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addiction, heroin
addiction, heroin-neurologic complications with
adrenergic blocker
adverse drug reaction
airway obstruction
akinetic mute
alpha adrenergic blocker
alpha-fetoprotein
alpha-synuclein
Alzheimer's disease
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anhidrosis
anticonvulsants
anticonvulsants, untoward effects of
apraxia of eye movements
areflexia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, truncal
atypical
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
baroreceptors
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
biologic markers
bladder dysfunction
blinking
blinking, reduced
botulism
bradykinesia
bradykinesia, facial
brainstem, atrophy
cachexia
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cauda equina, lesion of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
clonidine
cognition
cogwheel rigidty
cold hands sign
constipation
contractures, joint
controversies in neurology
cortical-basal ganglionic degeneration
CPAP
degenerative diseases of CNS
dementia
dementia, frontotemporal
dementia, thalamic
demyelinating disease
developmental retardation
diabetes mellitus
differential diagnosis
dopamine receptor
dopamine receptor, D2
drooling
dysarthria
dysphagia
dyspnea
dystonia
dystonia, face
enzyme, defect
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
falling
familial
fatal familial insomnia
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
gait disorder
gammaglobulin therapy, intravenous
gastrointestinal motility
gaze palsy, supranuclear
gaze palsy, vertical
gene
genetic linkage
genetic neurologic disorders
giant cell arteritis
glutamate dehydrogenase deficiency
grasp reflex
growth hormone
growth retardation
head injury
hemiparesis
Horner's syndrome
hot cross bun sign
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
hyperreflexia
hypophonia
hypotonia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
intrathecal medication
Jakob-Creutzfeldt disease
L-dopa
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leukemia
leukoencephalopathy
Lewy body
Lewy body disease, diffuse
life expectancy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
marche a petits pas
masked facies
memory, impairment of
mental retardation
microcephaly
midbrain
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
midodrine
mimics
Mini Mental Status Examination
misdiagnosis
morning glory sign
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, ADC maps
MRI, contrast enhanced
MRI, diffusion weighted
MRI, functional
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, volumetry
MRS
multiple sclerosis
multiple system atrophy
myoclonus
myoclonus, stimulus sensitive
nerve growth factor
nerve growth stimulating activity
neuroblastoma
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromyelitis optica (Devic's disease)
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, sensory, hereditary
nicotine
ocular motility, disorders of
old age, neurology of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, total
orbit, tomograms of
orthostatic hypotension
orthostatic hypotension, idiopathic
orthostatic hypotension, treatment of
parasympathetic nervous system
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, rapid progression
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
pheochromocytoma
pons, atrophy
postural abnormality
practice guidelines
prion disease
procainamide
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
proteinopathy
pupil
pupil, abnormality in neurologic disorders
pure autonomic failure
purple glove syndrome
purple hands
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
quadrigeminal plate
radiation hypersensitivity
rapidly progressing neurologic illness
respirations in CNS disease
respiratory failure
review article
rigidity
rigidity, axial
Riley-Day syndrome
Romberg's sign
seizure
sensory ganglia
sensory ganglia, abnormal
sexual behavior, disorder of
sexual dysfunction in neurologic disease
Shy-Drager syndrome
sinemet
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
spinal cord, injury of
spinal cord, injury, sexual dysfunction in
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
stare
stem cell transplantation
striatonigral degeneration
stridor
substantia nigra
sudden death
superior colliculus
sympathetic nervous system
syncope
synucleinopathy
systemic illness
tandem gait, ataxic
tau protein
tauopathy
telangiectases
thalamus, lesion of
tracheostomy
treatment of neurologic disorder
tremor
tremor, cerebellar
trinucleotide repeats
upgaze
upgaze, paralysis of
urinary incontinence
valsalva maneuver
vocal cord paralysis
walking, difficulty with
Wallerian degeneration
weight loss
wheelchair
white matter disease
wide based gait
Showing articles 0 to 50 of 70 Next >>

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

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

Bilateral Middle Cerebellar Peduncle Lesions:Neuroimaging Features and Differential Diagnoses
Brain Behav 10:e01778, Jiang,J.,et al, 2020

Intrathecal Administration of Autologous Mesenchymal Stem Cells in Multiple System Atrophy
Neurol 93:e77-e87, Singer, W.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

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

Purple Hands in Multiple System Atrophy
Neurol 86:2314, Coon, E.A.,et al, 2016

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

Degenerative Diseases of the Nervous System, Multiple System Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1095, Ropper, A.H.,et al, 2014

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

Treatment of Multiple System Atrophy Using Intravenous Immunoglobulin
BMC Neurol 12:131, Novak, P.,et al, 2012

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009

Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008

Sexual Function in Men and Women With Neurological Disorders
Lancet 369:512-525, Rees,P.M.,et al, 2007

Pupil Findings in a Consecutive Series of 150 Patients with Generalised Autonomic Neuropathy
JNNP 77:1163-1168, Bremner,F. &Smith,S., 2006

Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy
Magn Reson Med Sci 3:125-132, Adachi, M., et al, 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Constipation in Neurological Diseases
JNNP 74:13-19, Winge,K.,et al, 2003

Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
Neurol 60:922-927, Seppi,K.,et al, 2003

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Diffusion-weighted MRI Differentiates the Parkinson Variant of Multiple System Atrophy from PD
Neurol 58:575-580, Schocke,M.F.H.,et al, 2002

T2-weighted MRI Differentiates Multiple System Atrophy from Parkinson's Disease
Neurol 59;1265-1267, Kraft,E.,et al, 2002

Improved Accuracy of Clinical Diagnosis of Lewy Body Parkinson's Disease
Neurol 57:1497-1499, Hughes,A.J.,et al, 2001

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Prevalence of Progressive Supranuclear Palsy and Multiple System Atrophy:A Cross-Sectional Study
Lancet 354:1771-1775, Schrag,A.,et al, 1999

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Survival of Patients with Pathologically Proven Multiple System Atrophy:A Meta-Analysis
Neurol 48:384-393, Ben-Shlomo,Y.,et al, 1997

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

Distinction of Idiopathic Parkinson's Dis from Multi-Syst Atrophy by Stim of Growth-Hormone Release w Clonidine
Lancet 349:1877-1881, Kimber,J.R.,et al, 1997

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

Consensus Statement on the Definition of Orthostatic Hypotension, Pure Autonomic Failure, and Multiple System Atrophy
Neurol 46:1470, Schatz,I.J.,et al, 1996

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
Arch Neurol 52:179-185, Perani,D.,et al, 1995

Different of Multi Syst Atrophy from Idiopathic Parkinson's Disease Using Proton MR Spectroscopy
Ann Neurol 37:204-210, Davie,C.A.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Diff Diag of parkinson's Disease, Multiple Sys Atrophy, & Steele-Richardson-Olszewski Syndrome:Striatal F-Dopa PET Data
JNNP 57:278-284, Burn,D.J.,et al, 1994

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
Brain 115:1875-1888, Chen,R.,et al, 1992

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991



Showing articles 0 to 50 of 70 Next >>