Neudle.com: atrophy cerebellar

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abdominal contractions

abdominal distention

abducens nerve paralysis

abortion, spontaneous

acetylcholine

acoustic nerve

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acquired immunodeficiency syndrome, infants and children

acromicria

ACTH, ectopic syndrome of

acute disseminated encephalomyelitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

ageusia

aggression

agitation

Aicardi-Goutieres syndrome

alcohol

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic polyneuropathy

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

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amphiphysin antibodies

amphotericin B

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic lateral sclerosis

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, posterior fossa

angiotensin-converting enzyme

aniridia

ankle edema

ankle reflex, absent

ankylosing spondylitis

anorexia

anosmia

anterior inferior cerebellar artery

anterior inferior cerebellar artery occlusion

anterior inferior cerebellar artery syndrome

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti Hu antibody

anti Ma

anti mGluR1 encephalitis

antibodies to voltage-gated calcium channels

anticholinesterase

anticoagulant, complications of

anticoagulant, restarting

anticoagulant, reversal of

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antimetabolite

antineurofascin antibodies

antithyroid antibodies

apnea, primary central

apraxia of eye movements

apraxia of eyelid opening

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

Arnold Chiari malformation

arrhythmia, cardiac

arterial dissection, aorta

arteriopathy

arteriovenous malformation

arteriovenous malformation, cerebral

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

atypical

audiogram

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski-Nageotte syndrome

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, hemorrhage

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

basilar impression

basophilic stippling of red blood cells

bilirubin encephalopathy

biologic markers

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

blood pressure

blood pressure, control

blood pressure, lowering

blue tongue virus

bone marrow biopsy

Borrelia burgdorferi infection

brain biopsy, stereotaxic

brainstem, deformity of

brainstem, glioma

brainstem, glioma, adult

brainstem, hemorrhage, primary

brainstem, hypoplasia

brainstem, infarction of

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

Brazil

breech delivery

Brown Sequard syndrome

calcification, intracranial

calcification, intracranial, rim

calcification, intraventricular

calcification, periventricular

calcitonin

calcium channel dysfunction

cane

CAR syndrome

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of pancreas

CAT scan, cerebrovascular disease

CAT scan, contrast enhanced

CAT scan, contrast enhanced, subepend.

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, indications for

cataracts, congenital

cauda equina

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus, syndrome

CD4 counts

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar edema

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar infarction, bilateral

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellar pontine angle tumor

cerebellar tonsils

cerebellar vermis

cerebellitis

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebellum, neoplasms of

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral palsy

cerebral peduncle

cerebral vasculature

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture negative

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, bilateral

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, complications with

cerebrovascular accident, mass effect with

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, surgical treatment of

cerebrovascular accident, volume

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease, infant and childhood

cerebrovascular disease, premature

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choroid plexus, abnormality of

choroid plexus, tumor of

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

climate change

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

cognition

cogwheel rigidty

collapsin response mediator protein 5 IgG

color vision, impaired

coma

complications

compression fracture

compression neuropathy

cone-rod dystrophy

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital ocular motor apraxia

congestive heart failure

conjunctival biopsy

conjunctivitis

consanguinity

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

cornea, opacity of

coronary thrombolysis

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical ribbon sign

cortical-basal ganglionic degeneration

cough

CPAP

cranial nerve palsies

cranial nerve palsies, unilateral

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

craniectomy, decompressive

craniopharyngioma

craniotomy

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyst, arachnoid, posterior fossa

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

delay in diagnosis

delayed dentition

delivery, complicated

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

difficulty going down stairs

digits, abnormal

dilantin

dilantin, factors influencing metabolism of

dilantin, serum level

dilantin, toxicity

diplopia

disability, neurological

disease modifying agents

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

DPPX

DPPX, antibodies, encephalitis

drooling

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

drug overdose

dural sinus thrombosis

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

eclampsia, postpartum

ectatic basilar artery

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electrophoretic pattern, CSF

