Neudle.com: family function

Differential
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abdominal distention

abdominal muscle paralysis

abiotrophy

abscess, intracerebral

abscess, intracranial

abscess, perivalvular

abulia

acanthocytosis

aceruloplasminemia

acid maltase deficiency

acid maltase deficiency, adult

acoustic nerve, vestibular division of

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acral sensory symptoms

acrocyanosis

acromicria

activities of daily living

activities of daily living scale

Addison's disease

adducted thumb

adenosine deaminase deficiency

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

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

alcoholism

algorithm

alopecia

alpha galactosidase A deficiency

alpha glucosidase

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

alternative medicine

aluminum

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, age of onset

Alzheimer's disease, behavioral symptoms

Alzheimer's disease, conjugal

Alzheimer's disease, diagnosis of

Alzheimer's disease, driving with

Alzheimer's disease, early onset

Alzheimer's disease, early symptoms

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, telling patient diagnosis of

Alzheimer's disease, treatment of

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloid beta protein

amyloid imaging

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

aneurysm, asymptomatic

aneurysm, intracranial

aneurysm, intracranial, detection

aneurysm, intracranial, familial

aneurysm, intracranial, natural history

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

angiography, cerebral

angiography, posterior fossa

anterior horn cell disease

anterior tibial muscle weakness

antibiotic prophylaxis

anticholinergic drugs

anticholinesterase

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, hypersensitivity syndrome

anticonvulsants, rectal administration

anticonvulsants, selection of

anticonvulsants, untoward effects of

antidepressant

antiphospholipid antibodies

anxiety

aortic valve, bicuspid

aortic valve, lesion of

aphasia

aphasia, progressive

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arterial dissection, multiple

arterial dissection, recurrent

arterial dissection, renal artery

arterial dissection, ruptured

arterial dissection, vertebral

arteriopathy

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, pulmonary

arthralgia

arthropathy

arthropathy, neuropathic

artificial nutrition and hydration

aspartate aminotransferase

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autism

autism, screening for

autistic behavior

automatic implantable cardioverter-defibrillator

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

bacterial endocarditis, neurologic manifestations of

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavior

behavior modification

behavior, combative

behavioral disorder

benign essential tremor

benign essential tremor, refractory

bent spine syndrome

beta adrenergic blocker

bicaudate index

bilateral periventricular nodular heterotopia

biologic markers

biotin

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

biotin-responsive basal ganglia disease

bone density, increased

bone marrow transplantation

bone pain

bovine spongiform encephalopathy

brachial neuritis

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain transplantation

brainstem, atrophy

brainstem, hypoplasia

brainstem, lesion of

brainstem, neoplasms of

brainstem, vascular malformation of

Brugada syndrome

bruising

bulbar palsy

bulbar palsy, childhood

bulbar palsy, progressive

bulimia

buphthalmos

burning feet

burning feet, differential diagnosis of

calcification, intracranial

carbonic anhydrase II deficiency

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

carnitine deficiency myopathy

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, neck

CAT scan

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

CAT scan, muscle

cataplexy

cataracts

cataracts, congenital

catecholamine

caudate nucleus

caudate nucleus, atrophy

cavernous hemangioma

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

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 death

cerebral edema

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral vasculature

cerebral vasculature, calcification

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cost of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, rehabilitation of

cerebrovascular accident, time of presentation

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, surgical treatment of

ceruloplasmin, serum

Charcot-Marie-Tooth

Chediak-Higashi syndrome

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing movements

chilbran skin lesions

choline acetyltransferase

choroid plexus, abnormality of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate island sign

cirrhosis

cirrhosis, infancy

cisterna magna, enlarged

citalopram

Clinical Pathologic Conference(C.P.C.)

