Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
advances in neurology
algorithm
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
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
C9orf72
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, proteincytologic dissociation
cerebrovascular accident
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
children
chorea
chromosomal abnormality
chromosome 5
cognition
concussion
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
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dystonia
electromyogram
emotional lability
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
health insurance
hemiparesis
hemiplegia
hemiplegia, progressive
heralding manifestation
hospice
Huntington's chorea
hyperreflexia
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
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
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
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
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
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
stiff legs
superoxide dismutase
survival motor neuron gene
syringomyelia
tau protein
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
trauma
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 350 to 400 of 4644 << Previous Next >>

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Poliomyelitis-A Persistent Problem
NEJM 288:370, Weinstein,L., 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Neuropathy in Thyrotoxicosis-Correspondence-NEJM 289:219
1973., , 1973

Occult Normal Pressure Hydrocephalus Manifested by Parkinsonism-dementia Complex
Neurol 23:234-238, Sypert,G.W.,et al, 1973

Reversible Forms of Motor Neuron-Disease:Lead"Neuropathy"
Neurol 22:446, Boothby,J., 1972

Amyotrophic Lateral Sclerosis
Richard Kisonak, Associated Press, Boston Globe Apr 30972., , 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Neurological Disorders in Patients Following Surgery for Peptic Ulcer
Neurol 22:450, Hoffman,P., 1972

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Muscular Quivering
BMJ 3, 1972 Jan., , 1972

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Paramagnetic Rim Lesions and Development of Clinical MS in Radiologically Isolated Syndrome
JAMA Neurol 83:250-258, Lim,T.R.et al, 2026

Diagnostic Value of the Kappa Free light Chain Index to Distinguish MOGAD, NMOSD, and MS
Neurol 106:e214946, Tournier,A.,et al, 2026

Using Susceptibility-Based Imaging in highly ctive Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

The 2024 McDonld Criteria for Dignosis of Multiple Sclerosis, The Rubber meets the Road
Neurol 106:e214688, Miller, A.E., 2026

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

Infantile Epileptic Spasms Syndrome (West Syndrome)
Stat Pearls PMID:30725936, Smith,M.S.,et al, 2025

Frequency and Diagnostic Implications of Paramagnetic Rim Lesions in People Presenting for Diagnosis to a Multiple Sclerosis Clinic
Neurol 105:e213912, Remner,B.,et al, 2025

Diagnosis of Multiple Sclerosis: 2024 Revisions of the McDonald Criteria
Lancet Neurol 24:850-865, Montalban,X.,et al, 2025

The Optic Nerve Should Graduate to Be the Fifth Lesion Site for the Diagnosis of Multiple Sclerosis
Neurol 102:e207919, Galetta,S. & Brownlee, W., 2024

Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
Stroke 55:e77-e90, Saposnik,G.,et al, 2024

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

Diagnostic MRI Score to Differentiate Susac Syndrome from Primary Angiitis of the Central Nervous System and Multiple Sclerosis
Ann Neurol 96:846-854, Marrodan,M.,et al, 2024

Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
Ann Neurol 96:1086-1091, Fadda,G.,et al, 2024

Management of Possible Multiple Sclerosis
NEJM 388:2195-2190, , 2023

Kappa Free Light Chain Biomarkers are Efficient for the Diagnosis of Multiple Sclerosis
Neurol Neuroinflamm 10:e200049, Levraut,M.,et al, 2023



Showing articles 350 to 400 of 4644 << Previous Next >>