Neudle.com: ataxia progressive

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Differential
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abdominal distention

abdominal protrusion

abdominal reflex, absent

abdominal x-ray

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, brainstem

abscess, intracerebral

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acral sensory symptoms

acute ataxic sensory neuropathy

acyl CoA dehydrogenase deficiency

Addison's disease

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

akinesia of eyelid function

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alien hand syndrome

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

amaurosis fugax

aminoacidopathies

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

anemia, megaloblastic

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, spinal

angiotensin-converting enzyme

ankle reflex, absent

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti citrullinated antibody

anti GQ1b IgG antibody

anti Hu antibody

anti Ri antibody

anti Tr antibodies

anti Yo antibody

antiamphiphysin

anticonvulsants

anticonvulsants, selection of

antiganglioside antibodies

antineurofascin antibodies

antithyroid antibodies

antiviral agents

aorta, abdominal

aorta, abnormal

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

arm swing, reduced

arrhythmia, cardiac

arylsulfatase A

ascending paralysis

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic-dystonia syndromes

atherosclerosis, premature

atypical lymphocytes

auditory evoked brainstem potentials

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

automobile accidents

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

B 12 deficiency

B cell lymphoma

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

Behcet's syndrome

Bickerstaff's brainstem encephalitis

biologic markers

bitemporal visual field defect

bladder dysfunction

blinking, reduced

bone marrow biopsy

brachial plexus neuropathy

BRAF protooncogene

brain biopsy, negative

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar dysfunction

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calf hypertrophy

cancer, unknown origin

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of bladder

carcinoma of breast

carcinoma of cervix

carcinoma of lung

carcinoma of ovary

carcinoma of testis

carcinoma of unknown origin

carcinoma of uterus

carpal tunnel syndrome

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, dense artery sign

CAT scan, emission

CAT scan, emission, abnormal

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, adult

central hypoventilation

central nervous system, infection of

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 edema

cerebellar hemangioma

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, mechanical extraction

cerebral glucose metabolism

cerebral infarction

cerebral infarction, subcortical

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, recurrent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

cervical myelopathy

cervical spondylosis

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing movements

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

Cockayne's syndrome

coenzyme Q10 deficiency

cognition, slowed

cogwheel rigidty

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

concentration, impaired

conduction block

cone-rod dystrophy

confusional state, acute

congenital infection, CNS

congenital infection, viral

congenital myopathy

congenital paresis

congestive heart failure

conjunctival biopsy

contactin associated protein like 1 antibodies

contactin associated protein like 1 auto antibodies.(CNTN1)

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

cornea, abnormal

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crossed adductor reflex

crying, pathologic

cryopyrin-associated periodic syndrome

Cushing's syndrome

cyclic vomiting

cyst, neoplastic cerebellum

cyst, parenchymal

cystatin C mutation

deafness, bilateral

deafness, sudden

deafness, unilateral

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, transmissible

dementia, treatment of

demyelinating disease

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental disability

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis dementia

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

disability rating scale, neurological

disability, neurological

disease modifying agents

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

doll's head maneuver

dopa responsive dystonia

dopamine agonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

DPPX, antibodies, encephalitis

Dravet syndrome

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

dystonia, cervical

dystonia, focal

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electron microscopy

electronystagmography

electrophoretic pattern, CSF

electroretinograph

embolism, paradoxical

embolism, vertebral-basilar artery

emotional lability

encephalitis, amebic

encephalitis, autoimmune

encephalitis, balamuthia

encephalitis, brainstem

encephalitis, episodic

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, progressive

endovascular therapy

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

Erdheim-Chester disease

erectile dysfunction

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

extinction on double simultaneous stimulation

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye movement, disorders of

Fabry's disease

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

facioscapulohumeral syndrome

failure to thrive

family planning

FARS2 deficiency

fatal familial insomnia

fatty acid, elevated plasma content

fever, recurrent

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

food-borne infection

fourth ventricle, compression

fracture, long bone

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

glycogen storage disease

Gowers maneuver

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hallucination, auditory

hallucination, visual

hand-foot-mouth disease

Hand-Schuller-Christian disease

head circumference

headache, progressive

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing problems in children

heel-knee-shin test

hemangioblastoma

hematuria, microscopic

hemianopia, homonymous

hemidiaphragm, paralysis of

hemifacial spasm

hemimyoclonic jerks

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniation syndromes, intracranial

