Neudle.com: mental retardation familial

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abducens nerve paralysis

abscess, intracerebral

abscess, perivalvular

aceruloplasminemia

achilles tendon, enlarged

acid maltase deficiency

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

activities of daily living

activities of daily living scale

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, inappropriate

Aicardi-Goutieres syndrome

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

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

alkylating agents

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

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, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

aminoacidopathies

amnestic syndrome

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyloid plaques

amyloidosis, oculoleptomeningeal, familial

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, treatment of

anemia, hemolytic

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

aneurysm, intracranial, familial

Angelman syndrome

angiofibroma, facial

angiography, cerebral

angioid streaks

angiomyolipomas

animal exposure

ankle, swelling of

anorexia nervosa

anterior horn cell disease

anticholinergic drugs

anticholinesterase

anticonvulsants, selection of

antiphospholipid antibodies

aortic valve, bicuspid

aortic valve, lesion of

aphasia, progressive

aphasia, progressive, primary

apolipoprotein E

apraxia of eye movements

apraxia, constructional

arteriovenous malformation

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

Asperger's syndrome

asterixis, causes of

asterixis, unilateral

ataxia telangiectasia

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, premature

attention deficit disorder with hyperactivity

auditory and vestibular pathways

auditory evoked brainstem potentials

autism, screening for

autistic behavior

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

autosomal dominant leukodystrophy

axonal degeneration

axonal spheroid

B 12 deficiency

bacterial endocarditis, neurologic manifestations of

basal cell carcinoma

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

bent spine syndrome

bilateral periventricular nodular heterotopia

biologic markers

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

black toenail sign

bladder dysfunction

blinking, reduced

blood dyscrasias, neurologic findings with

blood transfusion

bone density, increased

bone marrow transplantation

bovine spongiform encephalopathy

brainstem, atrophy

brainstem, lesion of

burst suppression pattern, electroencephalogram

cafe au lait spots

calcification, gyral

calcification, intracranial

Canavan's disease

carbonic anhydrase II deficiency

carcinoembryonic antigen

cardiac surgery

carnitine deficiency

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, bilateral

CAT scan, abdomen

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

CAT scan, muscle

cataracts, congenital

caudate nucleus, atrophy

caudate nucleus, lesion of

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral glucose metabolism

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral vasculature

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glutamine

cerebrospinal fluid, glycine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

chewing movements

chilbran skin lesions

chorea, causes of

chorea, familial

choreoathetosis

choroid plexus, abnormality of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cingulate island sign

