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adolescent medicine
advances in neurology
adverse drug reaction
affect, flat
akathisia
alcohol, neurologic complications with
alcoholism
algorithm
alien hand syndrome
alpha-synuclein
anti IgLON5
aphasia
aphasia, progressive, primary
apraxia
apraxia, constructional
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autonomic cardiovascular reflexes
autonomic dysfunction
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
blacks
blinking, reduced
bradykinesia
brain atrophy
bulbar palsy
carbon monoxide poisoning
CAT scan, emission, abnormal
cavernous hemangioma
central hypoventilation
cerebellar atrophy, primary
cerebellar edema
cerebellar lesion
cerebellitis
cerebellum, disease of
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebrospinal fluid, elevated protein of
cerebrovascular accident
children
chorea
chromosomal abnormality
chromosome 19
cingulate island sign
cirrhosis
climate change
Clinical Pathologic Conference(C.P.C.)
coat-hanger pain
cognition
compulsivity
computers, medicine and
contractures, joint
controversies in neurology
corpus callosum, thinning
cortical-basal ganglionic degeneration
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
depression
developmental milestones, loss of
developmental retardation
dexterity, impaired
diagnostic criteria
differential diagnosis
diplopia
disorientation
distal muscle atrophy
diurnal variation
dopa responsive dystonia
dopamine agonist
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysphagia
dystonia
dystonia, cervical
dystonia, children
encephalitis
encephalitis, episodic
encephalitis, Powassan
encephalitis, viral
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
erectile dysfunction
evidence-based research
executive dysfunction
eye movement, disorders of
falling
familial
fatigue
fever
flavivirus
fluency
fluoxetine
foot deformity
fourth ventricle, compression
frontal behavioral spatial syndrome
frontotemporal dementia, behavioral variant
gait disorder
galactorrhea
gammaglobulin therapy, intravenous
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
grasp reflex
Hallervorden Spatz disease
hallucination
headache
hemangioma, brainstem
hemiatrophy
hemifacial spasm
hepatic failure
hepatolenticular degeneration, non-Wilsonian
HLA
hoarseness
hydrocephalus
hyperammonemic encephalopathy
hyperreflexia
hypertonia
hyperuricemia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypothyroidism
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunomodulation
impulsivity
inclusion bodies
inclusion bodies, intranuclear
incontinence, fecal
inflexibility, mental
insect sting
insomnia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
Jakob-Creutzfeldt disease
L-dopa
leg spasms, painful
lenticular nucleus, lesion of, bilateral
leukoencephalopathy
level of consciousness, decreased
Lewy body
Lewy body disease, diffuse
life expectancy
liver disease
lobar atrophy
loss of sympathy
malformation, vascular
malformation, vascular, cerebral
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningoencephalitis
mental status, abnormal
micrographia
mimics
misdiagnosis
mood change
mortality
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, paramagnetic effect
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
multiple system atrophy
muscle biopsy
muscle cramp
muscle spasm
muscle spasm, face
mutism
myelopathy
myelopathy, hepatic
myoclonus
nausea and vomiting
neck pain
neck stiffness
neurodegeneration with brain iron accumulation
neuroleptic, atypical
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neurologic testing
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuroprotective agents
New England
obsessive-compulsive disorder
ocular motility, disorders of
old age, neurology of
ophthalmoplegia, progressive external
orthostatic hypotension
pain, increased response
palliative care
PANK2 mutation
paraparesis, spastic
parasomnia
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, duration
Parkinson disease, dystonia with
Parkinson disease, etiology of
Parkinson disease, familial
Parkinson disease, heterogeneity of
Parkinson disease, juvenile
Parkinson disease, late onset
Parkinson disease, L-dopa nonresponsive
Parkinson disease, mode of onset
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, prognosis of
Parkinson disease, progression
Parkinson disease, rapid onset
Parkinson disease, rapid progression
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
Parkinsonism, freezing phenomena in
Parkinsonism-dementia complex
pathology
personality change
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
POLG1 gene
polyneuropathy
portal caval shunt
practice guidelines
PRKN gene
prognosis
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, bilateral
pyramidal tract dysfunction
Red flags
release phenomena
respirations in CNS disease
review article
rigidity
rodents
salivation, excessive
scoliosis
season
seizure
selective serotonin reuptake inhibitors
serologic testing
shoulder, pain in
sinemet
single photon emission computed tomography
sleep apnea, obstructive
sleep pathology and physiology
smell
SNCA duplication
speech disorder
speech disorder, childhood
standing difficulty
stereotyped behavior
stiff man syndrome
stimulation, deep brain
striatonigral degeneration
suicide
symptomatic
syncope
synucleinopathy
systemic illness
tandem gait, ataxic
tardive dyskinesia
tau protein
tauopathy
teleconsulting
telemedicine
teleneurology
temporal lobe, atrophy
tick bite
tick-borne encephalitis
toe walking
tonic foot response
treatment of neurologic disorder
tremor
tremor, jaw
tremor, postural
tremulousness
tripping
tyrosine hydroxylase deficiency
upgaze, paralysis of
uric acid, low
urinary incontinence
viral infection
virtual house calls
visual impairment
visuospatial disturbance
vocal cord paralysis
walking
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
word-finding difficulty
workup
Showing articles 0 to 50 of 2009 Next >>

