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Differential
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abdominal muscle paralysis

acetylcholine in CNS

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

acyl CoA dehydrogenase deficiency

adenosine deaminase deficiency

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agalsidase alfa

agranulocytosis

alpha galactosidase A deficiency

alpha glucosidase

Alzheimer's disease

aminoacidopathies

aminoacylase 1 deficiency

anemia, hemolytic

anesthesia, general

angina pectoris

angiography, cerebral, negative

angiography, neurologic complications with

angiotensin-converting enzyme

animal exposure

anorexia nervosa

anterior horn cell disease

anticholinergic drugs

anticoagulant, complications of

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antiphospholipid antibodies

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arthropathy, neuropathic

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

atherosclerosis, generalized

autonomic dysfunction

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

bone marrow infarction

bone marrow necrosis

bone marrow suppression

bone marrow transplantation

brain biopsy, false negative

brainstem, infarction of

brainstem, lesion of

burning feet, differential diagnosis of

burning paresthesia

calcification, intracranial

calf hypertrophy

Canavan's disease

cancer, cerebrovascular accident complicating patients with

carbamazepine, toxicity

carbamyl phosphate synthetase-I deficiency

carbonic anhydrase II deficiency

carcinoma of lung

cardiac catheterization, neurologic complications

cardiac surgery, neurologic complications with

CAT scan, abnormal

CAT scan, chest

CAT scan, false negative

caudate nucleus, lesion of

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, multiple

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, rapidly progressive

ceruloplasmin, serum

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choline acetyltransferase

choline chloride

choreoathetosis

chromosomal abnormality

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

compression fracture

congestive heart failure

contractures, joint

cooling therapy

copper metabolism, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

coronary artery bypass

corpus callosum, infarction of

cortical blindness

cranial nerve enlargement

cranial nerve palsies

crawl regression

C-reactive protein, elevated

creatine phosphokinase isoenzyme elevation

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

cyclophosphamide

cystoisospora belli

cytochrome c oxidase

cytochrome c oxidase, deficiency

decerebrate posture

decision analysis

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

dysdiadochokinesia

dysostosis multiplex

dystonia, children

dystonic reaction, acute

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electron microscopy

embolism, atheromatous

embolism, cholesterol

embolism, retinal

emergencies, medical

emergencies, neurologic

encephalomyelitis

encephalopathy, acute

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, marantic

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

Epstein-Barr virus

Epstein-Barr virus, negative

esophageal varices

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial weakness

failure to thrive

Farber's disease

fatty acid, elevated plasma content

feeding disorder

femoral artery catheterization

ferritin, elevated

fibrin split products

fingernails, abnormal

flow study, carotid artery

flu-like illness

fornix, lesion of

fracture, pathologic

frontal bossing

frontal lobe, behavior with disease of

frontal lobe, lesion of

fundus, abnormality of

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gangliosidosis GM2-AB variant

gastroenteritis

Gaucher's disease

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glutamate dehydrogenase deficiency

glutaric acidemia

glutaric aciduria

glycogen debranching enzyme deficiency

glycogen storage disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, auditory

headache, progressive

headache, severe

headache, thunderclap

heavy metal intoxication

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia, homonymous

hemoglobin abnormality, neurologic complications of

hemolytic-uremic syndrome

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

heterophile antibody test

hexosaminidase-A

hexosaminidase-A and B

histochemistry of muscle

human granulocytic anaplasmosis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

Hurler's syndrome

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hyperamylasemia

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hypersensitivity reaction

hypoalbuminemia

hypogammaglobulinemia

hypoglycorrhachia

hypokalemic paralysis

hypomyelination

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

infection, recurrent

infectious mononucleosis

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

interferon antibodies

interferon beta 1-a

interferon beta 1-b

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intracerebral hemorrhage

ischemic exercise test

Kayser-Fleischer ring

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lacunar infarction

Leber's hereditary optic neuropathy

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

Lesch-Nyhan syndrome

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

life expectancy

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

liver transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, cervical

lymphadenopathy, paraaortic

lymphocytic choriomeningitis

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

malignant hyperpyrexia

McArdle's disease

meconium staining

melanomatosis, primary malignant

memory, defect of recent

meningitis, aseptic

meningitis, plasma cell

menses, irregular

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

microangiopathic hemolytic anemia

microhemorrhage, intracerebral

microspherophakia

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve vegetation

molecular genetics

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, vessel wall

MRI, vessel wall enhancement

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, early onset

multiple sclerosis, relapsing

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle hypertrophy

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

mycoplasma pneumoniae

myocardial injury

myoclonic jerks

myopathy, distal, vacuolar

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, vacuolar

nausea and vomiting

neonatal screening, genetic neurologic disorders

neoplastic angioendotheliosis

nerve conduction studies

neuraminidase deficiency

neuritis, heavy metals causing

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromuscular disease, electrodiagnosis of

