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adenylate kinase 5 autoantibodies

advances in neurology

agitation

agnosia, visual

akinetic mute

Alice in Wonderland syndrome

alien hand syndrome

alternating rapid movement

aluminum

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, heterogeneity of

Alzheimer's disease, incidence

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, staging

Alzheimer's disease, treatment of

amnesia

amyloid

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, iatrogenic

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

aphasia, progressive, primary

apraxia of eyelid opening

apraxia, constructional

areflexia

arm swing, reduced

arthrogryposis multiplex

basal ganglia, lesion, bilateral

bovine spongiform encephalopathy

brain transplantation

CAT scan, emission, abnormal

cataplexy

cavum septi pellucidi

central core disease

central hypoventilation

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, secondary

cerebellar plaques, amyloid

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral glucose metabolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

Charcot-Marie-Tooth

choline acetyltransferase

chorea

choreoathetosis

chorioretinitis

chronic traumatic encephalopathy

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

cognition

color vision, impaired

complications

compulsivity

concussion

concussion, recurrent

confusion

controversies in neurology

cortical blindness

cortical-basal ganglionic degeneration

cough

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, screening for

dementia, subcortical

dementia, transmissible

depression

developmental milestones, loss of

differential diagnosis

electroencephalogram, abnormalities of

encephalitis

encephalitis, autoimmune

encephalitis, viral

encephalopathy

encephalopathy, post traumatic

epidemiology of neurology

executive dysfunction

eye movement, disorders of

falling

familial

Fazio-Londe's disease

fine motor function, impaired

finger nose finger test

flortaucipir

foam cells

football neurologic injuries

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait disorder

gait, apraxic

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

granulovacuolar degeneration

grasp reflex

Hallervorden Spatz disease

handwriting

head injury

head injury, mild

head injury, repetitive

head injury, return to play following

headache

headache, frontal

heavy metal intoxication

heel-knee-shin test

hemianopia, homonymous

hemifacial spasm

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes virus infection

hippocampal atrophy

hippocampus

hippocampus, hyperintense

hydrocephalus, normal pressure

hypophonia

iatrogenic neurologic disorders

immunoperoxidase staining

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deterioration

interferon

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jaundice

Kluver-Bucy syndrome

Kugelberg-Welander syndrome

language disorder in adults

L-dopa

lead poisoning

Lewy body

Lewy body disease, diffuse

limbic encephalitis

lipid storage disorder of CNS

manganese intoxication

masked facies

memory, defect of recent

memory, impairment of

meningitis

mental status, abnormal

mild cognitive impairment

mild cognitive impairment converting to Alzheimer's disease

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

molecular genetics

mongolism

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI

MRI pattern

MRI, abnormal

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, voxel-based morphometry

multiple system atrophy

nerve conduction studies

neurofibrillary degeneration

neurofibrillary degeneration, causes of

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic signs

neurologic symptoms

neurologic testing

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

nucleus basalis of Meynert

obsessive-compulsive disorder

old age, neurology of

olfactory bulb

ophthalmoplegia

ophthalmoplegia, total

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinsonism syndrome

PAS positive material in the brain

pathologic reflex

pathology

penguin silhouette sign

Pittsburgh Compound B

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

positional head-hanging test

preclinical

pregnancy, neurologic complications in

prion disease

prognosis

progressive neurologic disorder

progressive supranuclear palsy

prosopagnosia

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

proteinopathy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

pugilistic parkinsonism

punch-drunk syndrome

pursuit eye movements, abnormal

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

release phenomena

respirations in CNS disease

retrocollis

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

saccadic eye movements

saccadic eye movements, abnormal

salivation, excessive

screening

semantic dementia

senile plaques

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

sinemet

single photon emission computed tomography

sleep apnea, obstructive

sleep pathology and physiology

smell

Smell Identification Test

soccer

speech disorder

speech disorder, non aphasic

splenomegaly

spongy degeneration of brain

sports medicine, neurology of

square wave jerks

staining reactions in neuropathology

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

subacute sclerosing panencephalitis, adult onset

substantia nigra

symmetric brain lesions

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

toxoplasmosis, CNS

trauma

treatment of neurologic disorder

vibratory sensation, abnormal

visuospatial disturbance

vocal cord paralysis

voice, abnormality of

walking frame

walking, difficulty with

war

weight loss

Werdnig-Hoffman disease

word-finding difficulty

Showing articles 400 to 450 of 1005 << Previous Next >>

CSF Analysis in Patients With Sporadic CJD and Other Transmissible Spongiform Encephalopathies
Eur J Neurol 14:121-124, Green,A.,et al, 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

