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acetylcholine receptor antibody
acetylcholinesterase
acetylcholinesterase deficiency
Addison's disease
alveolar hypoventilation
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, myasthenic syndrome with
amyotrophic lateral sclerosis, treatment of
anterior interosseous neuropathy
anterior tibial muscle weakness
antibiotics
antibiotics, neurologic complications with
apnea
arm weakness
arthrogryposis multiplex
ataxia, cerebellar
autoimmune disease
benign congenital hypotonia
bitemporal visual field defect
botulism
brachial neuritis
bulbar palsy, acute
calcification, intracranial
calf atrophy
carpo-pedal spasm
central core disease
cerebrovascular accident
Charcot-Marie-Tooth
children
chronic polyneuritis, children
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
coma
complications
compression neuropathy
concussion
congenital myasthenic syndromes
congenital myopathy
congestive heart failure
controversies in neurology
cortical hand knob
cost
cost effectiveness
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
degenerative diseases of CNS
dementia
dermatomyositis
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diaphragmatic paralysis
differential diagnosis
diplopia
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
electromyogram
entrapment neuropathy
epidemiology of neurology
evidence-based research
exophthalmus
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
finger drop
finger weakness
foot drop
gammaglobulin therapy, intravenous
gene
genetic neurologic disorders
Guillain Barre syndrome
Guyon's canal
hallucination, auditory
hand weakness
Hand-Schuller-Christian disease
head injury
headache
heavy metal intoxication
hospice
hyperadrenalism
hypercalcemia
hypercapnia
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hyperkalemia
hyperparathyroidism
hyperthyroidism
hypokalemic periodic paralysis
hypoparathyroidism
hypothalamus
hypothalamus, disturbance of
immune complexes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
intrinsic hand muscles, wasting of
islet cell tumor
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, unilateral
level of consciousness, decreased
lid closure, weakness of
lordosis
median neuropathy
mental retardation
mimics
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, muscle
multiple sclerosis
muscle atrophy, progressive
muscle atrophy, static
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muscle diseases, characteristics of
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muscle weakness
muscle weakness, causes of
muscle weakness, proximal
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muscular dystrophy, cardiovascular changes with
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muscular dystrophy, differential diagnosis of
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muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
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myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, diagnosis
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myasthenia gravis, drug induced
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
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myasthenia gravis, treatment of
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myoedema
myopathy
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myopathy, mitochondrial
myopathy, thyroid disease causing
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myotonia dystrophica
myxedema coma
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neck weakness
nemaline rod myopathy
neoplasm, pituitary
neuritis, causes of
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pheochromocytoma
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porphyria
posterior interosseous neuropathy
practice guidelines
primary aldosteronism
prognosis
progressive muscular dystrophy
psychosis
ptosis
repetitive nerve stimulation
respiratory depression
respiratory failure
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
sarcoidosis
seizure
seizure, children
seizure, treatment of
sleep apnea
spinal cord, injury of
spinal muscular atrophy
stiff man syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
syringomyelia
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
teleconsulting
telemedicine
teleneurology
telestroke
tensilon test
tensilon test, false positive
tetany
thoracic outlet syndromes
thyrotoxicosis
torticollis
treatment of neurologic disorder
tricresylphosphate
trigger finger
Trousseau's sign
ulnar neuropathy
weakness
weakness, proximal
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
Showing articles 0 to 50 of 1164 Next >>

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

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Differential Diagnosis of Finger Drop
Neurologist 19:128-131, Varatharaj, A.,et al, 2015

Palliative Care and Neurology
Neurol 83:561-567, Boersma, I.,et al, 2014

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Myasthenic Hand
Neurol 51:913-914, Janssen,J.C.,et al, 1998

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

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

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

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

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

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

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Curtain Sign
NEJM 387:e7, Sherman, S.V., 2022

Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
Neurol 98:e2368-e2376, Molimard, A.,et al, 2022

A New Option is Approved for Patients with Myasthenia Gravis
JAMA 327:417, Voelker, R., 2022

Myasthenia Grais
www.mda.org, , 2021

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

Myasthenic Crisis Demanding Mechanical Ventilation
Neurol 94:e299-e313, Neumann, B.,et al, 2020

Long-Term Follow-Up, Quality of Life, and Survival of Patients with Lambert-Eaton Myasthenic Syndrome
Neurol 94:e511-e520, Lipka, A.F.,et al, 2020

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

Useful Bedside Testing for Myasthenia Gravis
Neurol 94:e1870-e1871, Gomes del Carvalho Neto, E.,et al, 2020

Thymectomy for Myasthenia Gravis
Neurol 94:705-709, Gronseth, G.S.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

The Face of Myasthenia Gravis
Neurol 95:89-90, Ruiter, A.M.,et al, 2020

Ptosis that Resolves with Application of an Ice Pack
BMJ 369:m1147, Chakraborty, A. & Jacob, J., 2020

Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, A.,et al, 2019

Long-Term Safety and Efficacy of Eculizumab in Generalized Myasthenia Gravis
Muscle Nerve 60:14-24, Muppidi, S.,et al, 2019

Drug Approved for Rare Muscle Weakening Syndrome
JAMA 321:239, Voelker, R., 2019

Pembrolizumab-Induced Myasthenia Gravis
Neurol 91:e1365-e1367, Algaeed, M.,et al, 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

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

Myasthenia Gravis Following Alemtuzumab Therapy for Multiple Sclerosis
Neurol 91:622-624, Midaglia, L.,et al, 2018

Acute demyelinating polyneuropathy induced by nivolumab
JNNP 89:435-437, Fukumoto, Y.,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

Rituximab as Treatment for anti-MuSK myasthenia gravis
Neurol 89:1069-1077, Hehir, M.K.,et al, 2017

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

Dont Fall for Pseudo-INO
Neurol 88:e205-e206, Traber, G.L.et al, 2017

Durability of the Rituximab Response in Acetylcholine Receptor Autoantibody-Positive Myasthenia Gravis
JAMA Neurol 74:60-66, Robeson, K.R.,et al, 2017



Showing articles 0 to 50 of 1164 Next >>