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Differential
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acetylcholine receptor
acetylcholine receptor antibody
acetylcholine receptor antibody, ganglionic
alcohol, neurologic complications with
alcoholism
amphiphysin antibodies
aneurysm, vertebral basilar system
antibodies to voltage-gated calcium channels
anticholinesterase
anticonvulsants, untoward effects of
aphasia
areflexia
Arnold Chiari malformation
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
autonomic neuropathy, idiopathic
azathioprine
bacterial infection
bone marrow transplantation
botulism
brainstem
brainstem, infarction of
brainstem, neoplasms of
calcium channel dysfunction
cancer, cerebrovascular accident complicating patients with
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
cavernous sinus, syndrome
central nervous system, infection of
central nervous system, infection, cancer patient
cerebellar degeneration
cerebral cortex
cerebral edema
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chemotherapy, CNS treatment and complications with
chorea
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
collapsin response mediator protein 5 IgG
coma
confusion
congenital myasthenic syndromes
contactin associated protein like 2 antibodies
cranial neuropathy, multiple
cyclosporine
cytomegalovirus infection
dementia
dermatomyositis
diabetes mellitus
dilantin
diplopia
dyspnea
ejection fraction
electromyogram
electromyogram, decremental response
emergencies, neurologic
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
ephedrine
extralimbic encephalitis
false negative
false negative VDRL
familial
fatigue
fever
Fisher's syndrome
fluorescent treponema antibody absorption(FTA-ABS)
fluorescent treponema antibody absorption/false positive
gait disorder
gammaglobulin therapy, intravenous
Guillain Barre syndrome
Guillain Barre syndrome, etiology of
headache
hepatomegaly
hepatosplenomegaly
Horner's syndrome
hydrocephalus
hypersomnia
hypertension
hypokinetic left ventricle
hyporeflexia
immunohistochemistry
immunologic disease
immunology and the nervous system
immunosuppressive agents
immunotherapy
inclusion body myositis
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
internuclear ophthalmoplegia, unilateral
intestinal pseudoobstruction
intracranial hypertension, benign
intracranial pressure, increased
intubation
leucine rich glioma inactivated 1 antibodies
leukocytosis
limbic encephalitis
lymphadenitis
malignancy screen
malignancy, occult
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningoencephalitis
mestinon
midbrain, infarction of
mononeuropathy
mortality
movement disorder
MRI, abnormal
multiple sclerosis
multiple sclerosis, etiology of
muscle pain
muscle weakness, proximal
mutism
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, congenital
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, neuromuscular junction in
myasthenia gravis, paraneoplastic
myasthenia gravis, presenting manifestations
myasthenia gravis, receptor site in
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenic syndrome
myasthenic syndrome, etiology
myelitis
myelopathy
myelopathy, necrotizing
myocarditis
myositis
nasopharyngeal carcinoma
neoplasm, metastatic to CNS
neoplasm, metastatic to CNS-hemorrhage into
neoplasm, primary of CNS
neoplasm, primary of CNS-hemorrhage in
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuronal cell surface antigen
neuronopathy, sensory
neuropathy
neuropathy, etiologies of
neuropathy, paraneoplastic
neuropathy, peripheral
neurosyphilis
NMDA antagonists
onconeural antibodies
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, cause of
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, unilateral
optic neuritis
papilledema
paraneoplastic cerebellar degeneration
pericarditis
peripheral nerve, lesion of
personality change
personality disorder
pituitary, apoplexy
plasmapheresis
pleocytosis of cerebrospinal fluid
polycythemia, primary
polymyositis
polyneuropathy, chronic inflammatory demyelinating
posterior inferior cerebellar artery syndrome
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychosis
ptosis
ptosis, bilateral
pulmonary edema
pulmonary infiltrates
pupil, abnormality in neurologic disorders
radiation therapy, CNS treatment and complications with
rash
rash, hand
Red flags
remote effect of cancer on the nervous system
repetitive nerve stimulation
respiratory distress syndrome, neurologic status with
respiratory failure
retinopathy
review article
rickettsial organism
Rocky Mountain spotted fever
screening
seizure
serologic test for syphilis
serologic testing
seronegative
spinal cord, compression of
spinal cord, lesion of
splenomegaly
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
syphilis, neurologic complications with
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
temporal lobe, lesion
tensilon test, false negative
thrombocytopenia
thymectomy
thymoma
thymus and neuromuscular function
tick bite
tonsillar herniation of cerebellum
treatment of neurologic disorder
trigeminal neuropathy
uncal herniation
vasculitides
viral infection
visual loss
weakness
weakness, fatiguable
weakness, generalized
weakness, proximal
Wernicke's encephalopathy
wheelchair
workup
xerostomia
Showing articles 50 to 100 of 2653 << Previous Next >>

