Neudle.com: cerebrovascular accident genetic

Differential
(Click to cross reference)

abdominal cramps

abdominal distention

abducens nerve paralysis

abscess, intracerebral

abscess, intracerebral, recurrent

abscess, intracranial

abscess, perivalvular

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acoustic nerve, vestibular division of

acoustic neurinoma

acral sensory symptoms

acrocyanosis

acromicria

ACTH

activated protein C resistance

acute disseminated encephalomyelitis

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of corpus callosum

agitation

agoraphobia

Aicardi-Goutieres syndrome

alpha galactosidase A deficiency

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement, impaired

alternative medicine

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, conjugal

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, incidence

Alzheimer's disease, misdiagnosis

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid plaques

amyloidosis

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

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, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia

anesthesia, general

aneurysm

aneurysm, asymptomatic

aneurysm, berry

aneurysm, intracranial

aneurysm, intracranial, familial

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

angiography, cerebral

angiography, posterior fossa

anterior horn cell disease

anti MAG antibodies

antibiotic prophylaxis

antibiotics

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, treatment

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiphospholipid antibodies

antithrombin III deficiency

anxiety

aortic valve, bicuspid

aortic valve, insufficiency

aortic valve, lesion of

aortic valve, stenosis

aphasia

aphasia, progressive, primary

apraxia of eye movements

arterial dissection, aorta

arterial dissection, carotid

arterial dissection, cerebral

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, recurrent

arterial dissection, renal artery

arterial dissection, ruptured

arterial dissection, vertebral

arteriopathy

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

aspartate aminotransferase

asymmetric crying facies

asymptomatic

asystole

ataxia

ataxia telangiectasia

atherosclerosis, premature

ATP1A3 gene

atrial enlargement

atrial fibrillation

atrial fibrillation, risk stratification

atrial myxoma

atrial paralysis

atrial septal defect

atrioventricular block

atrioventricular septal defect

attention

attention deficit disorder with hyperactivity

atypical

auditory and vestibular pathways

autism

autism, screening for

autistic behavior

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune meningitis

automatic implantable cardioverter-defibrillator

autonomic dysfunction

axonal spheroid

Babinski sign

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

baldness

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, hemorrhage

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior

behavior modification

behavior, combative

behavioral disorder

beta adrenergic agonist

beta adrenergic blocker

Binswanger disease

biologic markers

biotinidase deficiency

birth injury

bitemporal visual field defect

blood dyscrasias, neurologic findings with

bone marrow transplantation

bovine spongiform encephalopathy

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brain biopsy, stereotaxic

brain purpura

brain scan, abnormal

brain transplantation

brainstem, hypoplasia

brainstem, infarction of

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

brainstem, vascular malformation of

calcification, intracranial

calcification, muscle

calcium oxalate crystals

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

cardiac arrest

cardiac arrest and resuscitation

cardiac surgery

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency myopathy

carotid angiogram

carotid artery

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid artery stenosis, intracranial

CAT scan

CAT scan, abdomen

CAT scan, abnormal

CAT scan, abscess, cerebral

CAT scan, angiography

CAT scan, chest

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, indications for

cataracts, congenital

catecholamine

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous hemangioma

central core disease

central nervous system, infection of

central retinal artery occlusion

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellum, neoplasms of

cerebral arteries

cerebral atherosclerosis

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 edema, origin and treatment

