Neudle.com: dementia childhood

Differential
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abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abulia

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acrocyanosis

Addison's disease

adolescent medicine

adrenal crisis, acute

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

affect, inappropriate

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, driving with

Alzheimer's disease, visual variant

amaurosis fugax

AMPA receptor antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

ANA-negative systemic lupus erythematosus

anemia

anemia, megaloblastic

anesthesia, general

angiitis

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

ankle, swelling of

anorexia

antibiotics

antibiotics, neurologic complications with

antibodies to measles

anticardiolipin antibodies

anticoagulant, treatment

anticonvulsants, selection of

antiphospholipid antibodies

aqueduct of Sylvius, obstruction

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

bacterial infection, CNS

basal ganglia

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

bone marrow transplantation

burning feet, differential diagnosis of

burning paresthesia

cachexia

CAG repeats

calcification, intracranial

carcinoma

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

carcinoma of stomach

cardiomyopathy

carotid artery occlusion, neck

carotid artery stenosis

CAT scan, disappearing lesion on

CAT scan, emission, abnormal

CAT scan, false negative

cauda equina, enhancement

celiac disease, childhood

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

ceruloplasmin, serum

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 19

chronic progressive external ophthalmoplegia

cisterna magna

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

coma

complications

concentration, impaired

confusion

congenital infection, CNS

congenital infection, viral

conjunctival biopsy

consanguinity

contactin associated protein like 2 antibodies

corneal dystrophy

cortical blindness

cortical blindness, transient

cortical infarction

cortical infarction, small

coumarin

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy, multiple

C-reactive protein, elevated

crying

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyst, cortical parenchyma

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, cerebrovascular disease causing

dementia, childhood

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

depression

depth perception, impaired

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

dizziness

DPPX, antibodies, encephalitis

dysequilibrium syndrome

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electroencephalogram, video monitoring with

encephalitis, autoimmune

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post traumatic

encephalopathy, progressive

endemic area

enzyme, defect

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

eye movement, disorders of

Fabry's disease

facial weakness

faciobrachial dystonic seizure

familial hemiplegic migraine

fasciculation

fatigue

fatty acid, elevated plasma content

fenfluramine

fever

finger nose finger test

fingerprint bodies

fontanel, bulging

fourth ventricle, cyst

fracture, long bone

frontal lobe, pathologic signs of

fundus, abnormality of

fungal infection, CNS

gadolinium

gait disorder

gait, apraxic

gamma amino butyric acid receptor antibody

gangliosidosis GM2

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

glutamic acid decarboxylase, antibody

glycine receptor antibodies

granular atrophy, cerebral cortex

Hallervorden Spatz disease

hallucination

hallucination, visual

handwriting

head injury

head injury, pediatric

head injury, prognosis in

hearing loss, bilateral

hearing problems in children

heart block

heel-knee-shin test

helmets

helminthic infection of CNS

hemianopia

hemianopia, homonymous

hemiballismus

hemiparesis

hemiparesis, recurrent

hemiparesis, transient

hemiplegia

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

human immunodeficiency virus type 1, infants and children

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

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hyperekplexia

hyperkalemia

hyperphagia

hyperpigmentation of skin

hypotension, systemic

hypothermia

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

infant and newborn with distress, neurologic prognosis in

infant, evaluation of

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

iron, brain

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

jaundice

jaw contractures

Jewish

Kayser-Fleischer ring

Kearns-Sayre syndrome

lactic acidemia

lacunar infarction

Lafora's disease

language disorders in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

livedo reticularis

liver disease

liver transplantation

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

medical-legal aspects of neurology

melanoma, malignant

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, lymphomatous

meningitis, noninfectious

meningovascular syphilis

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

Mexican

Mexico

microangiopathy, brain

microangiopathy, retina

microcephaly

microinfarcts

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

molecular genetics

monoclonal antibodies

monoparesis

mood change

mortality

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography, false negative

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, FLAIR

MRI, high signal foci on

MRI, negative

MRI, orbit

MRI, paramagnetic effect

MRI, punctate pattern

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis, longitudinal

myelitis, transverse, recurrent

myocardial infarction

myopathy, mitochondrial

nausea and vomiting

neck pain

negative

neoplasm, intracranial, differential diagnosis of

neoplasm, metastatic

neoplasm, metastatic to eye

nerve biopsy

nerve conduction studies

neurexin-3 alpha antibodies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic examination, focal

neurologic signs

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuropathy, peripheral, treatment