electroretinograph

ELISA

embolism, vertebral-basilar artery

embryogenesis

emergencies, neurologic

emotional lability

encephalitis

encephalitis, amebic

encephalitis, autoimmune

encephalitis, balamuthia

encephalitis, brainstem

encephalitis, deer tick

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalocele

encephalomyelitis

encephalomyelitis, parainfectious

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, subacute bacterial

endolymphatic sac tumors

enzyme, defect

eosinophilia

ependymoma

epidemiology of neurology

episodic neurologic deficits

extraocular muscle lesion

eye movement, disorders of

eyelid opening, difficulty with

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

familial hemiplegic migraine

familial periodic ataxia

fetal alcohol syndrome

fibrinolytic agents, complications

fine motor function, impaired

finger nose finger test

fluorescein angiography

fluorescene in situ hybridization

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

fourth ventricle, compression

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal brain sagging syndrome

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

fungal infection

fungal infection, CNS

gadolinium

gait disorder

gait, spastic

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

general paresis of the insane

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

Gillespie syndrome

girdle sensation

gliadin antibodies

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

glutamate dehydrogenase deficiency

glutamic acid

glutamic acid decarboxylase, antibody

granular osmiphilic material

granule cell

granulomatous disease

grasping

gray hair

gray matter

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

hallucination

hallucination, auditory

Hand-Schuller-Christian disease

headache, progressive

headache, severe

headache, worst of life

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing loss, sudden, unilateral

hearing problems in children

hemianopia, transient

hemorrhage, intracranial, newborn

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniation syndromes, intracranial

herpes simplex virus

herpes zoster

herpes zoster, ophthalmicus

herpes zoster, oticus

highly active antiretroviral therapy

hippocampus

hippocampus, hyperintense

Hispanics

histochemistry

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Hoesch test

Horner's syndrome

Horner's syndrome, etiologies of

hot cross bun sign

human immunodeficiency virus type 1

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

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, treatment of

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperadrenalism

hyperammonemic encephalopathy

hyperbaric oxygen

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hypertensive encephalopathy

hypoglossal nerve paralysis

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism

hypogonadism, hypogonadotropic

hypokalemia

hypokalemic alkalosis

hypokalemic periodic paralysis

hypopigmentation of skin

hyporeflexia

hyposmia

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothalamus, lesion of

hypoxic encephalopathy

iatrogenic neurologic disorders

IgG4-related disease

imbalance

immediate recall

immune reconstitution inflammatory syndrome

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

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

inattention

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incoordination

infection

inferior vermian artery

influenza A virus

insect sting

intellectual deficit

intellectual deterioration

intelligence quotient

internal auditory artery

internal auditory artery, occlusion

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

interpeduncular cistern, compressed

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, incidence of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, location of

intracerebral hemorrhage, multiple

intracerebral hemorrhage, pathophysiology

intracerebral hemorrhage, progression of

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, treatment of

intracerebral hemorrhage, volume

intracranial hemorrhage

intracranial hypertension, benign

intracranial pressure monitoring

intracranial pressure, increased

intrathecal chemotherapy

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intravenous drug abuse

intraventricular hemorrhage

intraventricular hemorrhage, clot evacuation

intraventricular hemorrhage, treatment

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

jaundice

jaw pain

JC virus

JC virus cerebellar granule cell neuronopathy

JC virus encephalopathy

jittery baby

Joubert syndrome

karyotyping

Kearns-Sayre syndrome

kernicterus

Klumpke palsy

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lateral sinus thrombosis

laughing, pathologic

L-dopa

lead poisoning

Leber's congenital amaurosis

Leber's hereditary optic neuropathy

leg numbness

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

level of consciousness

level of consciousness, decreased

Lhermitte's sign

life expectancy

life support, withdrawal of

limbic encephalitis

lipid storage disorder of CNS

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphocytic meningoradiculitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

mastoid opacification

medial medullary syndrome

mediastinum, mass of

medulla oblongata

medulla oblongata, infarction of

medulla oblongata, lesion of

medulla oblongata, malformation

medulloblastoma

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningismus

meningitis

meningitis, actinomycotic

meningitis, adults

meningitis, aseptic

meningitis, aspergillus

meningitis, bacterial

meningitis, bacteriologic etiology of

meningitis, basilar

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, clinical features of

meningitis, coenurosis

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, factors influencing mortality in

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, granulomatous

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, leukemic

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neurologic aspects and complications of

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, spinal fluid smear and culture-negative

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

MERRF syndrome

MERS

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

methyl benzene

methylhydrazine derivatives

microangiopathy, brain

microangiopathy, retina

microcephaly

microglial nodules

microhemorrhage, intracerebral

microinfarcts

midbrain

midbrain, atrophy

midbrain, compression

midbrain, hemorrhage

midbrain, lesion of

midbrain, swollen

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, hemiplegic

Millard Gubler syndrome

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

molar tooth sign

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, abnormal, seizure causing

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, cortical enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, early changes in CVA

