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Differential
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abdominal reflex, absent

abducens nerve paralysis

abscess, spinal cord

abulia

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

addiction, heroin-neurologic complications with

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult T-cell leukemia-lymphoma

advances in neurology

adverse drug reaction

Africa

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol

alcohol injection

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

anemia, megaloblastic

anesthesia, general

aneurysm, vertebral basilar system

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angiography, neurologic complications with

angiography, spinal

ankle reflex, absent

ankylosing spondylitis

anterior horn cell disease

anterior spinal artery

antibiotics

anticonvulsants

anticonvulsants, untoward effects of

arteriovenous malformation

asterixis, unilateral

atherosclerosis, generalized

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

bacterial infection, CNS

ballismus, bilateral

Barkhof MR criteria for MS

basal ganglia

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

Benedict's solution test

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow biopsy

bone marrow transplantation

bowel urgency

brachial plexus neuropathy

brain atrophy

brain biopsy

brain biopsy, stereotaxic

brainstem

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

breast feeding

Brown Sequard syndrome

brucellosis

brucellosis, nervous system involvement with

bruit

bruit, spinal

bulbar palsy

bulbar palsy, progressive

burning feet

burning paresthesia

CAG repeats

calcification, intracranial

camptocormia

cane

carcinoma of pancreas

cardiac transplantation

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

cataracts

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral peduncle

cerebral venous thrombosis

cerebritis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, culture of

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, vascular territory involved

cerebrovascular disease

cervical myelopathy

cervical spine

cervical spine cyst

cervical spine injury, compression

cervical spondylosis

Charcot-Marie-Tooth

chilbran skin lesions

choroid plexus, tumor of

chromosomal abnormality

chromosome 2

chromosome 6

chronic progressive external ophthalmoplegia

cirrhosis

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clonus

clonus, finger

clubfoot as related to neurologic disease

coccidioidomycosis

cognition

color vision, impaired

coma

complications

compression fracture

concentration, impaired

confusion

congenital bilateral perisylvian syndrome

congenital infection, viral

congenital malformation

congenital malformation, non CNS

conjunctivitis

consanguinity

constipation

controversies in neurology

copper deficiency

cornea, opacity of

coronary artery bypass

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cough

Coxiella burnetti

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyanide poison

cyclophosphamide

cyst

cyst, epidermoid of CNS

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

dementia, subcortical

dementia, thalamic

dementia, treatment of

demyelinating disease

dental prostheses

dentate nuclei

dentate nuclei, lesion of

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diffuse idiopathic skeletal hyperostosis

digital subtraction angiography

digiti quinti sign

digits, abnormal

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

diplopia

disability, neurological

distal muscle atrophy

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria

dysarthria-clumsy hand syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystrophic calcification

ear, abnormal

ears of the Lynx MR sign

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

ELISA

embolization, therapeutic

emergencies, neurologic

emergency room

emotional lability

encephalitis

encephalitis lethargica

encephalitis, recurrent

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, metabolic

endemic area

endovascular therapy

enzyme, defect

enzyme, muscle disease

ependymoma

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

feeding disorder

ferric chloride test

fetal alcohol syndrome

fetus

fever

fibrillations

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

flexor spasm

fluorescent treponema antibody absorption(FTA-ABS)

fluorosis

folic acid

folic acid deficiency

foot deformity

foot drop

Friedreich's ataxia

frontal lobe, pathologic signs of

gadolinium

gag reflex, depressed

gamma amino butyric acid-mimetic drug

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

glutamine

gram negative rod

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

Guillain Barre syndrome

Haiti

Hallervorden Spatz disease

hearing problems in children

heart block

heart block, complete

hemangioma

hemangioma, vertebral

hematoma, epidural-spinal

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia

hemiparesis

hemoglobin abnormality, neurologic complications of

hemophagocytosis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

herniated disc

herniated disc, cervical

herniated disc, thoracic

herpes virus

herpes virus infection

human immunodeficiency virus type 1

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

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

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, viral induced

hyperammonemic encephalopathy

hypercalcemia

hyperhidrosis

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic intracranial pachymeningitis

hyperuricemia

hypoglycorrhachia

hypoglycorrhachia, causes of

hypogonadism

hypomyelination

hypopigmentation of skin

hypothalamus, disturbance of

hypothermia

hypothermia, causes of

hypothyroidism

hypotonia

iatrogenic neurologic disorders

imbalance

immunologic disease

immunology and the nervous system

immunosuppression

immunosuppressive agents

immunotherapy

impotence

impulsivity

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon

interferon alpha

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, multiple

intrathecal antispasticity drugs

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

iron, brain

irritability

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

klippel feil syndrome

konzo

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

language disorders in children

lathyrism

laughing, pathologic

leg numbness

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leukemia

leukemia, neurologic findings assoc.with

leuko-araiosis

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

lymphocytic pneumonitis

lymphoma

lymphoma involving CNS

lymphomatoid granulomatosis

Madonna facies

Maghreb

magnetic stimulation

magnetic stimulation, brain

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, dural

malformation, vascular, treatment of

maple syrup urine disease

medulla oblongata, lesion of

Melkersson's syndrome

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningeal sarcomatosis

meninges

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, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

meningovascular syphilis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, late-infantile

methyl benzene

methylmalonic acidemia

methylmalonic aciduria

microcephaly

microdontia

micrognathia

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

midline defect in children

Mills syndrome

mimics

misdiagnosis

mitochondrial disease

molecular genetics

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, contrast enhanced

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, emergent

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, T1 weighted high signal foci

