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acute disseminated encephalomyelitis

acute necrotizing encephalitis

advances in neurology

AMPA receptor antibodies

amyloid angiopathy, cerebral

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, false negative

angiography, cerebral, negative

animal exposure

anterior horn cell disease

antibodies to measles

antineutrophil cytoplasmic autoantibodies

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune basal ganglia encephalitis

autonomic dysfunction

axonal degeneration

B 12 deficiency

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

brachial neuritis

brain biopsy, negative

brainstem, infarction of

brainstem, lesion of

carbon monoxide poisoning

CAT scan, emission, abnormal

cauda equina, enhancement

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central nervous system, infection of

central nuclei, muscle

central pontine myelinolysis

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, women

chemotherapy, CNS treatment and complications with

choreoathetosis

chorioretinitis

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

cogwheel rigidty

collapsin response mediator protein 5 IgG

congenital myopathy

corpus callosum

corpus callosum, lesion of

cortical blindness

cortical ribbon sign

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cyclophosphamide

deafness, bilateral

deafness, sudden

deep gray nuclei

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentate nuclei, lesion of

diagnostic criteria

differential diagnosis

disability, neurological

DPPX, antibodies, encephalitis

dysdiadochokinesia

dyskinesia, facial

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

enterovirus infection of CNS

epidemiology of neurology

executive dysfunction

eye movement, disorders of

facial weakness

faciobrachial dystonic seizure

finger nose finger test

flaccid paralysis

fluorescein angiography

fundus, abnormality of

funduscopic exam

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

genetic testing

gliomatosis cerebri

granulomatosis with polyangiitis

Guillain Barre syndrome

gyrus, abnormal

hand-foot-mouth disease

headache, recurrent

hearing loss, bilateral

hearing loss, sudden, bilateral

heralding manifestation

herpes simplex encephalitis

hippocampus, hyperintense

histochemistry of muscle

human immunodeficiency virus type 1

hypertensive encephalopathy

hypoglycorrhachia

hypokalemic paralysis

immunohistochemistry

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

influenza A virus

intellectual deficit

intellectual deterioration

intranasal medication

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

life expectancy

limbic encephalitis

liver function enzymes

lymphoma involving CNS

lymphoma, primary of CNS

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, basilar

meningitis, leptospira

meningoencephalitis

mental status, abnormal

mesial temporal lobe

microaneurysm, retinal

microangiopathy, brain

microangiopathy, retina

midbrain, lesion of

middle cerebellar peduncle, lesion

mitochondrial disease

molecular genetics

monoclonal antibodies

movement disorder

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, false negative

MRI, gradient-echo

MRI, gray matter enhancement

MRI, high signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, misdiagnosis

myelitis, longitudinal

myelitis, transverse, recurrent

myoclonic jerks

myoclonus, stimulus sensitive

myopathy, centronuclear

nausea and vomiting

neoplasm, primary of CNS

nerve root enhancement

neurexin-3 alpha antibodies

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic signs

neurologic symptoms

neuronal cell surface antigen

neuroophthalmology

NMDA antagonists

ophthalmoplegia

oral ulcerations

osmotic demyelination syndrome

owl's eye sign of spinal cord

palate, paralysis-unilateral

palmomental response

paralysis, acute areflexic

Parkinsonism syndrome

patient information and support

persistent vegetative state

personality change

phenylketonuria

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pons, infarction of

pons, lesion of

posterior leukoencephalopathy syndrome

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive multifocal leucoencephalopathy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary edema

pulmonary embolism

pursuit eye movements, abnormal

pyloric stenosis

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

reflex, brainstem

reflex, brainstem, absent

remote effect of cancer on the nervous system

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinal microvascular disease

saccadic eye movements, abnormal

sarcoidosis, CNS

sensorineural hearing loss

serologic testing

serologic testing, false negative

serum alanine aminotransferase

sleep pathology and physiology

slow virus infection of CNS

small vessel disease

spinal cord, lesion of

spirochete infection

spongy degeneration of brain

square wave jerks

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, adult onset

substantia nigra

Susac's syndrome

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

travel, foreign

treatment of neurologic disorder

type 1 muscle fiber

upgaze, paralysis of

urinary incontinence

viral infection

viral infection, CNS

vision, blurred

visuospatial disturbance

walking, difficulty with

West Nile fever

Whipple's disease

white matter disease

white matter disease, subcortical

wide based gait

X-linked myopathy

Showing articles 350 to 400 of 8101 << Previous Next >>

Clinical Features of Nipah Virus Encephalitis Among Pig Farmers in Malaysia
NEJM 342:1229-1235, Goh,K.J.,et al, 2000

Poliomyelitic-Like Illness in Central European Encephalitis
Neurol 55:299-302, Schellinger,P.D. et al, 2000

Progressive Dementia and Gait Disorder in a 78 Year Old Woman
JNNP 68:526-531, Tagliati,M.,et al, 2000

Serotonin Sydrome
Medicine 79:201-209, Mason,P.J. et al, 2000

Incidence and Prevalence of Neurological Disorders Associated with HIV Since the Introduction of Highly Active Antiretroviral Therapy (HAART)
JNNP 69:376-380, Maschke,M. et al, 2000

Guillain-Barre Syndrome in a Patient with Non-Hodgkins Lymphoma
Ann Oncol 11:217-220, Schwenk,D.Re.,et al, 2000

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Simultaneous Bilateral Thalamic Hemorrhage: Case Report
Radiation Medicine 17:359-361, Sunada,I.,et al, 1999

Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
Neurol 50:764-767, Levin,M.I.,et al, 1998

A 35-Year-Old Bricklayer with Hemimyoclonic Jerks
Lancet 351:1926, Grunewald,T.,et al, 1998

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

Poliomyelitis-Like Illness Due to Japanese Encephalitis Virus
lancet 351:1094-1097, Solomon,T.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Coma in Fulminant Pneumococcal Meningitis:New MRI Observations
Neurol 51:1200-1202, Vernino,S.,et al, 1998

Steroid Myopathy in Cancer Patients
Neurol 48:1234-1238, Batchelor,T.T.,et al, 1997

Polymyalgia Rheumatica and Temporal Arteritis:Diagnosis and Management
BMJ 314:1329-1332, Swannell,A.J., 1997

A 9-Year-Old With Fever and Severe Muscle Pains
Lancet 349:1666, Punda-Polic,V.,et al, 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 1997

Intravenous Immune Globulin Therapy for Neurologic Diseases
Ann Int Med 126:721-730, Dalakas,M.C., 1997

An Infant with Encephalitis
Lancet 350:1594, Yeung,W.L.,et al, 1997

Guillain-Barre Syndrome Following Allogeneic Bone Marrow Transplantation
Neurol 49:1711-1714, Wen,P.Y.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Neuroradiographic Manifestations of Encephalitis
NEJM 337:1393-1394, Pfister,H-W.,et al, 1997

Myelinolysis After Correction of Hyponatremia
Ann Int Med 126:57-62, Laureno,R.&Karp,B., 1997

Epidemiology, Pathophysiology, & Management of Hyponatremic Encephalopathy
Am J Med 102:67-77, Fraser,C.L.,et al, 1997

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Subacute Sclerosing Panencephalitis:Evaluation with CT and MR
AJNR 17:761-772, Brismar,J.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Showing articles 350 to 400 of 8101 << Previous Next >>