herpes simplex virus

herpes virus infection

herpes, genital

hiccoughs, intractable

high arched feet

highly active antiretroviral therapy

hip flexor weakness

histochemistry of muscle

HIV CSF viral escape syndrome

Hodgkin's disease

homocysteine, serum

hot cross bun sign

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 2

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

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

hummingbird sign

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hyperadrenalism

hyperalimentation

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperinsulinism

hyperintense vessel sign

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypokalemic periodic paralysis

hypometric saccades

hypomyelination

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophosphatemia

hypotension, systemic

hypothalamus, disturbance of

iatrogenic neurologic disorders

ideomotor apraxia

IgG4-related disease

imbalance, postural

immune reconstitution inflammatory syndrome

immunodeficiency

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

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

inappropriate behavior

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incontinence, fecal

inferior olivary nucleus

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrathecal medication

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

jaw jerk, abnormal

JC virus cerebellar granule cell neuronopathy

JC virus encephalopathy

juvenile paresis

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

Lafora's disease

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy, 4H

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid abnormalities

lid closure, weakness of

life expectancy

light-near dissociation, causes of

limbic encephalitis

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

liver function enzymes

locked-in syndrome

long bone lesion

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macular degeneration

malformation, CNS, congenital

malignancy screen

malignancy, occult

manganese intoxication

marche a petits pas

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, neurologic aspects and complications of

meningitis-encephalitis PCR panel

meningoencephalitis

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microangiopathy, retina

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

missing piece sign

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

mitral valve lesion

mitral valve prolapse

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy multiplex

monoparesis, focal

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, FLAIR, hyperintense vessels

MRI, flow void, blood

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lumbosacral plexus

MRI, mouse ears

MRI, optic nerve

MRI, paramagnetic effect

MRI, punctate pattern

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle spasm, face

muscle stiffness

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycobacterial infection

mycobacterium bovis

mycotic aneurysm

myelitis, longitudinal

myelitis, transverse

myeloneuropathy

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myelopathy, vacuolar

myoclonic ataxia

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myoclonus, treatment of

myoclonus-ataxia syndrome

myopathy, genetic

myopathy, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, vacuolar

myositis, ocular

myotonia dystrophica

myxedema, neurologic manifestations of

nasal septum, perforation of

Native Americans

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nephrotic syndrome

nerve conduction studies

nerve conduction studies, motor

nerve hypertrophy

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, immune

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, onion bulb

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

Niemann-Pick disease

night blindness

NMDA antagonists

node of Ranvier

nodopathy, autoimmune

numb clumsy hands syndrome

numbness, ascending

numbness, extremity

numbness, generalized

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, upbeating on upgaze

nystagmus, vertical

obsessive-compulsive disorder

occipital cortex

occipital lobe, lesion of

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculodentodigital dysplasia

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy, bilateral

optic atrophy, hereditary

optic disc edema

optic nerve, enhancement

optic neuropathy

optical coherence tomography

oral ulcerations

orthostatic hypotension

otitis, neurologic complications with

overlap syndrome

pain, abdominal

pain, neuropathic

pain, testicular

palatal myoclonus

palmomental response

paralysis, acute

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, progressive

paraparesis, spastic

paraparesis, spastic, tropical

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

parenteral alimentation

paresthesias, feet

paresthesias, generalized

paresthesias, hands

parietal lobe, lesion of

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, on-off phenomena in

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal hemiplegia

paroxysmal neurologic deficits

patent foramen ovale

pathologic reflex

Pelizaeus Merzbacher

penguin silhouette sign

Penumbra System

periarteritis nodosa

perineum, numbness of

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral nerve, lesion of

pernicious anemia

peroxisomal disease

personality change

pheochromocytoma

picking at skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

pons, infarction of

pons, lesion of

pontocerebellar atrophy

portal caval shunt

position sensation

positional head-hanging test

posterior column disease

posterior fossa

posterior fossa, lesion of

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

prion protein gene

prisoners of war, neurologic complications in

progressive ataxia and palatal tremor

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive supranuclear palsy

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

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

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudohypertrophy

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

quadriplegia, transient

quality of life

radiation hypersensitivity

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

refractive errors

Refsum's disease

regional enteritis

relapsing polychondritis

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal transplantation

renal tubular acidosis

respirations in CNS disease

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal hemangioma

retinal infarction

retinitis pigmentosa

retroperitoneal mass

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rhomboencephalopathy

riboflavin transporter deficiency

rigidity, axial

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

Schmidt syndrome

sclerae, hyperpigmented

scleroderma, neurologic involvement with

sclerosis, bone

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, intractable

seizure, laughing as manifestation

seizure, paradoxical

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, leg

sensory loss, patchy

sensory nerve action potentials

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

simultanagnosia

single photon emission computed tomography

sinuses, diseases of

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

sleep apnea, obstructive

sleep pathology and physiology

sloped shoulders

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

sodium valproate

solitary scerlosis

somatosensory evoked potentials

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, cervical

spinal cord, compression of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenium of corpus callosum

