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adenylate kinase 5 autoantibodies
advances in neurology
agitation
agnosia, visual
akinetic mute
Alice in Wonderland syndrome
alien hand syndrome
alternating rapid movement
aluminum
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, familial
Alzheimer's disease, heterogeneity of
Alzheimer's disease, incidence
Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, staging
Alzheimer's disease, treatment of
amnesia
amyloid
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, iatrogenic
amyloid beta protein
amyloid imaging
amyloid plaques
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anomic aphasia
anorexia
anti IgLON5
anticholinesterase
anticonvulsants
antiviral agents
aphasia
aphasia, progressive, primary
apolipoprotein E
APP
applause sign
apraxia
apraxia of eyelid opening
apraxia, constructional
areflexia
arm swing, reduced
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
attention span
atypical
autoantibodies
automobile accidents
axonal injury
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
blast injury
blepharospasm
blinking, reduced
bovine spongiform encephalopathy
boxing
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brain transplantation
brain weight
bruxism
bulbar palsy
callosal angle
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
cavum septi pellucidi
central core disease
central hypoventilation
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, secondary
cerebellar plaques, amyloid
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral glucose metabolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS disease
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
Charcot-Marie-Tooth
choline acetyltransferase
chorea
choreoathetosis
chorioretinitis
chronic traumatic encephalopathy
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
cognition
color vision, impaired
complications
compulsivity
concussion
concussion, recurrent
confusion
controversies in neurology
cortical blindness
cortical-basal ganglionic degeneration
cough
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, screening for
dementia, subcortical
dementia, transmissible
depression
developmental milestones, loss of
dexterity, impaired
diagnostic criteria
dialysis
diarrhea
diet
differential diagnosis
diplopia
donepezil
downward gaze
dysarthria
dyschromatopsia
dysdiadochokinesia
dysmetria
dysnomia
dysphagia
dystonia
dystonia, focal
echolalia
efficacy
electroencephalogram
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalitis, viral
encephalopathy
encephalopathy, post traumatic
epidemiology of neurology
executive dysfunction
eye movement, disorders of
falling
familial
Fazio-Londe's disease
fine motor function, impaired
finger nose finger test
flortaucipir
foam cells
football neurologic injuries
frontal behavioral spatial syndrome
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, apraxic
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
granulovacuolar degeneration
grasp reflex
Hallervorden Spatz disease
handwriting
head injury
head injury, mild
head injury, repetitive
head injury, return to play following
headache
headache, frontal
heavy metal intoxication
heel-knee-shin test
hemianopia, homonymous
hemifacial spasm
hepatic failure
hepatosplenomegaly
heralding manifestation
herpes virus infection
hippocampal atrophy
hippocampus
hippocampus, hyperintense
histochemistry
HLA
hoarseness
hockey
Huntington's chorea
hydrocephalus, normal pressure
hypophonia
iatrogenic neurologic disorders
ideomotor apraxia
imbalance
imbalance, postural
immunohistochemistry
immunoperoxidase staining
impulsivity
inattention
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incoordination
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
interferon
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
jaundice
Kluver-Bucy syndrome
Kugelberg-Welander syndrome
language disorder in adults
L-dopa
lead poisoning
Lewy body
Lewy body disease, diffuse
limbic encephalitis
lipid storage disorder of CNS
lobar atrophy
logopenia
loss of sympathy
lymphadenopathy
macropsia
manganese intoxication
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental status, abnormal
mesial temporal lobe
metamorphopsia
micropsia
midbrain
midbrain, atrophy
mild cognitive impairment
mild cognitive impairment converting to Alzheimer's disease
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
molecular genetics
mongolism
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, FLAIR
MRI, negative
MRI, serial
MRI, volumetry
MRI, voxel-based morphometry
multiple system atrophy
muscle spasm, face
mutism
myasthenia gravis
myoclonic jerks
myoclonus
myotonia dystrophica
nerve conduction studies
neurofibrillary degeneration
neurofibrillary degeneration, causes of
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neurologic symptoms
neurologic testing
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
neurotransmitter
Niemann-Pick disease
nucleus basalis of Meynert
obsessive-compulsive disorder
old age, neurology of
olfactory bulb
ophthalmoplegia
ophthalmoplegia, total
optic atrophy
palmomental response
paranoia
parasomnia
Parkinson disease
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, dementia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, tremor, absence of
Parkinsonism syndrome
PAS positive material in the brain
pathologic reflex
pathology
penguin silhouette sign
perseveration
personality change
Pick bodies
Pick's disease
Pittsburgh Compound B
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, mercury
poison, neurologic problems with
positional head-hanging test
preclinical
pregnancy, neurologic complications in
prion disease
prognosis
progressive neurologic disorder
progressive supranuclear palsy
prosopagnosia
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pugilistic parkinsonism
punch-drunk syndrome
pursuit eye movements, abnormal
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
real-time quaking-induced conversion
release phenomena
respirations in CNS disease
retrocollis
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rigidity
rigidity, axial
risk factors
Romberg's sign
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
screening
semantic dementia
senile plaques
sequencing difficulty
serologic testing
serologic testing of cerebrospinal fluid
sinemet
single photon emission computed tomography
sleep apnea, obstructive
sleep pathology and physiology
smell
Smell Identification Test
soccer
speech disorder
speech disorder, non aphasic
splenomegaly
spongy degeneration of brain
sports medicine, neurology of
square wave jerks
staining reactions in neuropathology
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
substantia nigra
symmetric brain lesions
synucleinopathy
tandem gait, ataxic
tangential
tau protein
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of-bilateral
toxoplasmosis, CNS
trauma
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tricresylphosphate
tuberous sclerosis
ubiquitin
vaccine
vasculitides
vasculopathy
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual distortions
visual loss
visual symptoms
visuospatial disturbance
vocal cord paralysis
voice, abnormality of
walking frame
walking, difficulty with
war
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
wide based gait
Williams syndrome
word-finding difficulty
Showing articles 650 to 700 of 1005 << Previous Next >>

