantin, toxicity

diplopia

disability, neurological

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

dopa responsive dystonia

downward deviation of eyes

downward gaze, paralysis of

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

Dravet syndrome

driving

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

drug interactions

drug overdose

drug overdose, management of

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

dystonia, children

dystonia, delayed onset

dystonia, face

dystonia, focal

dystonia, psychogenic

dystonia, treatment of

dystonic reaction, acute

echolalia

eclampsia

eclampsia, postpartum

eczema

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

electromyogram

electroretinograph

ELISA

embolism, paradoxical

emergencies, neurologic

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, parainfectious

encephalopathy, post anoxic

encephalopathy, progressive

encephalopathy, septic

enterovirus infection of CNS

entrapment neuropathy

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

epsilon sarcoglycan gene

extralimbic encephalitis

extrapyramidal

extrapyramidal movement disorder, progressive

eye movement, disorders of

eye movement, painful

eye, pain in

facial appearance, abnormal

facial movement disorder

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

feeding disorder

fever

fibrillations

fine motor function, impaired

finger nose finger test

frontal lobe, anatomy and physiology

frontal lobe, pathologic signs of

fucosidosis

fundus, abnormality of

fungal infection, CNS

gadolinium

gag reflex, depressed

gait disorder

gait, apraxic

gait, spastic

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gamma hydroxybutyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gastrointestinal disease, neurologic complications

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

GluD2

glutamic acid decarboxylase, antibody

glycine receptor antibodies

glycoprotein

GM1 ganglioside antibodies

gout

gram positive rod

granular osmiphilic material

granuloma, pulmonary

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

gyrus, abnormal

hairline, abnormal

Hallervorden Spatz disease

hallucination

hallucination, auditory

hallucination, olfactory

hallucination, visual

hammertoes

hand weakness

handedness

hand-foot-mouth disease

head retraction reflex

headache

headache, cough

headache, sudden onset of

headache, throbbing

headache, vascular

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

heel-knee-shin test

helminthic infection of CNS

hemianopia

hemianopia, homonymous

hemiparesis, transient

hemiplegia

hemolytic-uremic syndrome

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, cervical

herpes simplex encephalitis

highly active antiretroviral therapy

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocysteine, serum

homocystinuria

hospice

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, normal pressure

hydroxyindole acetic acid 5(5HIAA)

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperammonemic encephalopathy

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypersomnia

hypertension

hypertensive encephalopathy

hyperthermia

hyperthyroidism

hypertonia

hypertonia, congential

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immune reconstitution inflammatory syndrome

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inability to stand on tiptoes

inappropriate behavior

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

incoordination

industrial neurologic disorders

infection

infection, recurrent

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deterioration

interferon alpha

internuclear ophthalmoplegia

interobserver agreement

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaw jerk, abnormal

Jewish

jumping Frenchman of Maine

juvenile distal and segmental muscular atrophy

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

kuru plaques

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Lafora body

Lafora's disease

laminar necrosis, cortical

laminectomy

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

lateropulsion

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

Leber's hereditary optic neuropathy

left handedness

leg numbness

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leprosy

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

level of consciousness, differential diagnosis in

levitation

Lewy body

Lewy body disease, diffuse

Lhermitte's sign

life expectancy

life support, withdrawal of

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lithium

liver biopsy

liver disease

liver function enzymes

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

Maghreb

malabsorption

malabsorption syndrome

malaise

malformation, CNS, congenital

malignancy screen

manganese intoxication

mediastinum, lymph-node biopsy

mediastinum, mass of

medical-legal aspects of neurology

medulla oblongata, lesion of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal gliomatosis

meningismus

meningitis

meningitis, aseptic

meningitis, CSF cell count-normal

meningitis, eosinophilic

meningitis, fungal

meningitis, neutrophilic

meningitis, syphilitic

meningitis, TB

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

mental status, abnormal, acute

methylmalonic acid, serum

methylmalonic acidemia

metoclopramide

metrizamide

metronidazole

microangiopathic hemolytic anemia

microangiopathy, brain

microcephaly

micrographia

microinfarcts

middle cerebellar peduncle, lesion

migraine

mild cognitive impairment

Mills syndrome

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

monoamine oxidase inhibitors

monoclonal antibodies

motor neuron disease, misdiagnosis

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, psychogenic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, contrast enhanced, subependymal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, false negative

