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Differential
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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 50 to 100 of 9396 << Previous Next >>

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

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Neurovascular Complications of Iatrogenic Fusarium solani Meningitis
NEJM 390:522-529, Strong, N.,et al, 2024

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

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,et al, 2024

Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
Neurol 103:e209586, Taborda,M.H.,et al, 2024

Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Primary Diffuse Leptomeningeal Melanocytosis, A Diagnoatic Conundrum
Neurol 101:e576-3580, Selvarajan,J.M.P.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
Neurol 100:1111-1116, Mankad,J.P. & Lavingia,J.R., 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Neuroimaging Findings in CHANTER Syndrome
AJNR 43:1136-1141, Mallikarjun, K.S.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Nitromethane-Induced Acute Reversible Encephalopathy
Neurol 97:e1361-e1362, Palumbo, G.,et al, 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A Case of Primary Leptomeningeal Lymphoma Presenting with Hydrocephalus Characterized by Disproportionately Large Fourth Vehicle
NMCCRJ 8:399-404, Nohira, S.,et al, 2021

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

Recurrent Perimesencephalic Nonaneurysmal Subarachoid Hemmorrhage Within a Short Period of Time:A Case Report
World J Clin Cases 16:3356-3364, Li,J.,et al, 2021

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

Central Nervous System Involvement in Erdheim-Chester Disease
Neurol 95:e2746-e2754, Aubart,F.C.,et al, 2020

Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency
Neurol 95:e3129-e3137, He, R.,et al, 2020



Showing articles 50 to 100 of 9396 << Previous Next >>