Free Protein S Deficiency in Acute Ischemic Stroke, A Case-Control Study
Stroke 24:224-227, Mayer,S.A.,et al, 1993

Neurologic Prognosis of Cytomegalovirus Polyradiculomyelopathy in AIDS
Neurol 43:493-499, Cohen,B.A.,et al, 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Infectious Prions or Cytotoxic Metabolites?
Lancet 341:159-161, Pablos-Mendez,A.,et al, 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

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Headache Caused by a Single Lesion of Multiple Sclerosis in the Periaqueductal Gray Area
Headache 33:452-455, Haas,D.C.,et al, 1993

Bacterial Spinal Epidural Abscess, Review of 43 Cases and Literature Survey
Medicine 71:369-385, Darouiche,R.O.,et al, 1992

Amyloidoma of the CNS. I. Clinical and Pathologic Study
Neurol 42:2019-2023, Cohen,M.,et al, 1992

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

The Molecular Pathogenesis of Alzheimer's Disease:Clinical Prospects
Lancet 340:1512-1515, Murphy,M., 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Bovine Gangliosides and Acute Motor Polyneuropathy
BMJ 305:1330-1331, Figueras,A.,et al, 1992

"Chronic Sensory Demyelinating Neuropathy":CIDP Presenting as a Pure Sensory Neuropathy
JNNP 55:677-680, Oh,S.J.,et al, 1992

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

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Plasma-Cell Dyscrasia with Polyneuropathy, The Spectrum of POEMS Syndrome
NEJM 327:1919-1923, Miralles,G.D.,et al, 1992

Cerebrospinal Fluid in Diseases of the Nervous System
W. B. Saunder Co, 2nd Ed, Phila, p. 185, 271, Fishman,R.A., 1992

Cerebral Venous Thrombosis
Neurol Clin 10:87-111, Ameri,A.&Bousser,M-G., 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Fatal Familial Insomnia:A Second Kindred with Mutation of Prion Protein Gene at Codon 178
Neurol 42:669-670, 1992, Medori,R.,et al, 1992

Prion Disease
NEJM 326:486-487, Johnson,R.T., 1992

Cerebral Infarction Associated with Protein C Deficiency
Stroke 23:108-111, Matsushita,K.,et al, 1992

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

A Correlative Triad of Gadolinium-DTPA MRI, EDSS, & CSF-MBP in Relapsing MS Treated with High-Dose Intravenous Methylprednisolone
Neurol 42:63-67, Barkhof,F.,et al, 1992

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

Myeloma and Benign Intracranial Hypertension
BMJ 304:685, Wasan,H.,et al, 1992

Clinicopath Conf
Multiple Myeloma, Presenting as Plasmacytoma of Bone Extending into Sphenoid Sinus, Case 21-1992, NE, M 31417-1424,1992., 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Human Herpesvirus-6:Clinical Implications of a Recently Discovered, Ubiquitous Agent
J Pediatr 121:173-181, Leach,C.T.,et al, 1992

Pure Sensory Guillain-Barre Syndrome
JNNP 55:411-415, Miralles,F.,et al, 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Protein Redistribution Diet Remains Effective in Patients with Fluctuating Parkinsonism
Arch Neurol 49:149-151, Karstaedt,P.J.&Pincus,J.H., 1992

Tuberculous Meningitis with Acellular Cerebrospinal Fluid in AIDS Patients
AIDS 6:1165-1167, Laguna,F.,et al, 1992

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Plasma Exchange in Polyneuropathy Associated with Monoclonal Gammopathy of Undetermined Significance
NEJM 325:1482-1486, Dyck,P.J.,et al, 1991

A Case of Myelinoclastic Diffuse Sclerosis in an Adult
Neurol 41:316-318, Dresser,L.P.,et al, 1991

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

Tuberculosis of the CNS (Spinal Cord Disease)
In Infections of the Central Nervous System, Raven Press, New York, p 44091., Zuger,A.&Lowry,F.D., 1991

Myasthenia Gravis in Mothers and Their Newborns
Clin Obstet Gynecol 34:82-99, Plauche,W.C., 1991

BA4 Amyloid Protein Deposition in Brain After Head Trauma
Lancet 338:1422-1423, Roberts,G.W.,et al, 1991

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

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991



Showing articles 650 to 700 of 1005 << Previous Next >>