MRI, FLAIR

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, negative

MRI, nodular enhancement

MRI, pelvis

MRI, punctate pattern

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

mycobacterium kansasii

myelination of nervous system

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelitis, transverse

myelitis, transverse, recurrent

myelogram

myelogram, complications of

myelogram, metrizamide

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myoclonus, differential diagnosis of

myoclonus, epilepsy

myoclonus, essential

myoclonus, face

myoclonus, multifocal

myoclonus, orthostatic

myoclonus, post anoxic

myoclonus, psychogenic

myoclonus, segmental

myoclonus, sleep

myoclonus, stimulus sensitive

myoclonus, treatment of

myoglobinuria

myopathy

myopathy, distal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, thyroid disease causing

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal abstinence syndrome

neoplasm, intracranial

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neuraminidase deficiency

neurexin-3 alpha antibodies

neuritis, causes of

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neuroblastoma

neuroendocrinology

neurogenic bladder

neurologic complications

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic examination

neurologic examination, video

neurologic history

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuron specific enolase

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathology, peripheral nerves

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neuroprotective agents

newborn, evaluation of

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

occupational neurologic disorders

ocular bobbing

ocular flutter

ocular motility, disorders of

ocular myoclonus

oculocephalic reflex

oculogyric crisis

oculomasticatory myorhythmia

odontoid process

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, total

opiate

opisthotonus

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

optical coherence tomography

oral ulcerations

organ transplantation

ornithine transcarbamylase deficiency

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

paramedian pontine reticular formation

paraneoplastic brainstem encephalitis

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, postencephalitic

Parkinson disease, psychogenic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

paroxysmal nonkinesigenic dyskinesia

PAS positive

PAS positive material in the brain

pathologic reflex

pathology

patient information and support

perivascular enhancement

pernicious anemia

perseveration

persistent vegetative state

phenothiazine, dyskinesia associated with

phenylketonuria

phonophobia

pigmentary retinopathy

piracetam

Pisa syndrome

pituitary stalk

pituitary stalk, lesion of

pituitary, hormones of

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

pleurisy

pneumoencephalogram(PEG)

pneumonia

POLR3B

polycythemia, secondary

polyglucosan body disease

polymerase chain reaction

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyneuropathy, uremic

polypharmacy

polyradiculoneuropathy

pons, lesion of

pontine hemorrhage

pontocerebellar atrophy

position sensation

positive sharp waves

post transplant lymphoproliferative disease

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

postinfectious

postpartum

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary lateral sclerosis

primitive neuroectodermal tumors

prion disease

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

propafenone

propranolol

proprioception

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, dilated, episodic

pupil, light reflex, abnormal

Purkinje cell

Purkinje cell surface antibody

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

rabies, nervous system involvement with

raccoon

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

rash

rash, hand

reading disorder, acquired

real-time quaking-induced conversion

recurrent

reflex, brainstem

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

remternetug

renal failure

renal stones

renal transplantation

respirator

respiratory depression

respiratory dyskinesias

respiratory failure

respiratory myoclonus

respiratory tract infection

restless leg syndrome

reticular formation

reticulum cell sarcoma

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rubeola, encephalitis

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, classification of

seizure, diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, EEG normal during

