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Differential
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accommodation
accomodation, abnormal
achilles tendon, enlarged
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
adverse drug reaction
affect, flat
alexia
algorithm
alien hand syndrome
Alzheimer's disease
amyotrophic lateral sclerosis
ANA
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
anomic aphasia
anticholinergic drugs
antiviral agents
aphasia
aphasia, classification of
aphasia, progressive, primary
apraxia
arthralgia
ataxia
ataxia, cerebellar
ataxia, frontal
ataxia, hereditary
ataxia, progressive
ataxic gait
autoimmune disease
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, degeneration
behavior modification
behavioral disorder
Bell's phenomenon
blinking
blinking, reduced
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, lesion of
C9orf72
cachexia
calcium antagonist
camptocormia
carbon monoxide poisoning
CAT scan, abnormal
CAT scan, angiography
CD4 counts
cerebellar atrophy, primary
cerebellar degeneration
cerebellitis
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
coma
complications
concentration, impaired
confusion
conjunctivitis
contractures, joint
convergence
convergence, impaired
conversion reaction
corpus callosum
corpus callosum, lesion of
cortical-basal ganglionic degeneration
Coxiella burnetti
crying, pathologic
cryopyrin-associated periodic syndrome
cystatin C mutation
degenerative diseases of CNS
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
depression
developmental retardation
diagnostic criteria
differential diagnosis
digital subtraction angiography
diplopia
disability, neurological
disconnection syndrome
dizziness
dopamine agonist
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, brainstem
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, delayed
episodic disorders
Erdheim-Chester disease
eye movement, disorders of
falling
familial
fasciculation
fatigue
fever
fever, recurrent
finger nose finger test
Fisher C.M.
foam cells
Friedreich's ataxia
frontal behavioral spatial syndrome
frontal bossing
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, apraxic
gait, festinating
gait, spastic
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
hallucination
hallucination, visual
handwriting
head circumference
headache
headache, awakened by
headache, awakening with
headache, bifrontal
headache, occipital
headache, recurrent
headache, severe
hearing loss
heel swelling
hemiparesis
highly active antiretroviral therapy
hip flexor weakness
histiocytosis
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hyperreflexia
hypersomnia
hypertrophic intracranial pachymeningitis
hypometric saccades
hypomyelination
hypophonia
hyporeflexia
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
immunosuppression
immunosuppressive agents
impulsivity
inattention
incontinence, fecal
infection
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
kinesia paradoxica
lacunar infarction
laughing, pathologic
L-dopa
leg dragging
leg weakness, bilateral
Legionnaires'disease
lethargy
Lewy body
lobar atrophy
lumbar drain
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, neurologic aspects and complications of
mental status, abnormal
micrographia
middle cerebellar peduncle, lesion
miosis
misdiagnosis
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, nodular enhancement
multimodal neuroimaging
multiple system atrophy
mutism
myelopathy
myoclonus
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neurologic symptoms
neuropathology
neuropathy, demyelinating
next-generation sequencing
nystagmus
nystagmus, gaze-evoked
nystagmus, upbeating on upgaze
ocular motility, disorders of
old age, neurology of
opportunistic infection, CNS
optic ataxia
optic atrophy
optic atrophy, bilateral
oscillopsia
paranoia
paraparesis, spastic
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
patient information and support
Pelizaeus Merzbacher
perivascular enhancement
Persistent postural-perceptual dizziness
personality change
pes cavus
photophobia
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
polymerase chain reaction, false negative
pons, lesion of
posterior leukoencephalopathy syndrome
precipitating factors
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
proprioception, abnormal
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
pupil
pupil, light reflex, abnormal
Q fever
rash
recurrent
red eye
reflex, cutaneous
release phenomena
respiratory tract infection
retropulsion
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rickettsial organism
rigidity
rooting reflex
seizure
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss
serologic testing
serotonin norepinephrine reuptake inhibitors
short stature
short steps
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull bone, thickening
slow virus infection of CNS
slurred speech
smell
snout reflex
somnolence
speech disorder
speech, soft
splenium of corpus callosum
spongy degeneration of brain
stare
startle myoclonus
startle reaction
steroid therapy, CNS treatment and complications with
stooped posture
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
subcortical U fibers
suck reflex
suicide
systemic illness
systemic lupus erythematosus
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, atrophy
thrombocytopenia
tongue, fasciculations of
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, resting
turning in bed
twins
upgaze
upgaze, paralysis of
urinary incontinence
vasculopathy
vasospasm, cerebral
ventriculostomy
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual impairment
voice, abnormality of
walking frame
walking, difficulty with
weakness, generalized
weight loss
wheelchair
white matter disease
wide based gait
writing
Showing articles 400 to 450 of 1434 << Previous Next >>

