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acetazolamide

acute disseminated encephalomyelitis

advances in neurology

adverse drug reaction

agitation

algorithm

amnesia

AMPA receptor antibodies

amphiphysin antibodies

anti GQ1b IgG antibody

anti Hu antibody

anti IgLON5

antibodies to voltage-gated calcium channels

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune encephalopathy

autoimmune epilepsy

autonomic dysfunction

autonomic neuropathy

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

calcium channel dysfunction

carcinoma

carcinoma of lung

CAT scan, emission, abnormal

catatonia

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central core disease

central nervous system, infection of

cerebellar degeneration

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, childhood

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

channelopathy

children

chloride channel dysfunction

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel rigidty

cold hands sign

collapsin response mediator protein 5 IgG

coma

complications

computers, neurologic diagnosis and

confabulation

confusion

constipation

contactin associated protein like 2 antibodies

controversies in neurology

creatine phosphokinase(CPK)elevated

cytochrome c oxidase

deep gray nuclei

degenerative diseases of CNS

delusion

dementia

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

differential diagnosis

disability, neurological

DPPX

DPPX, antibodies

DPPX, antibodies, encephalitis

electroencephalogram, abnormalities of

electromyogram

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, etiology

encephalitis, paraneoplastic

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalopathy

episodic neurologic deficits

extralimbic encephalitis

face, contractions

faciobrachial dystonic seizure

false negative

false positive

familial hemiplegic migraine

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gender

gene

gene mutation

genetic neurologic disorders

glutamic acid decarboxylase, antibody

glycine receptor antibodies

hallucination

hallucination, olfactory

headache

hemimyoclonic jerks

heralding manifestation

herpes simplex encephalitis

hyperkalemic periodic paralysis

hypersomnia

hypertension

hypokalemic periodic paralysis

hyponatremia

hyponatremia with cerebral disorders

immunologic disease

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

incidence

insomnia

intellectual deficit

intellectual deterioration

Isaacs syndrome

Jakob-Creutzfeldt disease

lateropulsion

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

level of consciousness, decreased

lymphoma, primary of CNS

malignancy screen

malignancy, occult

malignant hyperpyrexia

masked facies

memory

memory, defect of recent

memory, impairment of

meningeal enhancement

mental status, abnormal

mesial temporal lobe

mesial temporal sclerosis

mexiletine

migraine

mild cognitive impairment

mimics

misdiagnosis

molecular genetics

monoclonal antibodies

mood change

mortality

Morvan's fibrillary chorea

movement disorder

movement disorder, extrapyramidal

movement disorder, paroxysmal

MRI

MRI pattern

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, high signal intensity of basal ganglia

MRI, negative

muscle cramp

muscle diseases, characteristics of

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis, transverse, recurrent

myoclonic jerks

myoclonus

myoclonus, orthostatic

neurexin-3 alpha antibodies

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination, focal

neuromuscular junction

neuromyotonia

neuronal cell surface antigen

neuronopathy, sensory

neuropathy

neuropathy, paraneoplastic

old age, neurology of

onconeural antibodies

ophelia syndrome

ophthalmoplegic migraine

opsoclonus-myoclonus syndrome

paramyotonia congenita

paraneoplastic cerebellar degeneration

paresthesias

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal neurologic disorder

pathognomonic

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

periodic paralysis

peripheral nerve, lesion of

pleocytosis of cerebrospinal fluid

potassium channel antibodies

potassium channel dysfunction

practice guidelines

precipitating factors

prognosis

progressive neurologic disorder

pruritus

psoriasis

psychiatric problems in neurologic disorders

psychological testing

remote effect of cancer on the nervous system

retinopathy

reversible neurologic disorder

review article

rippling muscle disease

rituximab

safety

salivation, excessive

screening

seizure

seizure, adult onset

seizure, drug resistance

seizure, dystonic

seizure, focal

seizure, intractable

seizure, intractable, treatment of

seizure, psychomotor-temporal lobe

seizure, treatment of

seizure, unknown origin

serologic testing

serologic testing, false negative

seronegative

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

sleep pathology and physiology

sodium channel dysfunction

spinocerebellar ataxia

spinocerebellar ataxia type 6

standing difficulty

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

symmetric brain lesions

tangential

temporal lobe

temporal lobe, lesion

temporal lobe, lesion, bilateral

transient neurologic deficit

treatment of neurologic disorder

varicella zoster virus

white matter disease, subcortical

wide based gait

workup

Showing articles 50 to 100 of 251 << Previous Next >>

A Case of Voltage-Gated Potassium Channel Antibody-Related Limbic Encephalitis
Nat Clin Pract Neurol 2:339-343, Harrower,T., et al, 2006

Psychiatric Presentation of Voltage-Gated Potassium Channel Antibody-Associated Encephalopathy
Br J Psychiatry 189:182-183, Parathasarathi,U.D., et al, 2006

Voltage-gated Potassium Channel Antibody-Associated Encephalitis with Basal Ganglia Lesions
Neurol 66:1780-1781, Hiraga,A.,et al, 2006

Potassium Channel Antibody-Associated Encephalopathy: A Potentially Immunotherapy-Responsive Form of Limbic Encepahlitis
Brain 127:701-712, Vincent,A.,et al, 2004

Potentially Reversible Autoimmune Limbic ncephalitis with Neuronal Potassium Channel Antibody
Neurol 62:1177-1182,1040, Thieben,M.J.,et al, 2004

Amnesia, Cerebral Atrophy, and Autoimmunity
Lancet 361:1266, Schott,J.M., et al, 2003

Voltage-Gated Potassium Channel Antibodies in Limbic Encephalitis
Ann Neurol 54:530-533, Pozo-Rosich,P.,et al, 2003

Morvans Syndrome: Peripheral and Central Nervous System and Cardiac Involvement With Antibodies to Voltage-Gated Potassium Channels
Brain 124:2417-2426, Liguori,R., et al, 2001

Morvans Syndrome Associated With Voltage-Gated K+ Channel Antibodies
Neurol 54:771-772, Barber,P.A., et al, 2000

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

Acquired Neuromyotonia:Evidence for Autoantibodies Directed Against K+Channels of Peripheral Nerves
Ann Neurol 38:714-722, 7011995., Shillito,P.,et al, 1995

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

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

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

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

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

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

Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome)
Neurol 69:586-595, Fertleman,C.R.,et al, 2007

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Acute Tetrodotoxin-Induced Neurotoxicity After Ingestion of Puffer Fish
Ann Neurol 57:339-348, 309, Kiernan, M.C., et al, 2005

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

Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001

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

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

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

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Clinicopath Conf, Chronic Salicylate Toxicity
NEJM 388:264-272, Case Record 2, 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

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

Sequential Bilateral Vision Loss in a Woman with Scalp Tenderness and Jaw Claudication
JAMA Neurol 78:878-879, Kaufman, A.R.,et al, 2021

Aquaporin-4 and MOG Autoantibody Discovery in Idiopathic Transverse Myelitis Epidemiology
Neurol 93:e414-e420, Sechi, E.,et al, 2019

Eculizumab in Aquaporin-4-Positive Neuromyelitis Optica Spectrum Disorder
NEJM 381:614-625, Pittock, S.J.,et al, 2019

Area Postrema Syndrome
Neurol 91:e1642-e1651, Shosha, E.,et al, 2018

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

A 50-year-old Woman with SLE and a Tumefactive Lesion
Neurol 89:e140-e145, Choi, J.H.,et al, 2017

Showing articles 50 to 100 of 251 << Previous Next >>