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Differential
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abdominal cramps

abdominal distention

abdominal muscle paralysis

abdominal muscle spasms

abdominal protrusion

abdominal reflex, absent

abducens nerve paralysis

abscess, vertebral

acquired immunodeficiency syndrome

acute intermittant porphyria

Addison's disease

adverse drug reaction

alcohol, neurologic complications with

alternating hemiplegia

amaurosis fugax

amphiphysin antibodies

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, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anemia, megaloblastic

anesthesia, general

angina pectoris

angioneurotic edema

anterior horn cell disease

anti citrullinated antibody

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinergic drugs

antineutrophil cytoplasmic autoantibodies

antispasticity drugs

aqueduct of Sylvius, obstruction

arrhythmia, cardiac

arteritis, temporal

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

axonal degeneration

B 12 deficiency

bacterial infection

Balint's syndrome

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

benign essential tremor

blindness, sudden

blood brain barrier

bone demineralization

botulinum toxin

brachial plexus neuropathy

brainstem, infarction of

brainstem, lesion of

Brugada syndrome

bulbar palsy, acute

burning feet, differential diagnosis of

burning paresthesia

calcification, intracranial

calf hypertrophy

campylobacter infection

cancer, unknown origin

carcinoma of breast

carcinoma of lung

carcinoma of unknown origin

carnitine deficiency myopathy

carpal tunnel syndrome

carpo-pedal spasm

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, serial

cauda equina, enhancement

cecum perforation

celiac disease, adult

celiac disease, epilepsy and cerebral calcification

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

Charcot-Marie-Tooth

chest x-ray, abnormal

chewing, impaired

Chinese paralytic syndrome

chromosomal abnormality

Churg-Strauss syndrome

Clinical Pathologic Conference(C.P.C.)

clostridium tetani

clubfoot as related to neurologic disease

coenzyme Q10 deficiency

Cogan's syndrome

cold hands sign

collagen vascular disease

collagenous sprue

compression fracture

conduction block

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

corneal reflex, abnormal

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyclophosphamide

cylindrical spiral

cyst, cortical parenchyma

cyst, ventricular

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cystoisospora belli

cytomegalic inclusion disease

cytomegalovirus infection

deafness, unilateral

decerebrate posture

decorticate posture

deep gray nuclei

degenerative diseases of CNS

demyelinating disease

denervation of muscle

denervation potentials

dermatitis herpetiformis

dermatomyositis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic radiculopathy

dialysis disequilibrium syndrome

diarrhea, bloody

differential diagnosis

disability, neurological

disc space infection

disc space narrowing

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug abuse, neurologic complications of

drug induced neurologic disorders

dura, thickened

dysequilibrium syndrome

dystonia, cervical

dystonia, drug induced

dystonia, focal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electromyogram, incremental response

electrophoretic pattern, serum

emergencies, neurologic

emotional lability

empyema, epidural-spinal

encephalomyopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

entrapment neuropathy

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

evoked potentials

exercise intolerance

exercise-related muscle strength increase

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

face, numbness of

facial movement disorder

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

factitious disorder

fasciculation, benign

fatigable chewing

fine motor function, impaired

flaccid paralysis

fourth ventricle, cyst

frontal lobe, pathologic signs of

fundus, abnormality of

fungal infection, CNS

gamma amino butyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric dilatation, acute

gastroenteritis

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

glutamic acid decarboxylase, antibody

glycogen storage disease

GM1 ganglioside antibodies

gram positive rod

granuloma, eosinophilic

granulomatosis with polyangiitis

granulomatosis, allergic

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

hallucination, visual

headache, chronic

headache, chronic daily

headache, severe

headache, vascular

hearing loss, sudden, bilateral

heavy metal intoxication

heliotrope rash

helminthic infection of CNS

hematuria, microscopic

hemianopia, homonymous

hemiparesis, transient

hemorrhagic diathesis

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

herpes simplex virus

herpes virus infection

herpes, genital

hexosaminidase-A

hip flexor weakness

histochemistry of muscle

HMGcoA reductase inhibitors

H-reflex testing

human immunodeficiency virus type 1

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hyperamylasemia

hypereosinophilic syndrome(HES)

hyperexcitable peripheral nerve disorder

hypergammaglobulinemia

hyperkalemic periodic paralysis

hyperparathyroidism

hyperphosphatasia

hyperpigmentation of skin

hypersegmented polys

hypertensive crisis

hyperthyroidism

hypokalemic paralysis

hypokalemic periodic paralysis

hypomyelination

hyponatremia with cerebral disorders

hyponatremic encephalopathy

hypoosmolality of serum

hypoparathyroidism

hypoparathyroidism, idiopathic

hypoprothrombinemia

hypothalamus, disturbance of

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunomodulation

immunosuppression

immunosuppressive agents

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

intellectual deficit

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrinsic hand muscles, wasting of