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coat-hanger pain

cobalamin C deficiency

Cockayne's syndrome

codfish vertebrae

cognition, slowed

cogwheel rigidty

cold hands sign

compression fracture

compression neuropathy

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myopathy

congestive heart failure

contractures, joint

conversion reaction

copper deficiency

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corneal transplant

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cortical infarction

cost effectiveness

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cyst, odontogenic

cyst, parenchymal

cyst, porencephalic

cytomegalovirus infection

decerebrate posture

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

dementia, subcortical

dementia, thalamic

dementia, transmissible

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

digits, abnormal

disability rating scale, neurological

disability, neurological

disease modifying agents

disinhibition-dementia-parkinsonism-amyotrophic complex

distal muscle atrophy

diurnal variation

dopa responsive dystonia

dopamine agonist

down-beat nystagmus

Dravet syndrome

drug induced neurologic disorders

dysdiadochokinesia

dysostosis multiplex

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

dystonia, children

dystonia, etiology of

dystonia, painful

dystonia, treatment of

dystonic reaction, acute

ears of the Lynx MR sign

eating disorder

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electron microscopy

electronystagmography

electroretinograph

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis, viral

encephalomalacia

encephalopathy, acute

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, acute bacterial

entrapment neuropathy

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epistaxis, recurrent

epsilon sarcoglycan gene

erectile dysfunction

esophageal varices

ethics in neurology

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

face, elongated

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

failure to thrive

familial hemiplegic migraine

Farber's disease

FARS2 deficiency

fatal familial insomnia

fatty acid dehydrogenase deficiency

fatty acid, elevated plasma content

feeding disorder

ferric chloride test

ferritin, elevated

fetal alcohol syndrome

fever, recurrent

fibroma, ungual

fine motor function, impaired

finger nose finger test

fingerprint bodies

flow study, carotid artery

fluorescene in situ hybridization

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

gait, festinating

galactocerebrosidase

gamma amino butyric acid

gangliosidosis GM2

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geniculate body, lateral

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

Gilles de la Tourette syndrome

Gillespie syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutaric acidemia

glutaric aciduria

glycogen storage disease

Gorlin-Goltz syndrome

granular osmiphilic material

growth hormone deficiency

growth retardation

guanidinoacetate methyltransferase deficiency

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hallucination, auditory

hallucination, visual

head circumference

health insurance

hearing loss, bilateral

hearing problems in children

heart valve surgery

heat intolerance

heel-knee-shin test

hemangioblastoma

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hemianopia, homonymous

hemihypertrophy, congenital

hemochromatosis

hemochromatosis, primary

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hexosaminidase-A

hexosaminidase-A and B

hockey stick sign

holoprosencephaly

homovanillic acid

human immunodeficiency virus type 1

Hunter's syndrome

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's disease, children

Hurler's syndrome

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, viral induced

hyperglycinemia

hyperglycinemia, nonketotic

hyperhomocysteinemia

hyperostosis corticalis generalisata familiaris

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperthyroidism

hypertriglyceridemia

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypoalbuminemia

hypofibrinogenemia

hypoglycemic coma

hypoglycorrhachia

hypomelanosis of Ito

hypometric saccades

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotension, neurologic causes of

hypotension, systemic

hypothalamus, disturbance of

hypothermia, causes of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunodeficiency

immunofluorescence

immunologic disease

immunosuppression

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

inappropriate behavior

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

infantile bilateral striatal necrosis

infantile spasm

infection, recurrent

inflexibility, mental

influenza, avian

insulin resistance

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial pressure, increased

intrauterine infection

intrinsic hand muscles, wasting of

iron, serum, low

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

joint hypermobility

Kayser-Fleischer ring

KCNQ2 encephalopathy

Kearns-Sayre syndrome

kinesia paradoxica

Kluver-Bucy syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lacunar infarction

Lafora's disease

laminar necrosis, cortical

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

Leber's congenital amaurosis

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

lenticular nucleus, lesion of, bilateral

Lesch-Nyhan syndrome

leukemia, neurologic findings assoc.with

leukodystrophy, pigmented orthochromatic

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body disease, diffuse

libido, decreased

lid abnormalities

life expectancy

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

livedo reticularis

liver function enzymes

liver transplantation

long bone lesion

low birth weight

Lowe's syndrome

lumbar puncture

lymphadenopathy

lymphangiomyomatosis

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetic susceptibility

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

manic-depressive

maple syrup urine disease

marche a petits pas

Marinesco-Sjogren syndrome

medulloblastoma

melanomatosis, primary malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningoencephalopathy

mental retardation

mental retardation, etiology of

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylhydrazine derivatives

methylmalonic acidemia

methylmalonic aciduria

microangiopathy, brain

microhemorrhage, intracerebral

microspherophakia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine with aura

migraine, confusional state and delirium with

migraine, hemiplegic

migraine, mental disorder associated with

migratory lesion pattern

mild cognitive impairment

Miller-Dieker syndrome

Minamata disease

Mini Mental Status Examination

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

monoamine oxidase inhibitors

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

moyamoya, adult

MRI lesion location

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, functional

MRI, gradient-echo

MRI, gyral swelling

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle stiffness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelinolysis, extrapontine

