Neudle.com: copper deficiency

Differential
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aceruloplasminemia

Addison's disease

adverse drug reaction

alcohol, neurologic complications with

anticonvulsants, untoward effects of

Arnold Chiari malformation

ascites

ataxia

ataxia telangiectasia

basilar artery occlusion

blindness

blindness, nutritional

blood dyscrasias, neurologic findings with

brainstem, lesion of

burning feet

carcinoma

carcinoma of pancreas

CAT scan, abnormal

cataracts

ceftriaxone

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

copper metabolism, abnormal

corpus callosum

corpus callosum, lesion of

diabetic coma, diagnosis and treatment

diet

differential diagnosis

disability, neurological

disorientation

dissociated sensory loss

electrolyte imbalance

facial expression abnormality

gastrectomy, neurologic complications following

gastric partitioning

gene

gene mutation

genetic diagnosis, prenatal

genetic neurologic disorders

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hypotension, systemic

hypothyroidism

iatrogenic neurologic disorders

imbalance

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

infant, evaluation of

intellectual deficit

intellectual deterioration

internet

iron, brain

iron, serum, low

Jakob-Creutzfeldt disease

jaundice

Kayser-Fleischer ring

Leigh's disease

leukopenia

level of consciousness, decreased

Lhermitte's sign

lipid storage disorder of CNS

liver function enzymes

long bone lesion

lymphoma involving CNS

malabsorption

malabsorption syndrome

Marinesco-Sjogren syndrome

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

MRI, diffusion weighted

MRI, gradient-echo

MRI, negative

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, cognitive presenttion

myelitis, longitudinal

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myopathy

nausea and vomiting

neoplasm, intracranial

neoplasm, primary of CNS

nerve conduction studies

neuritis, causes of

neuroendocrinology

neurologic complications of, burns

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

nutritional deficiency

obesity

optic atrophy

optic neuropathy

optic neuropathy, nutritional

osmotic demyelination syndrome

paresthesias, generalized

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

pseudobulbar palsy

psychiatric disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

psychosis, cause of

quadriplegia

remote effect of cancer on the nervous system

renal stones

retinopathy

retroperitoneal hemorrhage

skull bone, thickening

slit lamp examination

small-bowel bypass

sodium valproate

somatosensory evoked potentials

spinal cord, cervical

spinal cord, lesion of

spinocerebellar degeneration

splenomegaly

subdural hematoma

swayback

symmetric brain lesions

syphilis, neurologic complications with

systemic lupus erythematosus

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiazide diuretic

thrombocytopenia

treatment of neurologic disorder

tremor

trichopoliodystrophy

trientine dihydrochloride

unconsciousness

urinary incontinence

visual loss

visual loss, progressive

vitamin A deficiency

vitamin deficiency

vitamin supplementation

vitamin, multiple

Von Hippel Lindau

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Wernicke's encephalopathy

wheelchair

white matter disease

zinc

Showing articles 1150 to 1200 of 1340 << Previous Next >>

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

The Intelligence of Hydrocephalic Children
Arch Neurol 38:607-615, Dennis,M.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Extramedullary Hematopoiesis & Spinal Cord Compression Complicating Polycythemia Rubra Vera
Ann Neurol 7:81-84, Rice,G.P.A.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Neonatal Polycythemia Causing Multiple Cerebral Infarcts
Arch Neurol 37:109-110, Amit,M.,et al, 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Cognitive Function in Patients With Multiple Sclerosis
Arch Neurol 37:577-579, Peyser,J.M.,et al, 1980

The Neuropsychiatry of Megaloblastic Anaemia
BMJ 281:1036-1038, Shorvon,S.D.,et al, 1980

Unreliability of Radiodilution Assays as Screening Tests for Cobalamin (Vitamin B12) Deficiency
JAMA 244:1942-1945, Cohen,K.L.,et al, 1980

Studies Of A Patient With Megaloblastic Anemia & An Abnormal Transcobalamin II
NEJM 303:1209-1212, Seligman,P.A.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Proximal Myopathy after Prolonged Total Therapeutic Starvation
BMJ 280:1212-1213, Scobie,I.N.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Wernicke's Encephalopathy in Patients With Tumors of the Lymphoid-Hemopoietic Systems
Arch Neurol 37:338-341, DeReuck,J.L.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Heterozygous Expression Of X-Linked Mental Retardation & X-chromosome Marker fra (X) (q27)
NEJM 303:662-664, Turner,G.,et al, 1980

Acquired Hemophilia, Meningioma, & Diphenyl-hydantoin Therapy
J Neurosurg 53:600-605, O'Reilly,R.A.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

The Fragile X-Chromosome Mental Retardation & Large Testes
Arizona Med 37:764-766, Hecht,F.,et al, 1980

X-Linked Mental Retardation
Am J Med Genet 7:407-415, Turner,G.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Cerebral Infarcts with Arterial Occlusion in Neonates
Ann Neurol 6:495-502, Barmada,M.A.,et al, 1979

Iatrogenic Night Blindness & Keratoconjunctival Xerosis
NEJM 301:943-944, Partamian,L.G.,et al, 1979

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Periodic Lateralized Epileptiform Discharges in Infants & Children
Ann Neurol 6:47-50, PeBenito,R.,et al, 1979

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Fetal Alcohol Syndrome & Related CNS Problems
Neurol 29:1429-1430, Wisniewski,K.,et al, 1979

Computerized Cranial Tomography in Wilson Disease
Neurol 29:866-868, Nelson,R.F.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Myasthenia Gravis, Pernicious Anemia, & Hashimoto's Thyroiditis
Arch Neurol 36:594-595, Krol,T.C., 1979

Visual Evoked Responses in Pernicious Anemia
Arch Neurol 36:168-169, Troncoso,J.,et al, 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Computed Tomography in Wilson Disease:Report of 2 Cases
Ann Neurol 5:102-103, Ropper,A.H.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Progressive Myelopathy Due to Extramedullary Hematopoiesis:Case Report & Review of the Literature
Ann Neurol 5:485-489, Stahl,S.M.,et al, 1979

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Showing articles 1150 to 1200 of 1340 << Previous Next >>