Neudle.com: primary cerebellar ataxia

Differential
(Click to cross reference)

abdominal distention

abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abortion, spontaneous

abscess, intracerebral

acanthocytosis

acetazolamide

acetylcholine

achilles tendon, enlarged

aciduria

acoustic nerve

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acromicria

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic polyneuropathy

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

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alkalosis

alkalosis, respiratory

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

AMPA receptor antibodies

amphiphysin antibodies

amphotericin B

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

aneurysm, vertebral basilar system

Angelman syndrome

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS, benign focal

angiography, posterior fossa

angiokeratoma

angiotensin-converting enzyme

anterior horn cell disease

anti GQ1b IgG antibody

anti Hu antibody

anti Ma

anti MAG antibodies

anti mGluR1 encephalitis

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticardiolipin antibodies

anticholinesterase

anticonvulsants, untoward effects of

antimetabolite

antineutrophil cytoplasmic autoantibodies

antioxidant

antithyroid antibodies

apnea, primary central

apraxia

apraxia of eye movements

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

aqueductal stenosis

areflexia

arenavirus

Arnold Chiari malformation

aspartate aminotransferase

ataxia telangiectasia

ataxia, truncal, associated with ocular oscillations

ataxic gait

ataxic hemiparesis

ataxic-dystonia syndromes

ataxin

ataxin-2

atherosclerosis, premature

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune GFAP astrocytopathy

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

ballismus, bilateral

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Bergmann's gliosis

bilirubin encephalopathy

biotin deficiency, juvenile form

biotinidase deficiency

bismuth

bitemporal visual field defect

bladder dysfunction

blindness

blindness, monocular

blood dyscrasias, neurologic findings with

bovine spongiform encephalopathy

brain biopsy, stereotaxic

brain scan

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, dysfunction, eye movement disorders with

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hematoma

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

calcification, periventricular

calcium channel dysfunction

cancer of colon

cane

CAR syndrome

carbon tetrachloride poisoning

carcinoembryonic antigen

carcinoma of pancreas

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

cataracts, congenital

cat-scratch disease

celiac disease, adult

celiac disease, childhood

central core disease

central nervous system, infection of

central pontine myelinolysis

central retinal artery occlusion

cephalosporins

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar calcification

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellar vermis

cerebellitis

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebellum, neoplasms of

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot

chest pain

chest x-ray, abnormal

chickenpox

children

chlorambucil

chloride channel dysfunction

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

collapsin response mediator protein 5 IgG

concentration, impaired

concussion

confusion

congenital infection, CNS

congenital infection, viral

congenital malformation

conjunctival biopsy

conjunctivitis

consanguinity

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conus medullaris, lesion of

conversion reaction

copper metabolism, abnormal

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical ribbon sign

cough

CPAP

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

creatinine, elevated

Creutzfeldt-Jakob disease, genetic

Crigler-Najjar disease, type I

cry, abnormal

cry, weak

cryptococcal meningitis

Cuba

cultured skin fibroblasts

Cushing's syndrome

cyst

cyst, peritumoral

cyst, benign intracranial

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cytochrome c oxidase, deficiency

degenerative diseases of CNS

dementia, differential diagnosis of

dementia, familial

dementia, frontotemporal

dementia, posttraumatic

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

dermatitis

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

diet

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, toxicity

diplopia

disability, neurological

disease modifying agents

disorientation

distal muscle atrophy

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

DPPX

DPPX, antibodies, encephalitis

drooling

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

dystonia, psychogenic

ear, pain in

eating disorder

efficacy

ejection fraction, abnormal

electrical injury of nervous system

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electrophoretic pattern, CSF

