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Differential
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adverse drug reaction
akinetic mute
alpha-synuclein
Alzheimer's disease
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anticonvulsants
anticonvulsants, untoward effects of
ataxia
ataxia, cerebellar
atypical
audiogram
auditory and vestibular pathways
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
biologic markers
blinking
blinking, reduced
botulism
bradykinesia
bradykinesia, facial
cachexia
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cauda equina, lesion of
cerebellar atrophy, primary
cerebellar lesion
cerebellar vermis
cerebrovascular accident
Clinical Pathologic Conference(C.P.C.)
clonidine
cognition
cogwheel rigidty
constipation
controversies in neurology
cortical-basal ganglionic degeneration
CPAP
dantrolene sodium
degenerative diseases of CNS
dementia
dementia, frontotemporal
diabetes mellitus
diet
differential diagnosis
dilantin
dopamine receptor
dopamine receptor, D2
droperidol
dysarthria
dysphagia
dystonia
dystonia, face
enzyme, defect
extrapyramidal movement disorder, progressive
facial appearance, abnormal
facial expression abnormality
falling
fasciculation
gait disorder
gastrointestinal motility
gaze palsy, supranuclear
gaze palsy, vertical
genetic neurologic disorders
glutamate dehydrogenase deficiency
grasp reflex
growth hormone
guanidine
head injury
hearing loss
hemiparesis
hot cross bun sign
Huntington's chorea
hyperhidrosis
hyperreflexia
hypophonia
imbalance
imbalance, postural
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
Isaacs syndrome
Jakob-Creutzfeldt disease
L-dopa
Lewy body
Lewy body disease, diffuse
life expectancy
marche a petits pas
masked facies
meclizine
memory, impairment of
midbrain
midbrain, atrophy
mimics
Mini Mental Status Examination
misdiagnosis
morning glory sign
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, ADC maps
MRI, diffusion weighted
MRI, functional
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, volumetry
MRS
multiple sclerosis
multiple sclerosis, diet in
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, static
muscle pain
muscle stiffness
muscle weakness
myasthenic syndrome
myasthenic syndrome, treatment of
myoclonus
myoclonus, stimulus sensitive
myokymia
nerve growth factor
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromyotonia
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuroprotective agents
neurosyphilis
ophthalmoplegia
ophthalmoplegia, total
orthostatic hypotension
orthostatic hypotension, idiopathic
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
pons, atrophy
postural abnormality
practice guidelines
prevention of neurologic disorders
prion disease
procainamide
prognosis
progressive neurologic disorder
progressive supranuclear palsy
proteinopathy
pure autonomic failure
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
rapidly progressing neurologic illness
review article
rigidity
rigidity, axial
Riley-Day syndrome
Romberg's sign
seizure
sexual behavior, disorder of
sexual dysfunction in neurologic disease
Shy-Drager syndrome
sinemet
single photon emission computed tomography
skin, biopsy
spinal cord, injury of
spinal cord, injury, sexual dysfunction in
spinal cord, lesion of
spinocerebellar ataxia type 1
stare
steroid therapy, CNS treatment and complications with
striatonigral degeneration
stridor
sweating
sweating, abnormality of
sympathetic nervous system
synucleinopathy
syphilis, neurologic complications with
systemic illness
tandem gait, ataxic
tau protein
tauopathy
tracheostomy
treatment of neurologic disorder
tremor
tremor, cerebellar
upgaze
upgaze, paralysis of
urinary incontinence
valium
vertigo
vertigo, cervical
vertigo, treatment of
walking, difficulty with
weight loss
wheelchair
wide based gait
Showing articles 0 to 50 of 11715 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

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

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

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

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

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

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

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

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

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

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

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

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

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

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

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

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Important Advances in Clinical Medicine
West J Med 123:128, Mosier,J.M.,et al, 1975

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

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

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

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

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

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

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015



Showing articles 0 to 50 of 11715 Next >>