Neudle.com: Babinski sign

Differential
(Click to cross reference)

abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

abulia

aceruloplasminemia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

addiction, heroin

Addison's disease

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

agenesis of corpus callosum

aggression

agitation

Aicardi-Goutieres syndrome

alcohol intolerance

algorithm

altered states of consciousness

alternating rapid movement

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

anemia, megaloblastic

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

atherosclerosis, generalized

atherosclerosis, premature

atrioventricular block

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign in new born

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bedridden

behavior modification

behavioral disorder

Behcet's syndrome

Bell's phenomenon

Bickerstaff's brainstem encephalitis

brain biopsy, false negative

brain biopsy, stereotaxic

brainstem

brainstem, atrophy

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis

brucellosis, nervous system involvement with

Brudzinski's sign

bruxism

bulbar palsy

bulbar palsy, progressive

burning feet

burning paresthesia

CAG repeats

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

cataracts

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, vascular territory involved

cerebrovascular disease

cherry red spot-myoclonus syndrome

chilbran skin lesions

choroid plexus, tumor of

chromosomal abnormality

chromosome 2

chromosome 6

chromosome 9

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

claudication, intermittent of cauda equina

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clivus

clonus

clonus, finger

cobalamin C deficiency

comprehension, impaired

compression fracture

concentration, impaired

confusion

congenital bilateral perisylvian syndrome

congenital malformation

congenital malformation, non CNS

consanguinity

constipation

controversies in neurology

convergence, impaired

conversion reaction

copper

copper deficiency

corneomandibular reflex

coronavirus

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

COVID-19

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

critical care unit

cry, abnormal

crying, pathologic

cryptococcal meningitis

cyst, epidermoid of CNS

cystatin C mutation

cysticercosis

cytomegalic inclusion disease

D-dimer

deafness

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

denture cream

depression

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digiti quinti sign

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dizziness

dopa responsive dystonia

Dravet syndrome

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, focal

dystonia, treatment of

ear, abnormal

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

emergencies, neurologic

emergencies, neurosurgical

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis

encephalitis lethargica

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, progressive

enzyme, defect

enzyme, muscle disease

eosinophilia

ependymal

ependymoma

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Erdheim-Chester disease

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

face, numbness of

facial anomalies

facial weakness

facial weakness, bilateral

fatal familial insomnia

fetal alcohol syndrome

fever

fine motor function, impaired

finger nose finger test

folic acid deficiency

Friedreich's ataxia, late onset

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gadolinium

gag reflex, depressed

gait disorder

gait, apraxic

gait, spastic

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

girdle sensation

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

glycogen storage disease

Google

granular osmiphilic material

grasp reflex

grasping

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hematoma, epidural-spinal

hemiparesis

hemiplegia

hemiplegia, progressive

hemosiderosis of CNS, superficial

hepatomegaly

hepatosplenomegaly

herniated disc

herniated disc, cervical

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hypercalcemia

hypercapnia

hypereosinophilic syndrome(HES)

hyperhidrosis

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypoglycorrhachia, causes of

hypomyelination

hypophonia

hyporeflexia

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

intellectual deterioration

interferon alpha

internal capsule

internet

internuclear ophthalmoplegia

interobserver agreement

intrauterine

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leukemia

leukemia, neurologic findings assoc.with

leuko-araiosis

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

life expectancy

lipid storage disorder of CNS

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

manganese intoxication

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, nocardia

meningitis, paracoccidioides

meningitis, pneumococcal

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

mental retardation

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

methyl benzene

methylmalonic acid, serum

methylmalonic acidemia

middle cerebellar peduncle, lesion

mitochondrial disease

molecular genetics

Montreal cognitive assessment

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, FLAIR

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, negative

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, ring sign

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, progressive

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myelitis, post infectious

myelopathy, chronic progressive

myelopathy, tract-specific

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

nerve root hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular dysmetria

ocular flutter

ocular motility, disorders of

oculogyric crisis

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opsoclonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