spongy degeneration of brain

square wave jerks

standing difficulty

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

stereotaxic surgery

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulant drugs

stooped posture

strokelike episodes

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

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

superior cerebellar peduncle

suprasellar lesion

survival motor neuron gene

Susac's syndrome

suspended sensory loss

sweating, abnormality of

symmetric brain lesions

synucleinopathy

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tendon, enlarged

teratoma, ovarian

testicular biopsy

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

third nerve palsy

thrombocytopenia

thrombophlebitis

tick-borne encephalitis

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

tonic foot response

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transient ischemic attack

transplacental virus infections

transverse smile

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, resting

tremor, writing

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

ulcerative colitis

ulcers, fingertip

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urinary retention

urinary sulfatidase excretion

urinary urgency

urine test for metabolic disorders

Usher's syndrome

valsalva maneuver

venous thrombosis, non-cerebral

ventricular enlargement

ventriculostomy

vestibular areflexia

vibratory sensation

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

visual loss, slow

visual symptoms

vitamin deficiency

vitamin E deficiency

vocal cord paralysis

voice, abnormality of

Von Hippel Lindau

walking, difficulty with

walking, difficulty with in dark

weakness, acute

weakness, episodic

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Wernicke's encephalopathy

Western immunoblot test

white matter disease

white matter disease, subcortical

whole body imaging

whole genome sequencing

wide based gait

winging of scapula

xanthoma, tendon

X-linked bulbospinal neuronopathy

Showing articles 2250 to 2300 of 3146 << Previous Next >>

Progressive Multifocal Leukoencephalopathy in AIDS
JAMA 264:79-82, Chaisson,R.E.&Griffin,D.E., 1990

AIDS-Assoc Progressive Multifocal Leukoencephalopathy (PML) :Comparison to Non-AIDS PML
Neurol 40:1073-1078, Aksamit,A.J.,et al, 1990

High-Intensity Basal Ganglia Lesions on T1-Weighted MR Images in Neurofibromatosis
AJR 154:369-373, Mirowitz,S.A.,et al, 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

Relative Increase of T Cells Expressing Gamma/Delta Rather than Alpha/Beta Receptor in Ataxia-Telangietasia
NEJM 322:73-76, 1241990., Carbonari,M.,et al, 1990

Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990

Ataxic Sensory Neuropathy and Dorsal Root Ganglionitis Associated with Sjogren's Syndrome
Ann Neurol 27:304-315, Griffin,J.W.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Progressive Multifocal Leukoencephalopathy-Remission with Cytarabine
J Infection 20:51-54, O'Riordan,T.,et al, 1990

Headahce and Acquired Immunodeficiency Syndrome
Neurol Clinics North America 8:947-960, Goldstein,J., 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Incomplete Unilateral Ophthalmoplegia as the Presenting Manifestation of Waldenstrom's Macroglobulinemia
Neurol 40:1801-1802, Lossos,A.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Neurological Sequelae of Cerebral Malaria in Children
Lancet 336:1039-1043, Brewster,D.R.,et al, 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
Roberts. R. G. , et al, Lancet 336:1523-1526., , 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Acute Ascending Myelopathy of the Spine
Spine 14:1084-1089, Yablon,I.G.,et al, 1989

Brain White-Matter Changes in the Elderly Prone to Falling
Arch Neurol 46:1292-1296, Masdeu,J.C.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Chronic Progressive Myelopathy Associated with HTLV-I:Oligoclonal IgG and Anti-HTLV-I IgG Antibodies in CSF & Serum
Neurol 39:1566-1572, Link,H.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Variables Predicting Surgical Outcome in Symptomatic Hydrocephalus in the Elderly
Neurol 39:1601-1604, Graff-Radford,R.N.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Progressive Multifocal Leukoencephalopathy in Patients with AIDS:Appearance on MR Images
Radiology 173:517-529, Mark,A.S.&Atlas,S.W., 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Central Nervous System Manifestations of Lyme Disease
Arch Neurol 46:790-795, Pachner,A.R.,et al, 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Randomized, Double-Blind Six-Month Trial of Prednisone in Duchenne's Muscular Dystrophy
NEJM 320:1592-1597, 1621-16231989., Mendell,J.R.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Showing articles 2250 to 2300 of 3146 << Previous Next >>