Neudle.com: cerebellar atrophy primary

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal contractions

abdominal distention

abducens nerve paralysis

abortion, spontaneous

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

ACTH, ectopic syndrome of

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

agenesis of aqueduct of Sylvius

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic amblyopia

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

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

alkylating agents

alpha-fetoprotein

alpha-synuclein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

aminoacidopathies

amphiphysin antibodies

amyloid plaques

amyotrophic lateral sclerosis

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

Angelman syndrome

angiitis, granulomatous of CNS

angiography, cerebral

angiotensin-converting enzyme

ankle reflex, absent

ankylosing spondylitis

anterior inferior cerebellar artery

anterior inferior cerebellar artery occlusion

anterior inferior cerebellar artery syndrome

anti Hu antibody

anti mGluR1 encephalitis

anti Ri antibody

anti Tr antibodies

anti Yo antibody

antibodies to voltage-gated calcium channels

anticholinesterase

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

apnea, primary central

apraxia of eye movements

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

aqueductal stenosis

Arnold Chiari malformation

arterial dissection, aorta

ataxia telangiectasia

ataxia, cerebellar

ataxia, congenital

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

auditory evoked brainstem potentials

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

autosomal dominant leukodystrophy

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavior, combative

behavioral disorder

Behcet's syndrome

Bergmann's gliosis

bilirubin encephalopathy

biologic markers

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

bladder dysfunction

blood dyscrasias, neurologic findings with

blue tongue virus

bone marrow biopsy

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, glioma

brainstem, glioma, adult

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown Sequard syndrome

Brueghel's syndrome

calcification, intracranial

calcification, intraventricular

calcification, periventricular

calcium channel dysfunction

carcinoembryonic antigen

carcinoma of breast

carcinoma of lung

carcinoma of ovary

carcinoma of pancreas

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, indications for

CAT scan, pelvis

cataracts, congenital

cauda equina, enhancement

cavernous sinus, syndrome

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemangioma

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellar lesion

cerebellar pontine angle tumor

cerebellar tonsils

cerebellar vermis

cerebellitis, autoimmune

cerebellum, disease of

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral folate deficiency syndrome

cerebral vasculature

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, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure low

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, prevention of

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease, infant and childhood

Chamberlane's line

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chorea, familial

chorea, Sydenham's

choreoathetosis

chorioretinitis

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coccidioidomycosis

Cockayne's syndrome

coenzyme Q10 deficiency

cogwheel rigidty

collapsin response mediator protein 5 IgG

compression neuropathy

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital ocular motor apraxia

conjunctival biopsy

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, epidermoid of CNS

cyst, parenchymal

cyst, porencephalic

cyst, subcortical

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, reversible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis herpetiformis

dermatoglyphics

dermatomyositis

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

digits, abnormal

dilantin, factors influencing metabolism of

dilantin, serum level

dilantin, toxicity

disease modifying agents

disseminated intravascular coagulation(DIC)

distal muscle atrophy

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

DPPX, antibodies, encephalitis

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dyssynergia cerebellaris myoclonica

