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Differential
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acanthocytosis
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
alternating hemiplegia
alternating hemiplegia of childhood
amimia
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
anterior tibial muscle weakness
antiviral agents
aphasia
areflexia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
ATP1A3 gene
attention deficit disorder with hyperactivity
atypical
autonomic dysfunction
Babinski sign
basal ganglia, lesion, bilateral
behavioral disorder
beta-D-glucon
bladder dysfunction
brain atrophy
brain biopsy
brainstem, atrophy
bronchoscopy
bulbar palsy
calcification, gyral
calcification, intracranial
candida albicans
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, etiology
cerebral palsy, work up
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, nonvascular territory
cerebrovascular accident, young adult
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Coats plus
cobalamin C deficiency
coma
coma, sudden onset
complications
confusion
congenital myasthenic syndromes
consanguinity
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
corpus callosum, thinning
cortical ribbon sign
cranial nerve enhancement
creatine phosphokinase(CPK)elevated
cyst
cyst, benign intracranial
cyst, cortical parenchyma
cyst, parenchymal
deafness
delay in diagnosis
dementia
dementia, presenile
developmental disability
developmental retardation
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
disease modifying agents
distal muscle atrophy
distal muscle weakness
DNA sequencing
double-cortex syndrome
dysarthria
dysmetria
dysmorphic
dysphagia
dystonia
electromyogram
encephalopathy
encephalopathy, acute
eosinophilia
executive dysfunction
exome sequencing
Fabry's disease
facial appearance, abnormal
facial weakness
falling
false negative
familial
fatal familial insomnia
fatigue
feeding disorder
fever
fish
floppy infant
fourth ventricle, compression
fungal infection
fungal infection, CNS
gait disorder
gait speed
gait, spastic
GAMT gene
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus, lesion of, bilateral
gram positive cocci
gray hair
hammertoes
headache
headache, awakening with
headache, positional
headache, progressive
hearing loss
helminthic infection of CNS
hemianopia, homonymous
hemiparesis, transient
hemophagocytic lymphohistiocytosis
hepatomegaly
hepatosplenomegaly
heterotopia
HHH syndrome
high arched feet
high arched palate
human genome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperammonemic encephalopathy
hyperhomocysteinemia
hyperreflexia
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
imbalance
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
incoordination
India
infection
insomnia
insular cortex
insular cortex, lesion
intellectual deficit
interstitial pulmonary fibrosis
intracerebral hemorrhage
intravenous drug abuse
intrinsic hand muscles, wasting of
jaundice
Jewish
Krabbe's disease
lactic acidemia
Leber's hereditary optic neuropathy
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
leukoencephalopathy with calcification and cysts
level of consciousness, decreased
lid
lid abnormalities
life expectancy
linear lesion
lipid storage disorder of CNS
lung nodule
lung-brain syndromes
lysosomal storage disease
malformation, CNS, congenital
McLeod syndrome
megalencephaly
MELAS syndrome
memory, impairment of
meningeal enhancement
meningeal sarcomatosis
meningitis
meningitis, basilar
meningitis, candida
meningitis, chronic
meningitis, fungal
meningitis, neutrophilic
mental retardation
mestinon
metabolic acidosis
methylmalonic acidemia
microcephaly
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
miglustat
mimics
mineralization
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
movement disorder
moyamoya
moyamoya, adult
MRI, abnormal
MRI, blooming effect
MRI, contrast enhanced
MRI, diffusion weighted
MRI, mass effect on
MRI, muscle
MRI, negative
MRI, nodular enhancement
MRI, spinal cord
muscle biopsy
muscle weakness, proximal
mutism
myelomalacia
myeloneuropathy
myelopathy
myoclonus
myopathy
nasal speech
nausea and vomiting
needle tracks
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathy
neuropathy, demyelinating
newborn, evaluation of
next-generation sequencing
Niemann-Pick disease
night blindness
normal
NOTCH2NLC
nystagmus
occipital lobe
ocular motility, disorders of
opened mouth
ophthalmoplegia
organomegaly
ornithine transcarbamylase deficiency
ovarian dysgenesis
pachygyria
papilledema
paragonimiasis
paraparesis, familial spastic
paraparesis, spastic
parasitic infection, CNS
Parkinsonism syndrome
paroxysmal neurologic deficits
peripheral blood smear
Perrault syndrome
pes cavus
philtrum, tented
phonophobia
photophobia
PICU
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
polyglucosan body disease
polymicrogyria
pons, lesion of
precipitating factors
prion disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
ragged-red fibers
recurrent
ReNU syndrome
respiratory tract infection
retinopathy
review article
risk factors
Romberg's sign
salivation, excessive
schizophrenia
scissors gait
scotoma
screening
sedimentation rate, elevated
seizure
seizure, focal
seizure, laughing as manifestation
sensorineural hearing loss
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sleep pathology and physiology
small vessel disease
spastic ataxia
spastic paraplegia, type 7
spasticity
speech disorder
speech, absence of
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
strokelike episodes
symmetric brain lesions
systemic illness
tandem gait, ataxic
telangiectases, retinal
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of-bilateral
tinnitus
toe walking
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
tripping
tumefactive lesion
urea-cycle enzymopathies
urinary urgency
vasculitides
vasculopathy
vegetarianism
vestibular migraine
vision loss, sequential
vision, blurred
visual loss
visual loss, transient
visual obscurations, transient
visuospatial disturbance
walking, delayed
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
white matter disease, unilateral
whole genome sequencing
wide based gait
workup
x-linked intellectual deficit
x-linked mental retardation
Showing articles 250 to 300 of 305 << Previous Next >>

