Neudle.com: trajectory of disease

Differential
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abdominal distention

abdominal protrusion

abducens nerve paralysis

abscess, intracerebral

abscess, spinal cord

abulia

achilles tendon, enlarged

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acute ataxia of childhood

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy, adult onset

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

amenorrhea

ammonia

amphiphysin antibodies

amyloid

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyloid beta protein

amyloid beta-related angiitis

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

aneurysm, cavernous sinus

aneurysm, cavernous sinus-bilateral

aneurysm, intracranial

angiitis

angiitis, isolated of CNS

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

anterior horn cell disease

anti citrullinated antibody

anti GQ1b IgG antibody

antibodies to measles

anticardiolipin antibodies

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, selection of

anticonvulsants, untoward effects of

antiganglioside antibodies

antineutrophil cytoplasmic autoantibodies

antiphospholipid antibody syndrome

antithyroid antibodies

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apraxia, constructional

aqueduct of Sylvius, stenosis

arterialization of conjunctival vessels

arteriopathy

arteriovenous malformation

arteriovenous malformation, pulmonary

ataxia telangiectasia

ataxic-dystonia syndromes

ataxin

ataxin-2

atheromatous branch disease, intracranial

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

automobile accidents

autonomic dysfunction

autonomic neuropathy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

Balint's syndrome

basal cell carcinoma

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder, acute

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

Borrelia miyamotoi infection

brain biopsy, false negative

brain biopsy, stereotaxic

brain purpura

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

Brown Sequard syndrome

Brown-Vialetto-Van Laere syndrome

bulbar palsy, progressive

calcification, intracranial

calcification, membrane

calcifying pseudoneoplasm of the neuraxis

calf hypertrophy

callosal angle

camptocormia

cancer associated CNS vasculitis

cane

capsular warning syndrome

carbon monoxide poisoning

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, myelogram with

cataplexy

cauda equina

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cavernous hemangioma

cavernous sinus

cavernous sinus, expansion

cavernous sinus, lesion of

cavernous sinus, syndrome

CD4 counts

celiac disease, adult

central hypoventilation

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar hemangioma

cerebellar lesion

cerebellitis

cerebellitis, autoimmune

cerebellum, disease of

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral hypoperfusion

cerebral infarction

cerebral infarction, subcortical

cerebral peduncle

cerebral vasculature

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, IgG index, elevated

cerebrospinal fluid, leak

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrospinal gliomatosis

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, stuttering

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cervical myelopathy

cervical osteophyte

cervical radiculopathy

cervical spine

cervical spine cyst

cervical spine disease

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

chemosis

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choreoathetosis, paroxysmal

chromosomal abnormality

chromosome 5

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

chronic traumatic encephalopathy

cigarette smoking

cingulate island sign

cirrhosis

Clarkson disease

climate change

Clinical Pathologic Conference(C.P.C.)

clonus

clubbing of fingers

coat-hanger pain

cobalamin C deficiency

collapsin response mediator protein 5 IgG

color vision, impaired

color vision, impaired, cerebral

computers, medicine and

concentration, impaired

confusional state, acute

congenital heart disease

congenital infection, CNS

congenital infection, viral

congestive heart failure

conjunctival injection

conjunctival vessel tortuosity

conjunctivitis

consanguinity

constipation

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

conversion reaction

copper deficiency

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical deafness

cortical hemorrhage

cortical-basal ganglionic degeneration

cost

cotton-wool spots

cough

cranial nerve enhancement

cranial nerve palsies

cranial nerves, toxins effecting

cranial neuropathy

cranial neuropathy, multiple

cranial neuropathy, progressive

craniectomy, decompressive

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cricopharyngeal bar

crying, pathologic

cryopyrin-associated periodic syndrome

cryptococcal meningitis

cryptococcal meningoencephalitis

cyst, neoplastic cerebellum

decompressive spinal cord surgery

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

delusion

dementia

dementia, advanced

dementia, age at onset

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

Dengue fever

dental procedure, neurologic complications with

dental prostheses

dentatorubral-pallidoluysian atrophy

denture cream

depression

depth perception, impaired

dermatomyositis

developmental disability

developmental milestones, loss of

developmental retardation

diamond on quadriceps

diarrhea

diencephalon

dietary supplement

differential diagnosis

difficulty climbing stairs

disability, neurological

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

dizziness

dopa responsive dystonia

down-beat nystagmus

downward deviation of eyes

DPPX

DPPX, antibodies, encephalitis

Dravet syndrome

drooling

drop metastasis

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dural sinus thrombosis

dyskinesia, buccal lingual facial

dystrophic calcification

dystrophin

ears of the Lynx MR sign

EDTA(ehtylenediamine tetraacetic acid)

