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acrocyanosis
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
algorithm
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, heterogeneity of
Alzheimer's disease, preclinical
Alzheimer's disease, treatment of
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
amyloid-related imaging abnormalities
amyotrophic lateral sclerosis
angiitis, granulomatous of CNS
angiography, cerebral
anomic aphasia
anticoagulant, treatment
antiphospholipid antibody syndrome
aphasia
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
APP
APP gene
apraxia
arteritides
ataxia
ataxic gait
autoimmune disease
axonal spheroid
B 12 deficiency
B12
Balint's syndrome
basal ganglia, calcification of
behavioral disorder
biologic markers
bone biopsy
bone survey
bradykinesia
brain atrophy
brain biopsy
brain biopsy, negative
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus, lesion of, bilateral
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebroretinal microangiopathy with calcifications and cysts
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
chorea
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 20
chromosome 21
clindamycin
Clinical Pathologic Conference(C.P.C.)
comorbidities
compulsivity
confusion
corneal dystrophy
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
coumarin
COVID-19
crying, pathologic
cyst, bone
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, transmissible
dementia, treatment of
depression
diagnostic criteria
differential diagnosis
disorientation
dizziness
dysdiadochokinesia
dysphagia
dystonia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electron microscopy
encephalopathy
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
executive dysfunction
exome sequencing
Fabry's disease
falling
false negative
familial
fasciculation
fever
fluency
fracture, pathologic
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontal lobe, lesion of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
Gerstmann-Straussler-Scheinker disease
gliadin antibodies
gliosis
grasp reflex
grasping
hallucination
hallucination, visual
handedness
head injury
headache
hearing loss
hemosiderosis of CNS, superficial
heralding manifestation
Hodgkin's disease
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, exvacuo
hydrocephalus, normal pressure
hyperreflexia
hypersomnia
hypertension
hypoglycorrhachia
imbalance
impulsivity
inappropriate behavior
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
incoordination
inflexibility, mental
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, young adult
Kluver-Bucy syndrome
Lafora body
Lafora's disease
language disorder in adults
laughing, pathologic
lecanemab
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
Lewy body
lipomembranous polycystic osteodysplasia
livedo reticularis
lobar atrophy
logopenia
loss of sympathy
lupus anticoagulant
manganese intoxication
memory, defect of recent
memory, impairment of
memory, impairment of, subjective
mental status, abnormal
microangiopathy, brain
microhemorrhage, intracerebral
mild cognitive impairment
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoclonal antibodies
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, functional
MRI, linear enhancement
MRI, serial
MRI, T1 weighted high signal foci
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
mutism
myoclonic jerks
myoclonus
neologism
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neurocutaneous disease
neurocutaneous melanosis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neurosyphilis
nutritional deficiency
nystagmus
obsessive-compulsive disorder
pain, increased response
paranoia
paraparesis, spastic
paraphasias
paratonia
Parkinson disease
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
perseveration
personality change
Pick bodies
Pick's disease
Pittsburgh Compound B
pleocytosis of cerebrospinal fluid
polycystic lipomembranous osteodysplasia
polymerase chain reaction
posterior cortical atrophy
practice guidelines
preclinical
presenilin-1 gene
presenilin-2 gene
prion disease
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive subcortical gliosis
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
real-time quaking-induced conversion
Red flags
release phenomena
reticulum antibodies
review article
roaming behavior
safety
schizophrenia
seizure
seizure, children
seizure, diagnosis of
seizure, intractable
seizure, teenager
semantic dementia
senile plaques
serologic testing
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
Sneddon's syndrome
spasticity
speech disorder
spongy degeneration of brain
startle myoclonus
stereotyped behavior
steroid therapy, CNS treatment and complications with
stuttering
stuttering following CVA
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tau protein
tauopathy
temporal lobe, atrophy
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
tissue plasminogen activator, intravenous
tongue, fasciculations of
transient neurologic deficit
treatment of neurologic disorder
uremia
urinary incontinence
vanishing white matter
vasculopathy
vegetarianism
vertigo
vertigo, episodic
vitamin deficiency
weight loss
wheelchair
Whipple's disease
white matter disease
word-finding difficulty
Showing articles 0 to 50 of 2211 Next >>

A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
Neurol 102:e209188, Bai,X.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

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

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

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

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

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

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Frontotemporal Dementia
BMJ 347:f4827, Warren, J.D.,et al, 2013

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

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

A 34-Year-Old Man With Progressive Behavioral and Language Disturbance
Neurol 68:68-74, Miller,B.L.,et al, 2007

Dementia and White-Matter Demyelination in Young Patient With Neurosyphilis
Lancet:368:2258, Brinar,V.V. &Habek,M., 2006

Young-Onset Dementia, A Practical Approach to Diagnosis
The Neurologist 12:2-13, Ridha,B. &Josephs,K.A., 2006

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
AJNR 27:1037-1039, Mascalchi,M.,et al, 2006

The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
Neurol 64:1502-1507, Klunemann,H.H.,et al, 2005

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

Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
Ann Neurol 50:665-668, Prass,K.,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

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

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

A Case of Sporadic Pick Disease With Onset at 27 Years
Arch Neurol 56:1289-1291, Jacob,J.,et al, 1999

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

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

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,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

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

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Reversible Dementia and Chorea in a Young Woman with the Lupus Anticoagulant
Neurol 46:1599-1603, Van Horn,G.,et al, 1996

Sneddon's Syndrome is a Thrombotic Vasculopathy:Neuropathologic and Neuroradiologic Evidence
Neurol 45:557-560, Geschwind,D.H.,et al, 1995

Familial Alzheimer's Disease
Ann Neurol 36:335-336, Bird,T.D., 1994

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

Familial Progressive Subcortical Gliosis
Neurol 44:1633-1643, Lanska,D.J.,et al, 1994

Electroencephalography as an Aid in the Exclusion of Alzheimer's Disease
Arch Neurol 51:280-284, Robinson,D.J.,et al, 1994

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

Presenile-Onset Cerebral Adrenoleukodystrophy Presenting as Balint's Syndrome and Dementia
Neurol 43:1249-1251, Uyama,E.,et al, 1993

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

Celiac Disease, Brain Atrophy, and Dementia
Neurol 41:372-375, Collin,P.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Early-Onset Dementia & Extrapyramidal Disease:Clinicopath Variant of Gerstmann-Straussler-Scheinker or Alzheimer's Disease?
JNNP 53:932-934, Hart,J.Jr.&Gordon,B., 1990

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 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



Showing articles 0 to 50 of 2211 Next >>