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Neurology Specific Literature Search

Differential
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abdominal cramps

abducens nerve paralysis

abscess, intracerebral

abscess, intracranial

abscess, perivalvular

acetylcholinesterase

acetylcholinesterase deficiency

achilles tendon, enlarged

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acoustic neurinoma, bilateral

activated protein C resistance

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

Addison's disease

adenosine deaminase deficiency

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

affect, inappropriate

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alpha glucosidase

alpha-fetoprotein

alpha-synuclein

alternating hemiplegia

alternating hemiplegia of childhood

alternative medicine

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

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, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, hemolytic

anesthesia, general

aneurysm, intracranial

aneurysm, intracranial, delayed cerebral ischemia with

aneurysm, intracranial, familial

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

aneurysm, unruptured

Angelman syndrome

angina pectoris

angiofibroma, facial

angiography, cerebral

angiomyolipomas

ankle reflex, absent

anterior horn cell disease

anterior tibial muscle weakness

antibiotic prophylaxis

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticholinesterase

anticoagulant, treatment

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, hypersensitivity syndrome

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

aortic valve, bicuspid

aortic valve, lesion of

apolipoprotein E

apraxia of eye movements

apraxia, constructional

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arterial dissection, vertebral

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, pulmonary

arthrogryposis multiplex

arylsulfatase A

aspartate aminotransferase

Asperger's syndrome

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

atidarsagene autotemcel

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autism, screening for

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

autosomal dominant nocturnal frontal lobe epilepsy

bacterial endocarditis, neurologic manifestations of

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

benign essential tremor, refractory

benign sexual headache

beta adrenergic agonist

beta adrenergic blocker

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

bitemporal visual field defect

bleeding disorder

blind spot, enlarged

blindness, sudden

blinking, reduced

blood dyscrasias, neurologic findings with

bone density, increased

bone marrow transplantation

botulinum toxin

brachial plexus neuropathy

brain transplantation

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, vascular malformation of

Brugada syndrome

bulbar palsy, acute

burning paresthesia

cafe au lait spots

calcification, gyral

calcification, intracranial

calcitonin gene related peptide

calcitonin gene-related peptide receptor blocker

calcium antagonist

calf hypertrophy

Canavan's disease

carcinoembryonic antigen

carcinoma of pancreas

cardiac surgery

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, neck

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

CAT scan, spine

cavernous hemangioma

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar hemorrhage

cerebellar lesion

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral ischemia

cerebral vasculature

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, childhood

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

chloride channel dysfunction

choline acetyltransferase

chorea, treatment of

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

clinical trials

clubbing of fingers

clubfoot as related to neurologic disease

cluster headache

cobalamin C deficiency

Cockayne's syndrome

coenzyme Q10 deficiency

cogwheel rigidty

cold temperature

collagen vascular disease

color vision, impaired

complete blood count

compression fracture

compression neuropathy

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation, non CNS

congenital myasthenic syndromes

congestive heart failure

contractures, joint

contraindications

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

cornea, opacity of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical vein thrombosis