dystonia musculorum deformens

eating disorder

ectatic basilar artery

electrical injury of nervous system

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

endocarditis, subacute bacterial

epidemiology of neurology

episodic neurologic deficits

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

failure to thrive

familial hemiplegic migraine

familial periodic ataxia

feeding disorder

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fingerprint bodies

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

Friedreich's ataxia

Friedreich's ataxia, late onset

frontotemporal brain sagging syndrome

frontotemporal dementia, behavioral variant

fundus, abnormality of

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

Gillespie syndrome

gliadin antibodies

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

hallucination, auditory

Hand-Schuller-Christian disease

hearing loss, bilateral

hearing loss, sudden, unilateral

hearing problems in children

heel-knee-shin test

hemianopia, transient

hemifacial atrophy

hemifacial spasm

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes simplex virus

heterochromia iridis

highly active antiretroviral therapy

histochemistry of muscle

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

Horner's syndrome, etiologies of

hot cross bun sign

human immunodeficiency virus type 1

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

hydranencephally

hydrocephalus, congenital

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism, hypogonadotropic

hypokalemic alkalosis

hypokalemic periodic paralysis

hypometric saccades

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypothalamus, damage to

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

immune reconstitution inflammatory syndrome

immunocompetent

immunodeficiency

immunologic disease

immunology and the nervous system

immunosuppression

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inferior vermian artery

influenza A virus

intellectual deficit

intellectual deterioration

internal auditory artery

internal auditory artery, occlusion

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

interpeduncular cistern, compressed

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, multiple

intracranial pressure, increased

intrathecal chemotherapy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

islet cell tumor

Jackson's syndrome

Jakob-Creutzfeldt disease

Joubert syndrome

Kearns-Sayre syndrome

Korsakoff's psychosis

labyrinthitis, acute

lactic acidemia

laughing, pathologic

Leber's congenital amaurosis

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukodystrophy, 4H

leukoencephalopathy

level of consciousness, decreased

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lymphadenopathy

lymphadenopathy, hilar

lymphocytic choriomeningitis

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macular degeneration

malabsorption syndrome

malformation, CNS, congenital

malignancy screen

malignancy, occult

marche a petits pas

Marchiafava-Bignami disease

Marinesco-Sjogren syndrome

mediastinum, mass of

medulloblastoma

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, leukemic

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

methylhydrazine derivatives

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, hemorrhage

midbrain, swollen

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

Millard Gubler syndrome

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molar tooth sign

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

mononeuritis multiplex

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, indications for

MRI, spinal cord

multiple sclerosis

multiple system atrophy

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelopathy, carcinomatous

myelopathy, necrotizing

myoclonic ataxia

myoclonic jerks

myoclonus, abdominal

myoclonus, cortical

myoclonus, epilepsy

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus-ataxia syndrome

myopathy, alcoholic

myopathy, mitochondrial

myxedema, neurologic manifestations of

Native Americans

nausea and vomiting

neonatal infection, viral

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial, children

neoplasm, metastatic to CNS-treatment of

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-intraventricular

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nephrotic syndrome

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal dystrophy, juvenile

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular junction

neuromyelitis optica (Devic's disease)

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, motor

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

neurotoxicity, acute

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

NMDA antagonists

nutritional deficiency

nystagmus, direction fixed

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, pendular

nystagmus, peripheral

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, spontaneous

nystagmus, upbeating on upgaze

nystagmus, vertical

occipital lobe, infarction

occipital lobe, lesion of

ocular bobbing, atypical

ocular bobbing, monocular

ocular dysmetria

ocular motility, disorders of

ocular myoclonus

ocular myorhythmia

old age, neurology of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic disc edema

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, nutritional

optical coherence tomography

oral ulcerations

orbit, tomograms of

orthostatic hypotension

otitis, neurologic complications with

ovarian dysgenesis

Paget's disease

pain, abdominal

palatal myoclonus

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parathyroid adenoma

paratrigeminal syndrome

parietal lobe, lesion of

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

parotid gland neoplasm

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

PAS positive material in the brain

peripheral nerve, lesion of

peroxisomal disease

Perrault syndrome

personality change

pheochromocytoma

photosensitivity, skin

pigmentary retinopathy

pituitary, lesion of

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

pons, flattened

pons, infarction of

pons, lesion of

pontocerebellar atrophy

Poretti-Boltshauser syndrome

positional head-hanging test

posterior cerebral artery

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior fossa, mass of

posterior inferior cerebellar artery occlusion

posterior inferior cerebellar artery syndrome

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

premature infant

prenatal diagnosis by amniocentesis

prepontine cistern, effaced

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

primary intracranial hypotension

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive pallidum atrophy

proprioception, abnormal

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, bilateral

puberty, delayed

pulmonary edema

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

radiation hypersensitivity

radiation necrosis

radiation therapy, CNS treatment and complications with

ragged-red fibers

Ramsay Hunt syndrome

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

reflex, brainstem

remote effect of cancer on the nervous system

respiratory depression

respiratory failure

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal detachment

retinal dysplasia

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sagging of the brain

salivation, excessive

sarcoidosis, CNS

scalp tenderness

scotomata, scintillating

sedimentation rate, elevated

seizure, children

seizure, neonatal

seizure, withdrawal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss, leg

serologic testing

serologic testing of cerebrospinal fluid

serum tumor markers

sheathing of retinal veins

shunt procedure, ventricular

shunt procedure, ventriculo-atrial

Shy-Drager syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

skull x-ray, abnormal

slow virus infection of CNS

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, injury of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 5