orthostatic hypotension

oscillopsia

osteomyelitis

osteomyelitis, spinal

palpebromandibular synkinesia

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraplegia

paraplegia, in flexion

paraplegia, progressive

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive

PAS positive material in the brain

past pointing

pathologic reflex

patient information and support

pediatric neurology

perivascular enhancement

pernicious anemia

perseveration

Persistent postural-perceptual dizziness

pituitary stalk, lesion of

plantar reflex

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymicrogyria

polyneuropathy

polyneuropathy, familial

pons, infarction of

pons, lesion of

pontine glioma

position sensation, abnormal

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

postictal neurologic deficits

postural abnormality

precipitating factors

precocious puberty

premature infant

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prion disease

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

pupil

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pure dysarthria

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

radiation therapy, CNS treatment and complications with

respiratory dyskinesias

respiratory failure

respiratory tract infection

reversible neurologic disorder

rubella encephalitis, progressive

saccadic eye movements, abnormal

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure, tonic-clonic

selective serotonin reuptake inhibitors

senile plaques

sensory level

sensory loss

sensory loss, cutaneous

serologic testing

serotonin norepinephrine reuptake inhibitors

severe acute respiratory syndrome

single photon emission computed tomography

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

slurred speech

sneeze

snout reflex

sodium channel dysfunction

somatosensory evoked potentials

somnolence

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

stiff legs

stooped posture

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

subdural effusion

substantia nigra

suck reflex

superior cerebellar artery infarction

superior sagittal sinus thrombosis

swallowing

symmetric brain lesions

syncope

syringomyelia

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

tonic foot response

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transilumination of skull

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

vaccination, neurologic complications with

valsalva maneuver

vegetarianism

ventricular enlargement

vertigo

vertigo, episodic

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual acuity, decreased

visual evoked response

visual fields, constricted

Vogt-Koyanagi-Harada syndrome

walking frame

walking, delayed

walking, difficulty with

Wallerian degeneration

watershed infarcts

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

wheelchair

white matter disease

white matter disease, periventricular

wide based gait

workup

x-linked mental retardation

x-ray, spine

x-ray, thoracic spine

zinc

zoonoses

Showing articles 1400 to 1450 of 2385 << Previous Next >>

Patterns of Lateral Medullary Infarction, Vascular Lesion-MR Imaging Correl of 34 Cases
Stroke 29:645-652, Kim,J.S.,et al, 1998

Respiratory Management in Acute Neurologic Illness
Neurol 50:11-20, Wijdicks,E.F.M.&Borel,C.O., 1998

Assisted Suicide
Euthanasia, and the Neurologist, The Ethics and Humanities Subcom of AAN, Neurol 50:596-59898., , 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

The HCFA New Exam Document Criteria:Mini Auditing Stnds for Neurol Exam to be Used by Payors
Neurol 50:497-500, 3261998., Newer,M.R.&Sigsbee,B., 1998

Persistent MR Contrast Enhancement of Calcified Neurocysticercosis Lesions
AJNR 19:79-82, Sheth,T.N.,et al, 1998

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

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

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

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

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Diagnosis and Treatment of Alzheimer Disease and Related Disorders
JAMA 278:1363-1371, Small,G.W.,et al, 1997

Patients'Awareness of Stroke Signs, Symptoms & Risk Factors
Stroke 28:1871-1875, Kothari,R.,et al, 1997

Granulomatous Angiitis of the Nervous System
In Vasculitis & The Nervous System, Neurol Clin 15:821-83497., Younger,D.S.,et al, 1997

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

Clinical and Neuroradiographic Manifestations of Eastern Equine Encephalitis
NEJM 336:1867-1874, Deresiewicz,R.L.,et al, 1997

A Case of Acute Monocytic Ehrlichiosis with Prominent Neurologic Signs
Neurol 48:1619-1623, Grant,A.C.,et al, 1997

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

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

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

Measuring Quality of Care in Neurology
Arch Neurol 54:1329-1332, 13271997., Ringel,S.P.&Vickrey,B.G., 1997

Predictors of Intracranial Path Findings in Pts Who Seek ER Care Because of Headache
Arch Neurol 54:1506-1509, Ramirez-Lassepas,M.,et al, 1997

Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
JNNP 63:321-326, McGrath,N.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

CSF Findings in Children with Lyme Disease-Associated Facial Nerve Palsy
Arch Pediatr Adolesc Med 151:1224-1228, 11831997., Belman,A.L.,et al, 1997

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

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

Taste and Smell Losses in Normal Aging and Disease
JAMA 278:1357-1362, Schiffman,S.S., 1997

Patterns of Sensory Dysfunction in Lateral Medullary Infarction, Clinical-MRI Correlation
Neurol 49:1557-1563, Kim,J.S.,et al, 1997

Melatonin"A Clinical Perspective
Ann Neurol 42:545-553, Penev,P.D.,et al, 1997

Evaluation of Malignancy in Ring Enhancing Brain Lesions on CT by Thallium-201 SPECT
JNNP 63:569-574, Kallen,K.,et al, 1997

"Pseudoocclusion"of the Internal Carotid Artery:A Pitfall on Intracranial MRA
J Comput Assist Tomogr 21:831-833, Okamoto,K.,et al, 1997

Diagnosing Syncope
Ann Int Med 126:989-996, Linzer,M.,et al, 1997

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

Causes and Mechanisms of Cerebellar Infarction in Young Patients
Stroke 28:2400-2404, Barinagarrementeria,F.,et al, 1997

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

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

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

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

Cerebral Tuberculosis in Pts with AIDS, Report of 6 Cases & Review
Medicine 76:423-431, Lesprit,P.,et al, 1997

The Risks and Benefits of Carotid Endarterectomy in Patients with Near Occlusion of the Carotid Artery
Neurol 48:911-915, Morgenstern,L.B.,et al, 1997

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Medial Medullary Stroke:Report of Seven Patients and Review of the Literature
Neurol 48:882-890, Bassetti,C.,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

Corticobasal Degeneration:Neuropathologic and Clinical Heterogeneity
Neurol 48:959-969, Schneider,J.A.,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

Showing articles 1400 to 1450 of 2385 << Previous Next >>