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral glucose metabolism

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral palsy, etiology

cerebral palsy, risk factors

cerebral palsy, work up

cerebral peduncle

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, etiology

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, childhood

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cryptogenic

cerebrovascular accident, etiology

cerebrovascular accident, familial occurrence

cerebrovascular accident, genetic

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, pathophysiology

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, silent

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

cerebrovascular disease, surgical treatment of

Chediak-Higashi syndrome

chelation therapy

chemical meningitis

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chilbran skin lesions

children

chloride channel dysfunction

choroid plexus, abnormality of

choroid plexus, cyst

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cluster headache

coagulopathy

cobalamin C deficiency

cocaine

Cockayne's syndrome

codfish vertebrae

coenzyme Q10 deficiency

cognition

cognition, slowed

coin lesion on chest X-ray

coinfection

COL4A1 related disorder

cold hands sign

cold temperature

coldness

collagen vascular disease

collateral circulation

compression neuropathy

compression neuropathy, recurrent

compulsivity

conduction block

confusion

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myopathy

congestive heart failure

controversies in neurology

copper

copper metabolism, abnormal

cornea, abnormal

cornea, opacity of

corneal dystrophy

coronary artery disease

corpus callosum

corpus callosum, atrophy of

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cranial nerve palsies

cranial nerve tumor

cranial neuropathy

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Cree leukoencephalopathy

Creutzfeldt-Jakob disease, genetic

cry, abnormal

cry, weak

crying, pathologic

cryptococcal meningitis

cryptorchidism

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, neoplastic cerebellum

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, transmissible

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

desmin

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

dexterity, impaired

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

diarrhea

dichlorphenamide

diet

differential diagnosis

difficulty climbing stairs

dilated aortic root

diplopia

disability rating scale, neurological

disability, neurological

disease modifying agents

dislocated hip, congenital

dissociated sensory loss

distal muscle weakness

dopa responsive dystonia

dopamine

dopamine agonist

dopaminergic dysfunction

doppler

down-beat nystagmus

drooling

dropped head syndrome

drug abuse

drug induced neurologic disorders

drug interactions

Duane syndrome

duplex ultrasound

dural sinus thrombosis

Durett hemorrhages

dying

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystrophin associated proteins

ears of the Lynx MR sign

ears, low set

eating disorder

echocardiogram

echocardiogram, contrast

echocardiogram, transesophageal

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

echolalia

ectatic basilar artery

edema, pedal

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electron microscopy

electronystagmography

electroretinograph

embolism

embolism, air

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

emergencies, neurologic

emergencies, ocular

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, Japanese

encephalitis, viral

encephalitis, viral-causes of

encephalocele

encephalomalacia

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis

endocarditis, acute bacterial

endocarditis, infectious

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

enterovirus

enterovirus infection of CNS

entrapment neuropathy

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

evidence-based research

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extracorporeal membrane oxygenation

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial asymmetry

facial expression abnormality

facial weakness, bilateral

Factor V Leiden

factor V, deficiency

factor VII, deficiency

familial hemiplegic migraine

familial mediterranean fever

familial rectal pain

fasciculation

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fibrinolytic agents, contraindications

fibroma, ungual

fibromuscular dysplasia

fine motor function, impaired

finger nose finger test

finger tapping

fingers, abnormal

fish

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fistula, arterio-venous, pulmonary

fluorescein angiography

fourth ventricle, enlargement of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

fucosidosis

fundus, abnormality of

gastrocnemius muscle weakness

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

Gaucher's disease

gaze palsy

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

Gilles de la Tourette syndrome

glabellar sign

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

GLUT1

GLUT1 deficiency syndrome

glutaric acidemia

glycogen storage disease

glycoprotein

GNAQ gene

Gowers maneuver

granular osmiphilic material

grimacing

growth hormone

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gynecomastia

gyrus, abnormal

hair analysis

Hallervorden Spatz disease

headache, sudden onset of

headache, throbbing

headache, thunderclap

headache, unilateral

hearing loss

hearing loss, bilateral

hearing loss, sudden, unilateral

hearing problems in children

heart block

heart block, complete

helminthic infection of CNS

hemangioblastoma

hemangioma

hemangioma, brainstem

hemangioma, facial

hemangioma, internal organs

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, congenital

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemoptysis

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhage, putamenal

hemorrhage, thalamic

hemorrhagic diathesis

hemorrhoids

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniation syndromes, intracranial

