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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 600 to 650 of 763 << Previous Next >>

Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
NEJM 314:547-551, Brown,P.,et al, 1986

Clinicopath. Conference
Subacute Sclerosing Panencephalitis, Due to Measles Virus, Case 25-1986, NEJM 314:1689-170086., , 1986

Isolation of HTLV-III from CSF & Neural Tissues of Patients with Neurologic Syndromes Related to AIDS
NEJM 313:1493-1497, 15381985., Ho,D.D.,et al, 1985

Cerebral MR & CT Imaging in Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 9:125-128, Kovanen,J.,et al, 1985

Creutzfeldt-Jakob Disease Prion Proteins in Human Brains
NEJM 312:73-78, Bockman,J.M.,et al, 1985

Neurologic Complications of Bone Marrow Transplantation
Neurol 35:300-306, Patchell,R.A.,et al, 1985

Ataxic Creutzfeldt-Jakob Disease:Diagnostic Techniques & Neuropathologic Observations in Early Disease
Neurol 35:254-257, Jones,H.R.,et al, 1985

Computed Tomography During Creutzfeldt-Jakob Disease
Neuroradiology 27:362-364, Westphal,K.P.&Schachenmayr,W., 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Human Growth Hormone & Creutzfeldt-Jakob Disease
Ann Int Med 103:288-289, Raiti,S., 1985

Creutzfeldt-Jakob Disease in a Young Adult with Idiopathic Hypopituitarism, Relation to Growth Hormone
NEJM 313:731-733, Koch,T.K.,et al, 1985

Clinical & Path Features & Lab Confirmation of Creutzfeldt-Jakob Disease with Pituitary Derived Human Growth Hormone
NEJM 313:734-738, Gibbs,C.J.,et al, 1985

Detection of Measles Virus RNA in Lymphocytes from Peripheral-Blood of Patients with Subacute Sclerosing Panencephalitis
NEJM 313:910-915, Fournier,J.,et al, 1985

Potential Epidemic of Creutzfeldt-Jakob Disease from Human Growth Hormone Therapy
NEJM 313:728-731, Brown,P.,et al, 1985

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) with Amyloid Angiopathy
JNNP 48:1175-1178, Keohane,C.,et al, 1985

Echocardiographically Documented Mitral-Valve Prolapse
NEJM 313:1305-1309, Nishimura,R.A.,et al, 1985

Ischemic Cerebrovascular Complications of Pregnancy
Arch Neurol 42:1106-1113, Wiebers,D.O., 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Neurological Complications of Thyrotoxicosis in the Elderly
Ann Neurol 15:608, Florin,T., 1984

Sodium Hydroxide Decontamination of Creutzfeldt-Jacob Disease Virus
NEJM 310:727, Brown,P.,et al, 1984

Creutzfeldt-Jakob Disease:A Case of 16 Years Duration
Ann Neurol 15:107-110, Cutler,N.R.,et al, 1984

Computed Tomography of the Brain in Subacute Sclerosing Panencephalitis
Ann Neurol 15:489-493, Krawiecki,N.S.,et al, 1984

Acute Kingella Kingae Endocarditis with Recurrent Cerebral Emboli in a Child with Mitral Prolapse
Ann Neurol 16:88-89, Lee,W.L.,et al, 1984

Bitemporal Hypometabolism in Creutzfeldt-Jakob Disease Measured by Positron Emission Tomography
J Comput Assist Tomogr 8:978-981, Friedland,R.P.,et al, 1984

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Measles & the Central Nervous System
Lancet 2:1406-1410, Kipps,A.,et al, 1983

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Acupuncture Needles as a Cause of Bacterial Endocarditis
BMJ 287:326-327, Jefferys,D.S.,et al, 1983

"Lhermitte's Sign"as a Presenting Symptom of Subacute Combined Degeneration of the Cord
Ann Neurol 13:215, Sandyk,R.,et al, 1983

Aseptic Meningoencephalitis in Primary Sjogrem's Syndrome
Neurol 33:593-598, Alexander,E.L.,et al, 1983

The Effect of Amantadine on Arousal & EEG Patterns of Creutzfeldt-Jakob Disease
Arch Neurol 40:555-559, Terzano,M.G.,et al, 1983

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

The Effect of Inosiplex on the Survival of Subacute Sclerosing Panencephalitis
Neurol 33:1053-1055, DuRant,R.H.,et al, 1983

Progressive CT Abnormalities Despite Clinical Improvement in SSPE Treated with Inosiplex
Ann Neurol l3:457-460, Noetzel,M.J.,et al, 1983

Endocarditis Manifesting as Bacterial Meningitis
Arch Int Med 143:1483-1484, Francioli,P.B.,et al, 1983

Twenty-Eight Years of Benign Recurring Mollaret Meningitis
Arch Neurol 40:42-43, Tyler,K.L.,et al, 1983

Meningeal Sarcomatosis & Multiple Astrocytomas
Arch Neurol 40:179-182, Lukes,S.A.,et al, 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Granulomatous Angiitis Presenting as Chronic Meningitis & Ventriculitis
Jr. , et al, Neurol 33:1609-161283., Reik,L., 1983

Recurrent Aseptic Meningitis due to Sulindac
Ann Int Med 99:343-344, FordhamVonReyn,C., 1983

Cerebral Ischemic Events in Patients with Mitral Valve Prolapse
Stroke 13:448-450, Sandok,B.A.,et al, 1982

Indications for Echocardiography in Patients with Ischemic Stroke
Neurol 32:1005-1011, Knopman,D.S.,et al, 1982

Lhermitte's Sign in Multiple Sclerosis:A Clinical Survey & Review of the Literature
JNNP 45:308-312, Kanchandani,R.,et al, 1982

Chemical Disinfection Of Creutzfeldt-Jakob Disease Virus
NEJM 306:1279-1282, Brown,P.,et al, 1982

Repeated Suppression Of Creutzfeldt-Jakob Disease With Vidarabine
Jr. , et al, Lancet 2:564-56582., Furlow,T.W., 1982

Long-Term Follow-up of Patients with Subacute Sclerosing Panencephalitis Treated with Inosiplex
Ann Neurol 11:359-364, Dyken,P.R.,et al, 1982

Chronic Mycotic Meningitis with Spinal Involvement (Arachnoiditis) :A Report of Five Cases
Ann Neurol 11:519-524, Stein,S.C.,et al, 1982

Meningitis Caused by Streptococcus bovis
Arch Neurol 39:307-308, Gavryck,W.A.,et al, 1982



Showing articles 600 to 650 of 763 << Previous Next >>