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Differential
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acetylcholine receptor
acetylcholine receptor antibody
adverse drug reaction
agammaglobulinemia
algorithm
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
antibodies to voltage-gated calcium channels
anticholinesterase
antistriational muscle antibody
arthrogryposis multiplex
autoimmune disease
azathioprine
Bell's phenomenon
bulbar palsy
carcinoma
carcinoma of lung
cerebrovascular accident, mimics
chewing, impaired
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Collier's sign
comorbidities
complications
congenital myasthenic syndromes
consanguinity
creatine phosphokinase(CPK)elevated
critical care unit
cyclosporine
dabrafenib
delay in diagnosis
developmental retardation
difficulty climbing stairs
diplopia
diplopia, transient
drug interactions
dysarthria
dysphagia
dysphonia
electromyogram
electromyogram, decremental response
encephalitis, autoimmune
epidemiology of neurology
exercise-related muscle strength increase
exome sequencing
eye closure
facial appearance, abnormal
facial weakness
familial
fasciculation
fatigable chewing
fatigue
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gene mutation
genetic testing
gynecomastia
heralding manifestation
high arched palate
HLA
hypophonia
hyporeflexia
iatrogenic neurologic disorders
immune checkpoint inhibitors
immune-related adverse events
immunosuppressive agents
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
lid abnormalities
lid closure, weakness of
lid twitch
limbic encephalitis
lipoprotein receptor-related protein 4
lymphadenopathy, hilar
mediastinum, mass of
melanoma, malignant
mestinon
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
monoclonal antibodies
mortality
motor neuron disease
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
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, familial incidence of
myasthenia gravis, misdiagnosis of
myasthenia gravis, neuromuscular junction in
myasthenia gravis, ocular
myasthenia gravis, presenting manifestations
myasthenia gravis, prognosis of
myasthenia gravis, receptor site in
myasthenia gravis, remission of
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenia gravis, unmasked
myasthenia gravis, variants
myasthenic crisis
myasthenic sneer
myasthenic syndrome
myocarditis
nasal regurgitation
nasal speech
nerve conduction studies
neurologic disease, diagnoses of
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)
neuroophthalmology
nystagmus
ocular motility, disorders of
old age, neurology of
opened mouth
ophthalmoplegia
oropharyngeal weakness
peek sign
penicillamine
plasmapheresis
practice guidelines
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
prostigmine
proximal muscle atrophy
pseudointernuclear ophthalmoplegia
pseudomyasthenia
ptosis
ptosis, bilateral
ptosis, unilateral
quality of life
quinine
ragged-red fibers
remote effect of cancer on the nervous system
repetitive nerve stimulation
respiratory failure
review article
rituximab
saccadic eye movements
saccadic eye movements, abnormal
seronegative
single-fiber electromyography
sleep
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
temporalis muscle wasting
tensilon
tensilon test
tensilon test, false negative
tensilon test, false positive
tensilon test, paradoxical
thymectomy
thymic hyperplasia
thymoma
thymus and neuromuscular function
thyroiditis
tongue, fasciculations of
tongue, weakness
trametinib
transverse smile
treatment of neurologic disorder
upgaze, paralysis of
voice, abnormality of
walking, difficulty with
weakness
weakness, end of day
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
xerostomia
Showing articles 0 to 13 of 13

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

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Myasthenia Gravis Following Dabrafenib and Trametinib for Metastatic Melanoma
Neurol 94:322-323, Zaloum, A.,et al, 2020

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

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinical Manifestations of Myasthenia Gravis
UptoDate Aug 2016, Bird, S.J., 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Myasthenia Gravis
BMJ 345:e8497, Spillane, J.,et al, 2012

Does This Patient Have Myasthenia Gravis?
JAMA 293:1906-1914, Scherer,K.,et al, 2005

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Myasthenia Gravis
NEJM 330:1797-1810, Drachman,D.B., 1994

Ocular Myasthenia:A Protean Disorder
Survey of Ophthalmology 39:169-210, Weinberg,D.A.,et al, 1994



Showing articles 0 to 13 of 13