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acetylcholine
advances in neurology
akinetic mute
algorithm
alien hand syndrome
Alzheimer's disease
anomic aphasia
anticholinesterase
anticonvulsants
anticonvulsants, selection of
aphasia
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-motor
apolipoprotein E
apraxia
apraxia of eye movements
apraxia, constructional
apraxia, speech
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonal injury
Babinski sign
baclofen
basal ganglia, degeneration
basal ganglia, lesion, bilateral
Bing-Neel syndrome
blindness
blinking, reduced
brachium pontis
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
Broca's aphasia
burning paresthesia
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, orbits
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
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cerebellar vermis
cerebellum
cerebral cortical atrophy
chemosis
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosome 12
chromosome 14
chromosome 6
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
cobalt toxicity
cognition
color vision, impaired
complications
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
cranial nerve enlargement
cranial nerve palsies
cranial nerve palsy, alternating
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dexterity, impaired
diagnostic criteria
differential diagnosis
diplopia
donut sign
down-beat nystagmus, primary position of gaze
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dysthyroidism
dystonia
dystonia, focal
edema, periorbital
ejection fraction, abnormal
enzyme, defect
ethics in neurology
evoked potentials
excitotoxin
exophthalmus
extraocular muscle enlargement
extraocular muscle lesion
eye movement, disorders of
eye movement, painful
eye, pain in
falling
familial
fragile-X syndrome
Friedreich's ataxia
frontal behavioral spatial syndrome
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glabellar sign
glioma
globus pallidus, lesion of
glutamate dehydrogenase deficiency
glutamic acid
granulomatosis with polyangiitis
Graves ophthalmopathy
headache
headache, unilateral
hearing loss
hip arthroplasty
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hyperthyroidism
hypothalamus
hypothalamus, lesion of
hypotonia
hypoxia
ibrutinib
IgG4, serum
IgG4-related disease
imbalance
imbalance, postural
immunotherapy
inattention
incidence
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracranial pressure, increased
Jakob-Creutzfeldt disease
jaw pain
jocularity
Lafora's disease
language disorder in adults
lateral rectus palsy
L-dopa
leukodystrophy
levitation
life expectancy
lobar atrophy
lymphoma
lymphoma involving CNS
macroglobulinemia
macular degeneration
malignant optic glioma of adulthood
masked facies
maxillary nerves
memory, defect of recent
memory, impairment of
meningitis
mental retardation
MERRF syndrome
methotrexate
midbrain
midbrain, atrophy
mimics
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
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MRI, nodular enhancement
MRI, optic nerve
MRI, orbit
multiple system atrophy
muscle biopsy, extraocular
mutism
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy, necrotizing
myopathy, steroid responsive
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myositis, ocular
myotonia dystrophica
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neuroophthalmology
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neuropathology, brain
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ocular motility, disorders of
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ophthalmoplegia, total
optic atrophy
optic canal
optic canal, enlargement of
optic chiasm, enlarged
optic chiasm, lesion of
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, lesion of
optic nerve, neoplasm of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, ischemic
optic neuropathy, ischemic, posterior
orbit
orbit, biopsy
orbit, fat
orbit, inflammation in
orbit, lesions of
orbit, mass
orbital apex
orthostatic hypotension
pain
palatal myoclonus
papilledema
paresthesias
paresthesias, feet
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, differential diagnosis of
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
perineuritis
perineuritis, optic
perivascular enhancement
personality change
photophobia
photosensitivity, skin
physostigmine
Pick's disease
pleocytosis of cerebrospinal fluid
polymerase chain reaction
pons, atrophy
pons, lesion of
pontocerebellar atrophy
postoperative neurologic complications
postoperative visual loss
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, unilateral
proteinopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
ptosis
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
rash
release phenomena
retinal degeneration
retinitis pigmentosa
retro-orbital pain
review article
rigidity
rigidity, axial
risk factors
rituximab
saccadic eye movements
saccadic eye movements, abnormal
salivary gland enlargement
scotoma
seizure
seizure, paradoxical
seizure, treatment of
sella turcica, enlargement of
sensorineural hearing loss
sensory loss
sensory loss, cortical
Shy-Drager syndrome
sialadenitis
sinuses, diseases of
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
sleep apnea
sleep pathology and physiology
speech disorder
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
steroid therapy, CNS treatment and complications with
striatonigral degeneration
subthalamic nucleus
suck reflex
synucleinopathy
tau protein
tauopathy
tram-track sign
trazodone
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
vasculitides
vision, blurred
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual field defect, altitudinal
visual loss
visual loss, progressive
visuospatial disturbance
Waldenstrom's macroglobulinemia
weight loss
Wernicke's aphasia
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 0 to 50 of 2217 Next >>

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

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

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

Posterior Ischemic Optic Neuropathy
UptoDate Aug, Tamhankar, M. & Volpe, N., 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1106, Ropper, A.H.,et al, 2014

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

Visuoperception Test Predicts Pathologic Diagnosis of Alzheimer Disease in Corticobasal Syndrome
Neurol 83:510-519, Boyd, C.D.,et al, 2014

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

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

MRI findings in Post-operative Bilateral Posterior Ischemic Optic Neuropathy
J Ophthalmol 3:51-53, Bhatt, N.P.,et al, 2013

Expanding the Clinical, Radiological and Neuropathological Phenotype of Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS)
JNNP 83:15-22, Simon, N.G.,et al, 2012

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Imaging-Pathologic Correlation in Corticobasal Degeneration
AJNR 30:1884-1892, Tokumaru,A.,et al, 2009

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Recent Developments in Thyroid Eye Disease
BMJ 329:385-390, Cawood,T.,et al, 2004

Correlation Between Antemortem Magnetic Resonance Imaging Findings and Pathologically Confirmed Corticobasal Degeneration
Arch Neurol 61:1881-1884, Josephs,K.A.,et al, 2004

Language Function and Dysfunction in Corticobasal Degeneration
Neurol 61:493-499, Graham,N.L.,et al, 2003

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

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

Language Disturbances in Corticobasal Degeneration
Neurol 54:990-992, Frattali,C.M.,et al, 2000

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Dementia as the Most Common Presentation of Cortical-Basal Ganglionic Degeneration
Neurol 53:1969-1974, Grimes,D.A.,et al, 1999

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

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
JNNP 64:184-189, Wenning,G.K.,et al, 1998

Atrophy of the Corpus Callosum, Cortical Hypometabolism, and Cognitive Impairment in Corticobasal Degeneration
Arch Neurol 55:609-614, Yamauchi,H.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

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

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Corticobasal Degeneration:Neuropathologic and Clinical Heterogeneity
Neurol 48:959-969, Schneider,J.A.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 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

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

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

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

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



Showing articles 0 to 50 of 2217 Next >>