cobalamin C deficiency

collagen vascular disease

compression neuropathy

congenital deformities

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital ocular motor apraxia

congestive heart failure

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cost

cost effectiveness

cranial nerve palsies

cranial nerve tumor

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cry, abnormal

cry, weak

crying, pathologic

cryopyrin-associated periodic syndrome

cryptorchidism

Cuba

cultured skin fibroblasts

cyst, neoplastic cerebellum

cytomegalovirus infection

degenerative diseases of CNS

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, thalamic

dementia, transmissible

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diaphragmatic paralysis

diarrhea

diazepam rectal gel

diet

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin

dilantin, hypersensitivity to

diplegia, brachial

diplopia

disability rating scale, neurological

disability, neurological

disconnection syndrome

disinhibition-dementia-parkinsonism-amyotrophic complex

disorientation

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine

dopamine agonist

dopaminergic dysfunction

Dravet syndrome

driving

drooling

drug induced neurologic disorders

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, etiology of

dystonia, focal

dystonia, painful

dystonia, treatment of

ears of the Lynx MR sign

eating disorder

echocardiogram

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

echolalia

ectatic basilar artery

Ehlers-Danlos syndrome

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

electromyogram

electron microscopy

electronystagmography

electroretinograph

embolism, paradoxical

embolism, septic

embolization, therapeutic

emergencies, neurologic

emergencies, ocular

emergency medical technicians

Emery-Dreifuss muscular dystrophy

encephalopathy, acute necrotizing

encephalopathy, acute necrotizing of childhood

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post traumatic

encephalopathy, progressive

endocarditis

endocarditis, acute bacterial

endocarditis, prophylaxis

endolymphatic sac tumors

endovascular therapy

enophthalmous

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

ependymoma

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

executive dysfunction

exercise

exercise intolerance

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

facioscapulohumeral syndrome

Fahr disease

failed medical management

familial hemiplegic migraine

fatal familial insomnia

fatigue

fatty acid dehydrogenase deficiency

fatty acid, elevated plasma content

fetal alcohol syndrome

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

finger nose finger test

finger tapping

fingerprint bodies

fish

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

floppy infant

flow study, carotid artery

fluctuate

fluency

flunarizine

fluorescein angiography

fluorescene in situ hybridization

fourth ventricle, enlargement of

fracture, pathologic

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fucosidosis

fundus, abnormality of

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

Gaucher's disease

Gaucher's disease, adult onset

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

Gilles de la Tourette syndrome

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

glutaric acidemia

glycine

glycogen storage disease

glycoprotein

Gorlin-Goltz syndrome

gout

Gowers maneuver

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

hallucination, visual

head injury, pediatric

headache, thunderclap

headache, unilateral

health insurance

hearing loss

hearing loss, bilateral

hearing loss, sudden, unilateral

hearing problems in children

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hemianopia

hemianopia, homonymous

hemianopia, transient

hemihypertrophy, congenital

hemiparesis

hemiparesis, transient

hemiplegia

hemochromatosis

hemochromatosis, primary

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemoptysis

hemorrhagic diathesis

hemorrhoids

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

heterotopia

hexosaminidase-A

hexosaminidase-A and B

Huntington's chorea, genetic counselling

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, presymptomatic detection of

Huntington's disease, children

Hurler's syndrome

hydrocephalus

hydrocephalus, communicating

hydrocephalus, complications with

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, exvacuo

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, treatment of

hyperglycinemia, nonketotic

hyperhidrosis

hyperhomocysteinemia

hyperostosis

hyperostosis corticalis generalisata familiaris

hyperphagia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypersensitivity reaction

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypokalemic periodic paralysis

hypopigmentation of skin

hyporeflexia

hyposmia

hypotension, neurologic causes of

hypotension, systemic

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

inappropriate behavior

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

incidental finding

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinentia pigmenti

incoordination

infant, evaluation of

infantile bilateral striatal necrosis

infantile spasm

infection

infection, recurrent

inflexibility, mental

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intraventricular hemorrhage

intrinsic hand muscles, wasting of

ischemic exercise test

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

jaundice

Jervell Lange-Neilson syndrome

Jewish

joint hypermobility

Joubert syndrome

juvenile myoclonus epilepsy

karyotyping

Kayser-Fleischer ring

Kearns-Sayre syndrome

Kugelberg-Welander syndrome

kuru

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

language disorder in adults

laughing

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

L-dopa, drug interactions with and side effects of

learning disability

learning disability, in children

Leber's congenital amaurosis

leg atrophy

leg spasms

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

lens, ectopic

lenticular nucleus, lesion of, bilateral

leukodystrophy, pigmented orthochromatic

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukopenia

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

Lhermitte-Duclos disease

libido, decreased

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

lifestyle modification

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

liver function enzymes

liver transplantation

LMNA gene

lobar atrophy

locus ceruleus, lesion of

lymphoma involving CNS

lysosomal storage disease

magnetic susceptibility

magnetoencephalography

malaise

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malignant hyperpyrexia

managed care

mania

manic-depressive

maple syrup urine disease

marche a petits pas

marihuana

Marinesco-Sjogren syndrome

masked facies

McArdle's disease

McLeod syndrome

medical-legal aspects of neurology

medulla oblongata, neoplasm of

medulloblastoma

megalencephaly

megalencephaly, idiopathic

melanomatosis, primary malignant

MELAS syndrome

memantine

memory

memory, defect of recent

memory, evaluation of

memory, impairment of

meningeal enhancement

meningioma

meningismus

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

mental retardation, etiology of

mental retardation, familial

mental retardation, family psychological problems in

mental status, abnormal

MERRF syndrome

mesial temporal lobe

mesial temporal lobe epilepsy

mesial temporal sclerosis

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylmalonic acidemia

metoprolol

metronidazole

microangiopathy, brain

microhemorrhage, intracerebral

micropolygyria

microspherophakia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mild cognitive impairment