cost effectiveness

cranial nerve palsies

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

creatine phosphokinase(CPK)elevated

crying, pathologic

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cyclic vomiting

cyst, peritumoral

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cyst, porencephalic

decerebrate posture

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia, autoimmune

dementia, childhood

dementia, frontotemporal

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diabetes mellitus

diagnostic criteria

diamond on quadriceps

dichlorphenamide

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin, hypersensitivity to

dilantin, toxicity

diplopia, transient

disability, neurological

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dopamine agonist

down-beat nystagmus

Dravet syndrome

dropped head syndrome

drug induced neurologic disorders

dural sinus thrombosis

Durett hemorrhages

dysarthria-clumsy hand syndrome

dyschromatopsia

dysdiadochokinesia

dysostosis multiplex

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, painful

dystonia, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

dystroglycanopathies

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

edema, periorbital

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, video monitoring with

electron microscopy

electronystagmography

electroretinograph

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

Embryonal tumors

emergencies, neurologic

emergencies, ocular

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, autoimmune

encephalitis, viral

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, acute bacterial

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epistaxis, recurrent

epsilon sarcoglycan gene

erythromelalgia

esophageal varices

ethics in neurology

executive dysfunction

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

Factor V Leiden

failed medical management

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

familial rectal pain

fatty acid, elevated plasma content

feeding disorder

ferric chloride test

fetal alcohol syndrome

fibrinolytic agents, contraindications

fibroma, ungual

fibromuscular dysplasia

fine motor function, impaired

fistula, arterio-venous, pulmonary

flail arm syndrome

flow study, carotid artery

fluorescein angiography

fornix, lesion of

fracture, long bone

fragile-X syndrome

fragile-X syndrome, carrier

fried egg appearance

Friedreich's ataxia

fundus, abnormality of

funduscopic exam

gait, festinating

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal bleeding

Gaucher's disease

gaze palsy, supranuclear

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

gests antagoniste

Gilles de la Tourette syndrome

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

glucose tolerance test, abnormal

GLUT1 deficiency syndrome

glutamic acid decarboxylase

glutaric acidemia

glycogen storage disease

glycosyltransferase

Gowers maneuver

granular osmiphilic material

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

head retraction reflex

headache, chronic

headache, persistent

headache, positional

headache, preventive treatment

headache, recurrent

headache, severe

headache, treatment of

headache, vascular

health insurance

hearing loss, bilateral

hearing loss, sudden, unilateral

heart valve surgery

heat intolerance

hemangioblastoma

hemangioma, brainstem

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hemianopia, transient

hemiparesis, transient

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniated disc, thoracic

high arched feet

high arched palate

history of neurology

hormone replacement

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Hurler's syndrome

hydrocephalus, viral induced

hyperbilirubinemia

hyperhomocysteinemia

hyperkalemic periodic paralysis

hyperpigmentation of skin

hypersensitivity reaction

hyperthyroidism

hypertriglyceridemia

hypertrophic cardiomyopathy

hypoalbuminemia

hypocholesterolemia

hypofibrinogenemia

hypoglycemic coma

hypoglycorrhachia

hypokalemic periodic paralysis

hypometric saccades

hypoparathyroidism

hypophosphatemia

hypopigmentation of skin

hypotension, systemic

hypotonia, infants

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

imbalance, postural

immunodeficiency

immunohistochemistry

immunologic disease

immunology and the nervous system

immunosuppression

implantable cardioverter defibrillator

in situ hybridization

inappropriate behavior

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

infantile bilateral striatal necrosis

infantile spasm

infection, recurrent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon beta 1-a

interferon beta 1-b

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrathecal chemotherapy

intraventricular hemorrhage

intrinsic hand muscles, wasting of

ischemic exercise test

islet cell tumor

JAK2 V617F mutation

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

jaw contractures

jaw jerk, abnormal

joint hypermobility

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa, drug interactions with and side effects of

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lens, dislocation of

lenticular nucleus, lesion of, bilateral

Lesch-Nyhan syndrome

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

liver transplantation

locus ceruleus, lesion of

long bone lesion

Lowe's syndrome

lumbar puncture

lymphadenopathy

lymphangiomyomatosis

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetic susceptibility

magnetoencephalography

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, screening for

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

Marcus Gunn pupil

marfanoid skeletal abnormalities

McArdle's disease

medulla oblongata, neoplasm of

medulloblastoma

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

methylmalonic acidemia

methylmalonic aciduria

microhemorrhage, intracerebral

migraine, children

migraine, chronic

migraine, hemiplegic

migraine, intractable

migraine, pathogenesis

migraine, prophylaxis

migraine, treatment of

mild cognitive impairment

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

molecular markers

monoclonal antibodies

monomelic amyotrophy

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, paroxysmal

movement disorder, treatment of

MRI, angiography

MRI, blooming effect

MRI, complications with

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, functional

MRI, gradient-echo

MRI, incidental finding

MRI, optic nerve

MRI, paramagnetic effect

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, venography

mucopolysaccharidoses

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, clinical patterns

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, pathogenesis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

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, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, infantile and juvenile

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, receptor site in

myasthenia gravis, treatment of

myasthenic syndrome

myelination of nervous system

myelitis, longitudinal

myelopathy, chronic progressive

myeloproliferative disorder

myoblast transfer

myocardial abscess

myocardial infarction

myoclonic dystonia

myoclonic jerks

myoclonus, action

myoclonus, epilepsy

myopathy, alcoholic

myopathy, distal

myopathy, genetic

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, proximal

myopathy, quadriceps

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonic crisis

myotonic discharges

N-acetylcysteine

narcotic analgesics

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neonatal screening, genetic neurologic disorders

neoplasm, intracranial

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, primary intracerebral

neoplasm, primary intracerebral, reoperation

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-aged

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-recurrent

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve growth factor

nerve hypertrophy

neurocardiology

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuroophthalmology

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral, treatment

neuropathy, work up for

neurotransmitter

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

nonsteroidal anti-inflammatory drug

nutritional deficiency

nystagmus, periodic

nystagmus, vertical

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

oculopharyngeal muscular dystrophy

oligodendroglioma

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic atrophy, hereditary

optic disc edema

optic nerve sheath fenestration

optic nerve, compression of

optic nerve, decompression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

ornithine transcarbamylase deficiency

pacemaker, cardiac-transvenous

pain, abdominal

palliative care

pancreatic cyst

paralysis, acute

paralysis, acute areflexic

paralysis, recurrent

paramyotonia congenita

paraparesis, acute

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, transient

paraplegia, recurrent

paraspinal muscle

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal exercise-induced dyskinesia