Isaacs syndrome

ischemic exercise test

jaw claudication

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

Kearns-Sayre syndrome

keratitis, interstitial

lactic acidemia

lactic dehydrogenase(LDH)

laughing, pathologic

lead and the nervous system

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

level of consciousness, decreased

limbic encephalitis

lipid lowering agent

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

long bone lesion

lymphadenopathy

lymphadenopathy, axillary

lymphocytic meningoradiculitis

lymphoma involving CNS

lysosomal storage disease

malabsorption syndrome

malignant hyperpyrexia

malignant papulosis

McArdle's disease

McArdle's disease, adult onset

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, chronic

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, leptospira

meningitis, noninfectious

meningoencephalitis

mental status, abnormal

metabolic disorder, primary

methylmalonic acid, serum

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuritis multiplex

mononeuropathy multiplex

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI, brachial plexus

MRI, contrast enhanced

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, spinal cord

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle atrophy, static

muscle cramp, nocturnal

muscle pain-fasciculation syndrome

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle relaxant

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle tenderness

muscle twitching

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker, carrier

myasthenia gravis

myasthenic syndrome

myelopathy, chronic progressive

myeloradiculitis

myocardial infarction

myocardial infarction, acute

myocardial injury

myoclonic jerks

myopathy, alcoholic

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, proximal

myopathy, thyroid disease causing

myopathy, vacuolar

myositis, ocular

myotonia congenita

nasal septum, perforation of

nausea and vomiting

neoplasm, primary of CNS-intraventricular

nephrotic syndrome

nerve conduction studies

nerve conduction studies, motor

neuroendocrinology

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, amyloid

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, thoracoabdominal

neuropathy, toxic

neuropathy, vasculitic, systemic

night blindness

nutritional deficiency

occupational neurologic disorders

oculomasticatory myorhythmia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

ophthalmoplegic migraine

optic neuritis, bilateral

oral contraceptives

oral ulcerations

orthostatic hypotension

osteomyelitis, spinal

otitis, neurologic complications with

overlap syndrome

pain, abdominal

pain, neuropathic

pain, testicular

palate, paralysis

palliative care

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

parasitic infection, CNS

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal neurologic disorder

PAS positive material in the brain

pediatric neurology

periarteritis nodosa

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

pheochromocytoma

phosphorylase b kinase deficiency

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, organophosphate

polymerase chain reaction

polymyalgia rheumatica

polymyositis, eosinophilic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyneuropathy, uremic

polyps, gastrointestinal tract

polyradiculoneuropathy

posterior column disease

posterior leukoencephalopathy syndrome

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

primary aldosteronism

progressive encephalomyelitis with rigidity syndrome

progressive neurologic disorder

progressive spinal muscular atrophy

protozoan infection

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

quadriplegia, transient

rabies, nervous system involvement with

radial nerve, palsy of

radiculoneuritis

ragged-red fibers

Raynaud's phenomenon

reflex sympathetic dystrophy

reflex, brainstem

reflex, brainstem, absent

refractory sprue

regional enteritis

remote effect of cancer on the nervous system

renal transplantation

repetitive nerve stimulation

respiratory failure

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal artery occlusion

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rippling muscle disease

risus sardonicus

Sabin-Feldman dye test

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, differential diagnosis of

sensorineural hearing loss

sensory loss, band distribution

sensory polyneuropathy

serologic testing

serum glutamic oxaloacetic transaminase

serum lipase, elevated

shoulder, pain in

shunt procedure, ventricular

sick sinus syndrome

single-fiber electromyography

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skin, thickened

sleep pathology and physiology

small vessel disease

spastic dysphonia

spasticity, treatment of

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, infarction of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar degeneration

spirochete infection

splinter hemorrhages

standing difficulty

startle reaction

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

stimulation, sensory

subarachnoid hemorrhage, prognosis

subcutaneous edema

subcutaneous nodules

subdural hematoma

suspended sensory loss

sweating, abnormality of

syncope, recurrent

systemic illness

tandem gait, ataxic

Tay-Sachs disease

temporal artery, biopsy

temporalis muscle wasting

testicular biopsy

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

tinnitus, pulsatile

tone, muscle, increased

tongue, fasciculations of

tongue, impaired movements of

tongue, swelling

tongue, weakness

toxic encephalopathy

toxins, nervous system

toxoplasma complement fixation test

toxoplasmosis, acquired

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient ischemic attack

travel, foreign

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, treatment of

tremor, writing

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

tropical disease

Trousseau's sign

truncal polyneuropathy

tubular aggregates, muscle

type 2 muscle fiber

ulcerative colitis

uremic encephalopathy

uremic twitching

urinary 17 hydroxycorticosteroids

urinary 17 ketosteroids

urinary catecholamines

urinary retention

urine osmolality, elevated

vanilmandelic acid, urine

vertebral erosion

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual impairment

visual loss, transient

vitamin D deficiency

vitamin deficiency

vocal cord paralysis

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, episodic

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Wernicke's encephalopathy

West Nile fever

Whipple's disease

white matter disease

whole body imaging

X-linked bulbospinal neuronopathy

X-linked myopathy

yersinia enterocolitica

Showing articles 1900 to 1950 of 3286 << Previous Next >>

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,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

