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abdominal distention

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

adverse drug reaction

affective disorders

alcoholic polyneuropathy

aminoacidopathies

amyloid angiopathy, cerebral

anemia, hemolytic

anemia, iron deficiency

anemia, megaloblastic

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anticonvulsants, untoward effects of

antiendomysial antibodies

arterial dissection, precipitating events

ascending paralysis

ataxia, cerebellar

ataxia, sensory

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

B 12 deficiency, infants

B 12 metabolism, defective

B12 binding protein, abnormal

bacterial infection

basal ganglia, lesion of

Behcet's syndrome

blood dyscrasias, neurologic findings with

burning feet, differential diagnosis of

burning paresthesia

carbon monoxide poisoning

carotid artery disease

carotid artery stenosis

CAT scan, dementia

CAT scan, emission, abnormal

celiac disease, adult

central nervous system, infection of

central pontine myelinolysis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral infarction

cerebral ischemia

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, prevention of

cerebrovascular disease, risk factors in

cervical spine injury

cervical spondylosis

chemotherapy, CNS treatment and complications with

chorea, causes of

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

collagen vascular disease

concentration, impaired

congestive heart failure

controversies in neurology

copper deficiency

corpus callosum

corpus callosum, lesion of

cortical blindness

C-reactive protein, elevated

dementia, clinical diagnosis

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dental procedure, neurologic complications with

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

differential diagnosis

dilantin, toxicity

disability, neurological

dissociated sensory loss

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dystonia, focal

electrical sensation

electroencephalogram

electrophoretic pattern, serum

emotional lability

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy, Hashimoto's

epidemiology of neurology

evidence-based research

evoked potentials

failure to thrive

fine motor function, impaired

folic acid deficiency

F-wave response

gastrectomy, neurologic complications following

gastric partitioning

gastric surgery

gastrointestinal disease, neurologic complications

genetic neurologic disorders

genetic testing

girdle sensation

gliadin antibodies

gliomatosis cerebri

glucose level, serum

glucose tolerance test, abnormal

gluten sensitivity

gluten-free diet

hallucination, auditory

helicobacter pylori

hemorrhagic diathesis

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

hip flexor weakness

histamine-2 receptor blockers

homocysteine, serum

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

hyperbilirubinemia

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hypertensive encephalopathy

hypopigmentation of skin

hypoproteinemia

hypoprothrombinemia

hypotonia, infants

iatrogenic neurologic disorders

incontinence, fecal

infant, evaluation of

infantile tremor syndrome

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intestinal biopsy

intracerebral hemorrhage

inverted V sign

iron, serum, low

laboratory values, normal

lactic dehydrogenase(LDH)

leg weakness, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lhermitte's sign

limbic encephalitis

liver function enzymes

long bone lesion

lymphoma involving CNS

lymphoma, primary of CNS

malabsorption syndrome

memory, defect of recent

memory, impairment of

mental status, abnormal

metabolic disorder, primary

methylmalonic acid, serum

methylmalonic acidemia

methylmalonic aciduria

midbrain, lesion of

Mini Mental Status Examination

mitochondrial disease

monoclonal gammopathy

movement disorder

movement disorder, extrapyramidal

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle weakness

myelitis, longitudinal

myeloma, osteosclerotic

myeloneuropathy

myelopathy, tract-specific

myelopathy, vacuolar

neoplasm, primary of CNS

nerve conduction studies

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuropathy, diabetic

neuropathy, etiologies of

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, work up for

neuropsychiatry

newborn, evaluation of

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

old age, neurology of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, nutritional

orthostatic hypotension

pain, abdominal

pain, neuropathic

paraparesis, spastic

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

personality change

phenothiazine, dyskinesia associated with

phenylketonuria

plasma R binder deficiency

polyradiculoneuropathy

position sensation, abnormal

posterior column disease

posterior leukoencephalopathy syndrome

posterior tibial nerve

posterior tibial nerve compression

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

proton pump inhibitors

pseudoathetosis

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, acute

psychotic behavior

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyridoxine deficiency

radiation therapy, CNS treatment and complications with

regional enteritis

remote effect of cancer on the nervous system

retinal hemorrhages

reversible neurologic disorder

sarcoidosis, CNS

sclerosis, bone

scotoma, central

sensory loss, cutaneous

sensory loss, glove-stocking

sickle cell disease

skin, darkening of

skin, discoloration

skin, lesions in neurologic disorders

somatosensory evoked potentials

speech, pressured

spinal cord, cervical

spinal cord, lesion of

substantia nigra

symmetric brain lesions

systemic illness

tarsal tunnel syndrome

thiamine deficiency

thyroid function tests

tongue, swelling

transcobalamin II, abnormal

transcobalamin II, hereditary absence of

transglutaminase antibodies

treatment of neurologic disorder

tremor, orthostatic

ulcerative colitis

urinary incontinence

vascular endothelial growth factor

Venereal Disease Research Laboratory test

vibratory sensation, abnormal

visual evoked response

visual loss, slow

vitamin D deficiency

vitamin deficiency

vitamin supplementation

vitamin therapy

walking, difficulty with

weakness, generalized

weakness, progressive

Wernicke's encephalopathy

Whipple's disease

white matter disease

wide based gait

word-finding difficulty

Showing articles 500 to 550 of 803 << Previous Next >>

Neurologic Presentation of Wilson Disease without Kayser-Fleischer Rings
Neurol 46:1040-1043, Demirkiran,M.,et al, 1996

Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease
Neurol 46:1485-1486, Vidaud,D.,et al, 1996

Presynaptic Dopaminergic Deficits in Lesch-Nyhan Disease
NEJM 334:1568-1572, 16021996., Ernst,M.,et al, 1996

Differentiation of Central Nervous System Lesions in AIDS Patients Using Positron Emission Tomography (PET)
Int J STD AIDS 7:337-346, Heald,A.E.,et al, 1996

Cranial MR in Wilson Disease:Abnormal White Matter in Extrapyramidal and Pyramidal Tracts
AJNR 16:2021-2027, van Wassenaer-van Hall,H.N.,et al, 1995

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,et al, 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

Evaluating Contrast-Enhancing Brain Lesions in Patients with AIDS by Using Positron Emission Tomography
Ann Int Med 123:594-598, Pierce,M.A.,et al, 1995

Complementary Positron Emission Tomographic Studies of the Striatal Dopaminergic System in Parkinson's Disease
Arch Neurol 52:1183-1190, Antonini,A.,et al, 1995

Early Differential Diagnosis of Parkinson's Disease with F-flurodeoxyglucose and Positron Emission Tomography
Neurol 45:1995-2004, Eidelberg,D.,et al, 1995

Clinical and[18F]dopa PET Findings in Early Parkinson's Disease
JNNP 59:597-600, Morrish,P.K.,et al, 1995

Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
J Pediatr 127:193-199, Majnemer,A.&Shevell,M.I., 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Seizure-Induced Transient Hippocampal Abnormalities on MR:Correl with Positron Emission Tomography & EEG
AJNR 16:1736-1738, Cox,J.E.,et al, 1995

Comparison of Ictal SPECT and Interictal PET in the Presurgical Evaluation of Temporal Lobe Epielspy
Ann Neurol 37:738-745, Ho,S.S.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Conditions That Mimic Stroke in the Emergency Department
Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Recovery from Wernicke's Aphasia:A Positron Emission Tomographic Study
Ann Neurol 37:723-732, Weiller,C.,et al, 1995

Correlations Between Triplet Repeat Expansion and Clinical Features in Huntington's Disease
Arch Neurol 113:749-753, Claes,S.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
JAMA 274:813-819, Tokgozoglu,L.S.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Neuropath Evid of Graft Survival & Striatal Reinnerva after Transpl of Fetal Mesencephalic Tissue in Parkinson's Dis
NEJM 332:1118-1124, 11631995., Kordower,J.H.,et al, 1995

Bilateral Fetal Nigral Transplantation Into the Postcommissural Putamen in Parkinson's Disease
Ann Neurol 38:379-388, Freemen,T.B.,et al, 1995

Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
Arch Neurol 52:179-185, Perani,D.,et al, 1995

A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
Arch Neurol 52:299-305, Wills,A.J.,et al, 1995

Imaging the Head:Functional Imaging
JNNP 58:132-144, Sawle,G.V., 1995

Zinc-Induced Deterior in Wilson's Disease Aborted by Trtm with Penicillamine, Dimercaprol, & A Novel Zero Copper Diet
Arch Neurol 52:10-11, Walshe,J.M.,et al, 1995

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995

Myotonic Dystrophy with No Trinucleotide Repeat Expansion
Neurol 35:269-272, 2551994., Thornton,C.A.,et al, 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

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

Structural and Functional Brain Imaging in Friedreich's Ataxia
Arch Neurol 51:349-355, Junck,L.,et al, 1994

Demetia with Leucoaraiosis and Dural Arteriovenous Malformation:Clinical and PET Case Study
JNNP 56:929-931, Nencini,P.,et al, 1994

The Neurogenetic Genie:Testing for Huntington's Disease Mutation
Neurol 44:1369-1373, 1533-15361994., Hersch,S.,et al, 1994

CAG Repeat Size and Clinical Presentation in Huntington's Disease
Neurol 44:1137-1143, Ashizawa,T.,et al, 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

Treatment of Wilson's Disease with Ammonium Tetrathiomolybdate
Arch Neurol 51:545-554, Brewer,G.J.,et al, 1994

Initial and Follow-up Brain MRI Findings and Correlation with the Clinical Course in Wilson's Disease
Neurol 44:1064-1068, Roh,J.K.,et al, 1994

Treatment with D-penicillamine Improves Dopamine D2-Receptor Binding and T2-Signal Intensity in de novo Wilson's Disease
Neurol 44:1079-1082, Schwarz,J.,et al, 1994

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

Parkinsonism Caused by Petroleum Waste Ingestion
Neurol 44:1051-1054, Tetrud,J.W.,et al, 1994

Worsening of Neurologic Syndrome in Patients with Wilson's Disease with Initial Penicillamine Therapy
Arch Neurol 44:490-493, Brewer,G.J.,et al, 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994

Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
Lancet 344:714-717, Davis,M.B.,et al, 1994

Showing articles 500 to 550 of 803 << Previous Next >>