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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
C0ORF72
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, leak
cerebrospinal fluid, pressure low
Charles Bonnet's syndrome
choreoathetosis
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cognition
coma
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
dizziness
drug withdrawal
dural tear
dysarthria
dysmetria
eating disorder
electromyogram
electron microscopy
emotional lability
epidural blood patch
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
headache, positional
hearing loss
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
meningeal enhancement
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, negative
MRI, serial
MRI, spine
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
nausea and vomiting
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
tinnitus
tinnitus, pulsatile
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 50 to 100 of 3968 << Previous Next >>

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

The Spectrum of Imaging and Neuropsychological Findings in Pick's Disease
Neurol 39:362-368, Knopman,D.S.,et al, 1989

Positron Emission Tomography & Histopathology in Pick's Disease
Neurol 37:439-445, Kamo,H.,et al, 1987

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

The Human Kluver-Bucy Syndrome
Neurol 33:1141-1145, Lilly,R.,et al, 1983

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

Kluver-Bucy Syndrome in Pick disease:Clinical & patho-logic Correlations
Neurol 31:1415-1422, Cummings,J.L.,et al, 1981

Clinical Neuropathological Conference
(Ed) , Dis Ner Sys 34:124, 1973, Pick's Disease., Aronson,S.&Aronson,B., 1973

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
Neurol 96:848-863, Katz, D.I.,et al, 2021

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

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

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Validation of Clinicoradiological Criteria for the Diagnosis of Cerebral Amyloid Angiopathy-Related Inflammation
JAMA Neurol 73:197-202, Auriel, E.,et al, 2016

Recognizing Autoimmune-Mediated Encephalitis in the Differential Diagnosis of Limbic Disorders
AJNR 36:2196-2205, da Rocha, A.J.,et al, 2015

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Cerebral Amyloid Angiopathy Related Inflammation: Three Case Reports and a Review
JNNP 82:20-26, Chung,K.K.,et al, 2011

Alzheimer Disease
JAMA 287:2335-2338, Cummings,J.L. &Cole,G., 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

New Variant Creutzfeldt-Jakob Disease Presenting with Loss of Taste and Smell
JNNP 71:412-413, Reuber,M.&Al-Din,A.S.N., 2001

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

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

BSE Linked to New Variant of CJD in Humans
BMJ 312:795, 791, 843, 85496., , 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
Ann Neurol 97:435-448, Berthet,E.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

Revised Criteria for Diagnosis and Staging of Alzheimers Disease: Alzheimers Association Workgroup
Alzheimers Dement 20:5143-5169, Jack,Jr.,C.R.,et al, 2024

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

Brexpiprazole for the Treatment of Agitation and Aggression in Alzheimers Disease
JAMA Neurol 80:1272-1273, Ballard,C., 2023

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

Alzheimers Disease
Lancet 397:1577-1590, Scheltens, P.,et al, 2021

Headache, Cognitive Decline, and a Curious Rim-Enhancing Lesion
JAMA Neurol 78:613-614, Beaman, C.B.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
NEJM 383:83-85, Brandel, J.P.,et al, 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020



Showing articles 50 to 100 of 3968 << Previous Next >>