Miller-Dieker syndrome

mimics

Minamata disease

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

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, incidental finding

MRI, negative

MRI, paramagnetic effect

MRI, punctate pattern

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, volumetry

MRS

mucopolysaccharidoses

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle phosphorylase deficiency

muscle spasm

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, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, familial incidence of

myasthenia gravis, misdiagnosis of

myelination of nervous system

myopathy, mitochondrial

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-recurrent

nerve biopsy

nerve conduction studies

nerve hypertrophy

neuritis

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neurocardiology

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic bladder

neurogenic vs.myopathic atrophy

neuroichthyosis

neuroleptic

neuroleptic, atypical

neurolipidosis IV

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

nevoid basal cell carcinoma syndrome

nevus

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

nigrostriatal pathway

obsessive-compulsive disorder

occipital lobe

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

oculodentodigital dysplasia

olanzapine

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic ataxia

optic atrophy

optic atrophy, bilateral

optic foramina

optic foramina, abnormal

optic nerve

optic nerve, hypoplasia of

optic neuropathy

optokinetic nystagmus, abnormal

organ rupture

orthopnea

orthostatic hypotension

osteopetrosis

osteoporosis

pacemaker, cardiac-transvenous

pain, increased response

pallido-ponto-nigral degeneration

pallidotomy

palmoplantar keratoderma

paralysis, acute areflexic

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paratonia

paresthesias

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, classification

Parkinson disease, dementia with

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, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, rapid progression

Parkinson disease, subtypes

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal extreme pain disorder

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathognomonic

pathology

patient information and support

pectus excavatum

Pelizaeus Merzbacher

penicillamine

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

periventricular leukomalacia

peroxisomal disease

perseveration

persistent vegetative state

phenylketonuria, adult onset

pheochromocytoma

phosphorylase b kinase deficiency

photophobia

photosensitivity, skin

physical therapy

physician assisted suicide

Pick's disease

pigmentary retinopathy

pimozide

Pittsburgh Compound B

pituitary, hormones of

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumothorax

poison, mercury

poison, neurologic problems with

POLR3B

polycystic kidneys

polycystic lipomembranous osteodysplasia

polydactyly

polyglucosan body

polyglucosan body disease

polyhydramnios

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, familial

polyps, gastrointestinal tract

Pompe's disease of glycogen storage

pons, atrophy

pontocerebellar atrophy

port wine nevus

portal caval shunt

positive sharp waves

posterior cerebral artery territory infarction

postural abnormality

potassium

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

preclinical

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary familial brain calcification

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive subcortical gliosis

propranolol

protein 14-3-3, cerebrospinal fluid

pseudohypoparathyroidism

pseudomyotonia

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

PTEN hamartoma tumor syndrome

ptosis

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pulmonary stenosis

pulvinar sign

Purkinje cell

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiculopathy

ragged-red fibers

raphe nuclei

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading problem, causes of

real-time quaking-induced conversion

rehabilitation for neurologic disorders

renal tubular acidosis

repetitive questioning

research

respirator

respiratory depression

respiratory failure

respiratory tract infection

retinal vasculopathy with cerebral leukodystrophy

retinitis pigmentosa

retinopathy

Rett's syndrome

reversible neurologic disorder

review article

RFLPs

rhabdomyolysis

rhabdomyosarcoma of heart

rippling muscle disease

risk factors

risk factors, modification

saccadic eye movements, abnormal

scoliosis, neurologic association with

second wind phenomena

seizure

seizure, cardiac arrhythmia causing

seizure, children

seizure, classification of

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, home treatment

seizure, incidence of

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, nonepileptic

seizure, paradoxical

seizure, photosensitive

seizure, prevalence of

seizure, prognosis in adults

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, repetitive

seizure, surgical treatment of

seizure, teenager

seizure, tonic-clonic

seizure, treatment of

seizure, workup of

selective serotonin reuptake inhibitors

self-mutilation

semialdehyde dehydrogenase deficiency

senile plaques

sensorineural hearing loss

sensory loss

sensory polyneuropathy

shadowing

shagreen patch

shaken infant syndrome

shaking

short stature

shoulder, pain in

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sibling

simian crease

sinemet

single photon emission computed tomography

Sjogren-Larsson syndrome

skin, biopsy

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

skull x-ray, bony defect on

sleep

sleep pathology and physiology

slit lamp examination

sloped shoulders

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

smell

Smell Identification Test

sodium channel dysfunction

sodium valproate

somatosensory evoked potentials

sore throat

Southern immunoblot test

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, soft

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord

spinal cord degeneration

spinal cord, infarction of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 17

