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Differential
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advances in neurology
affect, flat
agitation
akathisia
akinetic mute
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
angiitis, isolated of CNS
animal exposure
anorexia
anxiety
apraxia
apraxia, dressing
areflexia
arm weakness
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
autoantibodies
autoimmune disease
autonomic dysfunction
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
blood transfusion
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
burning paresthesia
CAT scan
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
chewing movements
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
coma
concentration, impaired
confabulation
confusion
cortical ribbon sign
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, diagnostic evaluation of
dementia, familial
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, screening for
dementia, thalamic
dementia, transmissible
depression
dexterity, impaired
diagnostic criteria
diet
differential diagnosis
diplopia
disorientation
driving
dysarthria
dysdiadochokinesia
dysmetria
dyspraxia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electron microscopy
electrophoretic pattern, CSF
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endoscopy
enolase
epidemic
epidemiology of neurology
exome sequencing
eye movement, disorders of
falling
false negative
familial
fasciculation
fatal familial insomnia
fatal sporadic insomnia
fatigue
finger nose finger test
frontal lobe, anatomy and physiology
gait disorder
gait, apraxic
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
grasp reflex
grasping
gray matter
growth hormone
gyrus, abnormal
hallucination
handwriting
head turning
hemianopia, homonymous
heralding manifestation
hockey stick sign
hyperhidrosis
hypertension
hyperthermia
hypophonia
hyporeflexia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
immunotherapy
inattention
incidence
incoordination
incubation period
insight, loss
insomnia
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, multiple
intracerebral hemorrhage, recurrent
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, unilateral
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
laminar necrosis, cortical
laughing, pathologic
life expectancy
linear lesion
masked facies
memory, defect of recent
memory, impairment of
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoparesis
mortality
motor cortex
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, FLAIR
MRI, high signal intensity of basal ganglia
MRI, indications for
MRI, negative
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
multiple sclerosis
multiple system atrophy
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
nasal brushings
neurofibrillary degeneration
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuropathology
neuropathology, brain
next-generation sequencing
nystagmus
occipital cortex
occipital lobe, lesion of
occupational neurologic disorders
old age, neurology of
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
pain
pain, leg
paresthesias
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinsonism syndrome
pathognomonic
pathologic reflex
perseveration
personality change
pituitary, hormones of
polymerase chain reaction
preclinical
prevention of neurologic disorders
prion disease
prion protein gene
procainamide
prognosis
progressive neurologic disorder
progressive supranuclear palsy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
protein 14-3-3, cerebrospinal fluid, false positive
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
remote effect of cancer on the nervous system
review article
risk factors
Romberg's sign
rooting reflex
roving eye movements
saccadic eye movements, abnormal
sarcoidosis, CNS
scrapie
seizure
senile plaques
sensory symptoms
single photon emission computed tomography
sleep pathology and physiology
snout reflex
somnolence
spinal cord
spinal cord, lesion of
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
striatum, lesion of
striatum, lesion of, bilateral
stuporous
symmetric brain lesions
tachycardia
tandem gait, ataxic
tau protein
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tonsil biopsy
toxic encephalopathy
treatment of neurologic disorder
tremor
urinary incontinence
viral infection, CNS
virus, slow
vision, blurred
visual loss
visual loss, progressive
walking, difficulty with
weakness, acute
weakness, focal
weight loss
West Nile fever
Western immunoblot test
wheelchair
wide based gait
Showing articles 1350 to 1400 of 2765 << Previous Next >>

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Neuropathies Associated with Paraproteinemia
NEJM 338:1601-1607, Ropper,A.H.&Gorson,K.C., 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Facial Nerve is Liable to Pressure Palsy
Neurol 51:320-322, Foloni,T.E.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Longitudinal Study of CSF Levels of Tau, A beta 1-40, and A beta 1-42 (43) in Alzheimer's Disease
Ann Neurol 44:17-26, 61998., Kanai,M.,et al, 1998

An Unusual Case of Creutzfeldt-Jakob Disease
Neurol 51:617-619, Vingerhoets,F.J.G.,et al, 1998

Clinicopath Conf
Sarcoidosis, Involving the Spinal Cord & Mediastinal Lymph Nodes, Case 8-1998, NEJM 338:747-754., , 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

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

Middle Cerebral Artery Main Stem Thrombosis in Two Siblings with Familial Thrombotic Thrombocytopenic Purpura
Neurol 50:1157-1160, Kelly,P.J.,et al, 1998

Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
BMJ 316:1500-1501, Ando,Y.,et al, 1998

Prognosis of patients with Primary Systemic Amyloidosis Who Present with Dominant Neuropathy
Am J Med 104:232-237, Rajkumar,S.V.,et al, 1998

Occult Giant Cell Arteritis:Ocular Manifestations
Am J Ophthalmol 125:521-526, Hayreh,S.S.,et al, 1998

High Risk of Cerebral-Vein Thromb in Carriers of Prothrombin-Gene Mutation & Users of Oral Contracept
NEJM 338:1793-1797, 18401998., Martinelli,I.,et al, 1998

SPECT in the Identif of New Variant Creutzfeldt-Jakob Disease:Case Reports
BMJ 316:593-594, 5631998., deSilva,R.,et al, 1998

The Role of 99m-Tc HMPAO SPECT in the Diagnosis of Creutzfeldt-Jacob Disease
AJNR 19:454-455, Miller,D.A.,et al, 1998

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

Optic Neuritis, Prognosis for Multiple Sclerosis from MRI, CSF, and HLA Findings
Neurol 50:708-714, Soderstrom,M.,et al, 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
Neurol 51:1226-1227, Wasay,M.,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

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
Neurol 51:1039-1045, Seale,C.G.,et al, 1998

Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
Neurol 51:944-948, Rpt of the Quality Stnds Subcmte AAN, 1998

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

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

Risk of Cerebral Sinus Thrombosis in Oral Contraceptive Users Who Are Carriers of Hered Prothrombotic Cond
BMJ 316:589-592, deBruijn,S.F.T.M.,et al, 1998

Cerebrovasc Dis Risk Factors:Neuroradiol Findings in Pts with Activated Protein C Resistance
Radiology 207:85-89, Provenzale,J.M.,et al, 1998

Dural Sinus Thrombosis Associated with Activated Protein C Resistance:MRI & Proband Ident
AJR 170:499-502, Provenzale,J.M.,et al, 1998

Chromosome 19 Single-Locus & Multilocus Haplotype Assoc with MS, Evid of New Suscept Locus in Caucasian & Chinese Pts
JAMA 278:1256-1262, 12821997., Barcellos,L.F.,et al, 1997

Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Psychiatric Features
Lancet 350:908-910, 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

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

Cavernous Angioma of the Brain Stem Mimicking Multiple Sclerosis
NEJM 336:875-876, Vrethem,M.,et al, 1997

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

Clinicopath Conf
Genetic Hemochromatosis, Micronodular Cirrhosis of Liver, Case 10-1997, NEJM 336:939-94797., , 1997



Showing articles 1350 to 1400 of 2765 << Previous Next >>