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Differential
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abdominal contractions

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acute disseminated encephalomyelitis

Addison's disease

advances in neurology

adverse drug reaction

altered states of consciousness

alternating hemiplegia

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

ammonia

AMPA receptor antibodies

amphiphysin antibodies

amyloid angiopathy, cerebral

angiitis, granulomatous of CNS

angiitis, isolated of CNS

antibiotics, neurologic complications with

antibodies to measles

anticholinergic drugs

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, cognitive function with

anticonvulsants, effectiveness

anticonvulsants, mechanism of action of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

apraxia of eye movements

apraxia, constructional

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder, acute

brain biopsy, false negative

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

burning feet

burning feet, differential diagnosis of

calcification, intracranial

CAR syndrome

carbon monoxide poisoning

cardiac arrest and resuscitation

CAT scan, complication with

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, pelvis

catatonia

ceftazidime

central nervous system, infection of

central pontine myelinolysis

cephalosporins

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellitis

cerebellum

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cervical spondylosis

chemotherapy, CNS treatment and complications with

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 2

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

contactin associated protein like 2 antibodies

cortical blindness

cortical ribbon sign

cortical-basal ganglionic degeneration

Creutzfeldt-Jakob disease, genetic

crying, pathologic

cytomegalic inclusion disease

cytomegalovirus infection

deep gray nuclei

degenerative diseases of CNS

dementia, rapidly progressive

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

disorientation

distal muscle atrophy

distal muscle weakness

DPPX, antibodies, encephalitis

dysequilibrium syndrome

dyskinesia

dyskinesia, buccal lingual facial

dystonia, delayed onset

dystonia, focal

dystonic reaction, acute

echolalia

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electromyogram

emergencies, neurologic

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, post anoxic

encephalopathy, progressive

enteritis

epidemiology of neurology

epilepsia partialis continua

escherichia coli

extralimbic encephalitis

eye movement, disorders of

faciobrachial dystonic seizure

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

gliomatosis cerebri

glutamic acid decarboxylase, antibody

glycine

granular osmiphilic material

hallucination, visual

handedness

head injury

headache

headache, sudden onset of

hemiparesis, transient

hemolytic-uremic syndrome

hepatitis

hepatomegaly

herpes simplex encephalitis

herpes virus

herpes zoster

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hyperammonemic encephalopathy

hypertensive encephalopathy

hypoglycorrhachia

hyponatremia

hypoxia, newborn

hypoxic encephalopathy

immunology and the nervous system

immunosuppression

immunotherapy

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

infantile spasm

insomnia

intellectual deficit

intellectual deterioration

intracranial pressure, increased

intrinsic hand muscles, wasting of

irritability

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

juvenile myoclonus epilepsy

lactic acidemia

laminectomy, cervical

language disorder in adults

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

levitation

life support, withdrawal of

lymphoma involving CNS

lymphoma, primary of CNS

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, fungal

meningitis, syphilitic

meningitis, TB

mental retardation

mesial temporal lobe

microangiopathic hemolytic anemia

microinfarcts

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

movement disorder, delayed onset

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, FLAIR

MRI, negative

MRI, pelvis

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple system atrophy

muscle biopsy

muscle cramp

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis

myelitis, transverse, recurrent

myoclonus, post anoxic

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

neoplasm, primary of CNS

nerve conduction studies

neurexin-3 alpha antibodies

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic signs

neurologic symptoms

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, paraneoplastic

occupational neurologic disorders

olivary degeneration, hypertrophic

onconeural antibodies

ophthalmoplegia

opsoclonus

opsoclonus-myoclonus syndrome

optic atrophy

ornithine transcarbamylase deficiency

paraneoplastic cerebellar degeneration

paratonia

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

penicillin

peripheral nerve, lesion of

persistent vegetative state

personality change

phenylketonuria

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

POEMS syndrome

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

potassium channel antibodies

precipitating factors

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

Red flags

remote effect of cancer on the nervous system

renal failure

renal transplantation

respiratory failure

restless leg syndrome

reticulum cell sarcoma

salivation, excessive

seizure, clicking sound with

seizure, drug resistance

seizure, drug-induced

seizure, precipitating factors

seizure, spinal

seizure, stimulus sensitive

seizure, tonic-clonic

seizure, treatment of

sensory loss

sensory loss, cortical

serologic testing

serologic testing of cerebrospinal fluid

serologic testing, false negative

Shiga toxin

short stature

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

sodium valproate

sodium valproate, intravenous

sodium valproate, toxicity

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, vascular malformation of

staphylococcal protein A column therapy

status epilepticus, intractable

status epilepticus, myoclonic

status epilepticus, nonconvulsive

steroid therapy, CNS treatment and complications with

stiff man syndrome

storage disease of CNS

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

stuttering

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, adult onset

subdural hematoma

symmetric brain lesions

tandem gait, ataxic

tauopathy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thrombotic microangiopathy

