Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
advances in neurology
algorithm
allodynia
Alzheimer's disease
aminoacidopathies
amyloid
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
angiostrongylus cantonensis
anterior horn cell disease
aphasia
aphasia, progressive, primary
areflexia
arm atrophy
arm weakness
ascending paralysis
aspiration
asthma
asthma, poliomyelitis-like syndrome with
ataxia
ataxia, progressive
Babinski sign
behavioral disorder
biologic markers
BiPAP
brain atrophy
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
burning feet
burning paresthesia
C0ORF72
CAG repeats
calf hypertrophy
camptocormia
cane
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
children
chorea
chromosomal abnormality
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cognition
concussion
confusion
congenital heart disease
constipation
controversies in neurology
cost
cost effectiveness
creatine phosphokinase(CPK)elevated
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
developmental retardation
dexterity, impaired
diagnostic criteria
differential diagnosis
diplegia, atonic
diplegia, brachial
disability, neurological
disorientation
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dystonia
electromyogram
emotional lability
encephalopathy
endemic area
eosinophilia
epidemiology of neurology
episodic neurologic deficits
evidence-based research
evoked potentials
exercise intolerance
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
finger weakness
flaccid paralysis
flail arm syndrome
fluency
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
hallucination
hand weakness
head injury
headache
headache, progressive
health insurance
helminthic infection of CNS
hemiparesis
hemiplegia
hemiplegia, progressive
heralding manifestation
hospice
Huntington's chorea
hyperreflexia
hypoglycorrhachia
hyporeflexia
hypotonia
hypotonia, infants
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, ubiquitin
inclusion body myositis
inflexibility, mental
intellectual deficit
internal capsule
intrinsic hand muscles, wasting of
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
lactic acidemia
laminectomy, cervical
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
leukodystrophy
Lewy body disease, diffuse
life expectancy
lobar atrophy
locked-in syndrome
lysosomal storage disease
meningismus
meningitis, eosinophilic
metabolic disorder, primary
Mills syndrome
mimics
misdiagnosis
mobility
mobility aids
molecular genetics
monomelic amyotrophy
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, functional
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
mutism
myasthenia gravis
myelopathy
myelopathy, ischemic
myopathy
myopathy, autoimmune
myopathy, quadriceps
myositis
nasal speech
neck weakness
nerve biopsy
neurologic complications of, surgery
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neurologic testing
neuronal degeneration
neuropathology
neuropathy
neuropathy, motor, multifocal
neuroprotective agents
next-generation sequencing
nusinersen
owl's eye sign of spinal cord
pain
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
parasitic infection
parasitic infection, CNS
paresthesias
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic deficits
patient information and support
peroxisomal disease
personality change
pes cavus
physical therapy
Pick's disease
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymyositis
practice guidelines
pregnancy, neurologic complications in
primary lateral sclerosis
prognosis
progranulin
progressive neurologic disorder
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
raw fish ingestion
release phenomena
respirator
respiratory failure
review article
riluzole
risk factors
saccadic eye movements, abnormal
scoliosis
scoliosis, neurologic association with
scooters
screening
seizure
shoulder, subluxation
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
SMN1 gene
snail
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord degeneration
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid therapy, CNS treatment and complications with
stiff legs
superoxide dismutase
survival motor neuron gene
sushi
syringomyelia
tau protein
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
trauma
travel history
travel, foreign
treatment of neurologic disorder
trinucleotide repeats
tripping
ubiquitin
urea-cycle enzymopathies
urinary incontinence
viral infection
viral infection, CNS
viral isolation
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
word-finding difficulty
X-linked bulbospinal neuronopathy
Showing articles 50 to 100 of 4573 << Previous Next >>

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

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

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

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

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

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

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,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

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

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

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

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

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Physician-Assisted Death
Neurol 87:1152-1160, Abrahao, A.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

Acute Flaccid Myelitis of Unknown Etiology in California 2012-2015
JAMA 314:2663-2671, Van Haren, K.,et al, 2015

Responsibilities of Health Care PRofessionals in Counseling and Educating Patients with Incurable Neurological Diseases Regarding "Stem Cell Tourism"
JAMA Neurol 72:1342-1345, Bowman, M.,et al, 2015

Differential Diagnosis of Finger Drop
Neurologist 19:128-131, Varatharaj, A.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Ischemic-Hypoxic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1133, Ropper, A.H.,et al, 2014

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Venous Thromboembolism in Amyotrophic Lateral Sclerosis
Neurol 82:1674-1677, Gladman, M.,et al, 2014

Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
Neurol 82:149-155, Mioshi, E.,et al, 2014

Degenerative Diseases of the Nervous System, Werdnig-Hoffman Disease, Spinal Muscular Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1116, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
Adams & Victors Principles of Neurology, Chp 39, pg 1118, Ropper, A.H.,et al, 2014

Macroglossia in Amyotrophic Lateral Sclerosis
JAMA Neurol 70:1432-1435, McKee, H.R.,et al, 2013

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Spectrum of Paraneoplastic Disease Associated With Lymphoma
Neurol 76:705-710, Briani,C.,et al, 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009

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

A Large-Scale International Meta-Analysis of Paraoxonase Gene Polymorphisms in Sporadic ALS
Neurol 73:16-24,11, Wills,A.-M.,et al, 2009

What Are the Prospects of Stem Cell Therapy for Neurology?
BMJ 337:1325-1327, Chandran,S., 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Palliative Care for Patients With Amyotrophic Lateral Sclerosis
JAMA 298:207-216,248, Mitsumoto,H. &Rabkin,J.G., 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Lead Poisoning From the Beauty Case: Neurologic Manifestations in an Elderly Woman
Neurol 69:929-930, Fluri,F.,et al, 2007

West Nile Virus: A Case Report with Flaccid Paralysis and Cervical Spinal Cord MR Imaging Findings
AJNR 26:26-29, Kraushaar, G., et al, 2005

Hemiplegic ALS:Mills Syndrome
Neurol 64:1984-1985, Rajabally,Y.A.,et al, 2005

Clinicopath Conf,Encephalomyelitis Due to West Nile Virus and CLL, Case 22-2005
NEJM 353:287-295, Hollande,H.,et al, 2005

Brachial Amyotrophic Diplegia in a Patient with Human Immunodeficiency Virus Infection
Arch Neurol 62:817-823, Berger,J.R.,et al, 2005

ALS Corticospinal Degeration on DWI
Neurol 62:1834, Cabello,J.P.,et al, 2004



Showing articles 50 to 100 of 4573 << Previous Next >>