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abdominal protrusion

acetylcholine receptor antibody

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

addiction, heroin

Addison's disease

adverse drug reaction

akinesia of eyelid function

amaurosis fugax

amphiphysin antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

anoctaminopathy

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti Hu antibody

anti MAG antibodies

anti Ri antibody

anti Yo antibody

anticholinergic drugs

anticoagulant, treatment

anticoagulant, treatment in CVD

apraxia of eyelid opening

aqueduct of Sylvius, obstruction

arrhythmia, cardiac

arthrogryposis multiplex

ascending paralysis

asthma, poliomyelitis-like syndrome with

ataxia, cerebellar

ataxia, progressive

autoimmune disease

autonomic dysfunction

autonomic neuropathy

azidodeoxythymidine

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

benign essential tremor

bent spine syndrome

bitemporal visual field defect

blepharophimosis

bone marrow suppression

botulinum toxin

brachial neuritis

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, lesion of

bulging of biceps

calcification, intracranial

carcinoma of breast

carcinoma of lung

carcinoma of ovary

cardiovascular disease

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, muscle

CAT scan, serial

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cogwheel rigidty

collagen vascular disease

collapsin response mediator protein 5 IgG

compression neuropathy

congenital myopathy

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

corpus callosum, atrophy of

cortical blindness

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, cortical parenchyma

cyst, ventricular

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytomegalovirus infection

delay in diagnosis

dementia, frontotemporal

dementia, rapidly progressive

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug withdrawal

dysferlinopathy

dystonia, cervical

dystonia, drug induced

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electron microscopy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalomyelitis

encephalopathy, progressive

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

evoked potentials

exercise intolerance

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial nerve palsy

facial weakness

fatigable chewing

fetal movements, reduced

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

flaccid paralysis

foot drop, bilateral

fourth ventricle, cyst

gammaglobulin therapy, intravenous

gastroenteritis

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

hallucination, auditory

Hand-Schuller-Christian disease

headache, severe

heat intolerance

heavy metal intoxication

helminthic infection of CNS

hemianopia, homonymous

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

high arched feet

hip flexor weakness

histochemistry of muscle

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

human immunodeficiency virus type 1, pathogenesis

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hyperadrenalism

hyperamylasemia

hyperinsulinism

hyperparathyroidism

hyperthyroidism

hypoglycorrhachia

hypokalemic periodic paralysis

hypoparathyroidism

hypothalamus, disturbance of

hypotonia, infants

immunologic disease

immunology and the nervous system

immunosuppression

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion body myositis

intellectual deficit

interstitial pulmonary fibrosis

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

jaw jerk, abnormal

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

laminar necrosis, cortical

leg weakness, bilateral

leg weakness, unilateral

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

lid closure, weakness of

life expectancy

limbic encephalitis

lipid storage disorder of CNS

liver function enzymes

lymphoma involving CNS

malignancy screen

malignancy, occult

Marinesco-Sjogren syndrome

median neuropathy

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, leptospira

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

mixed connective tissue disease

molecular genetics

monoclonal gammopathy

monomelic myositis

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, drug induced

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle hypertrophy, congenital

muscle stiffness

muscle swelling

muscle swelling, focal

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myasthenic crisis

myasthenic syndrome

myelopathy, vacuolar

myoclonic jerks

myoclonus, cortical

myoclonus, stimulus sensitive

myopathy, amyloid

myopathy, autoimmune

myopathy, axial

myopathy, carcinomatous

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, focal

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, monomelic

myopathy, necrotizing

myopathy, quadriceps

myopathy, radiation-induced

myopathy, thyroid disease causing

myopathy, vacuolar

myositis, bacterial

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

myositis, ocular

myositis, parasitic

myotonia dystrophica

myxedema, neurologic manifestations of

nausea and vomiting

neoplasm, pituitary

nerve conduction studies

nerve hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronopathy, sensory

neuroophthalmology

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, short-fiber

neuropathy, toxic

Niemann-Pick disease

NMDA antagonists

ocular myopathy

ocular myopathy, differential diagnosis

old age, neurology of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

optic neuropathy

overlap syndrome

Paget's disease

pain, abdominal

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic cerebellar degeneration

paraproteinemia

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinson disease

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

personality change

pheochromocytoma

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleural effusion

poliomyelitis vaccine

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyradiculoneuropathy

pons, lesion of

position sensation, abnormal

positive sharp waves

posterior interosseous neuropathy

postural abnormality

prevention of neurologic disorders

primary aldosteronism

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychological testing

psychosis, acute

pupil, abnormality in neurologic disorders

quadriceps atrophy

quadriceps weakness

quality of life

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory failure

respiratory tract infection

rheumatoid arthritis

rickettsial organism

Schwartz-Jampel syndrome

sclerosis, bone

sedimentation rate, elevated

sensorineural hearing loss

serologic testing

shunt procedure, ventricular

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

spinal cord, lesion of

spirochete infection

standing difficulty

status epilepticus

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tensilon test, false positive