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spinopontine atrophy, dominant

splenomegaly

spongy degeneration of brain

spontaneous remission

staphylococcus aureus

stem cell transplantation

steppage gait

stereotaxic surgery

stereotyped behavior

stereotyped behavior, drug induced

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stimulant drugs

stimulation, deep brain

stooped posture

storage disease of CNS

strabismus

streptococcal infection

streptococcus viridans

stress, emotional

striatum, lesion of

striatum, lesion of, bilateral

striopallidodentate calcifications, familial idiopathic

strokelike episodes

stuporous

Sturge-Weber syndrome

stuttering

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, prognosis

subcortical U fibers

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

suprascapular neuropathy

sural nerve

survival motor neuron gene

sweating

sweating, abnormality of

symmetric brain lesions

tapetoretinal degeneration

tau protein

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

telangiectases

telangiectases, retinal

temper tantrums

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tentorium cerebelli

term infant

testicular enlargement

thalamotomy

thalamus, focused ultrasound ablation

thalamus, atrophy of

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thyroid function tests

tomaculous neuropathy

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

toxins, nervous system

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

transverse smile

trauma

treatment of neurologic disorder

treatment, non-pharmacologic

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

trientine dihydrochloride

trinucleotide repeats

tripping

tuberin

tuberous sclerosis

tuberous sclerosis, screening for

tumor suppressor gene

umbilical-cord blood transplantation

unconsciousness

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uric acid, low

urinary catecholamines

urinary incontinence

urine test for metabolic disorders

vanishing white matter

varicose veins

vasculopathy

venous thrombosis, non-cerebral

ventricular tachycardia

ventriculostomy, endoscopic

vertebral-basilar insufficiency

vertigo

vertigo, episodic

very long chain fatty acids

vestibular function, tests of

vibratory sensation, abnormal

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, congenital

visual loss, slow

visuospatial disturbance

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

von Hippel-Lindau, screening

walking

walking frame

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Wernicke's aphasia

Wernicke's encephalopathy

West disease

wheelchair

white matter disease

white matter disease, subcortical

word-finding difficulty

workup

wound healing, poor

xeroderma pigmentosa

x-linked hydrocephalus

x-linked intellectual deficit

X-linked lissencephaly

x-linked mental retardation

zinc

Showing articles 250 to 300 of 8137 << Previous Next >>

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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
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Monomelic Amyotrophy
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Lower Cognitive Performance in Normal Older Adult Male Twins Carrying the Apolipoprotein E-E4 Allele
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Myotonic Dystrophy
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
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Cerebral Involvement in McLeod Syndrome
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Clinical Genetics in Neurological Disease
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Advances in Molecular Analysis of Fragile X Syndrome
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Familial Progressive Subcortical Gliosis
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Increased Risk of Alzheimer's Disease in Mothers of Adults with Down's Syndrome
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Familial Alzheimer's Disease
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
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The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
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Benign Familial Disease with Muscle Mounding and Rippling
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Shaken Baby Syndrome:Inflicted Cerebral Trauma
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Choroido-Cerebral Calcification Syndrome with Retardation
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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Use of Twin Cohorts for Research in Alzheimer's Disease
Neurol 43:261-267, Breitner,J.C.S.,et al, 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Infectious Prions or Cytotoxic Metabolites?
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Memory Evaluation in Alzheimer's Disease, Caregivers'Appraisals and Objective Testing
Arch Neurol 50:92-97, Koss,E.,et al, 1993

Home Ventilation for ALS Patients:Outcomes, Costs, and Patient, Family and Physician Attitudes
Neurol 43:438-443, Moss,A.H.,et al, 1993

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

Course and Outcome of Patients in Vegetative State of Nontraumatic Aetiology
JNNP 56:407-409, Sazbon,L.,et al, 1993

Questions People Ask About Stroke
Stroke 24:536-538, Hanger,H.C.&Mulley,G.P., 1993

Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
Arch Neurol 50:725-728, Randolph,C.,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

Time Until Institutionalization and Death in Patients with Dementia
Arch Neurol 50:643-650, Brodaty,H.,et al, 1993

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

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

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Familial Intracranial Aneurysms, A Review
Stroke 23:1024-1030, terBerg,H.W.M.,et al, 1992

The Bradford Community Stroke Trial:Results at Six Months
BMJ 304:1085-1089, Young,J.B.&Forster,A., 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Showing articles 250 to 300 of 8137 << Previous Next >>