Neudle.com: heredito degenerative diseases

Differential
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abiotrophy

abortion, spontaneous

acanthocytosis

acute disseminated encephalomyelitis

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, prognosis of

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

ammonia

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

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

anatomy of

angiitis, isolated of CNS

aphasia, progressive, primary

apnea

apnea, primary central

apraxia of eye movements

areflexia

arm swing, reduced

arthrogryposis multiplex

aspartocyclase

aspiration

ataxia

ataxia telangiectasia

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

blood dyscrasias, neurologic findings with

bone marrow biopsy

bovine spongiform encephalopathy

brain transplantation

brainstem, atrophy

brainstem, neoplasms of

bruxism

bulbar palsy

bulbar palsy, childhood

bulbar palsy, progressive

cafe au lait spots

CAG repeats

calcification, intracranial

Canavan's disease

cane

carbon monoxide poisoning

CAT scan, emission, abnormal

cataplexy

cataracts

cataracts, congenital

caudate nucleus, atrophy

celiac disease, adult

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, bilateral

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

children

choline acetyltransferase

chorea

chorea, familial

choreoathetosis

chromosomal abnormality

chromosome 14

chromosome 20

chromosome 5

chronic traumatic encephalopathy

claustrophobia

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel rigidty

Collier's sign

color vision, impaired

compulsivity

confusion

congenital birth defects

congenital malformation

congenital malformation, non CNS

consanguinity

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost

CPAP

crying, pathologic

cultured skin fibroblasts

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, cerebrovascular disease causing

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, screening for

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diet

differential diagnosis

diplopia

dopamine

dopamine agonist

dopaminergic dysfunction

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

emotional lability

employment

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, post traumatic

enkephalins

enzyme activity

enzyme, defect

epidemiology of neurology

executive dysfunction

exercise intolerance

eye movement, disorders of

familial periodic ataxia

fasciculation

Fazio-Londe's disease

feeding disorder

fetal tissue

fibrillations

fine motor function, impaired

football neurologic injuries

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

free radical

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glabellar sign

gliadin antibodies

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid

glutamic acid decarboxylase

glutaric acidemia

gluten sensitivity

gluten-free diet

glycogen storage disease

granular osmiphilic material

grasp reflex

growth hormone

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head injury, repetitive

heavy metal intoxication

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

highly active antiretroviral therapy

human immunodeficiency virus type 1

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

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

hypotension, systemic

hypothermia

hypotonia

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

insular cortex, lesion

intellectual deficit

intellectual deterioration

internet

intrathecal medication

intrinsic hand muscles, wasting of

inverse association

iron, brain

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kugelberg-Welander syndrome

kuru

lactic acidemia

language disorder in adults

laughing

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

learning disability, in children

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

Lesch-Nyhan syndrome

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic system

limbic-predominant age-related TDP-43 encephalopathy

liver disease

lobar atrophy

locus ceruleus, lesion of

logopenia

loss of sympathy

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

magnetic susceptibility

maple syrup urine disease

Marinesco-Sjogren syndrome

masked facies

memory, defect of recent

memory, impairment of

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mimics

minocycline

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, field strength

MRI, field strength, high

MRI, FLAIR

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, serial

MRI, spinal cord

MRI, spine

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle wasting, diffuse

muscular dystrophy

mutism

myasthenia gravis

myelination of nervous system

myoclonus, orthostatic

myopathy

myopathy, mitochondrial

myotonia dystrophica

N-acetyl-L-aspartic acid

Native Americans

negative

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuronal cell death

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal loss

neuronal migration disorder

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuroprotective agents

neurotoxic

neurotoxin

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

NMDA antagonists

NMDA receptors

nucleus basalis of Meynert

nystagmus

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

optic atrophy

optic atrophy, hereditary

orthostatic hypotension

osmotic demyelination syndrome

oxidative phosphorylation

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, familial

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

pathologic reflex

patient information and support

penguin silhouette sign

peptides, brain

perseveration

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

phakomatoses

phobias

physician assisted suicide

Pick bodies

Pick's disease

pigmentary retinopathy

pneumonia

poison, mercury

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

pontocerebellar atrophy

posterior column disease

posterior cortical atrophy

prevention of neurologic disorders

primary lateral sclerosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false positive

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

seizure, drug resistance

seizure, laughing as manifestation

semantic dementia

senile plaques

sensorineural hearing loss

sequencing difficulty

short stature

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

SMN1 gene

soccer

sodium-glucoe cotransporter-2 inhibitors

speech disorder, childhood

speech, loss of

spinal cord

spinal cord degeneration

spinal cord, infarction of

spinal cord, injury of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

startle myoclonus

status epilepticus

stem cell transplantation

stillbirth

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stridor

stuttering

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

survival motor neuron gene

symmetric brain lesions

temporal lobe, atrophy

tetracycline

thalamus, lesion of

thalamus, lesion of-bilateral

treatment of neurologic disorder

trinucleotide repeats

ventricular enlargement

vestibular function, tests of

visual acuity, decreased

visual evoked response

visual fields, constricted

visual impairment

visual loss

visual symptoms

visuospatial disturbance

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

web sites

weight loss

Werdnig-Hoffman disease

West disease

West Nile fever

Western immunoblot test

word-finding difficulty

workup

writing

X-linked bulbospinal neuronopathy

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