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

Hirschprung's disease

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

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

huntingtin

Huntington's chorea

Huntington's chorea, differential diagnosis

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's chorea, sporadic form

Huntington's disease, children

hydrocephalus

hydrocephalus, congenital

hypercoagulable state

hyperhomocysteinemia

hyperkalemic periodic paralysis

hyperlipidemia

hyperphagia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertension, cerebrovascular disease with

hypertrophic cardiomyopathy

hypoalbuminemia

hypofibrinogenemia

hypogammaglobulinemia

hypokalemic periodic paralysis

hypokinesia

hypometric saccades

hypophosphatemia

hypopigmentation of skin

hypothyroidism, congenital

hypoxic-ischemic leukoencephalopathy

hypsarrhythmia

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

implantable cardioverter defibrillator

impulsivity

inability to stand on tiptoes

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incoordination

India

infant, evaluation of

inflexibility, mental

insomnia

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

intelligence testing in children

interferon alpha

interferonopathy

internuclear ophthalmoplegia

interobserver agreement

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, small

intracerebral hemorrhage, work up

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intranasal medication

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

intrinsic hand muscles, wasting of

ipsilateral hemiplegia

ischemic exercise test

islet cell tumor

JAK2 V617F mutation

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

jaw jerk, abnormal

Jervell Lange-Neilson syndrome

joint hypermobility

juvenile myoclonus epilepsy

karyotyping

Kayser-Fleischer ring

Kearns-Sayre syndrome

klippel feil syndrome

Krabbe's disease

KRIT1 gene

kuru

kyphoscoliosis, neurologic causes of

laminar necrosis, cortical

laminopathies

language delay

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

leukocyte enzyme abnormality

leukoencephalopathy with calcification and cysts

leukoencephalopathy, hereditary diffuse

leukopenia

level of consciousness, decreased

levonorgestrel

Lewy body

Lhermitte-Duclos disease

lid closure, weakness of

life expectancy

lifestyle modification

limb-girdle weakness

limbic system

limbic-predominant age-related TDP-43 encephalopathy

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

liver transplantation

lumbosacral plexopathy

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

magnetic susceptibility

magnetoencephalography

malaise

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malformation, Vein of Galen

malignancy screen

malignant hyperpyrexia

mania

manic-depressive

maple syrup urine disease

medical-legal aspects of neurology

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

medulla oblongata, neoplasm of

medulloblastoma

megalencephaly

melanomatosis, primary malignant

MELAS syndrome

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, bacterial

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, diagnosis

meningitis, fungal

meningitis, helminthic

meningitis, leptospira

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral

meningitis, viral etiology in

meningitis-encephalitis PCR panel

mental retardation, familial

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylene tetrahydrofolate reductase

methylmalonic acidemia

microangiopathy, brain

microcephaly

micrographia

microhemorrhage, intracerebral

microspherophakia

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migratory lesion pattern

Mills syndrome

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

MNGIE syndrome

molecular genetics

mongolism

mononeuropathy multiplex

mononeuropathy, children

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, gyral enhancement

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, incidental finding

MRI, paramagnetic effect

MRI, perfusion

MRI, peripheral nerve

MRI, punctate pattern

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, volumetry

MRS

mucopolysaccharidoses

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, conjugal

multiple sclerosis, differential diagnosis of

multiple sclerosis, etiology of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple sclerosis, risk factors for

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myasthenic syndrome

myelin protein zero gene

myelitis, transverse

myelomeningocele

myelopathy

myelopathy, chronic progressive

myeloproliferative disorder

myocardial abscess

myocardial biopsy

myocardial infarction

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myotonia dystrophica, classification

myotonia dystrophica, type 2

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-aged

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-treatment of

nephritis

nephrocalcinosis

nerve biopsy

nerve biopsy, indication

nerve conduction studies

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neural tube defect

neurocardiology

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurofibromin

neuroleptic

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neuromuscular disease, electrodiagnosis of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, work up for

