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abdominal reflex, absent

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alternating rapid movement

Alzheimer's disease

amyloid plaques

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiography, spinal

ankle reflex, absent

anterior horn cell disease

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

atherosclerosis, premature

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

axonal spheroid

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

bladder dysfunction

bone marrow biopsy

brachial plexus neuropathy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

burning paresthesia

calcification, intracranial

carcinoma of pancreas

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts, congenital

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortical atrophy

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, cytology

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

choroid plexus, tumor of

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

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

cryptococcal meningitis

cyst, epidermoid of CNS

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, reversible

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

Dravet syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electron microscopy

emotional lability

encephalitis, viral

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, recurrent

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

fundus, abnormality of

gammaglobulin therapy, intravenous

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

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

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

hearing problems in children

heel-knee-shin test

hemosiderosis of CNS, superficial

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

high arched feet

Hodgkin's disease

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

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomyelination

hypotension, systemic

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

incontinence, fecal

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

lactic acidemia

laughing, pathologic

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

life expectancy

locked-in syndrome

lymphoma involving CNS

marche a petits pas

Marinesco-Sjogren syndrome

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal gliomatosis

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, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

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, contrast enhanced

MRI, diffusion weighted

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, spinal cord

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis

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 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 conduction studies

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic 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

nystagmus, rotary

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic neuropathy

optical coherence tomography

orthostatic hypotension

pain, abdominal

palatal myoclonus

palmomental response

paraparesis, familial spastic

paraparesis, familial spastic, classification

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, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Pelizaeus Merzbacher

pernicious anemia

personality change

photosensitivity, skin

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

pons, lesion of

portal caval shunt

posterior column disease

postural abnormality

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

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

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sarcoidosis, CNS

scalp tenderness

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

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

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 paraplegia, type 11

spastic paraplegia, type 7

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 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

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

subcortical U fibers

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

teeth, abnormal

teeth, number of in infants

tendon, enlarged

thalamus, lesion of

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tonsillar herniation of cerebellum

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

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

Vogt-Koyanagi-Harada syndrome

walking, difficulty with

weakness, progressive

weakness, proximal

Western immunoblot test

white matter disease

wide based gait

xanthoma, tendon

xeroderma pigmentosa

Showing articles 1150 to 1200 of 1533 << Previous Next >>

Neurologic Manifestations of Heatstroke at the Mecca Pilgrimage
Neurol 37:1004-1006, Yaqub,B.A., 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Clinicopath. Conf
Cryptococcal Meningitis & Septicemia, AIDS After Platelet Tranfusion, Case 41-1987, NEJM 317:946-953, , 1987

Delayed Cerebellar Ataxia:A New Complication of Falciparum Malaria
BMJ 294:1253-1254, Senanayake,N., 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Acute Trimethyltin Limbic-Cerebellar Syndrome
Neurol 37:945-950, Besser,R.,et al, 1987

Plasma R Binder Deficiency & Neurologic Disease
NEJM 317:1330-1332, Sigal,S.H.,et al, 1987

Myelopathy Hand
Editorial, Lancet 2:721-7221987., , 1987

Clinicopath Conf
Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Breast & Other Cancers in Families with Ataxia-Telangiectasia
NEJM 316:1289-1294, Swift,M.,et al, 1987

Cranial Magnetic Resonance Imaging in the Evaluation of Myelopathy of Undetermined Etiology
Neurol 37:840-843, Miska,R.M.,et al, 1987

The Neurologic Examination in Patients with Probable Alzheimer's Disease
Arch Neurol 44:929-932, Huff,F.J.,et al, 1987

Vitamin E Deficiency & Neurologic Disease in Adults with Cystic Fibrosis
Ann Int Med 107:51-54, Sitrin,M.D.,et al, 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Retrovirus-Associated Myelopathies
Arch Neurol 44:659-663, Roman,G.C., 1987

Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987

Familial Cases of HTLV-I-Associated Myelopathy
Ann Neurol 22:601-605, Miyai,I.,et al, 1987

Ataxic Hemiparesis with Contralateral Trigeminal Nerve Impairment Due to Pontine Hemorrhage
Stroke 18:244-245, Ambrosetto,P., 1987

Pontine Ataxic Hemiparesis Studied by a High Resolution Magnetic Resonance Imaging System
Ann Neurol 21:204-207, Nabatame,H.,et al, 1987

Urinary & Gait Disturbances as Markers for Early Multi-Infarct Dementia
Stroke 18:138-141, Kotsoris,H.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Neurologic Aspects of Boxing
Arch Neurol 44:453-459, Jordan,B.D., 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

Idiopathic Hypoparathyroidism with Extensive Brain Calcification & Persistent Neurologic Dysfunction
Neurol 37:307-309, Friedman,J.H.,et al, 1987

Clinical & Magnetic Resonance Features of Primary Intracranial Arachnoid Cysts
Ann Neurol 21:342-348, Gandy,S.E.&Heier,L.A., 1987

Long Term Exposure to Hydrogen Sulphide Producing Subacute Encephalopathy in a Child
BMJ 294:614, Gaitonde,U.B.&Sellar,R.J., 1987

Rett's Syndrome, Correlation of Electroencephalogram Characteristics with Clinical Staging
Arch Neurol 44:1053-1056, Glaze,D.G.,et al, 1987

The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
Neurol 37:910-915, Boustany,R.M.N.,et al, 1987

Ataxia After Severe Head Injury:The Pathological Substrate
Ann Neurol 22:77-79, Chester,C.S.&Reznick,B.R., 1987

Somatosensory Evoked Potentials in Lacunar Syndromes of Pure Motor & Ataxic Hemiparesis
Stroke 18:1093-1097, Kelly,M.A.,et al, 1987

Magnetic Resonance Imaging in Isolated Noncompressive Spinal Cord Syndromes
Ann Neurol 22:714-723, Miller,D.H.,et al, 1987

Tropical Spastic Paraparesis Associated with Human T Lymphotropic Virus Type I in an East African Naturalised in Sweden
BMJ 295:1380-1381, Ryberg,B.,et al, 1987

The Aetiology of Mirror Writing:A New Hypothesis
JNNP 50:1572-1578, Tashiro,K.,et al, 1987

Radiculomeningeal Vascular Malformations of the Spine:MR Imaging
Radiology 164:845-849, Nasaryk,T.J.,et al, 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Hyponatraemia as a Cause of Reversible Ataxia
et al BMJ 293:1346, Kelsey,S.M., 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Clinicopath Conf (Juvenile) Periarteritis Nodosa (Kawasaki Syndrome)
with Involvement of Subcutaneous ( & Cerebral) Arteries, Case 43-1986, NEJM 315:1143-1154, , 1986

Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986

Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
Lancet 2:1066-1067, Spencer,P.S.,et al, 1986

Chronic Idiopathic Ataxic Neuropathy
Ann Neurol 19:545-554, Dalakas,M.C., 1986

Clinicopathological Conference
Scurvy, Wernicke-Korsakoff Syndrome, Case 33-1986, NEJM 315:503-50886., , 1986

Showing articles 1150 to 1200 of 1533 << Previous Next >>