MRI, gray matter enhancement

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, indications for

MRI, lumbosacral plexus

MRI, mass effect on

MRI, negative

MRI, nodular enhancement

MRI, serial

MRI, skull bone changes

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, volumetry

MRS

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

mumps virus

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

mutism

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

myelopathy, carcinomatous

myelopathy, hepatic

myelopathy, necrotizing

myelopathy, tract-specific

myeloradiculitis

myeloschisis

myocardial infarction

myocardial infarction, acute

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myoedema

myopathy

myopathy, alcoholic

myopathy, mitochondrial

myopia

myotonia dystrophica

myxedema coma

myxedema, neurologic manifestations of

neonatal infection, viral

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial, children

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-intraventricular

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

nerve root, lumbar, lesion of

neuroaxonal degeneration

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic testing

neurological intensive care

neuromuscular junction

neuromyelitis optica (Devic's disease)

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, onion bulb

neuropathy, paraneoplastic

neuropathy, peripheral

next-generation sequencing

nodopathy, autoimmune

nonresponsive

nutritional deficiency

nystagmus

nystagmus, direction fixed

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, pendular

nystagmus, peripheral

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, spontaneous

nystagmus, upbeating on upgaze

nystagmus, vertical

obesity

obstetric neurologic injuries

occipital lobe, infarction

occipital lobe, lesion of

octreotide

ocular bobbing

ocular bobbing, atypical

ocular bobbing, monocular

ocular dysmetria

ocular flutter

ocular motility, disorders of

ocular myoclonus

ocular myorhythmia

old age, neurology of

oligophrenin 1

onconeural antibodies

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

optic atrophy, hereditary

optic atrophy, unilateral

optic neuropathy, bilateral

optic neuropathy, nutritional

optical coherence tomography

oral contraceptives

oral ulcerations

orbit, tomograms of

organ transplantation

orthostatic hypotension

oscillopsia

osteopetrosis

osteoporosis

otitis, neurologic complications with

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paratrigeminal syndrome

paresthesias

parietal lobe, lesion of

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

parvovirus

PAS positive

PAS positive material in the brain

periaqueductal lesion

pericarditis

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

perivascular enhancement

photosensitivity, skin

physostigmine

phytanic acid

pigmentary retinopathy

pituitary stalk, lesion of

pituitary, lesion of

plasmapheresis

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleurisy

pneumoencephalogram(PEG)

pneumonia

poison, mercury

poison, neurologic problems with

POLG1 gene

poliomyelitis

POLR3B

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

pontocerebellar atrophy

Poretti-Boltshauser syndrome

portal caval shunt

position sensation

positional head-hanging test

post hemorrhagic hydrocephalus

posterior cerebral artery

posterior cerebral artery territory infarction

posterior column disease

posterior fossa

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior fossa, mass of

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

postpartum

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prepontine cistern, effaced

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

proprioception

proprioception, abnormal

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, tonic

Purkinje cell

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyramidal tract, uncrossed

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

race

radiation hypersensitivity

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiculopathy

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

reading disorder, acquired

remote effect of cancer on the nervous system

renal failure

renal stones

renal transplantation

respiratory depression

respiratory failure

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

reversible splenial lesion syndrome

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

sagging of the brain

salivation, excessive

scoliosis, neurologic association with

scotoma

scotomata, scintillating

screening

season

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

seizure, prevention of

seizure, withdrawal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory nerve action potentials

serologic testing

serologic testing of cerebrospinal fluid

serum tumor markers

sheathing of retinal veins

shell fish poisoning

short stature

shunt procedure, lumboperitoneal

shunt procedure, lumboperitoneal-complications of

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, lesions in neurologic disorders