electrophoretic pattern, serum

embryogenesis

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalomyopathy

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, parainfectious

encephalopathy, progressive

enzyme, defect

eosinophilia

ependymoma

epidemiology of neurology

epinephrine

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

Erdheim-Chester disease

executive dysfunction

extraocular muscle lesion

eye movement, disorders of

eye, pain in

Fabry's disease

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

fine motor function, impaired

finger nose finger test

fluorescein angiography

fluorescene in situ hybridization

folic acid deficiency

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

fundus, abnormality of

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

glucose tolerance test, abnormal

glue sniffing

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

granular osmiphilic material

granule cell

granulomatous disease

grasp reflex

gray matter

growth hormone

growth hormone deficiency

growth retardation

Guillain Barre syndrome

gynecomastia

Hallervorden Spatz disease

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

hearing loss, bilateral

hearing problems in children

hematuria, microscopic

hemochromatosis, primary

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemorrhagic diathesis

hemosiderin

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herbs

herniated disc, thoracic

herpes simplex virus

herpes virus

herpes virus infection

herpes zoster

herpes zoster, disseminated

heterophile antibody test

hiccoughs

histiocytosis

histochemistry

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocysteine, serum

Horner's syndrome

hot cross bun sign

human immunodeficiency virus type 1

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

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

hydrocephalus, normal pressure

hydroxyglutaric aciduria

hydroxytryptophan L-5(L-5 HTP)

hyperactivity

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hypocalcemia, causes of

hypodontia

hypofibrinogenemia

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypopigmentation of skin

hypotension, systemic

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

immunization, neurologic complications with

immunocompetent

immunodeficiency

immunoelectrophoresis, serum

immunofluorescent exam of CSF cells

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

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

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

industrial neurologic disorders

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior vermian artery

intellectual deterioration

intelligence quotient

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, small

intracerebral hemorrhage, young adult

intracranial hypotension

intracranial pressure, increased

intrathecal chemotherapy

intrathecal medication

intrauterine

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kayser-Fleischer ring

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

Korsakoff's psychosis

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction, differential diagnosis of

laryngismus stridulus

lateropulsion

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

lead poisoning

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg numbness

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, toxic

leukopenia

levamisole

level of consciousness, decreased

lipid storage disorder of CNS

listeria monocytogenes

liver function enzymes

liver transplantation

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malabsorption syndrome

malaria

malformation, CNS, congenital

malignancy screen

malignancy, occult

malignant hyperpyrexia

mania

mannitol

maple syrup urine disease

marche a petits pas

Marchiafava-Bignami disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

mediastinum, mass of

medulla oblongata, neoplasm of

MELAS syndrome

memory, defect of recent

memory, impairment of

Meniere's disease

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningismus

meningitis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, cysticercosis

meningitis, echinococcal

meningitis, elderly

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metallic taste

methotrexate

methyl benzene

methylglutaconic aciduria

methylhydrazine derivatives

methylmalonic acid, serum

metronidazole

microangiopathy, brain

microangiopathy, retina

microcephaly

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

midbrain, hemorrhage

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, optic nerve

MRI, pelvis

MRI, punctate pattern

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, causes of

muscle weakness, proximal

mutism

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycophenolate

mycoplasma

mycoplasma pneumoniae

myelinolysis, extrapontine

myelitis

myelitis, autoimmune

myelitis, longitudinal

myelitis, transverse

myelomalacia

myelopathy

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy, mitochondrial

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

negative

neonatal infection, viral

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve conduction studies, sensory

neuraminidase deficiency

neuritis

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neuroaxonal leukodystrophy

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, surgery

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

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neurootology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, motor

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, monocular

nystagmus, pendular

nystagmus, periodic

nystagmus, periodic alternating

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, upbeating-in primary position of gaze

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculogyric crisis

oculomasticatory myorhythmia

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic nerve, enhancement

optic neuritis

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optical coherence tomography

optokinetic nystagmus, abnormal

oral ulcerations

orbit, tomograms of

organ transplantation

organomegaly

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteoblastic lesions, causes of

osteoporosis

otitis, neurologic complications with

ototoxicity

ovarian dysgenesis

ovarian insufficiency

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

parietal lobe, lesion of

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

parvovirus

PAS positive

PAS positive material in the brain

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

peripheral nerve, lesion of

peripheral pulse, absent

perivascular enhancement

pigmentary retinopathy

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleural effusion

pleurisy

pneumoencephalogram(PEG)

