Neudle.com: cerebrovascular accident hereditary

Differential
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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

activated protein C resistance

acyl CoA dehydrogenase deficiency

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

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, 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

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

aneurysm, asymptomatic

aneurysm, berry

aneurysm, intracranial

aneurysm, intracranial, familial

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

angiography, cerebral

angiography, cerebral, false negative

angiography, posterior fossa

anterior horn cell disease

anti MAG antibodies

antibiotic prophylaxis

antibiotics

anticholinergic drugs

anticoagulant, treatment

anticonvulsants

anticonvulsants, selection of

antiphospholipid antibodies

antithrombin III deficiency

anxiety

aorta, atherosclerosis

aortic valve, bicuspid

aortic valve, insufficiency

aortic valve, lesion of

aortic valve, stenosis

aphasia

aphasia, progressive, primary

apolipoprotein E

APP gene

apraxia

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

asterixis, unilateral

ataxia telangiectasia

atherosclerosis, premature

ATP1A3 gene

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

autism

autism, screening for

autistic behavior

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

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

basilar artery occlusion

Bassen-Kornzweig syndrome

behavior

behavior modification

behavior, combative

behavioral disorder

Behcet's syndrome

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

Binswanger disease

biologic markers

biotinidase deficiency

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, stereotaxic

brain purpura

brain scan, abnormal

brain transplantation

brainstem, dysfunction

brainstem, hypoplasia

brainstem, infarction of

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

brainstem, vascular malformation of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

calcification, muscle

calcium oxalate crystals

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

cardiac arrest

cardiac surgery

cardiac surgery, neurologic complications with

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

caries

carnitine deficiency

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

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, ring sign

cataracts

cataracts, congenital

catecholamine

caudate nucleus, atrophy

cavernous hemangioma

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

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, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral palsy, etiology

cerebral palsy, risk factors

cerebral peduncle

cerebral vasculature, calcification

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebritis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