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

neuropathy, toxic

neurotransmitter

nonsteroidal anti-inflammatory drug

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

optic chiasm, enlarged

optic nerve, enlarged

organ transplantation

ornithine transcarbamylase deficiency

pain, abdominal

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, hands

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

patient information and support

pectus excavatum

pediatric neurology

periarteritis nodosa

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

peroxisomal disease

personality change

phenylketonuria

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

polymerase chain reaction

Pompe's disease of glycogen storage

position sensation, abnormal

postpartum coma

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protozoan infection

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pulmonary function tests

pulmonary infiltrates

putamen, lesion of

pyramidal tract

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

renal failure, acute

renal transplantation

renal tubular acidosis

respiratory failure

respiratory tract infection

retinal degeneration

retinal hemorrhages

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

Reye's syndrome

rickettsial organism

salivation, excessive

Sandhoff's disease

Sanfilippo syndrome

scalp tenderness

scoliosis, neurologic association with

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, drug-induced

seizure, elderly

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

serologic testing

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

sickle cell disease

skin, lesions in neurologic disorders

slit lamp examination

small vessel disease

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 1

spinocerebellar degeneration

splinter hemorrhages

spongy degeneration of brain

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

striatum, lesion of

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcutaneous nodules

substantia nigra

superior cerebellar artery infarction

sweating, abnormality of

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

Tay-Sachs disease

temporal lobe, lesion

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, weakness

tranquilizers, neurologic complications with

transluminal angioplasty, coronary artery

treatment of neurologic disorder

trientine dihydrochloride

tyrosine hydroxylase deficiency

umbilical-cord blood transplantation

unconsciousness

urea-cycle enzymopathies

urinary incontinence

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vertebral infarction

vertebral-basilar insufficiency

vertigo, episodic

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

vitamin deficiency

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

white matter disease

winging of scapula

Showing articles 750 to 800 of 6400 << Previous Next >>

Pontine Ischemic Rarefaction
Ann Neurol 37:460-466, Pullicino,P.,et al, 1995

Serial Magnetic Resonance Imaging in Isolated Angiitis of the Central Nervous System
Neurol 45:1462-1465, Ehsan,T.,et al, 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Creutzfeldt-Jakob Disease after Liver Transplantation
Ann Neurol 38:269-272, Creange,A.,et al, 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Neuroimaging and Cerebrospinal Fluid Cytology in the Diagnosis of Leptomeningeal Metastasis
Ann Neurol 38:51-57, Frelich,R.J.,et al, 1995

Clinical Relevance and Frequency of Transient Stenoses of the Middle and Anterior Cerebral Arteries in Bacterial Meningitis
Stroke 26:1399-1403, Muller,M.,et al, 1995

Multifocal Inflammatory Leukoencephalopathy Associated with Levamisole Therapy
Neurol 45:374-376, Kimmel,D.W.,et al, 1995

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

Ischemic Stroke as First Manifestation of Essential Thrombocythemia, Report of Six Cases
Stroke 26:1463-1466, Arboix,A.,et al, 1995

Risk of Recurrent Stroke in Patients with Sickle Cell Disease Treated with Erythrocyte Transfusions
J Pediatr 126:896-899, Pegelow,C.H.,et al, 1995

Binswanger's Disease-Revisited
Neurol 45:626-633, Caplan,L.R., 1995

Systemic non-Hodgkin's Lymphoma Manifesting as Neurogenic Respiratory Failure
Neurol 45:589-590, Wolfe,G.I.,et al, 1995

Current Management of Primary Central Nervous Lymphoma
Oncology 9:63-78, DeAngelis,L.M., 1995

Eval of CSF EBV-DNA and IL-10 as Markers for In Vivo Dx of AIDS-Related Primary CNS Lymphoma
British J Haematology 90:844-849, DeLuca,A.,et al, 1995

Takayasu's Arteritis
Stroke Syndromes, Eds Bogousslavsky & Caplan, Cambridge Univ Press, Chp 48, p 439-442, Naritomi,H., 1995

Neurologic manifestations of intravascular lymphomatosis
Acta Neurol Scand 91:494-499, Chapin, J.E.,et al, 1995

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Mononeuritic Multiplex:A Harbinger of Acute Leukemia in Relapse
Arch Neurol 51:618-622, Lekos,A.,et al, 1994

Role of Stereotactic Biopsy in Multifocal Brain Lesions:Considerations on 100 Consecutive Cases
JNNP 57:957-960, Franzini,A.,et al, 1994

Combined-Modality Therapy in the Treatment of Primary Central Nervous System Lymphoma in AIDS
Neurol 44:1473-1479, Forsyth,P.A.,et al, 1994

Contrast-Enhanced Fast MRI in Differentiating Brain Toxoplasmosis and Lymphoma in AIDS Patients
J Comput Assist Tomogr 18:714-718, Laissy,J.P.,et al, 1994