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

triangle of Guillain and Mollaret

Trousseau's sign

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uremic encephalopathy

visuospatial disturbance

walking, difficulty with

Wernicke's encephalopathy

wheelchair

Whipple's disease

white matter disease

white matter disease, periventricular

white matter disease, subcortical

Showing articles 1000 to 1050 of 2208 << Previous Next >>

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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Familial Aggregation in Frontotemporal Dementia
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Angiographically Defined Primary Angiitis of the CNS, Is It Really Benign
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Neurological and Neuroradiological Findings in Long-Term Survivors of Allogeneic Bone Marrow Transplantation
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Cortical Myoclonus
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Meningoencephalomyelitis Caused by Herpes Simplex Virus-1 in Pt with Idiopathic T CD4+Lymphocytopenia
Neurol 50:569-570, Tumbarello,M.,et al, 1998

Clinicopath Conf
Cat Scratch Encephalitis Due to B. Quintana, Case 1-1998, NEJM 338:112-11998., , 1998

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

Incidence of Status Epilepticus in Rochester, Minnesota, 1965-1984
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Do Nonconvulsive Seizures Damage the Brain? Yes
Arch Neurol 55:117-120, Young,G.C.&Jordan,K.G., 1998

Do Nonconvulsive Seizures Damage the Brain? No
Arch Neurol 55:119-120, Aminoff,M.J., 1998

Isolated Weakness of the Fingers in Cortical Infarction
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Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
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A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
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Tiagabine for Complex Partial Seizures, A Randomized, Add-on, Dose-Response Trial
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Rhabdomyolysis and Hypoxia Associated with Prolonged Propofol Infusion in Children
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Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
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Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

Six-Month Evaluation of Carbatrol (Extended-Release Carbamazepine) in Complex Partial Seizures
Neurol 519:1727-1729, Mirza,W.U.,et al, 1998

Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
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Alzheimers Disease with Asymmetric Parietal Lobe Atrophy: A Case Report
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Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

Magnetic Resonance Imaging Features of Solitary Inflammatory Brain Masses
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Herpes Simplex Encephalitis (HSE) and the Immunocompromised: A Clinical and Autopsy Study of HSE in the Settings of Cancer and Human Immunodeficiency Virus-Type 1 Infection
Hum Pathol 29:215-222, Schiff,D. &Rosenblum,M.K., 1998

Herpes Simplex Virus Infections of the Central Nervous System in Human Immunodeficiency Virus-Infected Patients: Clinical Management by Polymerase Chain Reaction Assay of Cerebrospinal Fluid
CID 27:303-309, Cinque,P., et al, 1998

Risk of Unprovoked Seizure After Acute Symptomatic Seizure: Effect of Status Epilepticus
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Isolated Vagal Nerve Palsy Associated with a Dissection of the Extracranial Internal Carotid Artery
AJNR 19:1845-1847, Nusbaum, A.O.,et al, 1998

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
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AIDS Dementia Complex with Generalized Myoclonus
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Candidal Meningitis in HIV-Infected Patients: Analysis of 14 Cases
Clin Inf Dis 25:473-476, Casado, J.L.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
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Neuroimaging in Presumed Primary Headache Disorders
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Predictors of Intracranial Path Findings in Pts Who Seek ER Care Because of Headache
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Unilateral Hypnic Headache:A Case Study
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Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
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Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
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Nasal Benzodiazepines for Management of Acute Childhood Seizures
Lancet 349:222-223, Wallace,S.J., 1997

Status Epilepticus Amauroticus
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CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
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Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
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Epilepsy in Childhood
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Cognitive Recovery Instead of Decline After Acute Encephalitis:A Prospective Follow Up Study
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Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
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Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
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Correlation of MRI and Neuropathology in AIDS
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Showing articles 1000 to 1050 of 2208 << Previous Next >>