myeloneuropathy

myelopathy, chronic progressive

myelopathy, vacuolar

myocardial abscess

myocardial biopsy

myoclonic dystonia

myoclonic jerks

myoclonus, action

myoclonus, epilepsy

myopathy, alcoholic

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myotonia congenita

myotonia dystrophica

nasal bridge, wide

nausea and vomiting

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neuroichthyosis

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

neuropsychiatry

neurotransmitter

nevoid basal cell carcinoma syndrome

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

nitrogen mustard

Noonan Syndrome

nystagmus, monocular

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

ocular myopathy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic foramina, abnormal

optic nerve, hypoplasia of

optic neuropathy

optokinetic nystagmus, abnormal

ornithine transcarbamylase deficiency

orthostatic hypotension

ovarian insufficiency

pain, increased response

palatal myoclonus

pallido-ponto-nigral degeneration

palmoplantar keratoderma

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, rapid progression

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

patient information and support

pectus excavatum

Pelizaeus Merzbacher

periventricular leukomalacia

peroxisomal disease

personality change

phenylketonuria

phenylketonuria, adult onset

pheochromocytoma

philtrum, tented

photosensitivity, skin

pigmentary retinopathy

Pittsburgh Compound B

pituitary, hormones of

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polycystic kidneys

polycystic lipomembranous osteodysplasia

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, familial

polyps, gastrointestinal tract

pons, lesion of

pontocerebellar atrophy

port wine nevus

portal caval shunt

postpartum coma

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

prion protein gene

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive subcortical gliosis

progressive supranuclear palsy

prolactin, elevated

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

pseudohypoparathyroidism

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis, acute

psychosocial aspects

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary hypertension

pulmonary infiltrates

pulmonary stenosis

pursuit eye movements, abnormal

putamen, lesion of

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation encephalopathy, delayed

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

real-time quaking-induced conversion

reduplicative paramnesia

refractive errors

Refsum's disease

release phenomena

renal cell carcinoma

renal tubular acidosis

respirations in CNS disease

respiratory depression

respiratory failure

respiratory tract infection

retinal degeneration

retinal detachment

retinal hamartoma

retinal hemangioma

retinal hemorrhages

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rhabdomyosarcoma of heart

rigid spine syndrome

Riley-Day syndrome

saccadic eye movements, abnormal

salivation, excessive

Sandhoff's disease

Sanfilippo syndrome

Schilder's disease

scoliosis, neurologic association with

sea-blue histiocytes

seizure, children

seizure, drug resistance

seizure, familial

seizure, febrile

seizure, injury following

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, pyridoxine dependent

seizure, teenager

seizure, tonic-clonic

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory polyneuropathy

serologic testing

shoulder, pain in

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

skull x-ray, bony defect on

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

SNCA duplication

Sneddon's syndrome

sodium channel dysfunction

somatosensory evoked potentials

Southern immunoblot test

spastic diplegia

spastic dysphonia

spastic paraplegia, type 11

spastic paraplegia, type 15

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 17

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

staphylococcus aureus

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

stereotyped behavior

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stimulant drugs

stooped posture

storage disease of CNS

streptococcal infection

streptococcus viridans

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

subependymal nodules

substantia nigra

symmetric brain lesions

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

tardive dyskinesia

Tay-Sachs disease

teeth, wide-spaced

temper tantrums

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tentorium cerebelli

testicular enlargement

thalamic tumors

thalamic tumors, bilateral

thalamus, atrophy of

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thalassemia/mental retardation syndrome

thiamine deficiency

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

top of the basilar syndrome

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

treatment resistant

tremor, intention

tremor, resting

tremor, wing beating

trichopoliodystrophy

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis

tuberous sclerosis, screening for

tyrosine hydroxylase deficiency

ultrasonography

umbilical-cord blood transplantation

unconsciousness

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

vanishing white matter

vasospasm, cerebral

venous thrombosis, non-cerebral

vertigo, episodic

very long chain fatty acids

vibratory sensation, abnormal

vincristine neurotoxicity

violent behavior

viral infection

viral infection, CNS

viral isolation

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, congenital

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin deficiency

vitreous opacities

vocal cord paralysis

vomiting, recurrent

Von Hippel Lindau

walking, difficulty with

weakness, chronic

weakness, generalized

weakness, progressive

Wernicke's aphasia

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolff-Parkinson-White syndrome