efficacy

electrical sensation

electrocorticogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electromyogram, decremental response

electroretinograph

emergencies, neurologic

emergencies, neurosurgical

emergency room

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, balamuthia

encephalitis, brainstem

encephalitis, episodic

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, progressive

endarterectomy, carotid

enzyme, muscle disease

enzyme, serum

eosinophilia

epidemiology of neurology

epidural steroid

epilepsia partialis continua

episcleritis

episodic disorders

episodic neurologic deficits

episodic unconsciousness

epistaxis

Erdheim-Chester disease

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

Exserohilum rostratum

extralimbic encephalitis

extraocular muscle enlargement

extraocular muscle lesion

eye movement, disorders of

eye movement, painful

eye, pain in

face, numbness of

facial movement disorder

facial pain

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

failed medical management

fatal familial insomnia

fine motor function, impaired

finger nose finger test

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fistula, arterio-venous, pulmonary

fluorescein angiography

fluorosis

foam cells

folic acid deficiency

fourth ventricle, compression

fourth ventricle, floor

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

fungal infection

fungal infection, CNS

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

ganglionitis

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

genu of corpus callosum

geographic location

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

girdle sensation

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

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

GM1 ganglioside antibodies

GNAQ gene

gout

Gowers maneuver

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

gray matter

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hallucination

hallucination, olfactory

hallucination, visual

head injury, repetitive

headache, progressive

headache, recurrent

headache, severe

headache, sudden onset of

headache, unilateral

hearing loss

hearing loss, bilateral

hearing loss, rapidly progressive

hearing loss, sudden, bilateral

heel swelling

heel-knee-shin test

helminthic infection of CNS

hemangioblastoma

hemangioma

hemangioma, brainstem

hemangioma, leptomeningeal

hematoma, epidural-spinal

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemianopia, isolated homonymous

hemiatrophy

hemiatrophy, cerebral

hemifacial atrophy

hemifacial spasm

hemiparesis

hemiparesis, recurrent

hemiplegia

hemiplegia, progressive

hemispherectomy

hemolytic-uremic syndrome

hemophagocytosis

hemosiderosis of CNS, superficial

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniated disc

herniated disc, cervical

herniation syndromes, intracranial

heterochromia iridis

hiccoughs

high arched feet

highly active antiretroviral therapy

hip flexor weakness

hip pain

hippocampus

hippocampus, hyperintense

histiocytosis

histochemistry of muscle

HIV CSF viral escape syndrome

HLA

HMGcoA reductase inhibitors

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 2

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

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, exvacuo

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hydrocephalus, treatment of

hyperammonemic encephalopathy

hypercalcemia

hypereosinophilic syndrome(HES)

hyperesthesia

hyperhomocysteinemia

hyperpigmentation of skin

hypertrophic intracranial pachymeningitis

hypertrophic spinal pachymeningitis

hypotension, neurologic causes of

hypotension, systemic

iatrogenic neurologic disorders

immune checkpoint inhibitors

immune reconstitution inflammatory syndrome

immune reconstitution inflammatory syndrome, paradoxical

immune reconstitution inflammatory syndrome, unmasked

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impulsivity

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone

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

inappropriate behavior

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incontinence, fecal

incoordination

India

infant, evaluation of

infection

inferior olivary nucleus

inflexibility, mental

intellectual deterioration

internal auditory canal

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial hypotension

intracranial pressure, increased

intraocular pressure, increase

intrathecal medication

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

intubation

iron, brain

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

jugular foramen syndrome

juvenile distal and segmental muscular atrophy

Kaposi's sarcoma

kelch-like protein 11 antibodies

ketogenic diet

lactate

lactic acidemia

lactic dehydrogenase(LDH)

