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acetazolamide
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
akinetic mute
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
anorexia
areflexia
arm swing, reduced
arrhythmia, cardiac
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
atrial fibrillation
attention deficit disorder with hyperactivity
attention span
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
bone marrow transplantation
bradykinesia
brain atrophy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, syndrome
cardiomyopathy
CAT scan
CAT scan, abnormal
catalepsy
cataplexy
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congestive heart failure
consanguinity
corona radiata
cortical-basal ganglionic degeneration
cough
cranial neuropathy
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
depression
developmental milestones, loss of
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
disease modifying agents
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
electroencephalogram, abnormalities of
electromyogram
electrophoretic pattern, CSF
embolism
encephalitis
encephalopathy
epileptic encephalopathy
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial periodic ataxia
FARS2 deficiency
fatigue
fine motor function, impaired
finger nose finger test
finger numbness
foam cells
foot drop
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glabellar sign
granular osmiphilic material
hammertoes
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
hormone replacement
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hypertonia
hypogonadism
hypogonadism, hypogonadotropic
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
inattention
incoordination
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
Kayser-Fleischer ring
lacunar infarction
lacunar infarction, differential diagnosis of
lateropulsion
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
Lorenzo's oil
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomal storage disease
medulla oblongata, neoplasm of
memory, defect of recent
memory, impairment of
meningitis, CSF cell count-normal
microcephaly
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, spinal cord
MRI, spine
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
myelomalacia
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
nausea and vomiting
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
neurofibrillary degeneration
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, sensory
next-generation sequencing
Niemann-Pick disease
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
olivary degeneration, hypertrophic
optic atrophy
ovarian dysgenesis
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
Perrault syndrome
personality change
pes cavus
pons, infarction of
pontine hemorrhage
positional head-hanging test
prevention of neurologic disorders
prion disease
prion protein gene
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
pure dysarthria
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
release phenomena
retropulsion
review article
rigidity
risk factors
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella virus
saccadic eye movements, abnormal
salivation, excessive
scoliosis
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
sensory loss
serologic testing
serologic testing of cerebrospinal fluid
slit lamp examination
slurred speech
spastic ataxia
spastic diplegia
spasticity
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
splenomegaly
spontaneous remission
square wave jerks
staggering
strokelike episodes
suck reflex
superior cerebellar artery infarction
superior cerebellar artery syndrome
symmetric brain lesions
tandem gait, ataxic
tau protein
tauopathy
thalamus, lesion of-bilateral
titubation
toe walking
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vertigo, episodic
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
viral infection, CNS
vision, blurred
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
white matter disease
wide based gait
workup
Showing articles 350 to 400 of 1088 << Previous Next >>

A 27-year-old Man with Hand Numbness
Neurol 82:e80-e84, Vijayan, J.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, High-Altitude (mountain) sickness
Adams & Victors Principles of Neurology Chp 40, pg 1139, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hypercapnia Pulmonary Disease
Adams & Victors Principles of Neurology Chp 40, pg 1139, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Holmes Tremor in a Patient with Progressive Multifocal Leukoencephalopathy
Surg Neurol Int 5:5413-5415, Gunness, V.R.N.,et al, 2014

Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
Child Adolesc Pych Ment Health 8:20, Wouters,S.,et al, 2014

Misdiagnosis of Treatable Stroke Mimic: The Case for HIV Screening in Practice Guidelines
Neurohosp 3:125-130, Finelli, P.F., 2013

Erythromelalgia? A Clinical Study of People Who Experience Red, Hot, Painful Feet in the Community
Int J Vasc Med ID=864961, Friberg, D.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
Ann Neurol 74:648-654,627, Horisawa, S.,et al, 2013

Cheiro-Oral Syndrome Secondary to Thalamic Infarction
The Neurologist 19:22-25, Satpute, S.,et al, 2013

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

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

A Pilot Study of Focused Ultrasound Thalamotomy for Essential Tremor
NEJM 369:640-648, Elias, W.J.,et al, 2013

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
Neurol 81:1557, Trocello, J.M.,et al, 2013

Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Brainstem Abnormalities and Vestibular Nerve Enhancement in Acute Neuroborreliosis
BMC Res Notes 6:551, Farshad-Amacker,N.A.,et al, 2013

Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
Neurol 79:1466-1473, Weissenborn, K.,et al, 2012

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

Clinicopathologic Conference, Rocky Mountain Spotted Fever
NEJM 366:1434-1443, Case 11-2011, 2012

Hashimoto Encephalopathy
Neurol 78:e134, Afshari, M.,et al, 2012

A Musicians Dystonia
Lancet 379:2116, Vecchio, M.,et al, 2012

Teaching NeuroImages: Isolated Sensory Loss of the Arm Sparing Hand in Cortical Infarction
Neurol 76:e3, Cha,M.-J.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Fulminant Encephalopathy With Basal Ganglia Hyperintensities in HIV-Infected Drug Users
Neurol 76:787-794, Newsome,S.D.,et al, 2011

Fulminant Encephalopathy with Basal Ganglia Hyperintensities in HIV-infected Drug Users
Neurol 77:923, Finelli, P.F., 2011

Evidence-based guideline update: Treatment of Essential Tremor
Neurol 77:1752-1755, Zesiewicz, T.A.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

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

An Unusual Cause of Pseudomedian Nerve Palsy
Case Reports Neurol Med doi:10.1155/2011/474271, Manjaly, Z.M.,et al, 2011

Cerebral Toxoplasmosis in Acquired Immunodeficiency Syndrome (AIDS) Patients also Provides Unifying Pathophysiologic Hypotheses for Holmes Tremor
BMC Neurol 10:37, Lekoubou, A.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

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

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Is the Diagnosis at Hand?
The Lancet 375:1134, Holmes,M.V., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

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

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



Showing articles 350 to 400 of 1088 << Previous Next >>