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acetylcholine receptor
acetylcholine receptor antibody
acute intermittant porphyria
adverse drug reaction
agammaglobulinemia
ageusia
algorithm
alveolar hypoventilation
aminoglycoside
aminopyridine, 4
amphiphysin antibodies
ampicillin
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, myasthenic syndrome with
ANA
anesthesia, general
anesthesia, local
anosmia
anti Hu antibody
anti MAG antibodies
anti Ri antibody
anti Yo antibody
antiarrhythmic drugs
antibiotics
antibiotics, neurologic complications with
antibodies to voltage-gated calcium channels
anticholinergic drugs
anticholinergic drugs, side effects of
anticholinesterase
anticonvulsants
anticonvulsants, untoward effects of
apnea
areflexia
arm weakness
artane
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
azathioprine
beta adrenergic blocker
Bielschowsky head tilt test
botulism
brachial neuritis
burning paresthesia
calcium antagonist
calcium antagonist, side effects of
cancer associated myopathy
carcinoid tumor
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of ovary
cardiomyopathy
cardiotoxicity
CAT scan, chest
cerebellar degeneration
cerebellar lesion
cerebellum
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
chemotherapy, CNS treatment and complications with
children
Chinese paralytic syndrome
chloroquine
chlorpromazine
chronic progressive external ophthalmoplegia
ciguatera poisoning
ciprofloxacin
citrate
Clinical Pathologic Conference(C.P.C.)
cocaine
collapsin response mediator protein 5 IgG
comorbidities
complications
congenital myasthenic syndromes
constipation
contactin associated protein like 2 antibodies
contrast agents, neurotoxicity of
conversion reaction
cranial nerve palsies
cranial neuropathy
creatine phosphokinase(CPK)elevated
critical care unit
cyclosporine
deafness
demyelinating disease
dermatomyositis
developmental retardation
diaphragmatic paralysis
dilantin
dilantin, toxicity
diphtheria
diplopia
diplopia, transient
diplopia, vertical
drug abuse
drug abuse, neurologic complications of
drug induced neurologic disorders
dysarthria
dysphagia
dysphonia
electromyogram
electromyogram, decremental response
electromyogram, incremental response
electron microscopy
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
epidemiology of neurology
erythromycin
exercise
exercise-related muscle strength increase
eye movement, disorders of
face, numbness of
facial nerve palsy
facial weakness
familial
fasciculation
fatigue
fish poisoning
fluoroquinolones
fontanel, bulging
gait disorder
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
Graves ophthalmopathy
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
heat intolerance
heavy metal intoxication
HLA
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hormone replacement
hot bath test
H-reflex testing
hypercapnia
hypocalcemia
hyporeflexia
iatrogenic neurologic disorders
immune checkpoint inhibitors
immune-related adverse events
immunologic disease
immunology and the nervous system
immunosuppressive agents
immunotherapy
impotence
interferon
internuclear ophthalmoplegia
ipilimumab
Kearns-Sayre syndrome
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
level of consciousness, decreased
levonorgestrel
lid abnormalities
lid closure, weakness of
lid twitch
limbic encephalitis
lipoprotein receptor-related protein 4
lithium
magnesium salts
malignancy screen
malignancy, occult
Mary Walker phenomenon
melanoma, malignant
mestinon
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
monoclonal antibodies
mortality
motor neuron disease
MRI
MRI, abnormal
multiple sclerosis
muscle biopsy
muscle cramp
muscle pain
muscle relaxant
muscle strength, testing
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
MuSK antibodies
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, cold test for
myasthenia gravis, congenital
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, drug induced
myasthenia gravis, etiology of
myasthenia gravis, exacerbation
myasthenia gravis, familial incidence of
myasthenia gravis, misdiagnosis of
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, ocular
myasthenia gravis, paraneoplastic
myasthenia gravis, passive transfer of
myasthenia gravis, presenting manifestations
myasthenia gravis, prognosis of
myasthenia gravis, receptor site in
myasthenia gravis, sensory loss with
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenia gravis, unmasked
myasthenia gravis, variants
myasthenic crisis
myasthenic syndrome
myasthenic syndrome, treatment of
myocarditis
myopathy
myopathy, mitochondrial
myopia
myositis