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Diagnosis and Treatment of Parkinson Disease
JAMA 323:548-560, Armstrong, M.J. & Okun, M.S., 2020

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

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

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

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

National Randomized Controlled Trial of Virtual House Calls for Parkinson Disease
Neurol 89:1152-1161,1103, Beck, C.A.,et al, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

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

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Parkinsons Disease Beyond 20 Years
JNNP 86:849-855, Cilia, R.,et al, 2015

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

Progressive Parkinsonism, Balance Difficulties, and Supranuclear Gaze Palsy
JAMA Neurol 71:104-107, Erro, R.,et al, 2014

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

Serum Uric Acid and Clinical Progression in Parkinson Disease: Potential Biomarker for Nigrostriatal Failure
Arch Neurol 65:698-699, Schiess,M. &Oh,I., 2008

Invited Article: Changing Concepts in Parkinson Disease: Moving Beyond the Decade of the Brain
Neurol 70:1996-2003, Marras,C. &Lang,A., 2008

Practice Parameter: Diagnosis and Prognosis of New Onset Parkinson Disease (An Evidence-Based Review)
Neurol 66:968-975, Suchowersky,O.,et al, 2006

[123I]b-CIT SPECT is a Useful Method for Monitoring Dopaminergic Degeneration in Early Stage Parkinson's Disease
JNNP 74:294-298,287, Winogrodzka,A.,et al, 2003

Parkinson Disease With Old-Age Onset
Arch Neurol 60:529-533, Diederich,N.J.,et al, 2003

[123I]Beta-CIT SPECT Imaging Assessment of the Rate of Parkinson's Disease Progression
Neurol 57:2089-2094, Marek,K.,et al, 2001

Progression of Parkinsonian Signs in Parkinson Disease
Arch Neurol 56:334-337, Louis,E.D.,et al, 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Movement Disorders Associated with the Serotonin Selective Reuptake Inhibitors
J Clin Psychiatry 57:449-454, Leo,R.J., 1996

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

Prognostic Significance of the Onset Mode in Parkinsonism
Neurol 43:829-830, Rajput,A.H.,et al, 1993

Young-Onset Parkinson's Disease:A Clinical Review
Neurol 41:168-173, Golbe,L.I., 1991

Effect of Age at Onset on Progression and Mortality in Parkinson's Disease
Neurol 39:1187-1190, Diamond,S.G.,et al, 1989

Hemiparkinsonism with Hemiatrophy
Neurol 38:527-530, Buchman,A.S.,et al, 1988

Parkinsonism Death Rates by Race, Sex, and Geography
Neurol 38:1558-1561, Kurtzke,J.F.&Goldberg,I.D., 1988

Risk Factors for Progression in Parkinson's Disease
Neurol 38:1841-1844, Goetz,C.G.,et al, 1988

Progression of Parkinson's Disease Without Levodopa
Neurol 37:695-698, Coetz,C.G.,et al, 1987

The Heterogeneity of Parkinson's Disease:Clinical & Prognostic Implications
Neurol 35:522-526, Zetusky,W.J.,et al, 1985

Progress Toward Mitigating Disability Progression in Multiple Sclerosis
NEJM 392:1966-1968, Calabresi,P.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Endovascular Thrombectomy for Extracranial Internal Carotid Artery Occlusions with Large Ischemic Strokes
Neurol 104:e210269, Ortega-Gutierrez,S.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

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



Showing articles 0 to 50 of 2009 Next >>