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Differential
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accommodation
accomodation, abnormal
achilles tendon, enlarged
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
adverse drug reaction
affect, flat
alexia
algorithm
alien hand syndrome
Alzheimer's disease
amyotrophic lateral sclerosis
ANA
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
anomic aphasia
anticholinergic drugs
antiviral agents
aphasia
aphasia, classification of
aphasia, progressive, primary
apraxia
arthralgia
ataxia
ataxia, cerebellar
ataxia, frontal
ataxia, hereditary
ataxia, progressive
ataxic gait
autoimmune disease
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, degeneration
behavior modification
behavioral disorder
Bell's phenomenon
blinking
blinking, reduced
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, lesion of
C0ORF72
cachexia
calcium antagonist
camptocormia
carbon monoxide poisoning
CAT scan, abnormal
CAT scan, angiography
CD4 counts
cerebellar atrophy, primary
cerebellar degeneration
cerebellitis
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
coma
complications
concentration, impaired
confusion
conjunctivitis
contractures, joint
convergence
convergence, impaired
conversion reaction
corpus callosum
corpus callosum, lesion of
cortical-basal ganglionic degeneration
Coxiella burnetti
crying, pathologic
cryopyrin-associated periodic syndrome
cystatin C mutation
degenerative diseases of CNS
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
depression
developmental retardation
diagnostic criteria
differential diagnosis
digital subtraction angiography
diplopia
disability, neurological
disconnection syndrome
dizziness
dopamine agonist
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, brainstem
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, delayed
episodic disorders
Erdheim-Chester disease
eye movement, disorders of
falling
familial
fasciculation
fatigue
fever
fever, recurrent
finger nose finger test
Fisher C.M.
foam cells
Friedreich's ataxia
frontal behavioral spatial syndrome
frontal bossing
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, apraxic
gait, festinating
gait, spastic
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
hallucination
hallucination, visual
handwriting
head circumference
headache
headache, awakened by
headache, awakening with
headache, bifrontal
headache, occipital
headache, recurrent
headache, severe
hearing loss
heel swelling
hemiparesis
highly active antiretroviral therapy
hip flexor weakness
histiocytosis
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hyperreflexia
hypersomnia
hypertrophic intracranial pachymeningitis
hypometric saccades
hypomyelination
hypophonia
hyporeflexia
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
immunosuppression
immunosuppressive agents
impulsivity
inattention
incontinence, fecal
infection
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
kinesia paradoxica
lacunar infarction
laughing, pathologic
L-dopa
leg dragging
leg weakness, bilateral
Legionnaires'disease
lethargy
Lewy body
lobar atrophy
lumbar drain
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, neurologic aspects and complications of
mental status, abnormal
micrographia
middle cerebellar peduncle, lesion
miosis
misdiagnosis
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, nodular enhancement
multimodal neuroimaging
multiple system atrophy
mutism
myelopathy
myoclonus
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neurologic symptoms
neuropathology
neuropathy, demyelinating
next-generation sequencing
nystagmus
nystagmus, gaze-evoked
nystagmus, upbeating on upgaze
ocular motility, disorders of
old age, neurology of
opportunistic infection, CNS
optic ataxia
optic atrophy
optic atrophy, bilateral
oscillopsia
paranoia
paraparesis, spastic
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
patient information and support
Pelizaeus Merzbacher
perivascular enhancement
Persistent postural-perceptual dizziness
personality change
pes cavus
photophobia
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
polymerase chain reaction, false negative
pons, lesion of
posterior leukoencephalopathy syndrome
precipitating factors
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
proprioception, abnormal
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
pupil
pupil, light reflex, abnormal
Q fever
rash
recurrent
red eye
reflex, cutaneous
release phenomena
respiratory tract infection
retropulsion
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rickettsial organism
rigidity
rooting reflex
seizure
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss
serologic testing
serotonin norepinephrine reuptake inhibitors
short stature
short steps
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull bone, thickening
slow virus infection of CNS
slurred speech
smell
snout reflex
somnolence
speech disorder
speech, soft
splenium of corpus callosum
spongy degeneration of brain
stare
startle myoclonus
startle reaction
steroid therapy, CNS treatment and complications with
stooped posture
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
subcortical U fibers
suck reflex
suicide
systemic illness
systemic lupus erythematosus
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, atrophy
thrombocytopenia
tongue, fasciculations of
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, resting
turning in bed
twins
upgaze
upgaze, paralysis of
urinary incontinence
vasculopathy
vasospasm, cerebral
ventriculostomy
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual impairment
voice, abnormality of
walking frame
walking, difficulty with
weakness, generalized
weight loss
wheelchair
white matter disease
wide based gait
writing
Showing articles 650 to 700 of 1411 << Previous Next >>

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

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

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Characteristic Magnetic Resonance Imaging Findings in Machado-Joseph Disease
Arch Neurol 55:33-37, Murata,Y.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
JNNP 64:306-313, Talbot,P.R.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Clinicopath Conf,Sarcoidosis,with Involvement of Spinal Cord,Brain,Mediastinal Lymph Nodes and ? Lung,Case 35-1998
NEJM 339:1534-1541, , 1998

Adult Brainstem Gliomas
Neurol 51:1136-1139, Landolfi,J.C.,et al, 1998

Lateral Medullary Infarction
Stroke, Pathophysiology, Diagnosis and management, Churchhill Livingstone, NY 3rd Ed, Ch 22, p. 534, Amarenco,P.,et al, 1998

Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
Neurol 50:244-251, Tagliati,M.,et al, 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
Radiology 203:829-836, Ernst,T.,et al, 1997

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

A Blinding Headache
Lancet 350:182, Embil,J.J.,et al, 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

"Idiopathic"Cranial Hypertrophic Pachymeningitis Responsive to Antiotuberculous Therapy:Case Report
Neurosurg 41:965-971, Parney,I.F.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997



Showing articles 650 to 700 of 1411 << Previous Next >>