Positron Emission Tomography in Shy-Drager Syndrome
Ann Neurol 28:101-103, Bhatt,M.H.,et al, 1990

PET Study in Progressive Supranuclear Palsy, Hypometabolic Pattern
Arch Neurol 47:747-752, Blin,J.,et al, 1990

Positron Emission Tomography in Creutzfeldt-Jakob Disease
Arch Neurol 47:1035-1038, Holthodd,V.A.,et al, 1990

Transplantation of Human Fetal Dopamine Cells for Parkinson's Disease
Arch Neurol 47:505-512, Freed,C.R.,et al, 1990

National Cancer Institute Workshop Statement
Advances in Clinical Imaging Using Positron Emission Tomography, Arch Int Med 150:735-739, 729990., , 1990

Cerebral Metabolic Asymmetries & Assoc Neuro-psych Patterns in Early Dementia of the Alzheimer Type
Arch Neurol 47:753-760, Haxby,J.V., 1990

Infantile Spasms:I. PET Identified Focal Cortical Dysgenesis in Cryptogenic Cases for Surgical Treatment
Ann Neurol 27:406-413, Shields,W.D.,et al, 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990

Pituitary Microadenomas:A PET Study
Radiology 177:39-44, DeSouza,B.,et al, 1990

The Brain in Schizophrenia
JNNP 53:725-726, Ron,M.A.&Harvey,I., 1990

The Evaluation and Treatment of Seizures
NEJM 323:1468-1474, Scheuer,M.L.&Pedley,T.A., 1990

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

SPECT and PET in Epilepsy
Editorial, Lancet 1:135-1371989., , 1989

A Referendum on Clinical Trial Research in Multiple Sclerosis:Opinion of Jekyll Island Workshop
Neurol 39:977-981, Noseworthy,J.H.,et al, 1989

Immunological Treatment for Multiple Sclerosis
Editorial, Lancet 1:699-7011989., , 1989

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

Cerebral Glucose Metabolism in the Course of Subacute Sclerosing Panencephalitis
Arch Neurol 46:97-100, Huber,M.,et al, 1989

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

Normal-Pressure Hydrocephalus and the Saga of the Treatable Dementias
JAMA 262:2577-2581, 2592-25931989., Friedland,R.P., 1989

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

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

Immunotherapy of Multiple Sclerosis
Ann Neurol 23:211-223, Weiner,H.L.&Hafler,D.A., 1988

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

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

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

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

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

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

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

Wilson's Disease Studies with FDG & Positron Emission Tomography
Neurol 37:1707-1711, Hawkins,R.A.,et al, 1987

Total Lymphoid Irradiation in Multiple Sclerosis:Blood Lymphocytes & Clinical Course
Ann Neurol 22:634-638, Cook,S.D.,et al, 1987

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

Effect of Total Lymphoid Irradiation in Chronic Progressive Multiple Sclerosis
Lancet 1:1405-1409, Cook,S.D.,et al, 1986

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

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

Alzheimer's Disease & Down's Syndrome:New Insights
Ann Int Med 103:566-578, Cutler,N.R.,et al, 1985

Positron Emission Tomography & its Application to the Study of Cerebrovascular Disease in Man
Stroke 16:361-376, Powers,W.J.,et al, 1985

Pure Hemidystonia with Basal Ganglion Abnormalities on Positron Emission Tomography
Ann Neurol 15:228-233, Perlmutter,J.S.,et al, 1984

Parkinson's Disease, 1984
Lancet 1:829-830, Williams,D.,et al, 1984



Showing articles 250 to 300 of 305 << Previous Next >>