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Differential
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aminoacidurias
ammonia
anatomy of
anorexia
Arnold Chiari malformation
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
Behcet's syndrome
beriberi
beriberi, infantile
blood dyscrasias, neurologic findings with
brain atrophy
brainstem
brainstem, lesion of
bulimia
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, false negative
cataracts
caudate nucleus
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 atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
children
chorea
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
color vision, impaired
crying
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, congenital
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
differential diagnosis
dizziness
dysarthria
dystonia
electron microscopy
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
encephalopathy, neonatal
enkephalins
enzyme, defect
eye movement, disorders of
Fabry's disease
Fahr disease
failure to thrive
familial
flavivirus
fontanel, bulging
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
glioma
glutaric acidemia
gyrus, abnormal
head injury
head lag
headache
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hiccoughs
histochemistry
histochemistry of muscle
hyperglycemia
hyperphagia
hyperreflexia
hypoglycemia
hyponatremia
hypothermia
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
inborn errors of metabolism
infant and newborn with distress, neurologic prognosis in
infant, evaluation of
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal pseudoobstruction
intraventricular hemorrhage
iron, brain
irritability
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
magnetic susceptibility
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metronidazole
microhemorrhage, intracerebral
midbrain, lesion of
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, target sign
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle pain
myelitis, longitudinal
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
neoplasm, primary of CNS
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
neurotoxin
nutritional deficiency
nystagmus
nystagmus, rotary
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pancytopenia
paraparesis, spastic
Parkinson disease
pes cavus
pigmentary retinopathy
POLG1 gene
polyneuropathy
pons, lesion of
progressive infantile poliodystrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
remote effect of cancer on the nervous system
respiratory failure
restless leg syndrome
retinopathy
review article
Romberg's sign
seizure
seizure, children
sensorineural hearing loss
sensory loss
short stature
spasticity
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar degeneration
spongy degeneration of brain
status epilepticus
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
substantia nigra
suck, poor
symmetric brain lesions
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
titubation
tonic spasms
treatment of neurologic disorder
tremor
tremor, intention
urine test for metabolic disorders
visual acuity, decreased
vitamin deficiency
Von Hippel Lindau
weakness
weakness, progressive
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
wide based gait
workup
Showing articles 450 to 500 of 760 << Previous Next >>

Abnormal Eye Movements in Creutzfeldt-Jakob Disease
Ann Neurol 34:192-197, Grant,M.P.,et al, 1993

Creutzfeldt-Jakob Disease and Blood Transfusion
lancet 341:205-207, Esmonde,T.F.G.,et al, 1993

Positron Emission Tomographjy and Histopathology in Creutzfeldt-Jakob Disease
Neurol 43:1828-1830, Goldman,S.,et al, 1993

Mollarte's Meningitis Associated with Herpes Simplex Virus 2 Infection
Neurol 43:1722-1727, Picard,F.J.,et al, 1993

Complement Factor I Deficiency with Recurrent Aseptic Meningitis
Arch Int Med 153:1380-1383, Bonnin,A.J.,et al, 1993

Creutzfeldt-Jakob Disease in a Physician:A Review of the Disorder in Health Care Workers
Neurol 43:205-206, Berger,J.R.&David,N.J., 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

Clinicopath Conf
Subacute Bacterial Endocarditis with Multiple Cerebral Emboli and Mycotic Aneurysm, Case 10-1993, NE, M 8:717-725,1993., 1993

Persistence of Initial Infection in Recurrent Cryptococcus Neuformans Meningitis
Lancet 341:595-596, Spitzer,E.D.,et al, 1993

Acute Bacterial Meningitis in Adults, A Review of 493 Episodes
NEJM 328:21-28, Durand,M.L.,et al, 1993

Clinicopath Conf
Chronic Meningitis in a 51-Year-Old Man, Am J Med 94:85-921993., , 1993

Clinicopath Conf
Axonal Polyneuritis Assoc with IgA Lambda Multiple Myeloma, Case 21-1993, NEJM 328:1550-1558993., , 1993

Creutzfeldt-Jakob Disease in a Recipient of Human Pituitary-Derived Gonadotrophin:A Second Case
JNNP 55:1094-1095, Cochius,J.I.,et al, 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Plasma Vitamin B12 Level as a Potential Cofactor in Studies of HIV Type 1-Related Cognitive Changes
Arch Neurol 49:501-506, Beach,R.S.,et al, 1992

Cerebrovascular Syndromes Following Cardiac Transplantation
Neurol 42:819-823, Adair,J.C.,et al, 1992