pneumonia

POEMS syndrome

POLG1 gene

poliomyelitis-like illness

POLR3B

polydactyly

polymerase chain reaction

polymyositis

polyneuritis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

pontocerebellar atrophy

Poretti-Boltshauser syndrome

positional head-hanging test

post infectious cerebellar ataxia

post transplant lymphoproliferative disease

posterior cerebral artery

posterior column disease

posterior fossa, lesion of

posterior fossa, mass of

postinfectious

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary episodic ataxia

primary intracranial hypotension

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

propranolol

proprioception, abnormal

proptosis

protein 14-3-3, cerebrospinal fluid

proteinuria

pruritus

pseudobulbar palsy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

punch-drunk syndrome

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, tonic

pure motor hemiplegia

pure sensory stroke

Purkinje cell

purkinje cell cytoplastic autoantibody

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radial pulse, unilateral decrease of

radiation hypersensitivity

radiation induced neoplasm

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

real-time quaking-induced conversion

rehabilitation for neurologic disorders

release phenomena

remission

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

renal transplantation

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

review article

RFC1 gene

rheumatoid arthritis factor(R.A.factor)

rubella encephalitis, progressive

rubella syndrome

rubella virus

Sabin-Feldman dye test

saccadic eye movements, abnormal

safety

sagging of the brain

salivation, excessive

scotomata, scintillating

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, intractable

seizure, laughing as manifestation

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

seminoma

senile plaques

sensorimotor stroke

sensorineural hearing loss

sensory loss

sensory loss, asymmetric

sensory loss, leg

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

seronegative

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

shooting pain

short stature

shrimp sign

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

somatosensory evoked potentials

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinal cord, neoplasm

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 28

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

spirochete infection

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

spontaneous remission

sports medicine, neurology of

staphylococcal protein A column therapy

stem cell transplantation

stereotaxic surgery

steroid

steroid responsive encephalopathy

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

storage disease of CNS

strabismus

stress, emotional

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

stridor

striopallidodentate calcifications, familial idiopathic

strokelike episodes

stuttering

subconjunctival hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, acute

suck, poor

suicide

superior cerebellar artery syndrome

Susac's syndrome

symmetric brain lesions

syncope

synucleinopathy

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

teeth, wide-spaced

telangiectases

temper tantrums

temporal artery, biopsy

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

tetany

tetany, latent

tetany, normocalcemic

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, protrusion of

torticollis

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

tracheostomy

transglutaminase antibodies

transient neurologic deficit

treatment of neurologic disorder

trigeminal neuropathy

trigeminal neuropathy, sensory

trimethyltin

trinucleotide repeats

trisomes

trisomy 9p

trochlear nerve

trochlear nerve palsy

urea-cycle enzymopathies

urinary gonadotropin

urinary incontinence

urinary urgency

urine test for metabolic disorders

Usher's syndrome

uveitis

varicella zoster virus

varicella zoster virus, encephalitis

vertebral artery disease

vertebral artery stenosis

vertebral-basilar insufficiency

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

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 loss, sudden-unilateral

visuospatial disturbance

vitamin deficiency

vitamin E

vitamin E deficiency

vitamin supplementation

vitiligo

vitreous opacities

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

von Bonsdorff's sign

Von Hippel Lindau

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

Wernekinck commissure syndrome

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

wheelchair

Whipple's disease

white matter disease

white matter disease, subcortical

whole genome sequencing

x-linked intellectual deficit

x-linked mental retardation

Showing articles 200 to 250 of 6039 << Previous Next >>

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

BSE Linked to New Variant of CJD in Humans
BMJ 312:795, 791, 843, 85496., , 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Antineuronal Antibodies in Acute Cerebellar Ataxia Following Epstein-Barr Virus Infection
Neurol 44:1506-1507, Ito,H.,et al, 1994

Course and Outcome of Acute Cerebellar Ataxia
Ann Neurol 35:673-679, Connolly,A.M.,et al, 1994

Showing articles 200 to 250 of 6039 << Previous Next >>