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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 1650 to 1700 of 2801 << Previous Next >>

The Use of Albendazole in Patients with Single Lesions Enhanced on Contrast CT
NEJM 328:356-357, DelBrutto,O.H., 1993

Spasmodic Torticollis Occurring During Alcohol Withdrawal
Neurol 43:623-624, DeKeyser,J., 1993

Botulinum Toxin in the Treatment of Writer's Cramp, A Double-Blind Study
Neurol 43:183-185, Tsui,J.K.C.,et al, 1993

The Visual Variant of Alzheimer's Disease, A Clinicopathologic Case Study
Neurol 43:305-313, Levine,D.N.,et al, 1993

Asymmetry of Forearm Rolling as a Sign of Unilateral Cerebral Dysfunction
Neurol 43:1596-1598, Sawyer,R.N.,Jr.,et al, 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

MRI Pallidal Hyperintensity & Brain Atrophy in Cirrhotic Pts:2 Different MRI Patterns of Clin Deterior?
Neurol 43:2570-2573, Kulisevsky,J.,et al, 1993

Complex Partial Status Epilepticus in a Patient with Dural Metastases
Neurol 43:2389-2392, Steg,R.E.,et al, 1993

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Diagnosis of Medial Temporal Lobe Seizure Onset:Relative Specificity and Sensitivity of Quantitative MRI
Neurol 43:2117-2124, Spencer,S.S.,et al, 1993

Characvteristics of Medial Temporal Lobe Epilepsy:I. Results of History and Physical Examination
Ann neurol 34:774-780, French,J.A.,et al, 1993

Charact of Medial Temporal Lobe Epilepsy:Interictal & Ictal EEG, Neuropsych Test, Imaging, Surg Results & Path
Ann Neurol 34:781-787, Williamson,P.D.,et al, 1993

Reversible Paraneoplastic Limbic Encephalitis
Neurol 43:2418-2419, Kaniecki,R.&Morris,J.C., 1993

Focal Weakness Following Herpes Zoster
JNNP 56:1001-1003, Cockerell,O.C.&Ormerod,I.E.C., 1993

Discrete Cortical Infarction with Prominent Impairment of Thumb Flexion
Stroke 24:2118-2120, Terao,Y.,et al, 1993

Gabapentin as Add-On Therapy in Refractory Partial Epilepsy:A double-Blind, Placebo-Controlled, Parallel-Group Study
Neurol 43:2292-2298, Oommen,K.,et al, 1993

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
Brain 115:1875-1888, Chen,R.,et al, 1992

Pseudoradicular Syndrome in Multiple Sclerosis. 4 Cases Diagnosed by Magnetic Resonance Imaging
Revue Neurologique 148:692-695, Uldry,P.A.&Regli,F., 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

The Sit-up Test:An Alternative Clinical Test for Evaluating Pediatric Torticollis
Pediatrics 90:612-615, Caputo,A.R.,et al, 1992

Botulinum Toxin, Useful in Adult Onset Focal Dystonias
BMJ 305:1169-1170, Lees,A.J., 1992

Recurrent Status Epilepticus in Children
Ann Neurol 31:598-604, Shinnar,S.,et al, 1992

A Comparison of Valproate with Carbamazepine for the Treat of Complex Partial Seizures & Second General Seizures in Adults
NEJM 327:765-771, Mattson,R.H.,et al, 1992

Prolonged Sensory or Visceral Sympt:An Under-Dx Non-Convulsive Focal (Simple Partial) Status Epilepticus
JNNP 55:714-716, Manford,M.&Shorvon,S.D., 1992

Complex Partial Seizure-Induced Transient MR Enhancement
J Comput Assist Tomogr 16:814-816, Horowitz,S.W.,et al, 1992

Magnetic Resonance Imaging in Epilepsy
Lancet 340:343-344, 1992,, , 1992

The Localizing Value of Auras in Partial Seizures:A Prospective and Retrospective Study
Neurol 42:801-808, Palmini,A.&Gloor,P., 1992

Felbamate Monothrapy:Controlled Trial in Patients with Partial Onset Seizues
Ann Neurol 32:386-392, Sachdeo,R.,et al, 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest
Radiology 182:493-499, Barkovich,A.J.&Kjos,B.O., 1992

Nonconvulsive Status Epilepticus Following Electroconvulsive Therapy
Neurol 42:263-264, Varma,N.K.&Lee,S.I., 1992

Torticollis Due to Cervical Epidural Abscess and Osteomyelitis
Neurol 42:696-697, McKnight,P.&Friedman,J., 1992

Quadriplegia after Chiropractic Manip in Infant with Congen Torticollis by a Spinal Cord Astrocy
J Pediatr 120:266-269, Shafrir,Y.&Kaufman,B.A., 1992

Showing articles 1650 to 1700 of 2801 << Previous Next >>