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, nonvascular territory

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

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

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chilbran skin lesions

choroid plexus, abnormality of

choroid plexus, cyst

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

cognition, slowed

coin lesion on chest X-ray

COL4A1 related disorder

cold hands sign

cold temperature

collagen vascular disease

collateral circulation

compression neuropathy

compression neuropathy, recurrent

compulsivity

conduction block

confusion

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, viral

congenital malformation

congestive heart failure

controversies in neurology

copper

copper metabolism, abnormal

cornea, abnormal

cornea, opacity of

corneal dystrophy

coronary artery bypass

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

cost effectiveness

cough

coumarin

cranial nerve palsies

cranial nerve tumor

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, neoplastic cerebellum

deafness, bilateral progressive vs.unilateral acute

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

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, loss of

developmental retardation

developmental venous anomalies

dexterity, impaired

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

diarrhea

diet

differential diagnosis

difficulty climbing stairs

dilated aortic root

diplopia

disability rating scale, neurological

dislocated hip, congenital

dissociated sensory loss

distal muscle weakness

dopa responsive dystonia

dopamine

dopamine agonist

dopaminergic dysfunction

doppler

doppler, transcranial

down-beat nystagmus

drooling

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

Duane syndrome

duplex ultrasound

dural sinus thrombosis

Durett hemorrhages

dying

dysarthria

dysarthria-clumsy hand syndrome

dystrophin associated proteins

ear, abnormal

ear, pain in

early draining vein

ears of the Lynx MR sign

eating disorder

echocardiogram

echocardiogram, contrast

echocardiogram, transesophageal

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

echolalia

ectatic basilar artery

edema, pedal

efficacy

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

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

emergencies, ocular

Emery-Dreifuss muscular dystrophy

emotional lability

empty sella

empyema, epidural-spinal

encephalitis

encephalitis, autoimmune

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endarterectomy, carotid

endocarditis

endocarditis, acute bacterial

endocarditis, infectious

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

entrapment neuropathy

enzyme treatment

enzyme, defect

ependymoma

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

exercise-induced neurologic dysfunction

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

facial nevus

facial weakness

facial weakness, bilateral

Factor V Leiden

factor V, deficiency

factor VII, deficiency

Fahr disease

failed medical management

familial hemiplegic migraine

familial mediterranean fever

familial rectal pain

fasciculation

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

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

fluorescein angiography

flushing

foot deformity

foot drop

fourth ventricle, enlargement of

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

genetic screening

genetic testing

genioglossus

Gerstmann-Straussler-Scheinker disease

Gilles de la Tourette syndrome

glabellar sign

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

globus pallidus, lesion of, bilateral

glucocerebrosidase

GLUT1

GLUT1 deficiency syndrome

glutamine

glutaric acidemia

glycogen storage disease

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

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

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, putamenal

hemorrhage, thalamic

hemorrhagic diathesis

hemorrhoids

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatitis C virus

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

hereditary spherocytosis

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, 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

hypercoagulable state

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertension, cerebrovascular disease with

hypertrophic cardiomyopathy

hypoalbuminemia

hypofibrinogenemia

hypogammaglobulinemia

hypokalemic periodic paralysis

hypopigmentation of skin

hypothermia, causes of

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

inability to stand on tiptoes

inattention

inborn errors of metabolism

incidental finding

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incoordination

infant, evaluation of

inflexibility, mental

insulin resistance

intellectual deficit

intellectual deterioration

interferon alpha

internuclear ophthalmoplegia

interobserver agreement

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

intrauterine

intrauterine infection

intraventricular hemorrhage

intrinsic hand muscles, wasting of

ipsilateral hemiplegia

ischemic exercise test

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

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

kyphoscoliosis, neurologic causes of

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lens, dislocation of

lens, ectopic

lenticular nucleus, lesion of, bilateral

leukemia

leukocyte enzyme abnormality

leukoencephalopathy with calcification and cysts

leukoencephalopathy, hereditary diffuse

leukopenia

Lewy body

Lhermitte-Duclos disease

life expectancy

lifestyle modification

lightheaded

limb-girdle weakness

limbic system

limbic-predominant age-related TDP-43 encephalopathy

lipid storage disorder of CNS

lipid storage myopathy

Lisch nodules

livedo reticularis

liver disease

liver function enzymes

liver transplantation

lumbosacral plexopathy

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

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

malformation, venous

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

megalencephaly

melanomatosis, primary malignant

MELAS syndrome

memory, impairment of

meningeal enhancement

meningioma

meningismus

meningitis, brucellosis

meningitis, carcinomatous

menses

mental retardation

mental retardation, familial

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

methylene tetrahydrofolate reductase

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

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

MNGIE syndrome

molecular genetics

mongolism

mononeuropathy multiplex

mononeuropathy, children

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

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, high signal intensity of basal ganglia

MRI, incidental finding

MRI, indications for

MRI, negative

MRI, paramagnetic effect

MRI, perfusion

MRI, peripheral nerve

MRI, punctate pattern

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

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, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myasthenic syndrome

myelin protein zero gene

myelitis, transverse

myelomeningocele

myelopathy

myeloproliferative disorder

myocardial abscess

myocardial biopsy

myocardial infarction

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

nephrocalcinosis

nerve conduction studies

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neural tube defect

neurocardiology

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neurofibromatosis 2, presymptomatic

neurofibromin

neurogenic bladder

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, 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, classification of

