Neudle.com: ataxia progressive

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

abscess, lung

acanthocytosis

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

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

akinetic mute

alcohol intolerance

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

ANA

anemia

anemia, megaloblastic

aneurysm

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

angiography, cerebral, false negative

angiography, cerebral, negative

angiography, spinal

angiotensin-converting enzyme

anterior horn cell disease

anterior tibial muscle weakness

anti citrullinated antibody

anti GQ1b IgG antibody

anticonvulsants, selection of

antiganglioside antibodies

antineurofascin antibodies

antithyroid antibodies

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

ataxia telangiectasia

ataxic-dystonia syndromes

ataxin

ataxin-2

atherosclerosis, premature

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

automobile accidents

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

basal cistern

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

Bassen-Kornzweig syndrome

Bickerstaff's brainstem encephalitis

biologic markers

bismuth

bitemporal visual field defect

brachial plexus neuropathy

brain biopsy, negative

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

bromocriptine

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar dysfunction

bulbar palsy

bulbar palsy, progressive

calcification, intracranial

calf hypertrophy

callosal angle

cancer, unknown origin

cane

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of unknown origin

carcinoma of uterus

cardiomyopathy

carpal tunnel syndrome

CAT scan, angiography

CAT scan, chest

CAT scan, dense artery sign

CAT scan, emission

CAT scan, emission, abnormal

catalepsy

cataplexy

cataracts

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

CD4 counts

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

cerebellitis, autoimmune

cerebellum

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

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

chairbound

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chromosomal abnormality

chromosome 11

chromosome 20

chromosome 6

chronic progressive external ophthalmoplegia

Chvostek sign

cirrhosis

climate change

Clinical Pathologic Conference(C.P.C.)

clonus

clot retrieval

Coats syndrome

cobalamin C deficiency

Cockayne's syndrome

coenzyme Q10 deficiency

collagen vascular disease

collapsin response mediator protein 5 IgG

color vision, impaired

concentration, impaired

confusional state, acute

congenital infection, CNS

congenital infection, viral

congenital myopathy

congenital paresis

congestive heart failure

contactin associated protein like 1 antibodies

contactin associated protein like 1 auto antibodies.(CNTN1)

contactin associated protein like 2 antibodies

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cough

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

cyst, neoplastic cerebellum

degenerative diseases of CNS

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

depression

dermatitis

dermatomyositis

developmental disability

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis

dialysis dementia

diaphragmatic paralysis

diarrhea

diarrhea, bloody

diet

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

disability, neurological

disease modifying agents

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze

downward gaze, paralysis of

DPPX

DPPX, antibodies, encephalitis

Dravet syndrome

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dwarfism

dysarthria

dysarthria-clumsy hand syndrome

dyssynergia cerebellaris myoclonica

dystonia

dystonia musculorum deformens

dystonia, cervical

dystonia, focal

dystrophic calcification

dystrophin

ear, red

ear, swollen

ears of the Lynx MR sign

eczema

edema, pedal

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electron microscopy

electronystagmography

electrophoretic pattern, CSF

electroretinograph

ELISA

embolism, paradoxical

embolism, vertebral-basilar artery

encephalitis, autoimmune

encephalitis, balamuthia

encephalitis, brainstem

encephalitis, episodic

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, progressive

endemic area

endovascular therapy

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

epicanthal folds

epidemic

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

episodic unconsciousness

epistaxis

Epstein-Barr virus

equinovarus

Erdheim-Chester disease

erectile dysfunction

evoked potentials

executive dysfunction

exercise intolerance

exome sequencing

exophthalmus

extinction on double simultaneous stimulation

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye movement, disorders of

eye, pain in

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

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fever

fever, recurrent

fibrillations

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fisher C.M.

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flavivirus

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

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

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

ganglionitis

gangliosides

gargoylism

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

glioma

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

gluten ataxia

gluten sensitivity

gluten-free diet

glycogen storage disease

gout

Gowers maneuver

granular osmiphilic material

granulomatous disease

grasp reflex

gray matter

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

gynecomastia

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

hand-foot-mouth disease

Hand-Schuller-Christian disease

headache, progressive

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing problems in children

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemidiaphragm, paralysis of

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniation syndromes, intracranial