seizure, EEG pattern in

seizure, noise induced

seizure, paradoxical

seizure, photosensitive

seizure, precipitating factors

seizure, prognosis in adults

seizure, stimulus sensitive

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, withdrawal

selective serotonin reuptake inhibitors

senile plaques

sensorineural hearing loss

sensory loss

sensory loss, cortical

septicemia

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

serotonin

serotonin agonist

serotonin syndrome

serum alanine aminotransferase

serum gamma glutamyl transferase

severe acute respiratory syndrome

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

sodium valproate

somatosensory evoked potentials

speech disorder, childhood

speech, loss of

speech, unintelligible

sphingolipodoses

spinal cord

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinal stenosis

spinal stenosis, familial

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 16

spinocerebellar ataxia type 7

spirochete infection

splenium of corpus callosum

splenomegaly

spondylosis

spongy degeneration of brain

spontaneous remission

squirrels

standing difficulty

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, myoclonic

status epilepticus, nonconvulsive

steatorrhea

stem cell rescue

stem cell transplantation

steppage gait

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

stimulant drugs

storage disease of CNS

strabismus

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuporous

stuttering

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

subacute sclerosing panencephalitis, adult onset

subarachnoid hemorrhage

superior cerebellar peduncle

sweating

symmetric brain lesions

syncope

synucleinopathy

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syringomyelia

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

thrombotic microangiopathy

thymoma

thyroid stimulating immunoglobulins

tone, muscle, increased

tongue, atrophy

tongue, biting

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic cerebellar fits

tonic foot response

tonic spasms

tonsillar herniation of cerebellum

topiramate

torticollis

toxic encephalopathy

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

trauma

trazodone

treatment of neurologic disorder

triangle of Guillain and Mollaret

trichopoliodystrophy

tricyclic antidepressant

trigeminal nerve

trigeminal nerve, abnormality of

trigeminal neuralgia

trinucleotide repeats

unconsciousness, episodic

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uremic encephalopathy

urine test in toxic screen

venous thrombosis, non-cerebral

ventriculitis

verapamil

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo

vertigo, episodic

vibratory sensation, abnormal

vision, blurred, monocular

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight gain

weight loss

welder

Wernicke's encephalopathy

white matter disease, periventricular

white matter disease, subcortical

word-finding difficulty

x-ray, cervical spine

x-ray, spine

zinc

Showing articles 200 to 250 of 384 << Previous Next >>

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Serotonin Syndrome
Neurol 45:219-223, Bodner,R.A.,et al, 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

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

Myoclonus Associated with Propafenone
BMJ 308:113, Chua,T.P.,et al, 1994

Prognostic Value of Myoclonus Status in Comatose Survivors or Cardiac Arrest
Ann Neurol 35:239-243, Wijdicks,E.F.M.,et al, 1994

Ceftazidime-Related Nonconvulsive Status Epilepticus
Arch Int Med 154:586-589, Klion,A.D.,et al, 1994

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Anti-Ri Antibodies Associated with Opsoclonus and Progressive Encephalomyelitis with Rigidity
Neurol 44:1521-1522, Casado,J.L.,et al, 1994

Cortical Myoclonus in Huntington's Disease
Movement Disorders 9:633-641, Thompson,P.D.,et al, 1994

Encephalopathy from Abuse of Bismuth Subsalicylate (Popto-Bismol)
Neurol 43:1265, Jungreis,A.C.&Schaumburg,H.H., 1993

Ifosfamide-Induced Nonconvulsive Status Epilepticus
Arch Neurol 50:1104-1105, Wengs,W.J.,et al, 1993

Myoclonus Associated with Hyperthyroidism and Thymoma:A Case Report
Chin Med J 51:138-140, Liao,K-K.,et al, 1993

Novel Brainstem Syndrome Associated with Prostate Carcinoma
Neurol 43:2591-2596, Baloh,R.W.,et al, 1993

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Fatal Rabies Associated with Extensive Demyelination
Arch Neurol 50:317-323, Nelson,D.A.&Berry,R.G., 1993

Antineuronal (anti-Ri) Antibodies in a Pt with Steroid-Responsive Opsoclonus-Myoclonus
Neurol 43:207-211, Dropcho,E.J.,et al, 1993

Psychogenic Myoclonus
Neurol 43:349-352, Monday,K.&Jankovic,J., 1993

Klippel-Feil Syndrome:CT and MR of Acquired & Congen Abnormal of Cervical Spine & Cord
J Comput Assist Tomogr 17:215-244, Ulmer,J.L.,et al, 1993

Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Movement Disorders in Astrocytomas of the Basal Ganglia and the Thalamus
JNNP 55:1162-1167, Krauss,J.K.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Nicotine-Sensitive Paresis
Neurol 42:382-388, Yokota,T.,et al, 1992

Idiopathic Hemiparetic Parkinsonism, A Syndrome Distinct from Idiopathic Parkinsonism
Lancet 339:149-150, DeKeyser,J.,et al, 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Low Cerebrospinal Fluid Concentration of Free Gamma-Aminobutyric Acid in Startle Disease
Lancet 340:80-81, Dubowitz,L.M.S.,et al, 1992

Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
Ann Neurol 31:663-668, Ryan,S.G.,et al, 1992

The Role of Hypotension in Septic Encephalopathy Following Surgical Procedures
& Stevens, M. , Arch Neurol 49:653-656., Wijdicks,E.F.M., 1992

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
Brain 115:1875-1888, Chen,R.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Truncal Asterixis Associated with Ceftazidine, A Third-Generation Cephalosporin
Neurol 41:2008, Hillsley,R.E.&Massey,E.W., 1991

Cumulative Risks of Developing Extrapyramidal Signs, Psychosis, or Myoclonus in the Course of Alzheimer's Disease
Arch Neurol 48:1141-1143, Chen,J.,et al, 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

Myoclonus in Adult Huntington's Disease
Ann Neurol 29:213-215, Vogel,C.M.,et al, 1991

Multistate Outbreak of Poisonings Associated with Illicit Use of Gamma Hydroxy Butyrate
JAMA 265:447-448, , 1991

Showing articles 200 to 250 of 384 << Previous Next >>