Recurrent Aseptic Meningitis Complicating Intravenous Immunoglobulin Therapy for CIDP
Neurol 42:1636-1637, Vera-Ramirez,M.,et al, 1992

Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
Lancet 340:156-159, Mayer,R.J.,et al, 1992

Demonstration of the Transmissible Agent in Tissue From a Pregnant Woman with Creutzfeldt-Jakob Disease
NEJM 327:649, Tamai,Y.,et al, 1992

"Friendly Fire"in Medicine:Hormones, Homografts, and Creutzfeldt-Jakob Disease
Lancet 340:24-27, Brown,P.,et al, 1992

Histopathological Analysis of the Mechanisms of Intracranial Hemorrhage Complicating Infective Endocarditis
Stroke 23:843-850, Masuda,J.,et al, 1992

Clinicopath Conf
Metastatic Malignant Melanoma, "Encephalitic"Form, in Leptomeninges and Cerebral Cortex, Case 28-199, , NE27:107-116,1992., 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Is Cerebral Angiography Indicated in Infective Endocarditis?
Stroke 23:1662-1667, van der Meulen,J.H.P.,et al, 1992

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Central Nervous System Complications of Thermal Burns, A Postmortem Study of 139 Pts
Medicine 71:271-283, Winkelman,M.C.&Galloway,P.G., 1992

Long-Term Neurologic Consequences of Nutritional Vitamin B12 Deficiency in Infants
J Pediatr 121:710-714, Graham,S.M.,et al, 1992

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

Creutzfeldt-Jakob Disease in a Pathologist
Neurol 42:463, Gorman,D.G.,et al, 1992

Intraventricular Interferon and Oral Inosiplex in the Treatment of Subacute Sclerosing Panencephalitis
Neurol 42:488-491, Yalaz,K.,et al, 1992

A Controlled Trial of Fluconazole or Amphotericin B to Prevent Relapse of Cryptococcal Meningitis in Patients with AIDS
NEJM 326:793-798, Powderly,W.G.,et al, 1992

Subacute Necrotizing Myelopathy:MR Imaging in Four Pathologically Proved Cases
AJR 158:163-169, 1701992., Mirich,D.R.,et al, 1992

Vitamin B12 Metabolism in Multiple Sclerosis
Arch Neurol 49:649-652, Reynolds,E.H.,et al, 1992

Infective Endocarditis
In Braunwald, E. (Ed) Heart Disease, W. B. Saunders Co, Ch 35, p. 1097, Korzeniowski,O.M.&Kaye,D., 1992

CNS Complications of Infective Endocarditis
In Infections of CNS, Raven Press, New York, Ch 22, p5151., Francioli,P., 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

Neuroepithelial Cyst Presenting as Recurrent Aseptic Meningitis
Neurol 41:1834-1835, Kuroda,Y.,et al, 1991

Central Nervous System Complications of Infective Endocarditis
Stroke 22:1461-1463, Salgado,A.V., 1991

Herpes Simplex Virus Type 1 DNA in Cerebrospinal Fluid of a Patient with Mollaret's Meningitis
NEJM 325:1082-1085, Yamamoto,L.J.,et al, 1991

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991

Serial MR Imaging in Creutzfeldt-Jakob Disease
Neuroradiology 33:364-367, Uchino,A.,et al, 1991

Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
Lancet 337:1441-1442, Collinge,J.,et al, 1991

Creutzfeldt-Jakob Disease in a Patient with a Cadaveric Dural Graft
Neurol 41:940-941, Miyashita,K.,et al, 1991

Neurologic Complications of Infective Endocarditis
Neurol 41:1015-1020, Kanter,M.C.&Hart,R.G., 1991

Mortality, Neoplasia, & Creutzfeldt-Jakob Disease in Patients Treated with Human Pituitary Growth Hormone in the UK
BMJ 302:824-828, Buchanan,C.R.,et al, 1991

Cardiac Manifestations of Acquired Immune Deficiency Syndrome:A 1991 Update
Am Heart J 122:535-544, Kaul,S.,et al, 1991

Clinicopath Conf
CA of Lung, DIC, Marantic Endocarditis, Multiple CVA's, Case 36-1991, NEJM 325:714-726., , 1991

Multiple Sclerosis Associated with Vitamin B12 Deficiency
Arch Neurol 48:808-811, Reynolds,E.H.,et al, 1991

Screening for Dementia and Investigating Its Causes
Ann Int Med 115:122-132, Siu,A.L., 1991



Showing articles 450 to 500 of 760 << Previous Next >>