Neudle.com: "copper"

Differential
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aceruloplasminemia

acetylcholine receptor antibody

Addison's disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

aneurysm, intracranial

anticonvulsants, untoward effects of

anxiety

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

blindness

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

ceftriaxone

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

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

heavy metal intoxication

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

industrial neurologic disorders

infant, evaluation of

intellectual deficit

intellectual deterioration

internet

intracerebral hemorrhage

iron, brain

iron, serum, low

Jakob-Creutzfeldt disease

jaundice

jaw contractures

Kayser-Fleischer ring

L-dopa

lead and the nervous system

lead poisoning

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukoencephalopathy

leukopenia

level of consciousness, decreased

Lhermitte's sign

lipid storage disorder of CNS

liver biopsy

liver disease

liver function enzymes

liver transplantation

long bone lesion

lymphoma involving CNS

malabsorption

malabsorption syndrome

manganese intoxication

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, negative

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

muscle stiffness

myasthenia gravis

myelitis, longitudinal

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myoclonus

myopathy

nausea and vomiting

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neuritis, causes of

neuroendocrinology

neurofibromatosis 1

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

nutritional deficiency

obesity

occupational neurologic disorders

ocular motility, disorders of

oculogyric crisis

opened mouth

optic neuropathy

organ transplantation

osmotic demyelination syndrome

parenteral alimentation

paresthesias

paresthesias, generalized

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

progressive neurologic disorder

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

retroperitoneal hemorrhage

reversible neurologic disorder

salivation, excessive

serum alanine aminotransferase

single photon emission computed tomography

skin, darkening of

slit lamp examination

small-bowel bypass

sodium valproate

somatosensory evoked potentials

speech disorder

speech, slowed

spinal cord, cervical

spinal cord, lesion of

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

urinary incontinence

urine test for metabolic disorders

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Wernicke's encephalopathy

Showing articles 0 to 50 of 116 Next >>

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Wilson Disease Presenting with Catatonia
Neurol 96:e2781-e2782, Patel, R.A. & Bailey, M., 2021

Liver Transplantation as a Rescue Therapy for Severe Neurologic Forms of Wilson Disease
Neurol 94:e2189-e2202, Poujois, A.,et al, 2020

Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

Wilson Disease
NIDDK Oct2018, , 2018

Menkes Disease Mimicking Child Abuse
Pediat Dermatol 34:e132-e134, Droms, R.J.,et al, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

Copper Deficiency Clinical Case Conference: In Defense of Checklists
Ann Neurol 75:799, Finelli, P.F. & McCabe, A.L., 2014

Copper Deficiency
BMJ 348:g3691, Chhetri, S.K.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
Neurol 81:1557, Trocello, J.M.,et al, 2013

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

Teaching NeuroImages: MRI Reversal in Wilson Disease With Trientine Treatment
Neurol 74:e72, Park,H.K., et al, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

Acute and Bilateral Blindness Due to Optic Neuropathy Associated with Copper Deficiency
Arch Neurol 66:1025-1027, Naismith,R.T.,et al, 2009

Denture Cream: An Unusual Source of Excess Zinc, Leading to Hypocupremia and Neurologic Disease
Neurol 71:639-643, Nations,S.P.,et al., 2008

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Neuropathy Progressing to Myeloneuropathy 20 Years After Partial Gastrectomy
Neurol 66:1451, Everett,C.M.,et al, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Brain Metal Concentrations in Chronic Liver Failure Patients With Pallidal T1 MRI Hyperintensity
Neurol 67:1984-1989, Klos,K.J.,et al, 2006

Proton MR Spectroscopy in Wilson Disease: Analysis of 36 Cases
AJNR 26:1066-1071, Lucato,L.T.,et al, 2005

Copper Deficiency Myelopathy
Arch Neurol 61:762-766, Kumar,N.,et al, 2004

Copper Deficiency Myelopathy Produces a Clinical Picture Like Subacute Combined Degeneration
Neurol 63:33-39, Kumar,N.,et al, 2004

Clinical Correlation of Brain MRI and MRS Abnormalities in Patients with Wilson Disease
Neurol 63:638-643, Page,R.A.,et al, 2004

Treatment of Wilson Disease With Ammonium Tetrathiomolybdate, III. Initial Therapy in a Total of 55 Neurologically Affected Patients and Follow-up With Zinc Therapy
Arch Neurol 60:379-385, Brewer,G.J.,et al, 2003

Diffusion MR Imaging Changes Associated with Wilson Disease
AJNR 24:965-967, Sener,R.N., 2003

Myelopathy Due to Copper Deficiency Following Gastrointestinal Surgery
Arch Neurol 60:1782-1785, Kumar,N.,et al, 2003

Effect of Liver Transplantation on Neurological Manifestations in Wilson Disease
ArchNeurol 57:384-386, Stracciari,A.,et al, 2000

Cerebral Injury After Cardiac Surgery,Identification of a Group of Extraordinary Risk
Stroke 30:514-522, Wolman,R.L.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

Occupational Exposures to Metals as Risk Factors for Parkinson's Disease
Neurol 48:650-658, Gorell,J.M.,et al, 1997

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

Wilson Disease:Findings at MR Imaging and CT of the Brain with Clinical Correlation
Radiology 198:531-536, van Wassenaer-van Hall,H.N.,et al, 1996

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

Treatment of Wilson Disease with Ammonium Tetrathiomolybdate
Arch Neurol 53:1017-1025, Brewer,G.J.,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

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

Showing articles 0 to 50 of 116 Next >>