Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
airway obstruction
Alzheimer's disease
aminoacidopathies
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
analgesic
anxiety
aphasia
aphasia, progressive, primary
aphonia
apraxia
aqueduct of Sylvius, stenosis
aqueductal stenosis
asymptomatic
ataxia
atrioventricular block
basal ganglia, calcification of
behavioral disorder
benzodiazepine
blindness
bradycardia
brain atrophy
brain biopsy
bruit, supraclavicular
C9orf72
calcification, intracranial
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
cerebellar hypoplasia
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
cervical spine injury
cervical spondylosis
chorea
chronic progressive external ophthalmoplegia
claudication, extremity
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
concussion
contractures, joint
controversies in neurology
cornea, opacity of
corpus callosum
corpus callosum, thinning
cortical hand knob
cortical muscular atrophy
cost
cost effectiveness
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, cerebrovascular disease causing
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
developmental disability
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
dying
dyspnea
dyspraxia
dystonia
electromyogram
Emery-Dreifuss muscular dystrophy
encephalocele
encephalopathy
encephalopathy, progressive
episodic neurologic deficits
ethics in neurology
euthanasia
evidence-based research
evoked potentials
exercise intolerance
exercise-induced vascular symptoms
facial weakness, bilateral
familial
fasciculation
fetal movements, reduced
fetus
fibrillations
finger drop
floppy infant
fluency
foot drop
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontotemporal dementia, behavioral variant
gait disorder
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glioma
granular atrophy, cerebral cortex
gray matter
hallucination
head injury
headache
hearing loss
heart block
heart block, complete
heart murmur
hemiplegia
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
high arched feet
histochemistry
histochemistry of muscle
hospice
hunger
hydrocephalus
hydrocephalus, congenital
hypotonia
hypotonia, infants
inborn errors of metabolism
inflexibility, mental
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leukodystrophy
Lewy body disease, diffuse
life sustaining treatment
lissencephaly
lobar atrophy
locked-in syndrome
lysosomal storage disease
malformation, CNS, congenital
medical-legal aspects of neurology
MELAS syndrome
mental retardation
merosin
MERRF syndrome
metabolic disorder, primary
micrognathia
microinfarcts
micropthalmia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
MNGIE syndrome
molecular genetics
monomelic amyotrophy
morphine
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, susceptibility weighted
MRS
multiple sclerosis
multiple sclerosis, diagnosis of
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelopathy
myocardial infarction
myoclonus
myopathy
myopathy, distal
myopathy, mitochondrial
myotonia
myotonia congenita
myotonia dystrophica
negative
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neurologic testing
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, motor, multifocal
normal
ophthalmoplegia
optic atrophy
optic neuropathy
oxygen therapy
pacemaker, cardiac-transvenous
pain, increased response
palliative care
pancytopenia
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic deficits
peripheral vascular disease
peroxisomal disease
personality change
physician assisted suicide
pigmentary retinopathy
polyneuropathy
positive sharp waves
posterior interosseous neuropathy
practice guidelines
prognosis
progranulin
progressive neurologic disorder
proximal muscle atrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pyramidal tract
quality of life
ragged-red fibers
release phenomena
respiratory failure
retinal detachment
retinal dysplasia
retinopathy
review article
right to die
sedation
seizure
sensorineural hearing loss
short stature
single photon emission computed tomography
skin, lesions in neurologic disorders
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
speech, loss of
spinal cord, compression of
spinal cord, injury of
stereotyped behavior
sternocleidomastoid muscle
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subclavian artery stenosis
suck, poor
sudden death
symmetric brain lesions
syringomyelia
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
temporalis muscle wasting
term infant
thoracic outlet syndromes
toe walking
tongue, fasciculations of
treatment of neurologic disorder
trigger finger
trinucleotide repeats
ultrasonography
upgaze, paralysis of
urea-cycle enzymopathies
valium
visual field defect
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, progressive
weight loss
white matter disease
white matter disease, periventricular
winging of scapula
word-finding difficulty
Showing articles 100 to 150 of 9396 << Previous Next >>

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

A Woman with Monocular Vision Loss
Neurol 95:e1105-e1109, Danish, H.,et al, 2020

Headache, Confusion, and Somnolence in a 27-Year-Old Woman
JAMA doi:10-1001/JAMA.2020.10167, Sastry, R.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

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

Cerebellar Hippocampal and Basal Nuclei Transient Edema with Restricted Diffusion (CHANTER) Syndrome
Neurocrit Care 31:228-296, Jasne, A.S.,et al, 2019

Central Nervous System Infections Due to Coccidioidomycosis
J Fungi 5:2-12, Jackson, N.R.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Prolonged Microgravity Affects Human Brain Structure and Function
AJNR 40:1878-1885, Roberts,D.R.,et al, 2019

Optic Nerve Enhancement and Restricted Diffusion in Postoperative Visual Loss
Neuro-Ophthalmol 43:337-339, Finelli, P.F., 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

The Dangers of PRES
Neurol 92:e282-e285, Chaterine, C.,et al, 2019

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

Bobblehead-Doll Syndrome
NEJM 380:e5, Sacks, C.A., 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,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

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

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

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

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Multiple Sclerosis
NEJM 378:169-180, Reich, D.S.,et al, 2018

Deep Brain Nuclei T1 Shortening after Gadobenate Dimeglumine in Children: Influence of Radiation and Chemotherapy
AJNR 39:24-30, Kinner, S.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

A 30-year-old man with headache and sleep disturbance
Neurol 90:e1535-e1540, English, S.W.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

A Fatal Case of Undiagnosed Candida Meningitis-Role of Computer-assisted Diagnosis
Neurologist 23:138-140, Finelli, P.F., 2018

Alexander Disease with Features of Both Frontal and Bulbospinal Involvement
Neurol 91:e396-e397, Nam,T-S.,et al, 2018

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

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Atrophy Patterns in Cerebral Amyloid Angiopathy With and Without Cortical Superficial Siderosis
Neurol 90:e1751-e1758, Kim,J.,et al, 2018

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

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

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

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



Showing articles 100 to 150 of 9396 << Previous Next >>