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, vasculitic, systemic

newborn, evaluation of

next-generation sequencing

nigrostriatal pathway

nystagmus, dissociated

nystagmus, monocular

nystagmus, vertical

obesity

obsessive-compulsive disorder

occipital lobe

occipital lobe, infarction

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

oculopharyngeal muscular dystrophy

old age, neurology of

oligodendroglioma

operculum syndrome

operculum syndrome, bilateral

ophthalmic artery occlusion

ophthalmoplegia

ophthalmoplegia, progressive external

opiate

opisthotonus

optic atrophy

optic atrophy, hereditary

optic nerve

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

organ rupture

ornithine transcarbamylase deficiency

orthopnea

orthostatic hypotension

osmotic demyelination syndrome

osteogenesis imperfecta

osteoporosis

oxalosis, primary

pacemaker, cardiac-transvenous

pain, increased response

paralysis, acute areflexic

paraparesis

paraparesis, acute

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paraparesis, transient

paraplegia

paraplegia, recurrent

parenteral alimentation

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, misdiagnosis

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

PAS positive

PAS positive material in the brain

patent foramen ovale

pathognomonic

pathology

patient information and support

pectus excavatum

penicillamine

percussion induced muscle contraction

periodic limb movements

periodic movements during sleep

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

phosphorylase b kinase deficiency

photophobia

phytanic acid

PICU

pigmentary retinopathy

pimozide

pituitary, hormones of

platelet aggregation

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

polycythemia, primary

polycythemia, secondary

polyhydramnios

polymerase chain reaction

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

practice guidelines

Prader-Labhart-Willi syndrome

pramipexole

precipitating factors

preclinical

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

presenilin-2 gene

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

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

pulmonary infection

pulmonary infiltrates

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, episodic

putamen, lesion of

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

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

reversible neurologic disorder

rhabdomyosarcoma of heart

rigid spine syndrome

rigidity

riluzole

rippling muscle disease

risk factors

risk factors, modification

risk-benefit assessment

scoliosis, neurologic association with

screening

second wind phenomena

seizure

seizure, cardiac arrhythmia causing

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, nonepileptic

seizure, paradoxical

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, risk factors for

seizure, stimulus sensitive

seizure, treatment of

seizure, workup of

self-mutilation

sensorineural hearing loss

sensory loss

sensory nerve action potentials

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

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, biopsy

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

splenomegaly

spondylolysis

spondylosis

spongy degeneration of brain

spontaneous remission

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

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, prognosis

subarachnoid hemorrhage, recurrent

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

term infant

testicular atrophy

testicular enlargement

tetrahydrobiopterin

thalamic tumors

thalamic tumors, bilateral

thalamotomy

thalamus

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thrombotic thrombocytopenia purpura

thrombus, mural

thyroid function tests

thyrotoxicosis

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

tongue, red papules

tongue, weakness

torsades de points

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

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, high-intensity focused

ultrasonography, nerve

unconsciousness

unconsciousness, transient

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uremia

urinary catecholamines

urinary incontinence

urine test for metabolic disorders

ventricular septal defect

ventricular tachycardia

vertebral-basilar insufficiency

vertigo

vertigo, episodic

very long chain fatty acids

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision loss, sequential

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

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

Wernicke's encephalopathy

Western immunoblot test

wheelchair

white freckles

white matter disease

white matter disease, location

white matter disease, subcortical

wide based gait

Wildervanck's syndrome

Williams syndrome

winging of scapula

Wood's light

word-finding difficulty

workup

wound healing, poor

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

zinc

Showing articles 300 to 350 of 12641 << Previous Next >>

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

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

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
Neurol 44:823-828, Aylward,E.H.,et al, 1994

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

The Importance of Family History in Cerebrovascular Disease
Stroke 25:1599-1604, Graffagnini,C.,et al, 1994

Increased Risk of Alzheimer's Disease in Mothers of Adults with Down's Syndrome
Lancet 344:353-356, Schupf,N.,et al, 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
Stroke 25:889-903, Schievink,W.I.,et al, 1994

Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
Ann Int Med 120:133-134, Skinner,M.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
Neurol 44:399-405, Pettee,A.D.,et al, 1994

Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
Stroke 25:508-510, Papa,M.L.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Familial Atrioventricular Septal Defect:Possible Genetic Mechanisms
Br Heart J 71:79-81, Kumar,A.,et al, 1994

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Familial Aggregation of Stroke
Stroke 24:1366-1371, Kiely,D.K.,et al, 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

Conjugal Alzheimer's Disease:Is There an Increased Risk in Offspring?
Ann Neurol 34:396-399, Bird,T.D.,et al, 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993

Twin Birth is Not a Risk Factor for Seizures
Neurol 43:2515-2519, Berkovic,S.F.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
JAMA 270:2316-2320, MacCollin,M.,et al, 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Intracranial Aneurysms in Autosom Dominant Polycystic Kidney Disease
NEJM 327:916-920, 9531992., Chapman,A.B.,et al, 1992

A Study of Twins and Stroke
Stroke 23:221-223, Brass,L.M.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Showing articles 300 to 350 of 12641 << Previous Next >>