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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
advances in neurology
adverse drug reaction
age associated memory impairment
agitation
algorithm
alkalosis
alkalosis, respiratory
Alzheimer's disease
Alzheimer's disease, age of onset
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, early symptoms
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, pathogenesis
Alzheimer's disease, preclinical
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
amnesia
amphiphysin antibodies
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid deposition
amyloid imaging
amyloid plaques
amyloid-related imaging abnormalities
anti IgLON5
anticonvulsants, selection of
anticonvulsants, untoward effects of
aphasia
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
asymptomatic
ataxia
ataxia, truncal
autoantibodies
autoimmune disease
autoimmune epilepsy
autonomic dysfunction
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
blood transfusion
brain atrophy
brain damage
brain volume
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
caudate nucleus, atrophy
cerebellar plaques, amyloid
cerebral cortical atrophy
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, biochemical markers of CNS disease
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, neonatal
cerebrovascular accident, recurrent
cerebrovascular accident, seizure with
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 21
Chvostek sign
clindamycin
Clinical Pathologic Conference(C.P.C.)
cognition
collapsin response mediator protein 5 IgG
comorbidities
confusion
cortical blindness
cortical blindness, transient
cost
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, childhood
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, early detection
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, screening for
dementia, treatment of
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
dizziness
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
dyskinesia
dystonia
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis, autoimmune
encephalitis, paraneoplastic
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, post traumatic
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
epinephrine
erethism
evidence-based research
exercise
exercise intolerance
eye movement, disorders of
falling
familial
fasciculation
fever
florbetapir
fluency
frontotemporal dementia, behavioral variant
gait disorder
gamma amino butyric acid receptor antibody
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glycine receptor antibodies
hallucination
hallucination, visual
headache
hearing loss
hearing loss, bilateral
hemosiderosis of CNS, superficial
hepatomegaly
hippocampal atrophy
Huntington's chorea
Huntington's chorea, late onset
Huntington's chorea, misdiagnosis of
Huntington's disease, children
hyperreflexia
hyperventilation
hypocalcemia
hypocalcemia, causes of
hypomagnesemia
hypoparathyroidism
hypotension, systemic
hypotonia
imbalance
immunologic disease
immunotherapy
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
inflexibility, mental
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
intracerebral hemorrhage
lactic acidemia
Lafora body
Lafora's disease
laryngismus stridulus
lecanemab
Leigh's disease
lethargy
leucine rich glioma inactivated 1 antibodies
Lewy body
Lewy body disease, diffuse
life expectancy
limbic encephalitis
lobar atrophy
logopenia
lymphadenopathy
lysosomal storage disease
MELAS syndrome
memory
memory, evaluation of
memory, impairment of
memory, impairment of, subjective
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
microhemorrhage, intracerebral
mild cognitive impairment
mild cognitive impairment converting to Alzheimer's disease
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal antibodies
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, functional
MRI, negative
MRI, serial
MRI, volumetry
muscle biopsy
myoclonic jerks
myoclonus
myoclonus, epilepsy
neoplasm, intracranial
neoplasm, primary of CNS
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuroprotective agents
newborn, evaluation of
NMDA antagonists
normal
nystagmus
nystagmus, rotary
occipital lobe, lesion of
old age, neurology of
opportunistic infection
opportunistic infection, CNS
optic atrophy
pain, increased response
paratonia
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, familial
Parkinson disease, rapid progression
Parkinson disease, young onset
Parkinsonism syndrome
Parkinsonism-dementia complex
PAS positive
PAS positive material in the brain
patient information and support
personality change
Pittsburgh Compound B
posterior cortical atrophy
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
prevention of neurologic disorders
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychosocial aspects
pulmonary infiltrates
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
quality of life
ragged-red fibers
release phenomena
REM sleep
remote effect of cancer on the nervous system
retinal degeneration
retropulsion
review article
rigidity
risk factors
risk factors, modification
safety
salivation, excessive
Schilder's disease
schizophrenia
screening
seizure
seizure, adult onset
seizure, children
seizure, diagnosis of
seizure, drug-induced
seizure, elderly
seizure, etiology of
seizure, focal
seizure, hysterical
seizure, intractable
seizure, neonatal
seizure, nonconvulsive
seizure, prognosis in childhood
seizure, psychosocial aspects of
seizure, risk factors for
seizure, surgical treatment of
seizure, teenager
seizure, treatment of
seizure, treatment of, first
seizure, unknown origin
seizure, workup of
single photon emission computed tomography
skin, biopsy
sleep pathology and physiology
smell
Smell Identification Test
spasmophilia
spasticity
speech, loss of
status epilepticus
status epilepticus, nonconvulsive
status tetanicus
stereotyped behavior
steroid therapy, CNS treatment and complications with
striatonigral degeneration
striatonigral degeneration, infantile
term infant
tetany
tetany, latent
tetany, normocalcemic
tissue plasminogen activator, intravenous
titubation
toxoplasmosis, CNS
transient epileptic amnesia
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
Trousseau's sign
ventricular enlargement
visual acuity, decreased
visual fields, constricted
visual loss
visuospatial disturbance
von Bonsdorff's sign
weight loss
wide based gait
word-finding difficulty
workup
Showing articles 0 to 50 of 3804 Next >>