newborn, evaluation of

next-generation sequencing

NF1 gene

Niemann-Pick disease

night blindness

nigrostriatal pathway

obsessive-compulsive disorder

obstetric neurologic injuries

occipital lobe

occipital lobe, infarction

occipital lobe, lesion of

occupational neurologic disorders

ocrelizumab

ocular motility, disorders of

oculopharyngeal muscular dystrophy

old age, neurology of

oligodendroglioma

omeprazole

operculum syndrome

operculum syndrome, bilateral

ophthalmic artery occlusion

ophthalmoplegia

ophthalmoplegia, progressive external

opiate

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic atrophy, hereditary

optic chiasm, enlarged

optic nerve

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, enlarged

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

oral contraceptives

organ rupture

organomegaly

ornithine transcarbamylase deficiency

orthopnea

orthostatic hypotension

osteogenesis imperfecta

osteoporosis

ovarian insufficiency

oxalosis, primary

pacemaker, cardiac-transvenous

pain, increased response

paralysis, acute areflexic

paramyotonia congenita

paraparesis

paraparesis, acute

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, transient

paraplegia

paraplegia, recurrent

parasitic infection, CNS

paresthesias

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, classification

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, juvenile

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, subtypes

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal extreme pain disorder

paroxysmal hemiplegia

paroxysmal neurologic deficits

partruition

PAS positive

PAS positive material in the brain

patent foramen ovale

pathognomonic

pathology

patient information and support

pectus carinatum

pectus excavatum

penicillamine

percussion induced muscle contraction

periodic limb movements

periodic movements during sleep

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral nerve, lesion of

periventricular leukomalacia

phosphorylase b kinase deficiency

photophobia

phytanic acid

PICU

pigmentary retinopathy

pimozide

pituitary, hormones of

placebo effect

platelet aggregation

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

polycythemia, primary

polycythemia, secondary

polyhydramnios

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymicrogyria

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

Pompe's disease of glycogen storage

posterior cerebral artery territory infarction

posterior fossa, lesion of

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postural abnormality

potassium

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

pramipexole

precipitating factors

preclinical

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prethrombic state, screening for

prethrombotic state

prevention of neurologic disorders

primary episodic ataxia

primary lateral sclerosis

primary thrombocythemia

progressive myoclonic epilepsy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

proton pump inhibitors

proximal muscle atrophy

proximal myotonic myopathy

pruritus

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

PTEN hamartoma tumor syndrome

pulmonary hypertension

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, episodic

pyramidal tract

pyramidal tract dysfunction

pyramidal tract, uncrossed

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, acute

quadriplegia

quadriplegia, transient

quality of life

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

Rankin score

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

real-time quaking-induced conversion

repetitive nerve stimulation

research

respirator

respiratory failure

respiratory tract infection

restless leg syndrome

retina, abnormal

retinal artery tortuosity

retinal microvascular disease

retinal tumor

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retinitis pigmentosa

retinopathy

Rett's syndrome

reversible neurologic disorder

rhabdomyosarcoma of heart

rigid spine syndrome

rigidity

riluzole

rippling muscle disease

risk factors

risk factors, modification

risk-benefit assessment

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

screening

second wind phenomena

seizure

seizure, cardiac arrhythmia causing

seizure, children

seizure, complications following

seizure, crying as manifestation of

seizure, diagnosis of

seizure, differential diagnosis of

seizure, injury following

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, nonepileptic

seizure, paradoxical

seizure, pregnancy

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, risk factors for

seizure, stimulus sensitive

seizure, treatment of

seizure, treatment of, monotherapy

sensorineural hearing loss

sensory loss

sensory nerve action potentials

serologic testing

serologic testing of cerebrospinal fluid

shunt procedure, lumboperitoneal

single photon emission computed tomography

skin, biopsy

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

skull x-ray, abnormal

sleep

sleep apnea

sleep pathology and physiology

slit lamp examination

small vessel disease

small vessel disease, cerebral

smell

Smell Identification Test

sodium channel dysfunction

sodium valproate

somnolence

Southern immunoblot test

spastic ataxia

spastic paraplegia, type 11

spastic paraplegia, type 15

spasticity

spastin

speech disorder

speech disorder, childhood

speech, delayed development of

speech, soft

spina bifida

spinal cord

spinal cord degeneration

spinal cord, compression of

spinal cord, infarction of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenium of corpus callosum

