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Differential
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abdominal protrusion
activities of daily living
activities of daily living scale
agnosia
agnosia, visual
agraphia
akinetic mute
alexia
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, visual variant
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anomic aphasia
aphasia
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apolipoprotein E
apraxia
apraxia, constructional
arthralgia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
attention span
automobile accidents
B 12 deficiency
B12
behavioral disorder
binge eating
biologic markers
blepharospasm
bone biopsy
bone pain
bone scanning
brain atrophy
brain biopsy
bruxism
bulimia
C9orf72
calculations
CAT scan
CAT scan, abnormal
CAT scan, dementia
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar degeneration
cerebellar tonsils
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, pressure low
Charles Bonnet's syndrome
choreoathetosis
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cognition
comprehension, impaired
compulsivity
confusion
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
crying, pathologic
degenerative diseases of CNS
delirium
delusion
dementia
dementia, age at onset
dementia, clinical diagnosis
dementia, diagnostic classification
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
diagnostic criteria
differential diagnosis
difficulty climbing stairs
disinhibition-dementia-parkinsonism-amyotrophic complex
drug withdrawal
dysarthria
dysmetria
eating disorder
electromyogram
electron microscopy
emotional lability
executive dysfunction
falling
familial
fasciculation
fatigue
fibrillations
finger nose finger test
flail arm syndrome
fluency
foot drop
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal brain sagging syndrome
frontotemporal dementia, behavioral variant
gait disorder
gait, waddling
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
hallucination
hallucination, visual
hallucination, visual, benign
head injury
headache
headache, chronic
hemianopia, homonymous
herpes simplex encephalitis
hippocampus
House sign
Huntington's chorea
hyperreflexia
hypersomnia
imbalance
imbalance, postural
impulsivity
inappropriate behavior
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, ubiquitin
inflexibility, mental
initiative, lack of
insomnia
insular cortex
insular cortex, lesion
intellectual deficit
intellectual deterioration
interpeduncular cistern, compressed
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kluver-Bucy syndrome
language disorder in adults
laughing, pathologic
leg weakness, bilateral
Lewy body disease, diffuse
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
memory
memory, defect of recent
memory, impairment of
memory, recent
mental status, abnormal
mesial temporal sclerosis
midbrain, swollen
migraine
mimics
misdiagnosis
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, functional
MRI, serial
MRS
multiple system atrophy
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myopathy
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuropathology
neuropathology, brain
nutritional deficiency
nystagmus
obsessive-compulsive disorder
ophthalmoplegia
ophthalmoplegia, total
Paget's disease
pain, increased response
pallido-ponto-nigral degeneration
palmomental response
paranoia
paraparesis
paraphasias
paraplegia, in flexion
Parkinson disease
Parkinson disease, atypical
Parkinsonism syndrome
pathologic reflex
peduncular hallucinosis
perseveration
personality change
Pick bodies
Pick's disease
pons, flattened
posterior cortical atrophy
posterior leukoencephalopathy syndrome
prepontine cistern, effaced
primary intracranial hypotension
primary lateral sclerosis
prognosis
progranulin
progressive neurologic disorder
progressive subcortical gliosis
progressive supranuclear palsy
pruritus
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
quadriplegia
rapidly progressing neurologic illness
Red flags
release phenomena
repetition, impaired
respiratory failure
respiratory tract infection
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rigidity, axial
risk factors
roaming behavior
rooting reflex
sagging of the brain
sclerosis, bone
seizure
semantic dementia
sexual behavior, disorder of
simultanagnosia
single photon emission computed tomography
single photon emission computed tomography, false negative
sleep pathology and physiology
snout reflex
spasticity
speech disorder
speech, loss of
splenium of corpus callosum
splenium of corpus callosum, displaced
spongy degeneration of brain
stereotyped behavior
suck reflex
synucleinopathy
systemic illness
tangential
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
tongue, atrophy
tongue, fasciculations of
tonsillar herniation of cerebellum
trauma
treatment of neurologic disorder
ubiquitin
upgaze, paralysis of
urinary incontinence
vegetarianism
visual field defect
visuospatial disturbance
vitamin deficiency
weakness, progressive
wheelchair
white matter disease
wide based gait
Wingspan study
word-finding difficulty
Showing articles 1550 to 1600 of 2257 << Previous Next >>

New Neuropathological Criteria for Alzheimer Disease
Arch Neurol 55:1174-1176, Hyman,B.T., 1998

Acute Inflammatory Demyelinating Polyradiculopathy in Children:Clinical and Electrodiagnostic Studies
Ann Neurol 44:350-356, Delanoe,C.,et al, 1998

