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Differential
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aceruloplasminemia

acetylcholine receptor antibody

Addison's disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

aneurysm, intracranial

aorta, atherosclerosis

aphonia

Arnold Chiari malformation

artane

arthritis

ascites

aspartate aminotransferase

asymptomatic

ataxia

ataxia telangiectasia

ataxia, sensory

athetosis

athetosis, causes of

auditory evoked brainstem potentials

auditory evoked potentials

B 12 deficiency

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavioral disorder

Behcet's syndrome

benign essential tremor

blepharospasm

blood dyscrasias, neurologic findings with

bone marrow suppression

calcification, intracranial

carbon monoxide poisoning

carcinoma

carcinoma of pancreas

CAT scan, emission, abnormal

cataracts

catatonia

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral infarction, hemorrhagic

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

chromosomal abnormality

cirrhosis

cirrhosis, causes of childhood

claustrum

Clinical Pathologic Conference(C.P.C.)

copper metabolism, abnormal

cornea, abnormal

coronary artery bypass

corpus callosum

corpus callosum, lesion of

Cushing's syndrome

deep gray nuclei

degenerative diseases of CNS

diabetic coma, diagnosis and treatment

diet

differential diagnosis

disability, neurological

disorientation

dissociated sensory loss

diuretic

DNA probes

DNA sequencing

dopa responsive dystonia

dopamine receptor, D2

drooling

drug induced neurologic disorders

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dysphagia

dyspraxia

dystonia

dystonia musculorum deformens

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

DYT1 mutation

edema, pedal

electrolyte imbalance

electromyogram

emotional lability

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalopathy

epidemiology of neurology

eye movement, disorders of

Fabry's disease

facial expression abnormality

frontal lobe, lesion of

gait disorder

gastrectomy, neurologic complications following

gastric partitioning

gaze fixation, distractable

gene

gene mutation

gene therapy

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

glioma

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), late onset

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hypotension, systemic

hypothyroidism

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

impulsivity

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

incoordination

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

iron, brain

iron, serum, low

Jakob-Creutzfeldt disease

jaundice

jaw contractures

Kayser-Fleischer ring

L-dopa

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukoencephalopathy

leukopenia

level of consciousness, decreased

lipid storage disorder of CNS

liver biopsy

liver disease

liver function enzymes

liver transplantation

lymphoma involving CNS

malabsorption

Marinesco-Sjogren syndrome

masked facies

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, face of giant panda sign on

MRI, false negative

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

neoplasm, intracranial

neoplasm, primary of CNS

neuroendocrinology

neurofibromatosis 1

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease, diagnoses of

nutritional deficiency

obesity

ocular motility, disorders of

oculogyric crisis

opened mouth

optic neuropathy

optic neuropathy, nutritional

organ transplantation

osmotic demyelination syndrome

parenteral alimentation

Parkinson disease

Parkinson disease, misdiagnosis

Parkinsonism syndrome

phenylketonuria, adult onset

pheochromocytoma

polyneuropathy

polyradiculoneuropathy

pons, lesion of

porphyria

posterior column disease

postural abnormality

pregnancy, neurologic complications in

prognosis

proprioception, abnormal

prothrombin time, prolonged

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

psychosis, cause of

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

quadriplegia

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

renal failure

renal stones

retinopathy

reversible neurologic disorder

salivation, excessive

serum alanine aminotransferase

single photon emission computed tomography

skin, darkening of

slit lamp examination

somatosensory evoked potentials

speech disorder

speech, slowed

spinal cord, cervical

spinocerebellar degeneration

splenomegaly

spongy degeneration of brain

stimulation, deep brain

striatum, lesion of

striatum, lesion of, bilateral

subdural hematoma

suicide

swayback

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

thrombus, mural

thymus and neuromuscular function

tongue, protrusion of

torticollis

treatment of neurologic disorder

trientine dihydrochloride

unconsciousness

uric acid, low

urine test for metabolic disorders

walking, difficulty with

weight loss

Wernicke's encephalopathy

Showing articles 450 to 500 of 13505 << Previous Next >>

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

MRI of Spinal Cord and Brain Lesions in Subacute Combined Degeneration
Neuroradiology 11:716-719, Katsaros,V.K.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Permanent Cortical Damage Detected by Flumazenil Positron Emission Tomography in Acute Stroke
Stroke 29:454-461, Heiss,W.,et al, 1998

Imaging the Brain, Part 1 & 2
NEJM 338:812-820, 889-8961998., Gilman,S., 1998

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

Characterizing the Target of Acute Stroke Therapy
Stroke 28:866-872, Fisher,M., 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Measurement of Acetylcholinesterase by PET in the Brains of Healthy Controls & Pts with Alzheimer's Disease
Lancet 349:1805-1809, Iyo,M.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Spontaneous Neurological Recovery After Stroke and the Fate of the Ischemic Penumbra
Ann Neurol 40:216-226, Furlan,M.,et al, 1996

Clinicopath Conf
Focal Cortical Dysplasia, Case 7-1996, NEJM 334:586-592996., , 1996

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

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
J Pediatr 128:770-775, Levy,H.L.,et al, 1996

Leukoencephalopathy Associated with Cobalamin Deficiency
Neurol 46:832-834, Chatterjee,A.,et al, 1996

Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
Arch Neurol 53:493-497, Zappacosta,B.,et al, 1996

Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
NEJM 334:752-758, 7911996., Reiman,E.M.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,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

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

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

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

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

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

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

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

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

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

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

Showing articles 450 to 500 of 13505 << Previous Next >>