paroxysmal exertion-induced dyskinesia

paroxysmal extreme pain disorder

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

patient information and support

pectus excavatum

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

phosphorylase b kinase deficiency

photosensitivity, skin

pigmentary retinopathy

Pittsburgh Compound B

pituitary, adenoma

platelet aggregation

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polycystic kidneys

polycythemia, primary

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

Pompe's disease of glycogen storage

port wine nevus

portal caval shunt

posterior cerebral artery territory infarction

posterior column disease

postural abnormality

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

primary lateral sclerosis

primary thrombocythemia

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protein S deficiency

proximal muscle atrophy

pseudobulbar palsy

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosocial aspects

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary infection

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

quadriparesis, acute

quadriplegia, transient

quality of life

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

reading problem, causes of

recombinant DNA

refractive errors

Refsum's disease

renal cell carcinoma

respirations in CNS disease

respiratory depression

respiratory failure

respiratory tract infection

restless leg syndrome

retinal degeneration

retinal hamartoma

retinal hemangioma

retinal ischemia

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rhabdomyoma, cardiac

rhabdomyosarcoma of heart

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rippling muscle disease

risk factors, modification

risus sardonicus

Romano-Ward syndrome

saccadic eye movements, abnormal

salivation, excessive

sarcoglycanopathy

Schilder's disease

scoliosis, neurologic association with

scotoma, central

second wind phenomena

sedimentation rate, elevated

seizure, cardiac arrhythmia causing

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, etiology of

seizure, familial

seizure, febrile

seizure, hereditary

seizure, intractable

seizure, maternal

seizure, neonatal

seizure, nocturnal

seizure, paradoxical

seizure, photosensitive

seizure, prognosis in adults

seizure, psychomotor-temporal lobe

seizure, psychosocial aspects of

seizure, stimulus sensitive

seizure, treatment of

seizure, workup of

sensorineural hearing loss

serotonin agonist

serotonin antagonist

sexual intercourse

shunt procedure, lumboperitoneal

sick sinus syndrome

single photon emission computed tomography

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, translucent

skull x-ray, abnormal

skull x-ray, bony defect on

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

sodium channel dysfunction

sodium valproate

somatosensory evoked potentials

spastic dysphonia

speech disorder

speech disorder, childhood

speech, delayed development of

spinal cord degeneration

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar degeneration

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

staphylococcus aureus

startle reaction

stem cell transplantation

stent, venous sinus

stereotaxic surgery

stereotyped behavior

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus viridans

stress, emotional

striatal encephalitis

striatonigral degeneration

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, treatment of

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

superoxide dismutase

suprascapular neuropathy

survival motor neuron gene

symmetric brain lesions

syncope, recurrent

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tapetoretinal degeneration

tardive dystonia

telangiectases, retinal

temporal lobe, lesion

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tendon, enlarged

teratogenic drugs

testicular atrophy

tetrahydrobiopterin

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombophlebitis

thyroid function tests

tic, chronic multiple

tinnitus, pulsatile

tissue plasminogen activator, intravenous

tomaculous neuropathy

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tonic foot response

torticollis, post traumatic

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

treatment resistant

tremor, cerebellar

tremor, intention

tremor, postural

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

trichopoliodystrophy

trientine dihydrochloride

trigeminal nerve, lesion of

trigeminal neuropathy

trigeminovascular system

trinucleotide repeats

tuber, cortical

tuberous sclerosis

tuberous sclerosis, screening for

tumor suppressor gene

tyrosine hydroxylase deficiency

umbilical-cord blood transplantation

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary catecholamines

urinary sulfatidase excretion

urinary urgency

urine test for metabolic disorders

Usher's syndrome

vasospasm, cerebral

venous thrombosis, non-cerebral

ventricular tachycardia

vertigo, episodic

vertigo, migraine causing

vertigo, treatment of

very long chain fatty acids

violent behavior

viral infection

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual field testing

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, transient

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vitamin, multiple

vitreous opacities

Von Hippel Lindau

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking, delayed

walking, difficulty with

weakness, acute

weakness, chronic

weakness, episodic

weakness, fatiguable

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Wernicke's encephalopathy

Western immunoblot test

white matter disease

wide based gait

winging of scapula

Wiskott-Aldrich syndrome

wound healing, poor

xanthoma, tendon

x-linked mental retardation

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Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
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Showing articles 1000 to 1050 of 11821 << Previous Next >>