Lecanemab in Early Alzheimers Disease
NEJM 388:9-21,80, van Dyck,A.H.,et al, 2023

Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Practice Guide Update Summary: Mild Cognitive Impairment
Neurol 90:126-135, Petersen, R.C.,et al, 2018

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Prevalence of Cerebral Amyloid Pathology in Persons without Dementia
JAMA 313-1924-1938,1913, Jansen, W.J.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
AJNR 34:2075-2082, Desikan, R.S.,et al, 2013

Predicting Alzheimer Disease with �-Amyloid Imaging: Results from the Australian Imaging, Biomarkers, and Lifestyle Study of Ageing
Ann Neurol 74:905-913, Rowe, C.C.,et al, 2013

Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
NEJM 367:795-804,864, Bateman, R.J.,et al, 2012

Changing Concepts of Alzheimer Disease
JAMA 35:2458-2459, McKhann, G.M., 2011

Conversion of Amyloid Positive and Negative MCI to AD over 3 Years: An 11C-PIB PET Study
Neurol 73:754-760, 744, Okello,A.,et al, 2009

Clinical Syndromes Associated with Posterior Atrophy: Early Age at Onset AD Spectrum
Neurol 73:1571-1578, Migliaccio,R.,et al, 2009

Genetic Aspects of Alzheimer Disease
The Neurologist 15:80-86, Williamson,J.,et al, 2009

CSF Biomarkers and Incipient Alzheimer Disease in Patients with Mild Cognitive Impairment
JAMA 302:385-393,436,452, Mattsson,N.,et al, 2009

Frequent Amyloid Deposition Without Significant Cognitive Impairment Among the Elderly
Arch Neurol 65:1509-1517, Aizenstein,H.J.,et al, 2008

Disease-Modifying Therapies for Alzheimer Disease: Challenges to Early Intervention
Neurol 69:1622-1634, Cummings,J.L.,et al, 2007

Variability of Age at Onset in Siblings With Familial Alzheimer Disease
Arch Neurol 64:1743-1748, G�mez-Tortosa,E.,et al, 2007

Mild Cognitive Impairment
Lancet 367:1262-1270, Gauthier,S.,et al, 2006

A 10-Item Smell Identification Scale Related to Risk for Alzheimers Disease
Ann Neurol 58:155-160, Taberr,M.H.,et al, 2005

Neonatal Brain Injury
NEJM 351:1985-1995, Ferriero,D.M., 2004

Early Alzheimer's Disease
NEJM 349:1056-1063, Kawas,C.H., 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

Functional Deficits in Patients with Mild Cognitive Impairment
Neurol 58:758-764, Tabert,M.H.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Incidence and Outcome of Mild Cognitive Impairment in a Population-Based Prospective Cohort
Neurol 59;1594-1599, Larrieu,S.,et al, 2002

Early Detection of Dementia: Mild Cognitive Impairment (an Evidence-based Review)
Neurol 56:1133-1142, 1131, Petersen,R.C.,et al, 2001

The Value of Informant Versus Individual's Complaints of Memory Impairment in Early Dementia
Neurol 55:1724-1726, Carr,D.B.,et al, 2000

Mild Cognitive Impairment, Clinical Characterization and Outcome
Arch Neurol 56:303-308, Petersen,R.C.,et al, 1999

Functional Magnetic Resonance Imaging in Neuropsychiatry
BMJ 319:1551-1554, Longworth,C.,et al, 1999

The Genetics of Alzheimer Disease, Current Status and Future Prospects
Arch Neurol 55:294-296, Blacker,D.&Tanzi,R.E., 1998

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

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

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Seizures and Epilepsy in the Elderly
Arch Int Med 157:605-617, Thomas,R.J., 1997

High Apolipoprotein E e4 Allele Frequency in Age-Related Memory Decline
Ann Neurol 39:548-551, Blesa,R.,et al, 1996

Dementia and Adult-Onset Unprovoked Seizures
Neurol 46:727-730, Hesdorffer,D.C.,et al, 1996

A Low, "Normal"Score on the Mini-Mental State Exam Predicts Development of Dementia after Three Years
JAGS 43:656-661, Braekhus,A.,et al, 1995

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
Ann Neurol 36:362-367, Haltia,M.,et al, 1994

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

A Follow-up Study of Intractable Seizures in Childhood
Ann Neurol 28:699-705, Huttenlocher,P.R.&Hapke,R.J., 1990

Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
Neurol 40:395-403, Farrer,L.A.,et al, 1990

Advanced Alzheimer's Disease is a Risk Factor for Late-Onset Seizures
Arch Neurol 47:847-850, Romanelli,M.F.,et al, 1990

Predisposing Locus for Alzheimer's Disease on Chromosome 21
Lancet 1:352-355, Goate,A.M.,et al, 1989



Showing articles 0 to 50 of 3804 Next >>