MRI, target sign

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, chronic progressive

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, etiology of

multiple sclerosis, late-onset

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple system atrophy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis

myelitis

myelitis, longitudinal

myelopathy, ascending

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, necrotizing

myelopathy, radiation induced

myelopathy, transverse

myelopathy, vacuolar

myelopathy, venous hypertensive

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 culture

nerve root enhancement

neuritis, causes of

neurocutaneous disease

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, vasculitic, systemic

neuroradiology

neuroradiology, interventional

neurosyphilis

neurotoxin

next-generation sequencing

nitrous oxide

nonverbal

numb clumsy hands syndrome

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

occupational neurologic disorders

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

odontoid process

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

opsoclonus

optic ataxia

optic atrophy

optic atrophy, hereditary

optic nerve, lesion of

organ transplantation

orthostatic hypotension

palatopharyngeal incompetence

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

peripheral blood smear, abnormal

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

phenylketonuria, adult onset

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, organophosphate

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymicrogyria

polymyositis

polyneuropathy

polyneuropathy, familial

pons, lesion of

pontine glioma

portal caval shunt

posterior column disease

posterior inferior cerebellar artery syndrome

posterior longitudinal ligament, ossification of

postural abnormality

precocious puberty

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prion disease

prisoners of war, neurologic complications in

progeria

prognosis

progressive neurologic disorder

proprioception, abnormal

proteinuria

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pure dysarthria

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

Q fever

quadriparesis

quadriparesis, progressive

quadriplegia

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

rectal sphincter tone, decreased

recurrent

regional enteritis

release phenomena

remote effect of cancer on the nervous system

renal stones

respiratory dyskinesias

respiratory failure

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

retrovirus

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rubella encephalitis, progressive

saccadic eye movements, abnormal

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure

seizure, advice to parents and teachers regarding

seizure, psychosocial aspects of

seizure, tonic-clonic

seizure, treatment of

sensorineural hearing loss

sensory level

sensory loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

single photon emission computed tomography

Sjogren-Larsson syndrome

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

snout reflex

sodium channel dysfunction

sodium valproate

solitary scerlosis

somatosensory evoked potentials

spartin

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity

spasticity, treatment of

spastin

speech disorder

speech disorder, childhood

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, extramedullary cyst of

spinal cord, herniation

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, injury, prognosis in

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, meningioma

spinal cord, neoplasm, neurofibroma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal epidural arteriovenous malformation

spinal stenosis

spinal stenosis, cervical canal

spinal xanthomatosis

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

startle reaction

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

stiff legs

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

strokelike episodes

stuttering

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

subarachnoid hemorrhage

subcortical U fibers

substantia nigra

superior cerebellar artery infarction

sural nerve

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transposition of the great vessels

trauma

treatment of neurologic disorder

trinucleotide repeats

ultrasonography, head, fetus-neonate

ultrasonography, spinal

urine test for metabolic disorders

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual loss

vitamin deficiency

Vogt-Koyanagi-Harada syndrome

walking frame

walking, difficulty with

Wallerian degeneration

war

weakness

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

Werner's syndrome

West disease

Western immunoblot test

wheelchair

white matter disease

white matter disease, periventricular

x-linked hydrocephalus

x-ray, spine

zinc

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Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
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Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Natural History of Human T-Lymphotropic Virus 1-Associated Myelopathy: A 14-Year Follow-Up Study
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Hereditary Spastic Paraplegia
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The Hereditary Spastic Paraplegias
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Post-transplantation HTLV-1 Myelopathy in Three Recipients From a Single Donor
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Dysarthria in Acute Ischemic Stroke
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Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Progressive Necrotic Myelopathy
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Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Hereditary Spastic Paraparesis: A Review of New Developments
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Clinical Correlates of Vascular Parkinsonism
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Spastic Paraparesis after Anaesthesia
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HTLV-I-Associated Myelopathy:Acute Progression and Atypical MR Findings
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Spontaneous Thoracic Spinal Cord Herniation Through an Anterior Dural Defect
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Transdural Spinal Cord Herniation:Imaging and Clinical Spectra
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MR Appearance of an Intracranial Dural Arteriovenous Fistula Leading to Cervical Myelopathy
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Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
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Neurologic Manifestations of Spinal Epidural Arteriovenous Malformations
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Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
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Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
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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

Neurological Signs and Frontal White Matter Lesions in Vascular Parkinsonism
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Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,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

MR of Childhood Metachromatic Leukodystrophy
AJNR 18:733-738, Kim,T.S.,et al, 1997

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

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
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Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
Arch Neurol 53:940-942, Kompoliti,A.,et al, 1996

Interferon-Alpha is Effective in HTLV-I-Associated Myelopathy:A Multicenter, Randomized, Double-Blind, Controlled Trial
Neurol 46:1016-1021, Izumo,S.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

The Babinski Sign:100 Years On
BMJ 313:1029-1030, Ditunno,J.F.&Bell,R., 1996

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

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

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

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

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