Diagnosis of Intracranial Lymphoma in Patients with AIDS:Value of 201TI Single-Photon Emission Computed Tomography
AJR 163:417-421, O'Malley,J.P.,et al, 1994

Neurological Complications of Peripheral and Cutaneous T-Cell Lymphomas
Ann Neurol 36:625-629, Kaufman,D.K.,et al, 1994

Use of Thallium-201 Brain SPECT to Differentiate Cerebral Lymphoma from Toxoplasma Encephalitis in AIDS Pts
AJNR 15:1885-1894, Ruiz,A.,et al, 1994

Assessment of Fetal Tissue Transplantation in Parkinson's Disease:Does PET Play a Role
Neurol 44:1777-1780, Martin,W.R.W.&Perlmutter,J.S., 1994

AIDS-Associated Malignant Lymphoma
In Textbook of AIDS Medicine, Williams & Wilkins, Balt p. 431., Knowles,D.M.&Dalla-Favera,R., 1994

Lymphoma:Clin Char & Diagn
In AIDS Knowledge Base, 2nd Ed, Little, Brown & Co, Boston, 7:5-1, Kaplan,L.D., 1994

Acute Lumbosacral Polyradiculopathy in Acquired Immunodeficiency Syndrome:Experience in 23 Patients
Ann Neurol 35:53-58, So,Y.T.&Olney,R.K., 1994

Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
Stroke 25:508-510, Papa,M.L.,et al, 1994

Association of 1800 cGy Cranial Irradiation with Intellectual Function in Children with Acute Lymphoblastic Leukaemia
Lancet 344:224-227, Jankovic,M.,et al, 1994

Intravascular Lymphomatosis:A Clinicopathological Study of Three Cases
J Cancer Res Clin Oncol 120:164-168, Liszka,U.,et al, 1994

Diabetes Insipidus as First Manifestation of Primary Central Nervous System Lymphoma
Neurol 44:358-359, Balmaceda,C.M.,et al, 1994

Evidence for Long-Term Survival and Function of Dopaminergic Grafts in Progressive Parkinson's Disease
Ann Neurol 35:172-180, Lindvall,O.,et al, 1994

Neuronal Migration Disorders:Positron Emission Tomography Correlations
Ann Neurol 35:290-297, Lee,N.,et al, 1994

Clinicopath Conf
Multiple Myeloma with Epistaxis, Confusion and Central Retinal Vein Thrombosis, Case 13-1994, NEJM 3, 0:9927,1994., 1994

Detection of Intracranial Abnormalities in Patients with Chronic Fatigue Syndrome:Comparison of MR Imaging and SPECT
AJR 162:935-941, Schwartz,R.B.,et al, 1994

Primary Central Nervous System Lymphoma
Recent Results Cancer Res 135:155-169, DeAngelis,L.J., 1994

Clinicopath Conf
Cysticercosis Involving Basal Cisterns of Brain, Case 8-1993, NEJM 328:566-573993., , 1993

Clinicopath Conf
B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Infilt of Orbital Muscle, Case 4, 193,NEJM 328:266-275,1993., 1993

Primary T-Cell Lymphoma of the Brainstem
Neurol 43:377-381, McCue,M.P.,et al, 1993

The Clinical Spectrum of Ocular Lymphoma
Cancer 72:843-849, Peterson,K.,et al, 1993

Primary Central Nervous System Lymphoma
Ann Int Med 119:1093-1104, Fine,H.A.&Mayer,R.J., 1993

Expression of Epstein-Barr Virus Proteins in Primary CNS Lymphoma in AIDS Patients
Neurol 43:2358-2362, Bashir,R.,et al, 1993

Use of Thallium-201 Brain SPECT to Differentiate Cerebral Lymphoma from Toxoplasma Encephalitis in AIDS Patients
ASNR (Abstract) , p. 232, May 1993., Ruiz,A.,et al, 1993

Epilepsy and Pregnancy
BMJ 307:492-495, O'Brien,M.D.&Gilmour-White,S., 1993

Focal Hyperintensities in Cerebral White Matter on MR Images of Asymptomatic Volunteers:Correl with Social & Medical Histories
AJR 161:855-858, Yetkin,F.Z.,et al, 1993

Neurosurgical Management of the Acquired Immunodeficiency Syndrome
West J Med 158:249-253, Andrews,B.T.&Kenefick,T.P., 1993

Epstein-Barr Virus DNA in Cerebrospinal Fluid from Patients with AIDS-Related Primary Lymphoma of the Central Nervous System
Lancet 342:398-401, Cinque,P.,et al, 1993

Natural Killer Cell Leukemia Presenting with a Peripheral Neuropathy
Neurol 43:1853-1854, Bobker,D.H.&Deloughery,T.G., 1993

Showing articles 750 to 800 of 6400 << Previous Next >>