neurosyphilis

newborn, evaluation of

occipital lobe, lesion of

octreotide

old age, driving and

old age, neurology of

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic neuritis

optic neuritis, bilateral

optic neuropathy

orthostatic hypotension

overlap syndrome

owl's eye sign of spinal cord

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

penicillin

pericarditis

peripheral vascular disease

peroxisomal disease

persistent vegetative state

personality change

phenylketonuria

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

POLG1 gene

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognosis

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

ptosis

ptosis, bilateral

pulmonary infiltrates

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading

reading disorder, acquired

reading problem, causes of

rectal biopsy

recurrent

release phenomena

remote effect of cancer on the nervous system

renal failure

renal transplantation

respirations in CNS disease

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal branch artery occlusion

reversible neurologic disorder

rubella encephalitis, progressive

sedimentation rate, elevated

seizure, prognosis in childhood

seizure, treatment of

sensorineural hearing loss

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

short stature

shunt procedure, ventricular

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

slow virus infection of CNS

slurred speech

small vessel disease

small vessel vasculitis

Sneddon's syndrome

snout reflex

somatosensory evoked potentials

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, slowed

spinal cord, embolism of

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 7

splenomegaly

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

status epilepticus, intractable

steatorrhea

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

symmetric brain lesions

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic lupus erythematosus

tapetoretinal degeneration

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

third nerve palsy

Three territory sign

thromboangiitis obliterans cerebri

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

transport of patient

trauma

treatment of neurologic disorder

tremor

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

tumor necrosis factor

ulcerative colitis

upgaze, paralysis of

uremia

uremic encephalopathy

uremic twitching

urinary incontinence

urine test for metabolic disorders

ventricular enlargement

vertigo

vertigo, episodic

very long chain fatty acids

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual symptoms

visuospatial disturbance

vitritis

walking, difficulty with

weakness

weight loss

Wernicke's encephalopathy

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

workup

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The Clinical Features, MRI Findings, and Outcome of Optic Neuritis in Children
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Incidence, Cause, and Short-Term Outcome of Convulsive Status Epilepticus in Childhood: Prospective Population-Based Study
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Evolution of Cerebral Arteriopathies in Childhood Arterial Ischemic Stroke
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Behavioral Effects of Memantine in Alzheimer Disease Patients Receiving Donepezil Treatment
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Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
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Interferon beta-1a Treatment in Childhood and Juvenile-Onset Multiple Sclerosis
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Iatrogenic Creutzfeldt-Jakob Disease: The Waning of an Era
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Treatment of Childhood Migraine Attacks With Oral Zomitriptan and Ibuprofen
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Sinus Venous-Type Atrial Septal Defect: A Rare Curable Cause of Recurrent Transient Neurological Deficits
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Episodic Neurologic Dysfunction with Migraine and Reversible Imaging Findings After RadiationRRH
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Reversible Dementia with Parkinsonian Features Associated with Budesonide Use
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Effects of Oxcarbazepine on Cognitive Function in Children and Adolescents with Partial Seizures
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CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
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Atypical Antipsychotics in the Elderly with Parkinson Disease and the "Black Box" Warning
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Creutzfeldt-Jakob Disease: Comparative Analysis of MR Imaging Sequences
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Mitochondrial DNA Polymerase-y and Human Disease
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Multiple Simultaneous Cerebral Infarctions in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Dopamine-Responsive Dystonia
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Embolic Stroke Due to a Left Atrial Thrombus Two Years After Placement of an Atrial Septal Defect Closure Device
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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Neurological presentation of intravascular lymphoma: report of two cases and discussion of diagnostic challenges
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Dural Sinus Thrombosis after Minor Head Injury in a Child
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Discontinuing Prophylactic Transfusions Used to Preven Stroke in Sickle Cell Disease
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Adrenoleukodystrophy
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Clinicopath Conf., MELAS Syndrome
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Patent Foramen Ovale in Young Adults with Unexplained Stroke
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Neuroblastoma -- from Genetic Profiles to Clinical Challenge
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Clinical Features and Diagnosis of Primary Central Nervous System Lymphoma
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Global Prevalence of Dementia: A Delphi Consensus Study
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Diagnosis and Management of Dementia with Lewy Bodies
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Atomoxetine Treatment in Chidlren and Adolescents with ADHD and Comorbid Tic Disorders
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Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
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Risk of Death With Atypical Antipsychotic Drug Treatment for Dementia, Meta-analysis of Randomized Placebo-Controlled Trials
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Tuberculous Meningitis in BCG Vaccinated and Unvaccinated Children
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Delayed Neurotoxicity in Primary Central Nervous System Lymphoma
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Herbal Energy Drinks, Phenylpropanoid Compounds, and Cerebral Vasculopathy
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Long-Term Hemorrhage Risk in Chidlren Versus Adults With Brain Arteriovenous Malformations
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Acute Disseminated Encephalomyelitis
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Systematic Review of Misdiagnosis of Conversion Symptoms and "Hysteria"
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Neurological and Neuromuscular Disease as a Risk Factor for Respiratory Failure in Children Hospitalized With Influenza Infection
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Early Posttraumatic Subarachnoid Hemorrhage Due to Dissecting Aneurysms in Three Children
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Lipid Lowering Agents Are Associated With a Slower Cognitive Decline in Alzheimers Disease
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Update on Primary Central Nervous System Lymphoma
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Showing articles 1250 to 1300 of 4115 << Previous Next >>