Lafora body

Lafora's disease

laminectomy

laminectomy, cervical

language disorder in adults

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Legionella pneumophilia

Legionnaires'disease

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

level of consciousness, decreased

Lewy body

Lhermitte's sign

lid closure, weakness of

life expectancy

ligamentum flavum, ossification of

limb-girdle weakness

limbic encephalitis

linear lesion

lipid storage myopathy

liver disease

liver function enzymes

lumbar puncture, indications for

lumbosacral plexopathy

lumbosacral radiculopathy

Lyme disease

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, cutaneous

lymphoma, primary of CNS

lymphopenia

lysosomal storage disease

malabsorption syndrome

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

manganese intoxication

memory, defect of recent

memory, impairment of

memory, recent

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningeal gliomatosis

meningeal sarcomatosis

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, eosinophilic

meningitis, fungal

meningitis, lymphomatous

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, noninfectious

meningitis, treatment of

meningoencephalitis

meningomyelitis

mental status, abnormal

mental status, abnormal, acute

MERRF syndrome

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metamyelocytes

methotrexate

methylmalonic acid, serum

methylmalonic acidemia

methylmalonic aciduria

microaneurysm, retinal

microangiopathy, brain

microcephaly

micrographia

microhemorrhage, intracerebral

microinfarcts

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

monoparesis

Montreal cognitive assessment

motor neuron disease, misdiagnosis

motor symptoms

motor system

movement disorder

movement disorder, extrapyramidal

movement disorder, paroxysmal

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, false negative

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, eye of tiger sign

MRI, false negative

MRI, field strength, high

MRI, FLAIR

MRI, gradient-echo

MRI, gray matter enhancement

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lumbosacral plexus

MRI, mass effect on

MRI, muscle

MRI, negative

MRI, nodular enhancement

MRI, optic nerve

MRI, orbit

MRI, paramagnetic effect

MRI, pelvis

MRI, perfusion

MRI, peripheral nerve

MRI, punctate pattern

MRI, ring sign

MRI, ring sign, open

MRI, serial

MRI, skull bone changes

MRI, snowball lesions

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multinucleated giant cell

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, epidemiology of

multiple sclerosis, lesion location

multiple sclerosis, pathogenesis

multiple sclerosis, relapsing

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

mutism

myasthenia gravis

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelination of nervous system

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myoglobinuria

myopathy

myopathy, distal

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, primary of CNS

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve enlargement

nerve root biopsy

nerve root compression

nerve root enhancement

nerve root hypertrophy

nerve root, metastasis

neuritis, causes of

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurodegeneration with brain iron accumulation

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, multiple

neurologic disease, tempo

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyotonia

neuromyotonia and axonal neuropathy

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, chronic

neuropathy, demyelinating

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

numbness, generalized

nusinersen

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, primary position of gaze

nystagmus, upbeating on upgaze

nystagmus, vertical

obesity

obsessive-compulsive disorder

ochronosis

ocular motility, disorders of

oculocephalic reflex

oculomasticatory myorhythmia

old age, neurology of

olivary degeneration, hypertrophic

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, bilateral, acute

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

ophthalmoplegia, unilateral

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic ataxia

optic atrophy

optic atrophy, bilateral

optic chiasm, enhancement

optic disc edema

optic nerve

optic nerve, biopsy

optic nerve, enhancement

optic nerve, enlarged

optic nerve, neoplasm of

optic neuritis

optic neuropathy

optical coherence tomography

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

oral ulcerations

organomegaly

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteoarthrosis

osteoporosis

ovarian tumor

owl's eye sign of spinal cord

pachymeningitis, cranial

pain, increased response

palate, paralysis-unilateral

paralysis, asymmetric

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, flaccid

paraparesis, painful

paraparesis, progressive

paraparesis, spastic

paraphasias

paraplegia

paraplegia, progressive

paraspinal muscle weakness

paresthesias

paresthesias, facial

paresthesias, feet

paresthesias, generalized

paresthesias, hands

parietal lobe, lesion of

Parkinson disease

Parkinson disease, atypical

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

parotid gland swelling

PAS positive

PAS positive material in the brain

past pointing

pathologic reflex

pathology

patient information and support

peripheral blood smear

peripheral nerve, lesion of

pernicious anemia

perseveration

persistent vegetative state

plasma cell dyscrasia

plasmacytoma

plasmapheresis

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, lymphomatous

pons, infarction of

pons, lesion of

pontine warning syndrome

pontocerebellar atrophy

port wine nevus

portal caval shunt

position sensation

positional head-hanging test

positive sharp waves

posterior column disease

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postural abnormality

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

primary intracranial hypotension

primary lateral sclerosis

progressive ataxia and palatal tremor

progressive encephalomyelitis with rigidity syndrome

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

propionic aciduria

proprioception

proprioception, abnormal

proptosis

proptosis, unilateral

protein 14-3-3, cerebrospinal fluid

proteinuria

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudomyasthenia

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pupil, dilated and fixed, unilateral