narcolepsy
nasal speech
neck weakness
nerve conduction studies
neuroendocrinology
neuroleptic
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic examination
neurologic history
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuromyelitis optica (Devic's disease)
neuronal cell surface antigen
neuronopathy, sensory
neuroophthalmology
neuropathy
neuropathy, acute
neuropathy, diphtheritic
neuropathy, iatrogenic
neuropathy, medication induced
neuropathy, paraneoplastic
neuropathy, peripheral
neurotoxic
neurotoxin
nicotine
nivolumab
NMDA antagonists
ocular motility, disorders of
onconeural antibodies
ophthalmoplegia
opsoclonus-myoclonus syndrome
optic neuritis
oral contraceptives
orbicularis oculi muscle
ototoxicity
paraneoplastic cerebellar degeneration
paresthesias
Parkinson disease
peek sign
pembrolizumab
penicillamine
peripheral nerve, lesion of
phenothiazine
plasmapheresis
plasmapheresis, complications of
pleocytosis of cerebrospinal fluid
POEMS syndrome
polymyositis
polyneuropathy, chronic inflammatory demyelinating
porphyria
postoperative neurologic complications
practice guidelines
pregnancy, neurologic complications in
premarin
procainamide
progesterone
prognosis
progressive neurologic disorder
propranolol
prostigmine
pseudointernuclear ophthalmoplegia
pseudomyasthenia
psychosis
ptosis
ptosis, alternating
ptosis, bilateral
ptosis, unilateral
Purkinje cell
quality of life
quinidine
quinine
ragged-red fibers
Red flags
remote effect of cancer on the nervous system
renal failure
repetitive nerve stimulation
respiratory depression
respiratory failure
respiratory paralysis, pharmacologic
retinopathy
review article
rheumatoid arthritis, neurologic complications of
rituximab
saccadic eye movements
saccadic eye movements, abnormal
screening
seizure
sensory loss
seronegative
shell fish poisoning
single-fiber electromyography
sleep
sleep apnea
spinal cord, injury of
steroid
steroid therapy, CNS treatment and complications with
superior oblique myokymia
superior oblique palsy
systemic lupus erythematosus
tensilon test
tensilon test, false positive
tetanus antitoxin
third nerve palsy
thymectomy
thymic hyperplasia
thymoma
thymus and neuromuscular function
thyroiditis
thyrotoxicosis
tick paralysis
timolol
tinnitus
treatment of neurologic disorder
trochlear nerve palsy
verapamil
vertigo
viral infection
vision, blurred
visual loss
weakness
weakness, end of day
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Wernicke's encephalopathy
wheelchair
workup
xerostomia
Showing articles 500 to 550 of 2789 << Previous Next >>

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 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 Septuagenarian With Painless Ulceration on the Fingertip
Neurol 101:e1473 - e1477, Iyer,V.G., 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

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

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Multisystem Involvement in Post-Acute Sequelae of Coronavirus Disease 19
Ann Neurol 91:367-379, Novak, P.,et al, 2022

A 73-Year-Old Woman with Episodic Dysarthria and Horizontal Binocular Diplopia
Neurol 98:767-772, Bower, A.S.,et al, 2022

A Comprehensive Review of Cluneal Neuralgia as a Cause of Lower Back Pain
Orthopedic Reviews doi:10.52965/001c-35505, Anderson,D.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,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

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

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

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

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, 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

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

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

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

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

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,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

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

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

A case of COVID-19-associated pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
Neurol 95:978-983, Liberatore, G.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,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

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

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Distal Symmetric Polyneuropathy in 2020
JAMA 324:90-92, Callaghan, B.C.,et al, 2020



Showing articles 500 to 550 of 2789 << Previous Next >>