Development of Wernicke-Korsakoff Syndrome After Long Intervals Following Gastrectomy
Arch Neurol 55:1242-1245, Shimomura,T.,et al, 1998

A 55-Year-Old Man with Attention-Deficit/Hyperactivity Disorder
JAMA 280:1086-1092, Biederman,J., 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,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

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Evaluation and Management of Intracranial Mass Lesions in AIDS
Rpt of Quality Stnds Subcomm of the AAN, Neurol 50:21-261998., , 1998

An Algorithm (Decision Tree) for the Management of Parkinson's Disease:Trtm Guidelines
Neurol 50:S1-S57, Olanow,C.W.&Koller,W.C., 1998

Stereotactic pallidotomy for Trtm of Parkinson's Disease, Efficacy & Adverse Effects at 6 Mo in 26 Pts
Neurol 50:434-438, Shannon,K.M.,et al, 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Dyslexia
NEJM 338:307-312, Shaywitz,S.E., 1998

Subacute Postictal Aggression
Neurol 50:384-388, Gerard,M.E.,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

Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Tardive Dyskinesia:Diagnosis, Pathogenesis, and Management
The Neurologist 4:180-187, Trugman,J.M., 1998

Alzheimers Disease with Asymmetric Parietal Lobe Atrophy: A Case Report
J Neurol Sci 160:96-99, Kaida,K.-I.,et al, 1998

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

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 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

Cryptic Vascular Malformations:Controversies in Terminology, Diagnosis, Pathophysiology, and Treatment
AJNR 18:1839-1846, Dillon,W.P., 1997

Multifocal Motor Neuropathy, Serum IgM Anti-GM1 Ganglioside Antibodies Detected Using Linkage of GM1 to ELISA Plates
Neurol 49:1289-1292, Pestronk,A.&Choksi,R., 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Transmissible Spongiform Encephalopathies
NEJM 337:1821-1828, Haywood,A.M., 1997

Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
JNNP 63:321-326, McGrath,N.,et al, 1997

Laboratory Evaluation in the Diagnosis of Lyme Disease
Ann Int Med 127:1109-1123, 1106-11081997., Tugwell,P.,et al, 1997

A 56-Year-Old Woman with Chronic Fatigue Syndrome
JAMA 278:1179-1185, Komaroff,A.L., 1997

Brain magnetic Resonance Diffusion Abnormalities in Creutzfeldt-Jakob Disease
Arch Neurol 54:1411-1415, Bahn,M.M.,et al, 1997

Diffusion-Weighted Magnetic Resonance Imaging in Creutzfeldt-Jakob Disease
Lancet 349:847-848, Demarerel,P.,et al, 1997

The 14-3-3 Brain Protein and Transmissible Spongiform Encephalopathy
NEJM 336:873-875, Moussavian,M.,et al, 1997

Small-Vessel Vasculitis
NEJM 337:1512-1523, Jennette,J.C.&Falk,R.J., 1997

New Variant Creutzfeldt-Jakob Disease:Psychiatric Features
Lancet 350:908-910, Zeidler,M.,et al, 1997

Lumbar Puncture Still Has an Important Role in Diagnosing Subarachnoid Heemorrhage
BMJ 315:1598-1599, Wasserberg,J.&Barlow,P., 1997

Color Duplex Ultrasonography in the Diagnosis of Temporal Arteritis
NEJM 337:1336-1386, 13851997., Schmidt,W.A.,et al, 1997

Granulomatous Angiitis of the Nervous System
In Vasculitis & The Nervous System, Neurol Clin 15:821-83497., Younger,D.S.,et al, 1997

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

Genetic Testing of Children at Risk for Huntington's Disease
Neurol 49:1048-1053, Nance,M.A.,et al, 1997

The Effect of Different Diagnostic Criteria on the Prevalence of Dementia
NEJM 337:1667-1674, Erkinjuntti,T.,et al, 1997

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

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Electrophysiologic Findings in Multifocal Motor Neuropathy
Neurol 48:700-707, Katz,J.S.,et al, 1997

Practice Guidelines for the Use of Imaging in Transient Ischemic Attacks and Acute Stroke
Stroke 28:1480-1497, Culebras,A.,et al, 1997

Presymptomatic Hypertension is a Major Feature in the Diagnosis of Progressive Supranuclear Palsy
Arch Neurol 54:1104-1108, Ghika,J.&Bogousslavsky,J., 1997

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

Long-Term Cognitive Impairment Associated with Caudate Stroke
Stroke 28:970-975, Bokura,H.&Robinson,R.G., 1997



Showing articles 1550 to 1600 of 2257 << Previous Next >>