herpes simplex virus

herpes virus

herpes virus infection

herpes, genital

hiccoughs

hiccoughs, intractable

high arched feet

highly active antiretroviral therapy

hip flexor weakness

hip fracture

histiocytosis

histochemistry of muscle

HIV CSF viral escape syndrome

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

huntingtin

Huntington's chorea

Huntington's disease, children

Hurler's syndrome

hydrocephalus

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hyperadrenalism

hyperalimentation

hyperammonemic encephalopathy

hyperintense vessel sign

hyperkalemia

hyperparathyroidism

hyperpigmentation of skin

hypertrophic intracranial pachymeningitis

hypokalemic periodic paralysis

hypoparathyroidism, idiopathic

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypothermia

hypothyroidism

hypotonia

iatrogenic neurologic disorders

immune reconstitution inflammatory syndrome

immunodeficiency

immunohistochemistry

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

impulsivity

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

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

inappropriate behavior

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incontinence, fecal

incoordination

infection

inferior olivary nucleus

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

intravenous

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

jaundice

jaw jerk, abnormal

JC virus

JC virus cerebellar granule cell neuronopathy

JC virus encephalopathy

Jewish

juvenile paresis

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

keratoconus

Kernig's sign

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg numbness

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

lethargy

leucine rich glioma inactivated 1 antibodies

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

Lhermitte's sign

lid

lid abnormalities

lid closure, weakness of

life expectancy

light-near dissociation, causes of

limbic encephalitis

linear lesion

lipid storage disorder of CNS

listeria monocytogenes

listeriosis, CNS

liver disease

liver function enzymes

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphopenia

lysosomal storage disease

malformation, CNS, congenital

malignancy screen

malignancy, occult

manganese intoxication

marche a petits pas

masked facies

mastoiditis

medulla oblongata, lesion of

MELAS syndrome

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

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

MERCI trial

MERRF syndrome

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metamyelocytes

methcathinone

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microangiopathy, retina

microcephaly

microdontia

micrographia

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

miglustat

migraine

mimics

Mini Mental Status Examination

misdiagnosis

missing piece sign

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

mitral valve lesion

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

motor neuron disease, misdiagnosis

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, eye of tiger sign

MRI, false negative

MRI, FLAIR

MRI, FLAIR, hyperintense vessels

MRI, flow void, blood

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lumbosacral plexus

MRI, paramagnetic effect

MRI, pelvis

MRI, punctate pattern

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

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

mutism

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

mycobacterial infection

myelitis, longitudinal

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myoclonus, stimulus sensitive

myoclonus, treatment of

myoclonus-ataxia syndrome

myopathy, mitochondrial

myxedema, neurologic manifestations of

nasal septum, perforation of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve hypertrophy

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuritis

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

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

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

nodopathy, autoimmune

nonresponsive

nonverbal

NOTCH2NLC

numb clumsy hands syndrome

numbness, ascending

numbness, extremity

numbness, generalized

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, primary position of gaze

nystagmus, upbeating on upgaze

nystagmus, vertical

obesity

obsessive-compulsive disorder

occipital cortex

occipital lobe, lesion of

ochronosis

ocular bobbing

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculocephalic reflex

oculodentodigital dysplasia

olivary degeneration, hypertrophic

onconeural antibodies

one and a half syndrome

opened mouth

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus-myoclonus syndrome

optic ataxia

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic disc edema

optic nerve

optic nerve, enhancement

optic neuritis

optic neuropathy

optical coherence tomography

oral ulcerations

organomegaly

orthopnea

orthostatic hypotension

otitis, neurologic complications with

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, progressive

paraparesis, spastic

paraparesis, spastic, tropical

paraspinal muscle weakness

parathyroid adenoma

parenteral alimentation

paresthesias

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

penguin silhouette sign

perineum, numbness of

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral nerve, lesion of

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumonia

poison, neurologic problems with

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

pons, infarction of

pons, lesion of

pontine glioma

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

potassium channel antibodies

practice guidelines

precipitating factors

preclinical

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

prion disease

prion protein gene

prisoners of war, neurologic complications in

PRKN gene

progeria

prognosis

progressive ataxia and palatal tremor

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

progressive supranuclear palsy

proprioception

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

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

proteinuria

proximal muscle atrophy

pseudoretinitis pigmentosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pupil, tonic