skull bone, erosion

skull x-ray

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

sphenoid sinus

spinal cord

spinal cord, compression of

spinal cord, injury of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

splenium of corpus callosum

splenium of corpus callosum, displaced

splenomegaly

spondylolysis

spongy degeneration of brain

staggering

staphylococcal protein A column therapy

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

strabismus

straight sinus

streptokinase

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stridor

stuporous

stuttering

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

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

suboccipital decompression

superior cerebellar artery infarction

superior cerebellar peduncle

superior orbital fissure syndrome

superior petrosal sinus

suprasellar lesion

Susac's syndrome

symmetric brain lesions

syncope

syndactyly

synucleinopathy

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

syringomyelia

systemic illness

systemic lupus erythematosus

teeth, number of in infants

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

thiamine

Thies's sign

third nerve palsy

third ventricle, wall

thyroiditis

thyrotoxicosis

tick bite

tick-borne encephalitis

tinnitus

tissue plasminogen activator, intravenous

titubation

toe walking

tongue, hemiatrophy of

tongue, protrusion of

tonsillar herniation of cerebellum

tonsillectomy

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

trazodone

treatment of neurologic disorder

trinucleotide repeats

trochlear nerve palsy

upward deviation of eyes

upward transtentorial herniation

urea-cycle enzymopathies

urinary gonadotropin

urinary incontinence

urinary urgency

urine test for metabolic disorders

uveitis

vasculitides

vasculopathy

Venereal Disease Research Laboratory test

ventriculitis

ventriculostomy

ventriculostomy, endoscopic

vertebral artery occlusion

vertebral-basilar insufficiency

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

viral infection

viral infection, CNS

viral infection, CNS, treatment of

viral isolation

Virchow-Robin spaces, dilated

virus, slow

vision, failure of in childhood

visual acuity, decreased

visual cortex

visual evoked response

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Von Hippel Lindau

voriconazole

Walker-Warburg syndrome

walking frame

walking, delayed

walking, difficulty with

walking, difficulty with in dark

Wallerian degeneration

watershed infarcts

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Weber's syndrome

weight loss

Wernicke's encephalopathy

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

whole genome sequencing

X-linked bulbospinal neuronopathy

x-linked mental retardation

Zika virus infection

Showing articles 300 to 350 of 3367 << Previous Next >>

Intracranial Hemorrhage in the Term Newborn
Arch Neurol 41:30-34, Fenichel,G.M.,et al, 1984

Autonomic Dysfunction & Sleep Apnea in Olivoponto Cerebellar Degeneration
Arch Neurol 41:926-931, Chokroverty,S.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Multifocal Central Nervous System Damage Caused by Toluene Abuse
Neurol 33:1337-1340, Lazar,R.B.,et al, 1983

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Neuro-Ophthalmologic Signs in the Angiitic Form of Neurosarcoidosis
Neurol 33:1130-1135, Caplan,L.,et al, 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Unilateral Cerebellar Hypoplasia
J Comput Assist Tomogr 7:1077-1078, Mendelsohn,D.B.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Downbeating Nystagmus
Arch Neurol 40:777-784, Halmagyi,G.M.,et al, 1983

Cerebellar Atrophy in Epilepsy & Headache:Lack of Relationship to Phenytoin
Neurol 32:910-912, Ballenger,C.E.,et al, 1982

Cerebellar Strokes:Mortality, Surgical Indications, & Results Of Ventricular Drainage
Lancet 2:429-432, Shenkin,H.A.,et al, 1982

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Cerebellar Degeneration With Hodgkin's Disease
Arch Neurol 38:253-256, Brazis,P.W.,et al, 1981

Computed Tomography in Ataxia-Telangiectasia
J Comput Assist Tomogr 5:660-661, Assencio-Ferreira,V.J.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Remission of Cerebellar Dysfunction After Pneumonectomy For Bronchogenic Carcinoma
NEJM 302:156, Paone,J.F.,et al, 1980

Cerebellar Degeneration Due to Chronic Phenytoin Therapy
Ann Neurol 7:18-23, McLain,L.W.,et al, 1980

Cerebellar Softening
Ann Neurol 8:133-140, Scotti,G.,et al, 1980

Alcoholic Downbeat Nystagmus
Ann Ophthalmol 1127-1131, October 1980., Costin,J.A.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Acute Hydrocephalus in Cerebellar Infarct & Hemorrhage
Neurol 29:409-413, Greenberg,J.,et al, 1979

Optic Neuropathy & Ophthalmoplegia in Herpes Zoster Oticus
Neurol 29:726-729, Carroll,W.M.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
Arch Neurol 35:143, Gilroy,J.,et al, 1978

Cranial Computerized Tomography & Marie's Ataxia
Arch Neurol 35:55, Aita,J.F., 1978

Intracranial Arteriovenous Malformations in Childhood
Ann Neurol 3:338, Kelly,J.J.,et al, 1978

Phenytoin-related Cerebellar Degeneration Without Seizures
II, et al, Ann Neurol 2:437977., Rapport,R.L., 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Downbeating Nystagmus & Hereditary Cerebellar Degeneration, Levin DB, et al, In Neuro-ophthalmology Update
Masson Publishing USA, INC. 1977 P 337-338., Smith,J.L., 1977

Showing articles 300 to 350 of 3367 << Previous Next >>