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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 600 to 650 of 13505 << Previous Next >>

Cyanide-Induced Parkinsonism:Clinical, MRI, and 6-Fluorodopa PET Studies
Neurol 39:142-144, Rosenberg,N.L.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

PET Scanning, Provides Information on Function
BMJ 298:692-694, Frackowiak,R.S.J.&Jones,T., 1989

Cerebral Glucose Metabolism in Wernicke's Broca's, and Conduction Aphasia
Arch Neurol 46:27-34, Metter,E.J.,et al, 1989

Surgical Treatment of Intractable Neonatal-Onset Seizures:The Role of Positron Emission Tomography
Neurol 38:1178-1188, Chugani,H.T.,et al, 1988

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Brain Glucose Metabolism in Thalamic Syndrome
JNNP 51:427-428, Laterre,E.C.,et al, 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Disconnection & Cerebral Metabolism, The Case of Conduction Aphasia
Arch Neurol 45:275-279, Kempler,D.,et al, 1988

Diagnosis & Treatment of Aphasia, Part I & Part II
JAMA 259:1043-1047, 1205-12101988., Albert,M.L.&Helm-Estabrooks,N., 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

Positron Emission Tomography-A New Approach to Brain Chemistry
JAMA 260:2704-2710, Jacobson,H.G., 1988

Response of Human-Immunodeficiency-Virus-Associated Neurological Disease to 3'-Azido-3'-Deoxythymidine
Lancet 1:132-135, Yarchoan,R.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Positron Emission Tomography Studies of Cerebral Glucose Metabolism in Chronic Partial Epilepsy
Ann Neurol 22:480-486, Abou-Khalil,B.W.,et al, 1987

Borderzone Ischemia
Ann Neurol 22:707-713, Leblanc,R.,et al, 1987

Differences in Cerebral Blood Flow & Glucose Utilization in Vegetative Versus Locked-in Patients
Ann Neurol 22:673-682, Levy,D.E.,et al, 1987

The Metabolic Pathology of the AIDS Dementia Complex
Ann Neurol 22:700-706, Rottenberg,D.A.,et al, 1987

Metabolic & Clinical Correlates of Acute Ischemic Infarction
Neurol 37:1103-1110, Kushner,M.,et al, 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

Differentiation of Cerebral Radiation Necrosis from Tumor Recurrence by[18F]FDG & 82RB PET Scan
J Comput Assist Tomogr 11:563-570, Doyle,W.K.,et al, 1987

Lesions of the Putamen:Their Relevance to Dystonia
Neurol 37:1125-1129, Fross,R.D.,et al, 1987

Plasma R Binder Deficiency & Neurologic Disease
NEJM 317:1330-1332, Sigal,S.H.,et al, 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
NEJM 316:357-362, Mazziotta,J.C.,et al, 1987

Positron Emission Tomography & Histopathology in Pick's Disease
Neurol 37:439-445, Kamo,H.,et al, 1987

The Lennox-Gastaut Syndrome:Metabolic Subtypes Determined by FDG Positron Emission Tomography
Ann Neurol 21:4-13, Chugani,H.T.,et al, 1987

Cerebral Glucose Metabolism in the Lennox-Gastaut Syndrome
Ann Neurol 21:14-21, Theodore,W.H.,et al, 1987

Primary Progressive Aphasia-Differentiation from Alzheimer's Disease
Ann Neurol 22:533-534, Mesulam,M.M., 1987

Magnetic Resonance Imaging in Intractable Partial Epilepsy:Correlative Studies
Ann Neurol 20:57-62, Sperling,M.R.,et al, 1986

Positron Emission Tomography in Alzheimer's Disease
Neurol 36:879-887, Duara,R.,et al, 1986

Positron Emission Tomography in the Early Diagnosis of Huntington's Disease
Neurol 36:888-894, Hayden,M.R.,et al, 1986

Normal Pressure Hydrocephalus
BMJ 293:837-838, Anderson,M., 1986

Slowly Progressive Aphasia without Generalized Dementia:Studies with Positron Emission Tomography
Ann Neurol 19:68-74, Chawluk,J.B.,et al, 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

PET Studies of Cerebral Glucose Metabolism in Idiopathic Torticollis
Neurol 36:653-657, Stoessl,A.J.,et al, 1986

PET, CT, & MR Imaging in Cerebrovascular Disease
J Comput Assist Tomogr 10:903-911, Heiss,W.D.,et al, 1986

PET Scan Investigations of Huntington's Disease:Cerebral Metabolic Corr. of Neuro & Funct Decline
Ann Neurol 20:296-303, Young,A.B.,et al, 1986

Comparison of PET, MRI, & CT with Pathology in a Proven Case of Alzheimer's Disease
Neurol 36:1569-1574, McGeer,P.L.,et al, 1986

Positron Emission Tomography in Dementia of the Alzheimer Type
Arch Int Med 146:2045-2049, Berg,G.,et al, 1986

Brain Dopamine Metabolism in Patients with Parkinson's Disease Measured with Positron Emission Tomography
JNNP 49:853-860, Leenders,K.L.,et al, 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Showing articles 600 to 650 of 13505 << Previous Next >>