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,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

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

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

Electrodiagnosis Reliability in the Diagnosis of Infant Botulism
J Pediatr 120:747-749, Graf,W.D.,et al, 1992

Nerve Agents:A Review
Neurol 42:946-950, Gunderson,C.H.,et al, 1992

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

CNS Mycosis Fungoides:CT and MR Findings
J Comput Assist Tomogr 16:529-533, Tein,R.D.,et al, 1992

Unilateral Diaphragmatic Paralysis:An Electrophysiological Study
JNNP 55:316-318, Lagueny,A.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Upper Arm Radial Nerve Palsy after Muscular Effort:Report of Three Cases
Neurol 42:1632-1634, Streib,E.,et al, 1992

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

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Aluminium Intoxication in Undialysed Adults with Chronic Renal Failure
JNNP 55:697-700, Russo,L.S.,et al, 1992

MRI of Intracranial Neurovascular Compression
J Comput Assist Tomogr 16:503-505, Furuya,Y.,et al, 1992

Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992

Endovascular Treatment of Vertebral Arteriovenous Fistula
Radiology 183:361-367, Beaujeux,R.L.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
J Pediatr 121:845-851, Sebire,G.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Lyme Disease Associated with Fibromyalgia
Ann Int Med 117:281-285, Dinerman,H.&Steere,A.C., 1992

The Role of Hypotension in Septic Encephalopathy Following Surgical Procedures
& Stevens, M. , Arch Neurol 49:653-656., Wijdicks,E.F.M., 1992

Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis
NEJM 326:1380-1384, Miller,F.W.,et al, 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Improvement of Motor Performance of HIV-Positive Patients Under AZT Therapy
Neurol 42:891-896, Arendt,G.,et al, 1992

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

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Fibromyalgia:The Copenhagen Declaration
Lancet 340:663-664, Csillag,C., 1992

Chronic Daily Headache
Neurol 42:32-36, Sheftell,F.D., 1992

Interrelations Between Migraine and Tension-Type Headache in the General Population
Arch Neurol 49:914-918, Rasmussen,B.K.,et al, 1992

Early Guillain-Barre Syndrome without Inflammation
Arch Neurol 49:979-981, Ropper,A.H.&Adelman,L., 1992

Pure Sensory Guillain-Barre Syndrome
JNNP 55:411-415, Miralles,F.,et al, 1992

Plasma Exchange In Guillain-Barre Syndrome:One-Year Follow-up
French Coop Group on Plasma Exchange in Guillain-Barre Syndrome, Ann Neurol 32:94-971992., , 1992

A Randomized Trial Comparins Intravenous Immune Globulin and Plasma Exchange in Guillain-Barre Syndrome
NEJM 326:1123-1129, VanDerMeche,F.G.A.,et al, 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Generalized Myositis in Behcet Disease:TReatment with Cyclosporine
Ann Int Med 116:651-653, Lingenfelser,T.,et al, 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Persistent Paralysis in Critically Ill Patients after Long-Term Administration of Vecuronium
NEJM 327:524-528, Segredo,V.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

'De Novo'Absence Status of Late Onset:Report of 11 Cases
Neurol 42:104-110, Thomas,P.,et al, 1992

Complications of Acute Stroke
Lancet 339:721-724, Oppenheimer,S.&Hachinski,V., 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Pure Motor Stroke:A Reappraisal
Neurol 42:789-798, Melo,T.P.,et al, 1992

Neonatal Idiopathic Cerebral Venous Thrombosis:An Unrecognized Cause of Transient Seizures or Lethargy
Ann Neurol 32:51-56, Rivkin,M.J.,et al, 1992

Relationship of Cardiac Disease to Stroke Occurrence, Recurrence, and Mortality
Stroke 23:1250-1256, Broderick,J.P.,et al, 1992

Spontaneous Vertebal Artery Dissection Initially Mimicking Myocardial Infarction
Stroke 23:1021-1023, Linden,D.,et al, 1992

The Risk of Stroke in Patients with Acute Myocardial Infarction after Thrombolytic and Antithrombotic Treatment
NEJM 327:1-6, Maggioni,A.P.,et al, 1992

Showing articles 1900 to 1950 of 3286 << Previous Next >>