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Opsoclonus and Multiple Cranial Neuropathy as a Manifestation of Neuroborreliosis
Neurol 77:1013-1014, Sabien Van Erp, W.,et al, 2011

A Rare Cause of Gait Ataxia
Lancet 378:1274, Rous, C.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Basal Ganglia Involvement in Wernicke Encephalopathy: Report of 2 Cases
AJNR 32:E129-E131, Zuccoli, G.,et al, 2011

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

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Frontal Headache
JAMA 306:317-318, Chang,H.J.,et al, 2011

N-methyl-D-aspartate Receptor Autoimmune Encephalitis Presenting With Opsoclonus-Myoclonus
Arch Neurol 68:1069-1072, Smith, J.H.,et al, 2011

An Acutely Confused Young Woman
Lancet 378-456, Casetta, I,.et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Arch Neurol 67:118-121, Kurian,M.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

Assessment: Symptomatic Treatment for Muscle Cramps (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 74:691-696, Katzberg,H.D.,et al, 2010

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

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

A Meta-Regression of the Long-Term Effects of Deep Brain Stimulation on Balance and Gait in PD
Neurol 75:1292-1299, St. George,R.J.,et al, 2010

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Sensory Ganglionopathy Due to Gluten Sensitivity
Neurol 75:1003-1008, Hadjivassiliou,M.,et al, 2010

Primary Central Nervous System Post-Transplantation Lymphoproliferative Disorder
CANCER 16:863-870, Cavaliere, R.,et al, 2010

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

MR Imaging Findings in 56 Patients with Wernicke Encephalopathy: Nonalcoholics May Differ from Alcoholics
AJNR 30:171-176, Zuccoli,Z.,et al, 2009

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Clinicopath Conf. Rickets Due to Vitamin D Deficiency
NEJM 360:398-407, Case 3-2009, 2009

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

Neurosarcoidosis: A Study of 30 New Cases
JNNP 80:297-304, Joseph,F.G. &Scolding,N.J., 2009

Slurred Speech and Spirochaetes
Lancet 373:978, Thukral,A.,et al, 2009

High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
BMJ 338:653, Beau-Salinas,F.,et al, 2009

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
NEJM 360:1960-1970, Bockenhauer,D.,et al, 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Frequency, Characteristics, and Risk Factors for Amiodarone Neurotoxicity
Arch Neurol 66:865-869, Orr,C.F. &Ahlskog,E., 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

A 54-Year-Old Woman with Progressive Gait Disturbance and MRI Abnormalities
Neurol 73:466-474, Hochberg,F.H.,et al, 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

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

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

Reversible Extralimbic Paraneoplastic Encephalopathies with Large Abnormalities on Magnetic Resonance Images
Arch Neurol 66:268-271, McKeon,A.,et al, 2009

Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
JNNP 79:672-677, Wagner,J.N.,et al, 2008

Reversible Parkinsonism and Ataxia Associated With High-Dose Octreotide
Neurol 70:2345-2346, Espay,A.J., 2008

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

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008



Showing articles 400 to 450 of 1434 << Previous Next >>