splenomegaly

spondylolysis

spondylosis

spongy degeneration of brain

spontaneous remission

SPRED1 mutation

staphylococcus aureus

stem cell transplantation

stent, venous sinus

stereotaxic surgery

stereotyped behavior

stereotyped behavior, drug induced

steroid

steroid therapy, CNS treatment and complications with

stimulation, deep brain

strabismus

straight sinus

streptococcal infection

streptococcus viridans

stress, emotional

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

Sturge-Weber syndrome

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, prognosis

subarachnoid hemorrhage, recurrent

subcortical U fibers

subdural hematoma

subdural hematoma, neonates and infants

sudden infant death syndrome

superior sagittal sinus thrombosis

superoxide dismutase

survival motor neuron gene

sweating

sweating, abnormality of

symmetric brain lesions

tapetoretinal degeneration

tau protein

TDP-43 proteinopathy

telangiectases

telangiectases, retinal

temper tantrums

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular enlargement

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thrombotic thrombocytopenia purpura

thyroid function tests

thyrotoxicosis

thyroxine

tic

tic, chronic multiple

tinnitus

tinnitus, pulsatile

tissue plasminogen activator, intravenous

titinopathy

toe walking

tomaculous neuropathy

tongue, atrophy

tongue, biting

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

toxoplasmosis, congenital

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

transplacental virus infections

trauma

travel, foreign

treatment of neurologic disorder

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis, screening for

tumor suppressor gene

ultrasonography, carotid artery

ultrasonography, head

ultrasonography, head, fetus-neonate

ultrasonography, nerve

unconsciousness

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uremia

urinary catecholamines

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

vanishing white matter

ventricular septal defect

ventricular tachycardia

vertebral-basilar insufficiency

vertigo

vertigo, episodic

very long chain fatty acids

vestibular migraine

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual field testing

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

visuospatial disturbance

vital capacity

vitamin E deficiency

vitamin K

vitamin supplementation

vitreous opacities

vomiting, recurrent

Von Hippel Lindau

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking frame

walking, difficulty with

water channel antibodies

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Werner's syndrome

Western immunoblot test

white matter disease, location

white matter disease, subcortical

whole genome sequencing

wide based gait

Wildervanck's syndrome

Williams syndrome

winging of scapula

Wolff-Parkinson-White syndrome

Wood's light

word-finding difficulty

workup

wound healing, poor

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked intellectual deficit

x-linked mental retardation

Zika virus infection

zinc

Showing articles 50 to 100 of 12622 << Previous Next >>

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Smoking Causes Fatal Subarachnoid Hemorrhage
Stroke 51:3018-3022, Rautalin, I.,et al, 2020

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
AJNR 41:167-173, Bhatia,K.D.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Clinical Metagenomic Sequencing for Diagnosis of Meningitis and Encephalitis
NEJM 380:2327-2340, Wilson, M.R.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

CRAO and Silent Brain Infarcts caused by Cardiac Myxomas in Carney Complex
Neurol 92:e286-e287, Huang, L-T.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

Acute Encephalitis in Immunocompetent Adults
Lancet 393:702-716, Venkatesan, A.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

Chronic Meningitis Investigated via Metagenomic Next-Generation Sequencing
JAMA Neurol 75:947-955,915, Wilson,M.R.,et al, 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Adult-Onset Vanishing White Matter Disease
Neurol 90:e1091-e1092, Villar-Quiles, R.N.,et al, 2018

Cranial Cavernous Malformations
Stroke 49:1029-1035, Stapleton, C.J. & Barker, F.G., 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

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

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

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017

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

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

A Young Man with Progressive Vision and Hearing Loss
JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016

Showing articles 50 to 100 of 12622 << Previous Next >>