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

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

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

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

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

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

Acute demyelinating polyneuropathy induced by nivolumab
JNNP 89:435-437, Fukumoto, Y.,et al, 2018

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

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

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

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

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

Myasthenia Gravis Exacerbation after Discontinuing Mycophenolate
Neurol 86:1159-1163, Oskarsson, B.,et al, 2016

Myasthenia Gravis Treated with Autologous Hematopoietic Stem Cell Transplantation
JAMA Neurol 73:652-658,624, Bryant, A.,et al, 2016

A Randomized Controlled Trial of Methotrexate for Patients with Generalized Myasthenia Gravis
Neurol 87:57-64, Pasnoor, M.,et al, 2016

Randomized Trial of Thymectomy in Myasthenia Gravis
NEJM 375:511-522,576, Wolfe, G.I.,et al, 2016

International Consensus Guidance for Management of Myasthenia Gravis
Neurol 87:419-425, Sanders, D.B.,et al, 2016

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

Neurological, Respiratory, Musculoskeletal, Cardiac and Ocular Side-Effects of Anti-PD-1 Therapy
Eur J Cancer 60:210-225, Zimmer, L.,et al, 2016

Myasthenia Gravis after Botulinum Toxin Type A Injection
Turk J Neurol 22:143-144, Tekce, H.D.,et al, 2016

Two Cases of Congenital Myasthenic Syndrome with Vocal Cord Paralysis
Neurol 84:1281-1282, Al-Shahoumi, R.,et al, 2015

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

Paraneoplastic Neurologic Disorders in Small Cell Lung Carcinoma
Neurol 85:235-239, Gozzard, P.,et al, 2015

Clinical Utility of Acetylcholine Receptor Antibody Testing in Ocular Myasthenia Gravis
JAMA Neurol 72:1170-1174, Peeler, C.E.,et al, 2015

Myasthenia in Pregnancy: Best Practice Guidelines from a UK Multispecialty Working Group
JNNP 85:538-543, Norwood, F.,et al, 2014

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

Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

Overlooked non-motor Symptoms in Myasthenia Gravis
JNNP 84:989-994, Suzuki, S.,et al, 2013

Clinicopathologic Conference, Inflammatory Myopathy and Myasthenia Gravis Assoc. with Thymoma
NEJM 369:764-773, Case 26-2013, 2013

Long-lasting Treatment Effect of Rituximab in MuSK Myasthenia
Neurol 78:189-193, Diaz-Manera,J.,et al, 2012

Evidence-based Guideline: Intravenous Immunoglobulin in the Treatment of Neuromascular Disorders
Neurol 78:1009-1015, Patwa,H.S.,et al, 2012

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

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Evidence-Based Guideline Update: Plasmapheresis in Neurologic Disorders: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 76:294-300, Cortese,I.,et al, 2011

The use of rituximab in myasthenia gravis and Lambert--Eaton myasthenic syndrome
JNNP 82:671-673, Maddison, P.,et al, 2011

Use and monitoring of low dose rituximab in myasthenia gravis
JNNP 82:659-663, Blum, S., et al, 2011

Myasthenia Gravis as a Cause of Head Drop in Parkinson Disease
The Neurologist 17:144-146, Uludag, I.F.,et al, 2011

Comparison of IVIg and PLEX in patients with myasthenia gravis
Neurol 76:2017-2023, Barth, D.,et al, 2011

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

Comparative Analysis of Therapeutic Options Used for Myasthenia Gravis
Ann Neurol 68:797-805, Mandawat,A.,et al, 2010

Autoimmune Targets of Heart and Skeletal Muscles in Myasthenia Gravis
Arch Neurol 66:1334-1338, 1322, Suzuki,S.,et al, 2009

Tempo of Disease. In Merritts Neurology. Signs and symptoms in neurologic diagnosis: Approach to the patient
, Rowland, L.P.,et al, 2009

Incidence and Mortality Rates of Myasthenia Gravis and Myasthenic Crisis in US Hospitals
Neurol 72:1548-1554, Alshekhlee,A.,et al, 2009

A Case with Myasthenia Gravis, Brain Stem Multiple Infarcts, Fracture of Vertebrai Th6 and discal hernia to the Th7/Th8
Radiol Oncol 43:3:170-174, KuKaj,V.,et al, 2009

Treatment of Ocular Symptoms in Myasthenia Gravis
Neurol 71:1335-1341, Bhanushali,M.J.,et al, 2008

SOX1 Antibodies Are Markers of Paraneoplastic Lambert-Eaton Myasthenic Syndrome
Neurol 70:924-928, Sabater,L.,et al, 2008

A Trial of Mycophenolate Mofetil With Prednisone as Initial Immunotherapy of Myasthenia Gravis
Neurol 71:394-399,390, The Muscle Study Group, 2008



Showing articles 50 to 100 of 2653 << Previous Next >>