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Differential
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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acute intermittant porphyria
advances in neurology
algorithm
alien hand syndrome
alpha-fetoprotein
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
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
antidepressant
antiviral agents
aphasia
aphasia, progressive, primary
aphonia
apnea
applause sign
apraxia
apraxia of eye movements
areflexia
arm atrophy
arm swing, reduced
arm weakness
ascending paralysis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autoimmune disease
automatic behavior
automobile accidents
autonomic dysfunction
Babinski sign
basophilic stippling of red blood cells
behavioral disorder
BiPAP
blepharospasm
bone marrow biopsy
botulism
brachial amyotrophic diplegia
bradykinesia
brain atrophy
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
cachexia
CAG repeats
cane
carcinoembryonic antigen
carcinoma
CAT scan, emission, abnormal
catalepsy
CD4 counts
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
chills
Chinese paralytic syndrome
chondroitin sulfate C
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
coma, episodic
compulsivity
conduction block
confusion
constipation
conversion reaction
cortical-basal ganglionic degeneration
cranial neuropathy
crying, pathologic
cyclophosphamide
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
denervation of muscle
denervation potentials
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diphtheria
diplegia, atonic
diplegia, brachial
diplopia
distal muscle atrophy
distal muscle weakness
dog bite
downward gaze
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, Japanese
encephalitis, viral
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
evoked potentials
executive dysfunction
exercise
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
finger weakness
fish poisoning
flaccid paralysis
fluency
foot drop
frontal behavioral spatial syndrome
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, apraxic
gamma amino butyric acid
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
GM1 ganglioside antibodies
grasp reflex
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hallucination
hand weakness
headache
heavy metal intoxication
heralding manifestation
highly active antiretroviral therapy
hippocampus
HLA
hoarseness
hospice
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hypocretin
hypophonia
hyporeflexia
hypothalamus
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunohistochemistry
immunosuppression
immunosuppressive agents
immunotherapy
impulsivity
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
India
inflexibility, mental
intellectual deficit
intrinsic hand muscles, wasting of
laminectomy, cervical
laughing, pathologic
L-dopa
lead and the nervous system
lead poisoning
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
leukemia
life expectancy
lobar atrophy
locked-in syndrome
loss of sympathy
Lyme disease
lymphoma
lymphoma involving CNS
Man-In-The-Barrel syndrome
masked facies
masseter muscle wasting
meningitis
mental retardation
mental status, abnormal
midbrain
midbrain, atrophy
mimics
misdiagnosis
modafinil
monoclonal gammopathy
monomelic amyotrophy
mood change
mortality
motor neuron disease
motor neuron disease, misdiagnosis
motor neuron disease, spontaneous recovery
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sleep latency test
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelomalacia
myelopathy
myelopathy, ischemic
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myopathy
myopathy, autoimmune
myopathy, quadriceps
myopathy, steroid responsive
myositis
narcolepsy
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal loss
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
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
night sweats
obsessive-compulsive disorder
ocular motility, disorders of
osteomalacia
pain
pain, abdominal
pain, increased response
pain, leg
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paranoia
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraspinal muscle
parathyroid adenoma
Parkinson disease, axial symptoms
Parkinson disease, L-dopa nonresponsive
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
patient information and support
penguin silhouette sign
personality change
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymerase chain reaction, false negative
polymyositis
polyneuropathy, chronic inflammatory demyelinating
polysomnogram
porphyria
positive sharp waves
primary lateral sclerosis
progeria
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
progressive supranuclear palsy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
rabies, nervous system involvement with
radial nerve, palsy of
radiation hypersensitivity
release phenomena
REM sleep
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal cell carcinoma
renal stones
respirator
respiratory failure
respiratory tract infection
retrocollis
retrovirus
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rigidity
rigidity, axial
riluzole
risk factors
saccadic eye movements, abnormal
screening
sensory symptoms
sequencing difficulty
shell fish poisoning
sinemet
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep
sleep offset paralysis
sleep onset paralysis
sleep paralysis
sleep pathology and physiology
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid
stimulant drugs
syringomyelia
tandem gait, ataxic
tau protein
tauopathy
telangiectases
temporal lobe, atrophy
tick paralysis
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
toxins, nervous system
trauma
travel, foreign
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
undiagnosed
urinary incontinence
viral infection
viral infection, CNS
viral isolation
vision, blurred
visual symptoms
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, progressive
weight gain
weight loss
West Nile fever
wheelchair
word-finding difficulty
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 50 to 100 of 4074 << Previous Next >>

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Misdiagnosis of Myasthenia Gravis
J Nat'l Medical Assoc, 79:425-4291987., Wheeler,S.D., 1987

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

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

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

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

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
Neurol 102:e209260, Young,A. & Johnston,J.L., 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 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

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

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

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

Re-Emergency of Poliovirus in the United States:Considerations and Implications
Ann Neurol 92:725-728, Russo,G.B.,et al, 2022

What All Physicians Need to Know About the Polio Resurgence in New York State
JAMA online e1-e3, Larkin, H., 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

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

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

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

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

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

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

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Isolated Oculomotor Nerve Palsy due to Pituitary Apoplexy Missed on CT scan
Neurol 94:e1774-e1777, Marzoughi, S.,et al, 2020

Contrast-Induced Encephalopathy Following Coronary Angiography
Neurol 94:e2491-e2494, Harada, Y.,et al, 2020

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

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

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

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

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, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 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

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

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

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019



Showing articles 50 to 100 of 4074 << Previous Next >>