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abdominal reflex, absent

abducens nerve paralysis

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, infants and children

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alcohol injection

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alternating rapid movement

Alzheimer's disease

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

angiography, spinal

ankle reflex, absent

anterior horn cell disease

aqueduct of Sylvius, stenosis

aqueductal stenosis

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

benign essential tremor

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

brachial plexus neuropathy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

burning paresthesia

calcification, intracranial

carcinoma of breast

carcinoma of pancreas

carotid angiogram

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, spine

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortex

cerebral folate deficiency syndrome

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spondylosis

chenodeoxycholic acid

chorea, causes of

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cold hands sign

color vision, impaired

concentration, impaired

congenital infection, CNS

controversies in neurology

conversion reaction

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

diplegia, spastic cerebral

disability, neurological

distal muscle atrophy

distal muscle weakness

Dravet syndrome

drug abuse, inhalation

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystonia, focal

dystonia, painful

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electron microscopy

emotional lability

encephalitis lethargica

encephalitis, viral

encephalomalacia

encephalomyelitis

endovascular therapy

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatal familial insomnia

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescent treponema antibody absorption(FTA-ABS)

folic acid deficiency

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

fundus, abnormality of

gammaglobulin therapy, intravenous

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycogen storage disease

granulomatosis with polyangiitis

granulomatous disease

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

headache, intermittent

health insurance

hearing problems in children

heel-knee-shin test

hemangioma, vertebral

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

herniated disc, cervical

high arched feet

human immunodeficiency virus type 1

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

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

Huntington's chorea

Huntington's disease, children

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypomyelination

hypotension, systemic

immunosuppression

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

iodine deficiency

Isaacs syndrome

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

jaw jerk, abnormal

lactic acidemia

laminectomy, cervical

laughing, pathologic

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

life expectancy

locked-in syndrome

lymphoma involving CNS

lymphomatoid granulomatosis

malformation, vascular

marche a petits pas

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal gliomatosis

meningitis, CSF cell count-normal

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

methylglutaconic aciduria

methylmalonic acidemia

microangiopathy, brain

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

molecular genetics

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, spinal cord

MRI, T1 weighted high signal foci

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis

myelitis, longitudinal

myeloneuropathy

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myelopathy, vacuolar

myoclonic jerks

myoclonus, epilepsy

myopathy, vacuolar

myositis, ocular

myxedema, neurologic manifestations of

Native Americans

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-treatment of

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuropathology, brain

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

night blindness

numb clumsy hands syndrome

numbness, extremity

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

optical coherence tomography

oral ulcerations

orthostatic hypotension

pain, abdominal

palatal myoclonus

palmomental response

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

paraspinal muscle

paresthesias, feet

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

Pelizaeus Merzbacher

pernicious anemia

personality change

photosensitivity, skin

physical therapy

pleocytosis of cerebrospinal fluid

poison, organophosphate

polyglucosan body

polyglucosan body disease

polymerase chain reaction

pons, lesion of

portal caval shunt

posterior column disease

postural abnormality

practice guidelines

precipitating factors

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

Raynaud's phenomenon

regional enteritis

release phenomena

remote effect of cancer on the nervous system

respiratory dyskinesias

reticulum cell sarcoma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

risk-benefit assessment

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sclerae, hyperpigmented

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, intractable

seizure, neonatal

seizure, tonic-clonic

sensorineural hearing loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

shunt procedure, ventricular

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

solitary scerlosis

somatosensory evoked potentials

spastic diplegia

spastic dysphonia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity, treatment of

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subcortical U fibers

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

teeth, abnormal

teeth, number of in infants

tendon, enlarged

thalamus, lesion of

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tonic foot response

tonsillar herniation of cerebellum

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

tremor, treatment of

trinucleotide repeats

ulcerative colitis

ulcers, fingertip

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urinary urgency

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

vitamin deficiency

walking, difficulty with

weakness, progressive

weakness, proximal

Western immunoblot test

white matter disease

wide based gait

word-finding difficulty

xanthoma, tendon

xeroderma pigmentosa

Showing articles 1450 to 1500 of 2715 << Previous Next >>

Investigations of Disorders of Balance
JNNP 59:568-578, Rudge,P.&Bronstein,A.M., 1995

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Psychogenic Parkinsonism
Arch Neurol 52:802-810, Lang,A.E.,et al, 1995

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Low Back Pain
BMJ 310:929-932, Jenner,J.R.&Barry,M., 1995

Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
Neurol 45:1309-1313, Hurst,R.W.,et al, 1995

Reversible Downbeat Nystagmus and Ataxia in Felbamate Intoxication
Neurol 45:845, Hwang,T.L.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Increased Incidence of Levodopa Therapy Following Metoclopramide Use
JAMA 274:1780-1782, Avorn,J.,et al, 1995

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Asymmetrical Skin Temperature in Ischemic Stroke
Stroke 26:1543-1547, Korpelainen,J.T.,et al, 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Neuroleptic Drug Exposure and Treatment of Parkinsonism in the Elderly:A Case-Control Study
Am J Med 99:48-54, Avorn,J.,et al, 1995

Drug Treatment of Parkinson's Disease
BMJ 310:575-579, Quinn,N., 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Low-Dose Clozapine in the Treatment of Levodopa-Induced Mental Disturbances in Parkinson's Disease
Neurol 45:432-434, Rabey,J.M.,et al, 1995

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

Exacerbation of Idiopathic Parkinson's Disease by Naproxen
BMJ 311:422, Shaunak,S.,et al, 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 1995

Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle
Ann Neurol 38:355-356, Duvoisin,R.C.&Golbe,L.I., 1995

A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation
Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995

Cigarette Smoking and Protection from Parkinson's Disease:False Association or Etiologic Clue?
Neurol 45:1041-1051, Morens,D.M.,et al, 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

Occurrence of Different Cancers in Patients with Parkinson's Disease
BMJ 310:1500-1501, Moller,H.,et al, 1995

Neuropath Evid of Graft Survival & Striatal Reinnerva after Transpl of Fetal Mesencephalic Tissue in Parkinson's Dis
NEJM 332:1118-1124, 11631995., Kordower,J.H.,et al, 1995

Bilateral Fetal Nigral Transplantation Into the Postcommissural Putamen in Parkinson's Disease
Ann Neurol 38:379-388, Freemen,T.B.,et al, 1995

Stereotactic Ventral Pallidotomy for Parkinson's Disease
Neurol 45:753-761, Dogali,M.,et al, 1995

Electroconvulsive Therapy for the Physical Signs of Parkinson's Disease Without Depressive Disorder
JNNP 58:641-642, Pridmore,S.,et al, 1995

Psychosis in Advanced Parkinson's Disease:Treatment with Ondansetron, a 5-HT3 Receptor Antagonist
Neurol 45:1305-1308, Zoldan,J.,et al, 1995

Parkinsonism Unmasked by Lovastatin
Ann Neurol 37:685-686, Muller,T.,et al, 1995

Showing articles 1450 to 1500 of 2715 << Previous Next >>