word-finding difficulty

xanthoma, tendon

xeroderma pigmentosa

x-linked hydrocephalus

x-linked intellectual deficit

X-linked lissencephaly

x-linked mental retardation

Showing articles 700 to 750 of 5363 << Previous Next >>

Acute Toxic Limbic Encephalopathy Following Glyphosate Intoxication
Neurol 92:534-536, Planche, V.,et al, 2019

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

Bismuth Neurotoxicity from Use of Topical Bismuth Dressing for Burns
Neurol 92:680-681, Saini, V.,et al, 2019

A 71-year-old Man Receiving Treatment for Cryptococcal Meningitis, Developing New-Onset Lethargy
Neurol 92:815-820, Peng, T.J.,et al, 2019

Clinicopathologic Conference, Ingestion of Isopropyl Alcohol
NEJM 380:1657-1665, Case 13-2019, 2019

A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
Neurol 92:863-867, Patel, N.M.,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

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Pathophysiology and Management of Hyperammonemia in Organ Transplant Patients
Am J Kidney Dis PMID:31040091, Seethapathy, H. & Fenves, A.Z., 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

The Dangers of PRES
Neurol 92:e282-e285, Chaterine, C.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

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

Clinical Epidemiology of Familial Sarcoidosis
Respir Med 149:36-41, Terwiel, M. & Van Moorsel, C.H.M., 2019

Lyme Disease: What the Neuroradiologist Needs to Know
AJNR 40:1998-2000, Valand, H.A.,et al, 2019

A Patient with Psychiatric Illness and Multiple Hemorrhages
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Cerebellar Hippocampal and Basal Nuclei Transient Edema with Restricted Diffusion (CHANTER) Syndrome
Neurocrit Care 31:228-296, Jasne, A.S.,et al, 2019

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

Anti-LG11 Limbic Encephalitis Presenting as an Expanding Insular Lesion
Can J Neuro Sci 46:770-772, Sitwell,L.D.,et al, 2019

Bilateral Basal Ganglia Necrosis Secondary to Methamphetamine
MDCP 5:55-556, Sanchez,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

Thalamic Strokes that Severely Impair Arousal Extend Into the Brainstem
Ann Neurol 84:926-930, Hindman, J.,et al, 2018

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

Cerebral Fat Embolism Syndrome in Sickle Cell Disease Without Evidence of Shunt
eNeurologicSci 14:19-20, Nathan, C.L.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Nivolumab-Induced Autoimmune Encephalitis in Two Patients with Lung Adenocarcinoma
Case Rep Neurol Med 2018;doi:10.1155/2018/2548528, Shah, S.,et al, 2018

Cognitive Impairment Before Intracerebral Hemorrhage is Associated with Cerebral Amyloid Angiopathy
Stroke 49:40-45, Banerjee, G.,et al, 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

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

Clinicopathologic Conference, Pulmonary Adenocarcinoma, Complicated by a Hypercoagulable State with a Nonbacterial Thrombotic Endocarditis
NEJM, Case 33-2018, 2018

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

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Prodromal Symptoms of Multiple Sclerosis in Primary Care
Ann Neurol 83:1162-1173, Disanto,G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Ethical, Palliative, and Policy Considerations in Disorders of Consciousness
Neurol 91:471-475, Fins, J.J. & Bernat, J.L., 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Neurologic Abnormalities After Atrial Fibrillation Ablative Procedure
JAMA Neurol 75:1144-1145, Stanton, R.J.,et al, 2018

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

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

Intrasellar Herniation
Neurol 91:889-890, Pacheco, F.T.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Showing articles 700 to 750 of 5363 << Previous Next >>