thalamus, infarction, bilateral

thalamus, lesion of

thoracic outlet syndromes

thrombocytopenia

tongue, fasciculations of

tongue, weakness

torticollis, post traumatic

toxoplasmosis, CNS

transient ischemic attack

travel, foreign

treatment of neurologic disorder

trigeminal neuralgia

Trousseau's sign

ulnar neuropathy

ultrasonography

upgaze, paralysis of

urinary retention

urine test in toxic screen

viral infection

viral infection, CNS

vision, blurred

visual evoked response

visual field defect

walking, difficulty with

weakness, acute

weakness, congenital

weakness, fatiguable

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

West Nile fever

white matter disease

wide based gait

Showing articles 1950 to 2000 of 2801 << Previous Next >>

Long-Term Cognitive Sequelae of Acyclovir-Treated Herpes Simplex Encephalitis
Arch Neurol 47:646-647, Gordon,B.,et al, 1990

MR Findings in Neonatal Herpes Simplex Encephalitis Type II
J Comput Assist Tomogr 14:453-457, Enzmann,D.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Fluctuating MR Images with Mitochondrial Encephalopathy, Lactic Acidosis, Stroke-Like Syndrome (MELAS)
Neuroradiology 32:77, Abe,K.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Mitochondrial Encephalomyopathy (MELAS) with Mental Disorder, CT, MRI and SPECT Findings
Neuroradiology 32:74-76, Suzuki,T.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Poliomyelitis Outbreak in Isreal in 1988:A Report with two Commentaries
Lancet 335:1192-1198, Slater,P.E.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Evolution of Brain MRI Abnormalities in Limbic Encephalitis
Neurol 40:1304-1306, Dirr,L.Y.,et al, 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

The Headache Profile of Idiopathic Intracranial Hypertension
Cephalgia 10:331-335, Wall,M., 1990

Challenges in the Diagnosis of Acute Headache
Headache 30 Suppl 2:537-540, Edmeads,J., 1990

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Valproate Prevents the Recurrence of Absence Status
Neurol 39:1294-1297, Berkovic,S.F.,et al, 1989

Partial Seizures with Visual Disturbance Treated by Radiotherapy of Cavernous Hemangioma
Ann Neurol 26:782-785, Lance,J.W.&Smee,R.I., 1989

Serum Prolactin During Status Epilepticus
JNNP 52:1435-1437, Tomson,T.,et al, 1989

Sciatic Nerve Damage Due to Toilet Seat Entrapment:Another Saturday Night Palsy
JNNP 52:1113-1114, Tyrrell,P.J.,et al, 1989

Trochanteric Sciatic Neuropathy
Neurol 39:1539-1541, Crisci,C.,et al, 1989

Chiari Type I Malformation in Children
J Pediatr 115:573-576, Dure,L.S.,et al, 1989

Complex Partial Status Epilepticus Associated with Cyclosporin A Therapy
JNNP 52:1068-1071, Appleton,R.E.,et al, 1989

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Seizures after Liver Transplantation:A Clinicopathologic Study
Neurol 39:1297-1301, Estol,C.J.,et al, 1989

Post-Traumatic Torticollis
Neurol 39:1642-1643, Isaac,K.&Cohen,J.A., 1989

Complex Partial Status Epilepticus Provoked by"Crack"Cocaine
Ann Neurol 26:785-786, Ogunyemi,A.O.,et al, 1989

Efficacy of MR vs CT in Epilepsy
AJR 152:347-352, Heinz,E.R.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Prolonged Intermittent Drooling & Oromotor Dyspraxia in Benign Childhood Epilepsy with Centrotemporal Spikes
Epilepsia 30:564-568, Roulet,E.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

The Spectrum of Imaging and Neuropsychological Findings in Pick's Disease
Neurol 39:362-368, Knopman,D.S.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Showing articles 1950 to 2000 of 2801 << Previous Next >>