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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
atypical
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
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
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, 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
headache, severe
headache, throbbing
hearing loss
hemianopia, homonymous
herpes simplex encephalitis
hippocampus
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
intellectual deficit
intellectual deterioration
interpeduncular cistern, compressed
intracranial hypotension
intrathecal chemotherapy
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kluver-Bucy syndrome
language disorder in adults
laughing, pathologic
leukemia
level of consciousness, decreased
Lewy body disease, diffuse
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
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
pituitary hyperemia
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
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
quadriplegia
radiation therapy, CNS treatment and complications with
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
stem cell transplantation
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
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 0 to 50 of 2221 Next >>

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Spontaneous Intracranial Hypotension
NEJM 385:2173-2178, Schievink, W.I., 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

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

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
AJNR 37:774-781, Winton-Brown, T.T.,et al, 2016

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

Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
AJNR 37:1256-1261, Capizzano, A.A.,et al, 2016

A 50-year-old Man with Headache and Cognitive Decline
Neurol 85:e182-e186, Batra, A. & Berkowtiz, A., 2015

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

Degenerative Diseases of the Nervous System, Behavioral Variant FTLD
Adams & Victors Principles of Neurology, Chp 39, pg 1074, Ropper, A.H.,et al, 2014

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

Frontotemporal brain sagging syndrome
Neurol 76:1377-1382, Wicklund, M.R.,et al, 2011

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

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

Binge Eating is Associated With Right Orbitofrontal-Insular-Striatal Atrophy in Frontotemporal Dementia
Neurol 69:1424-1433, Woolley,J.D.,et al, 2007

Frontotemporal Dementia: Clinicopathological Correlations
Ann Neurol 59:952-962, Forman,M.S.,et al, 2006

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

Frontotemporal Lobar Degeneration
Arch Neurol 62:925-930, Johnson,J.K.,et al, 2005

Different Patterns of Magnetic Resonance Imaging Atrophy for Frontotemporal Lobar Degeneration Syndromes
Arch Neurol 62:1106-1110, Short,R.A.,et al, 2005

Most Cases of Dementia with Hippocampal Sclerosis May Represent Frontotemporal Dementia
Neurol 63:538-542, Hatanpaa,K.J.,et al, 2004

Spontaneous Intracranial Hypotension Causing Reversible Frontotemporal Dementia
Neurol 58:1285-1287, Hong,M.,et al, 2002

Utility of Clinical Criteria in Differentiating Frontotemporal Lobar Degeneration (FTLD) From AD
Neurol 58:1608-1615, Rosen,H.J.,et al, 2002

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

Clinicopath Conf., Pick's Disease, Case 11-2000
NEJM 342:1110-1117, , 2000

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

A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
JNNP 64:306-313, Talbot,P.R.,et al, 1998

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

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,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

Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
Radiology 203:829-836, Ernst,T.,et al, 1997

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

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
AJNR 18:367-378, Kitagaki,H.,et al, 1997

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

The Pathology and Nosology of Primary Progressive Aphasia
Neurol 44:2065-2072, Kertesz,A.,et al, 1994

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

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



Showing articles 0 to 50 of 2221 Next >>