pure akinesia

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

quadriplegia, transient

quality of life

quinine

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

relapsing polychondritis

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

renal failure

renal stones

renal transplantation

renal tubular acidosis

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

reversible neurologic disorder

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rhinorrhea

rhomboencephalopathy

riboflavin

riboflavin transporter deficiency

rubella encephalitis, progressive

saccadic eye movements

saccadic eye movements, abnormal

safety

salivation, excessive

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure

seizure, children

seizure, intractable

seizure, laughing as manifestation

seizure, paradoxical

seizure, treatment of

self-mutilation

semialdehyde dehydrogenase deficiency

seminoma

sensorineural hearing loss

sensory level

sensory 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

short stature

short steps

shrimp sign

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

simultanagnosia

sinemet

single photon emission computed tomography

sinuses, diseases of

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, biopsy

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

slurred speech

small vessel disease

small vessel disease, cerebral

snout reflex

sodium valproate

solitary scerlosis

somatosensory evoked potentials

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

spastin

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

sphenoid sinus

Spielmeyer Vogt syndrome

spinal cord

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

splenomegaly

spondylolysis

spongy degeneration of brain

stem cell transplantation

steppage gait

stereotaxic surgery

steroid

steroid therapy, CNS treatment and complications with

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

subarachnoid hemorrhage

superior cerebellar peduncle

suprasellar lesion

survival motor neuron gene

Susac's syndrome

suspended sensory loss

sweating

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tachycardia

tandem gait, ataxic

tapetoretinal degeneration

teeth, number of in infants

telangiectases

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

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

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

urinary sulfatidase excretion

urinary urgency

urine test for metabolic disorders

venous thrombosis, non-cerebral

ventricular enlargement

vibratory sensation, abnormal

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

voice, abnormality of

Von Hippel Lindau

walking

walking frame

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

weight loss

Wernicke's encephalopathy

Western immunoblot test

wheelchair

white matter disease

white matter disease, subcortical

whole body imaging

whole genome sequencing

X-linked bulbospinal neuronopathy

Showing articles 1600 to 1650 of 3146 << Previous Next >>

The Therapeutic Dilemma of Inclusion Body Myositis
Neurol 48:567-568, Barohn,R.J., 1997

HTLV-Associated Myelopathy in a Cohort of HTLV-I and HTLV-II Infected Blood Donors
neurol 48:315-320, Murphy,E.L.,et al, 1997

High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
JNNP 62:88-91, Waragai,M.,et al, 1997

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

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Neuro-Ophthalmic Presentation of Non-Hodgkins Lymphoma
Neurol 48:784-785, Finelli,P.F.&Lesser,R.L., 1997

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

The Impact of Inpatient Rehabilitation on Progressive Multiple Sclerosis
Ann Neurol 42:236-244, Freeman,J.A.,et al, 1997

Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

Improvement of Stiff-Man Syndrome with Vigabatrin
Neurol 48:1133-1134, Prevett,M.C.,et al, 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

Progressive Multifocal Leukoencephalopathy in an HIV-Infected Child
Neuroradiology 39:142-144, Morriss,M.C.,et al, 1997

Progressivge Multifocal Leukoencephalopathy Presenting as Human Immunodeficiency Virus Type 1 (HIV) -Assoc Dementia
Neurol 49:263-265, Zunt,J.R.,et al, 1997

Immunologic Analysis of Spinal Cord-Biopsy Specimen from a Pt with HTLV-I-Associated Neurologic Disease
NEJM 336:839-845, Levin,M.C.,et al, 1997

2-5 Yr Remission of AIDS-Assoc Progressive Multifocal Leukoencephalopathy with Combined Antiretroviral Therapy
Lancet 349:850, Elliot,B.,et al, 1997

Apolipoprotein E Genotypes in Primary Progressive Aphasia
Neurol 49:51-55, Mesulam,M.M.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Presymptomatic Hypertension is a Major Feature in the Diagnosis of Progressive Supranuclear Palsy
Arch Neurol 54:1104-1108, Ghika,J.&Bogousslavsky,J., 1997

Characterizing Swallowing Abnormalities in Progressive Supranuclear Palsy
Neurol 48:1654-1662, Litvan,I.,et al, 1997

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

Generalised Motor Neuron Disease as an Unusual Manifestation of Borrelia Burgdorferi Infection
JNNP 63:257-258, Hemmer,B.,et al, 1997

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
Arch Neurol 54:888-894, Rudnik-Schoneborn,S.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
Ann Neurol 42:249-253, Mora,M.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 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

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

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

Showing articles 1600 to 1650 of 3146 << Previous Next >>