Neudle.com: postural visual loss

Differential
(Click to cross reference)

abducens nerve paralysis

acetylcholine receptor antibody

acute intermittant porphyria

Adies pupil

adverse drug reaction

agnosia, color

akathisia

alcohol intolerance

alexia without agraphia

alien hand syndrome

alternating rapid movement

amnesic stroke

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

anticoagulant, treatment

aphasia

applause sign

apraxia

apraxia, constructional

aspartate aminotransferase

autoimmune autonomic ganglionopathy

autoimmune disease

automobile accidents

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

autonomic neuropathy, idiopathic

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

calcification, intracranial

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, myelogram with

CAT scan, venography

cataracts

cavernous sinus

cavernous sinus, metastasis to

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar infarction

cerebellar lesion

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, leak

cerebrospinal fluid, pressure

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

cis-platinum

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

Cornelia de Lange syndrome

cortical blindness

cortical blindness, transient

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, rapidly progressive

depression

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disability, neurological

dizziness

downward gaze

drug induced neurologic disorders

EDTA(ehtylenediamine tetraacetic acid)

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electron microscopy

embolization, therapeutic

emergencies, neurologic

encephalopathy, metabolic

epidemiology of neurology

extinction on double simultaneous stimulation

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

fine motor function, impaired

finger nose finger test

fingerprint bodies

fistula, arterio-venous, dural

fludarabine

fluorouracil

foot drop

fourth ventricle, compression

fracture, long bone

fungal infection

fungal infection, CNS

gait disorder

gait, apraxic

gammaglobulin therapy, intravenous

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

genetic neurologic disorders

Guillain Barre syndrome

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hallucination

hallucination, visual

hammertoes

handwriting

headache

headache, awakening with

headache, episodic

headache, positional

headache, progressive

headache, severe

headache, throbbing

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

hemianopia, homonymous

heralding manifestation

Hispanics

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, non-communicating(obstructive)

iatrogenic neurologic disorders

intellectual deterioration

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial hypotension

intracranial pressure, increased

intravenous drug abuse

iritis

iron, brain

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, variant

Kearns-Sayre syndrome

keratitis, interstitial

Klinefelter's syndrome

Korsakoff's psychosis

lactic acidemia

language disorder in adults

L-dopa

lead and the nervous system

lead poisoning

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

level of consciousness, decreased

lipid storage disorder of CNS

liver disease

liver function enzymes

lobar atrophy

lymphadenopathy

lymphoma

lymphoma, primary of CNS

lysosomal storage disease

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, neutrophilic

meningitis, noninfectious

meningoencephalitis

mental status, abnormal

MERRF syndrome

metabolic disorder, primary

metachromatic leukodystrophy

midbrain

midbrain, atrophy

midbrain, infarction of

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuritis multiplex

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, mass effect on

MRI, negative

MRI, nodular enhancement

MRI, optic nerve

MRI, paramagnetic effect

myelin protein zero gene

myelogram

myelopathy

myelopathy, tract-specific

myoclonic jerks

myoclonus

myopathy

myopathy, mitochondrial

nausea and vomiting

neck pain

needle tracks

neoplasm, intracranial with metastasis extracranially

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve conduction studies

neuroendocrinology

neurologic complications of, systemic cancer

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

occipital lobe, lesion of

old age, neurology of

orthostatic hypotension

Parkinson disease, axial symptoms

Parkinson disease, drug induced

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

phonophobia

photophobia

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polymyositis

pons, lesion of

porphyria

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior column disease

postural abnormality

pretectal syndrome

prevention of neurologic disorders

primary intracranial hypotension

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

proptosis

proptosis, unilateral

pruritus

pseudobulbar palsy

psoriatic arthritis

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

ptosis

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex of

pupil, light reflex, abnormal

pupil, light reflex, reversed

pupil, tonic

pure autonomic failure

pure sensory stroke

pursuit eye movements

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

rash

rash, hand

reading disorder, acquired

real-time quaking-induced conversion

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, children

seizure, laughing as manifestation

sensorineural hearing loss

sensory loss

sensory loss, cutaneous

sequencing difficulty

serum alanine aminotransferase

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

speech disorder, childhood

spinal cord

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 7

square wave jerks

stem cell rescue

stem cell transplantation

stent, venous sinus

steroid therapy, CNS treatment and complications with

stooped posture

subdural hygroma

suprasellar lesion

sweating, abnormality of

symmetric brain lesions

syncope

syncope, recurrent

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tau protein

tauopathy

thalamus, infarction of

thalamus, lesion of-bilateral

transient ischemic attack

transient neurologic deficit

transient neurologic deficit, benign syndrome in young adults

transverse sinus stenosis

trauma

travel, foreign

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

vasculitis, cutaneous

ventricular enlargement

vertigo

vertigo, episodic

vibratory sensation, abnormal

viral infection

vision, blurred

vision, cloudy

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields

visual fields, constricted

visual impairment

visual loss

visual loss, postural

visual loss, progressive

visual loss, slow

visual loss, transient

visual obscurations, transient

visual symptoms

visuospatial disturbance

vitamin deficiency

walking frame

walking, difficulty with

weakness

weakness, generalized

weight loss

wheelchair

white matter disease

whole genome sequencing

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Clinical and Immunological Features of Limbic Form of Hashimotos Encephalopathy
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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Paroxysmal Dystonia as a Manifestation of Multiple Sclerosis
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