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

splenium of corpus callosum

splenium of corpus callosum, displaced

spongy degeneration of brain

staphylococcal protein A column therapy

startle myoclonus

status epilepticus

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

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

subarachnoid hemorrhage

subdural hematoma

subthalamic nucleus

superior cerebellar peduncle

Susac's syndrome

synucleinopathy

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

teeth, wide-spaced

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratogenesis, viral

teratoma, ovarian

testicular germinoma

testicular teratoma

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, protrusion of

tonsillar herniation of cerebellum

toxoplasmosis, acquired

toxoplasmosis, CNS

transglutaminase antibodies

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, writing

trigeminal neuralgia

trinucleotide repeats

trochlear nerve

trochlear nerve palsy

Trousseau's sign

upgaze, paralysis of

urea-cycle enzymopathies

urinary gonadotropin

urinary incontinence

urinary urgency

urine test for metabolic disorders

vertebral-basilar insufficiency

vertigo, positional

vestibular areflexia

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral infection, CNS, treatment of

viral isolation

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss, progressive

visual loss, slow

vitamin E deficiency

vitreous opacities

vocal cord paralysis

Vogt-Koyanagi-Harada syndrome

voice, abnormality of

Walker-Warburg syndrome

walking, difficulty with

walking, difficulty with in dark

Wallerian degeneration

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Weber's syndrome

Wernicke's encephalopathy

Western immunoblot test

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

whole genome sequencing

wide based gait

Wolfram syndrome

x-linked mental retardation

Zika virus infection

Showing articles 550 to 600 of 7385 << Previous Next >>

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Absent Pachymeningeal Gadolinium Enhancement on Cranial MRI Despite Symptomatic CSF Leak
Neurol 53:402-404, Mokri,B.,et al, 1999

Hypoxic/Ischaemic Brain Damages, Especially Pallidal Lesions, in Heroin Addicts
Forensic Sci Int 102:51-59, Andersen,S.N. &Skullerud,K., 1999

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Predicting Neurologic Deterioration in Patients with Cerebellar Hematomas
Neurol 511:1364-1369, St. Louis,E.K.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Amyloid Neuropathy Simulating Lower Motor Neuron Disease
Neurol 51:600-602, Quattrini,A.,et al, 1998

Temporal Lobe Epilepsy in Childhood:Clin, EEG, & Neuroimag Findings & Synd Class in a Cohort with New-Onset Szres
Neurol 49:960-968, Harvey,A.S.,et al, 1998

Cerebellum in Attention-Deficit Hyperactivity Disorder
Neurol 50:1087-1093, Berquin,P.C.,et al, 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Thrombolysis-Related Intracranial Hemorrhage, Analysis of 224 Cases from GUSTO-1 Trial with Clin Correl
Stroke 29:563-569, Gebel,J.M.,et al, 1998

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

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

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

Preliminary Results of Linear Accelerator Radiosurgery for Acoustic Schwannomas
J Neurosurg 85:1013-1019, Mendenhall,W.M.,et al, 1997

The Variable MR Appearance of Primary Lymphoma of the Central Nervous System:Comparison with Histopathologic Features
AJNR 18:563-572, Johnson,B.A.,et al, 1997

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

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 1997

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

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

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

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

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

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

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

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

MR Imaging of the Meninges, Part II, Neoplastic Disease
Radiology 201:605-612, Fukui,M.B.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

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

Clinicopath Conf
Noncaseating Granulomas Consistent with Sarcoidosis, Case 37-1996, NEJM 335:1668-1674996., , 1996

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Twelfth-Nerve Palsy:Analysis of 100 Cases
Arch Neurol 53:561-566, Keane,J.R., 1996

Showing articles 550 to 600 of 7385 << Previous Next >>