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Differential
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acetazolamide
alternating hemiplegia
alternating hemiplegia of childhood
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, etiology of
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
ataxia
ataxia, paroxysmal
atenolol
autoantibodies
autoimmune disease
autonomic dysfunction
azathioprine
calcium antagonist
calcium antagonist, side effects of
calcium channel dysfunction
carcinoma
carcinoma of lung
CAT scan, chest
central core disease
cerebellar degeneration
cerebrospinal fluid, childhood
children
chloride channel dysfunction
choreoathetosis
chromosomal abnormality
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
concentration, impaired
confusion
dementia
dementia, autoimmune
dementia, rapidly progressive
dichlorphenamide
difficulty climbing stairs
diltiazem
diplopia
dysgeusia
dysosmia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
electromyogram, decremental response
electromyogram, incremental response
encephalitis, autoimmune
encephalopathy
epidemiology of neurology
episodic neurologic deficits
exercise-related muscle strength increase
familial
familial hemiplegic migraine
fatigue
flunarizine
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze deviation
gene
gene mutation
genetic neurologic disorders
hallucination
headache
hemiparesis
hemiparesis, transient
hemiplegia
H-reflex testing
hyperkalemic periodic paralysis
hypokalemic periodic paralysis
hyporeflexia
immunologic disease
immunology and the nervous system
immunosuppressive agents
infantile hemiplegia
insomnia
intellectual deficit
intellectual deterioration
limbic encephalitis
lymphadenopathy, hilar
malignancy, occult
malignant hyperpyrexia
memory
memory, impairment of
mental retardation
mexiletine
migraine
migraine, hemiplegic
molecular genetics
movement disorder
MRI, abnormal
muscle cramp
muscle diseases, characteristics of
muscle strength, testing
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenic syndrome
myasthenic syndrome, etiology
myasthenic syndrome, seronegative
myotonia
myotonia congenita
neck weakness
nerve conduction studies
neuroblastoma
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
nifedipine
nystagmus
nystagmus, monocular
old age, neurology of
ophthalmoplegia
paralysis
paramyotonia congenita
paraneoplastic cerebellar degeneration
paroxysmal neurologic deficits
periodic paralysis
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
potassium channel antibodies
potassium channel dysfunction
precipitating factors
prognosis
psychological testing
ptosis
quadriplegia
rapidly progressing neurologic illness
remote effect of cancer on the nervous system
repetitive nerve stimulation
review article
seizure
serologic testing
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid
steroid therapy, CNS treatment and complications with
stop working
thiazide diuretic
transient neurologic deficit
treatment of neurologic disorder
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
white matter disease
xerostomia
Showing articles 0 to 50 of 4338 Next >>

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

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

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

A 35-Year-Old Woman with Acute Seizures and Behavior Change
Neurol 81:e55-e59, Rejeski, J.J.,et al, 2013

Diagnosis and New Treatment in Muscle Channelopathies
JNNP 80:360-365, Meola,G.,et al, 2009

Seronegative Lambert-Eaton Myasthenic Syndrome
Neurol 59:1773-1775, Nakao,Y.K.,et al, 2002

The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
NEJM 345:17-24,57, Ducros,A.,et al, 2001

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

A News Locus for Hemiplegic Migraine Maps to Chromosome 1q31
Neurol 49:1231-1238, 11931997., Gardner,K.,et al, 1997

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Calcium-Channel Antibodies in the Lambert-Eaton Syndrome and Other Paraneoplastic Syndromes
NEJM 332:1467-1474, Lennon,V.A.,et al, 1995

Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
Ann Neurol 37:S63-S73, Sanders,D.B., 1995

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Alternating Hemiplegia of Childhood
J Pediatr 122:673-679, Bourgeois,M.,et al, 1993

Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
Neurol 43:36-41, Silver,K.&Andermann,F., 1993

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Paraneoplastic Cerebellar Degener III, Cerebellar Degener, Cancer & Lambert-Eaton Myasthenic Synd
Neurol 42:1944-1950, Clouston,P.D.,et al, 1992

Atenolol Compared with Nifedipine:Effect on Cognitive Function and Mood in Elderly Hypertensive Patients
Ann Int Med 116:615-623, Skinner,M.H.,et al, 1992

Calcium Channel Autoantibodies in the Lambert-Eaton Myashenic Syndrome
Ann Neurol 29:307-314, Leys,K.,et al, 1991

Specificity of Calcium Channel Autoantibodies in Lambert-Eaton Myasthenic Syndrome
Lancet 2:640-643, Sher,E.,et al, 1989

Autoantibody Activity in Lambert-Eaton Myasthenic Syndrome
Editorial, Lancet 1:9201988., , 1988

Dysosmia, Dysguesia, & Nifedipine
Ann Int Med 102:135-136, 7171985., Levenson,J.L.&Kennedy,K., 1985

MR Imaging Findings in Anti-Leucine-Rich Glioma Inactivated Protein 1 Encephalitis:A Systematic Review and Meta-Analysis
AJNR 45:977-986, Almeida,F.C.,et al, 2024

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

Glucose Hypermetabolism in the Basal Ganglia
Neurol 101:90-91, Kim,Y.E.,et al, 2023

A New Case of Neuromyelitis Optica Spectrum Disorders with Unknown Fever and Subacute Cognitive Decline with Normal Images
Cureus 14:e24950, Furuya,K. & Itoh,M., 2022

CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
Neurol 94:e2290-e2301,953, Syrbe, S.,et al, 2020

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

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Investigations in GABA? Receptor Antibody-Associated Encephalitis
Neurol 88:1012-1020,1010, Spatola, M.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Anti-DPPX Encephalitis,Pathogenic Effects of Antibodies on Gut and Brain Neurons
Neurol 85:890-897, Piepgras,J.,et al, 2015

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Effect of Rituximab in Patients with Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy
JAMA Neurol 71:896-900, Irani, S.R.,et al, 2014

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013

Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
JAMA Neurol 70:932-936, Sharma, V.,et al, 2013

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
AJNR 33:1403-1410, Marder, C.P.,et al, 2012

Autoimmune Epilepsy
Arch Neurol 69:582-593,565, Quek, A.M.L.,et al, 2012

Morvan Syndrome: Clinical and Serological Observations in 29 Cases
Ann Neurol 72:241-255, Irani, S.R.,et al, 2012



Showing articles 0 to 50 of 4338 Next >>