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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acute intermittant porphyria
advances in neurology
algorithm
allodynia
amyloid
amyloidosis
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
anemia
angiostrongylus cantonensis
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
antiviral agents
aphasia
aphasia, progressive, primary
aphonia
apnea
areflexia
arm atrophy
arm weakness
ascending paralysis
ataxia
ataxia, progressive
ataxic gait
autoantibodies
autonomic dysfunction
Babinski sign
basophilic stippling of red blood cells
behavioral disorder
BiPAP
bone marrow biopsy
botulism
brachial amyotrophic diplegia
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
burning feet
burning paresthesia
cachexia
CAG repeats
cane
carcinoma
CAT scan, emission, abnormal
CD4 counts
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
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
Chinese paralytic syndrome
chondroitin sulfate C
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
coma, episodic
conduction block
confusion
constipation
conversion reaction
cranial neuropathy
creatine phosphokinase(CPK)elevated
crying, pathologic
cyclophosphamide
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
denervation of muscle
denervation potentials
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diphtheria
diplegia, atonic
diplegia, brachial
disorientation
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electromyogram
electrophoretic pattern, serum
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
endemic area
eosinophilia
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
evoked potentials
exercise
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
finger weakness
fish poisoning
flaccid paralysis
fluency
foot drop
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
GM1 ganglioside antibodies
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hallucination
hand weakness
headache
headache, progressive
heavy metal intoxication
helminthic infection of CNS
heralding manifestation
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hypophonia
hyporeflexia
imbalance
immunohistochemistry
immunosuppressive agents
immunotherapy
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
inflexibility, mental
intellectual deficit
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
laminectomy, cervical
laughing, pathologic
lead and the nervous system
lead poisoning
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
lid closure, weakness of
life expectancy
lobar atrophy
locked-in syndrome
Lyme disease
lymphoma
lymphoma involving CNS
Man-In-The-Barrel syndrome
masseter muscle wasting
meningismus
meningitis, eosinophilic
mimics
misdiagnosis
monoclonal gammopathy
monomelic amyotrophy
mortality
motor neuron disease
motor neuron disease, misdiagnosis
motor neuron disease, spontaneous recovery
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelogram
myelomalacia
myelopathy
myelopathy, ischemic
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myopathy
myopathy, autoimmune
myopathy, quadriceps
myopathy, steroid responsive
myositis
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuropathology
neuropathology, peripheral nerves
neuropathy
neuropathy, acute
neuropathy, amyloid
neuropathy, diphtheritic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, painful
neuropathy, peripheral, treatment
neuropathy, toxic
neuroprotective agents
neurotoxin
next-generation sequencing
osteomalacia
pain
pain, abdominal
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paranoia
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraproteinemia
parasitic infection
parasitic infection, CNS
paraspinal muscle
parathormone
parathyroid adenoma
paresthesias
Parkinsonism syndrome
pathology
patient information and support
personality change
Pick's disease
pleocytosis of cerebrospinal fluid
poison, mercury
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyradiculoneuropathy
porphyria
positive sharp waves
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
radial nerve, palsy of
raw fish ingestion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal cell carcinoma
renal stones
respirator
respiratory failure
respiratory tract infection
retrovirus
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
riluzole
risk factors
screening
seizure
sensory symptoms
shell fish poisoning
single photon emission computed tomography
sleep
sleep pathology and physiology
snail
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid
steroid therapy, CNS treatment and complications with
sushi
syringomyelia
tandem gait, ataxic
tick paralysis
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
toxins, nervous system
trauma
travel history
travel, foreign
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
viral infection
viral infection, CNS
viral isolation
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
word-finding difficulty
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 350 to 400 of 4087 << Previous Next >>

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

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

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

Muscular Quivering
BMJ 3, 1972 Jan., , 1972

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

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

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

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

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

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

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,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

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

Radiologically Isolated Syndrome: A Review for Neuroradiologists
AJNR 41:1542-1549, Hosseiny, M.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

A Patient with a History of Weight Loss Presenting with Seizures
Neurol 95:e2038-e2042, Tang, G. & Benavides, D.R., 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Evaluation of the Central Vein Sign as a Diagnostic Imaging Biomarker in Multiple Sclerosis
JAMA Neurol 76:1446-1456, Sinnecker, T.,et al, 2019

"Better Explanations" in Multiple Sclerosis Diagnostic Workup
Neurol 92:e2527-e2537, Calabrese, M.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

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

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Misdiagnosis of Multiple Sclerosis
Neurol 92:15-16, Brownlee, W.J., 2018

A 56-year-old woman with acute vertigo and diplopia
Neurol 90:748-752, Sharma, R.,et al, 2018

IgG4-Related Disease and Intracranial Hypertension: Case Report of a Novel Mechanistic Association
J Neurol Sci 385:75-77, Healy, J.,et al, 2018

Late Onset Neuromyelitis Optica Mimicking an Acute Stroke in an Elderly Patient
J Neuroimmunol 309:1-3, Suchdev, K.,et al, 2017

A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
Neurol 89:e231-e234, Gutman, J.M.,et al, 2017



Showing articles 350 to 400 of 4087 << Previous Next >>