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriparesis, acute

quadriparesis, progressive

quadriplegia

quality of life

rabies, nervous system involvement with

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

reading

reading disorder, acquired

real-time quaking-induced conversion

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

renal stones

renal tubular acidosis

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal hemangioma

retinal lesion

retinal microvascular disease

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rhomboencephalopathy

riboflavin

riboflavin transporter deficiency

rubella encephalitis, progressive

rubella syndrome

rubella virus

rubeola virus

saccadic eye movements, abnormal

saddle anesthesia

safety

salivary gland enlargement

salivation, excessive

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

sclerosis, bone

scoliosis

scoliosis, neurologic association with

screening

scurvy

season

sedimentation rate, elevated

seizure

seizure, children

seizure, drug resistance

seizure, focal

seizure, intractable

seizure, laughing as manifestation

seizure, paradoxical

seizure, recurrent

seizure, repetitive

seizure, surgical treatment of

seizure, teenager

seizure, treatment of

selenium

semantic dementia

seminoma

sensorineural hearing loss

sensory level

sensory loss

sensory loss, asymmetric

sensory loss, leg

sensory loss, patchy

sensory nerve action potentials

serologic testing

serologic testing of cerebrospinal fluid

seronegative

serum alanine aminotransferase

shoulder-girdle wasting

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

simultanagnosia

sinemet

single photon emission computed tomography

skin, lesions in neurologic disorders

skull bone, thickening

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

small vessel disease

small vessel vasculitis

somatosensory evoked potentials

somnolence

sonophobia

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, pressured

speech, slowed

speech, unintelligible

spinal accessory nerve palsy

spinal cord

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, extramedullary cyst of

spinal cord, herniation

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, neurofibroma

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

spinal pachymeningitis

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spine, infection of

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splenomegaly

spondylolysis

spondylosis

spongy degeneration of brain

sports medicine, neurology of

Spurling test

squamous cell carcinoma of head and neck

status epilepticus, intractable

steatorrhea

stem cell transplantation

steroid therapy, CNS treatment and complications with

stiff legs

stiff man syndrome

stimulation, deep brain

stool, loose

stooped posture

straight sinus

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

stroke, progression of

strokelike episodes

Sturge-Weber syndrome

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

subarachnoid hemorrhage

subcortical U fibers

sudden death

suicide

superior cerebellar peduncle

superior sagittal sinus thrombosis

Susac's syndrome

sweet taste

symmetric brain lesions

symptomatic

syncope

syndrome of the sinking skin flap

synovitis

synucleinopathy

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

temporal artery, biopsy

temporal lobe

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, partial

third nerve palsy, pupil sparing in

tick-borne encephalitis

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

toxins, nervous system

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, limb shaking

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

ulcers, fingertip

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uremia

urinary incontinence

urinary retention

urinary sulfatidase excretion

vascular endothelial growth factor

vasculitides

vasculopathy

Vemurafenib

Venereal Disease Research Laboratory test

venous hypertension

venous thrombosis, non-cerebral

ventricular enlargement

vibratory sensation, abnormal

vision, blurred, monocular

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin A

vitamin A deficiency

vitamin deficiency

vitamin supplementation

voice, abnormality of

walking, difficulty with

walking, difficulty with in dark

water channel antibodies

weakness, fluctuating

weakness, focal

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

weight gain

weight loss

welder

Werdnig-Hoffman disease

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

Showing articles 150 to 200 of 309 << Previous Next >>

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Multiple Sclerosis
NEJM 378:169-180, Reich, D.S.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

Clinical Reasoning: A 66-year-old Woman with Seizures and Progressive Right-Sided Weakness
Neurol 90:e435-e439, St-Pierre, B.D.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A 50-year-old Woman with SLE and a Tumefactive Lesion
Neurol 89:e140-e145, Choi, J.H.,et al, 2017

National Randomized Controlled Trial of Virtual House Calls for Parkinson Disease
Neurol 89:1152-1161,1103, Beck, C.A.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Showing articles 150 to 200 of 309 << Previous Next >>