Spontaneous Spinal Cerebrospinal Fluid Leaks and Intracranial Hypotension
JAMA 295:2286-2296, Schievink,W.I., 2006

Dementia and White-Matter Demyelination in Young Patient With Neurosyphilis
Lancet:368:2258, Brinar,V.V. &Habek,M., 2006

Detection of CSF 14-3-3 Protein in Guillain-Barr Syndrome
Neurol 67:2211-2216, Bersano,A.,et al, 2006

Multiple Sclerosis with and without CSF Bands:Clinically Indistinguishable but Immunogenetically Distinct
Neurol 67:1062-1064, Imrell,K.,et al, 2006

Clinical Presentation and Pre-Mortem Diagnosis of Variant Creutzfeldt-Jakob Disease Associated With Blood Transfusion: A Case Report
Lancet 368:2061-2067, Wroe,S.J.,et al, 2006

Clinicopath Conf., Degoss Disease
NEJM 355:2575-2584, Case 38-2006, 2006

Concomitant Chronic Inflammatory Demyelinating Polyneuropathy and Myasthenia Gravis Following Cytomegalovirus Infection
J Neurol Sci 240:103-106, Mori, M.,et al, 2006

Plasma Exchange in Neuroimmunological Disorders: Part 2. Treatment of Neuromuscular Disorders
Arch Neurol 63:1066-1071, Lehmann,H.C.,et al, 2006

Poststroke C-Reactive Protein Is a Powerful Prognostic Tool Among Candidates for Thrombolysis
Stroke 37:1205-1210, Montaner,J.,et al, 2006

Kuru in the 21st Century--An Acquired Human Prion Disease With Very Long Incubation Periods
Lancet 367:2068-2074, Collinge,J.,et al, 2006

Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
Neurol 67:538-539, Hohler,A.D. &Flynn,F.G., 2006

Episodic Neurologic Dysfunction with Migraine and Reversible Imaging Findings After RadiationRRH
Neurol 67:676-678, Pruitt,A.,et al, 2006

Neuropathology of the Neuroradiologist: Rosenthal Fibers
AJNR 27:958-961, Wippold,F., II,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

CSF Findings in 250 Patients with Serologically Confirmed West Nile Virus Meningitis and Encephalitis
Neurol 66:361-365, Tyler,K.L.,et al, 2006

Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord
Neurol 66:494-498,468, van der Knaap,M.S.,et al, 2006

Clinically Isolated Syndromes, A New Oligoclonal Band Test Accurately Predicts Conversion to MS
Neurol 66:576-578, Masjuan,J.,et al, 2006

Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
Neurol 65:650-651, Horvath,J.,et al, 2005

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

Protein S Deficiency in HIV Associated Ischaemic Stroke:An Epiphenomenon of HIV Infection
JNNP 76:1455-1456,1331, Mochan,A.,et al, 2005

Evaluation of C-Reactive Protein Measurement for Assessing the Risk and Prognosis in Ischemic Stroke
Stroke 36:1316-1329, Di Napoli,M.,et al, 2005

Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
NEJM 352:686-691, de Jong,M.D., et al, 2005

Recommended Standard of Cerebrospial Fluid Analysis in the Diagnosis of Multiple Sclerosis, A Consensus Statement
Arch Neurol 62:865-870, Freedman,M.S.,et al, 2005

Update on Susacs Syndrome
Curr Opin Neurol 18:311-314, Gross,M. &Eliashar,R., 2005

Unusual Presentation of Central Nervous System Cryptococcal Infection in an Immunocompetent Patient
AJNR 26:2522-2526, Saigal,G.,et al, 2005

Diagnosis, Treatment, and Prognosis of Mycoplasma Pneumoniae Childhood Encephalitis: Systematic Review of 58 Cases
J Child Neurol 19:865-871, Daxboeck,F., et al, 2004

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

Diffusion-Weighted MRI Abnormalities as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease
Neurol 63:443-449,410, Shiga,Y.,et al, 2004

Sensitivity of 14-3-3 Protein Test Varies in Subtypes of Sporadic Creutzfeldt-Jakob Disease
Neurol 63:436-442,410, Castellani,R.J.,et al, 2004

Novel Methods for Disinfection of Prion-Contaminated Medical Devices
Lancet 364:521-526, Fichet,G.,et al, 2004

Preclinical vCJD After Blood Transfusion in a PRNP Codon 129 Heterozygous Patient
Lancet 364:527-529, Peden,A.H.,et al, 2004

Systemic Inflammatory Response Depends on Initial Stroke Severity but is Attenuated by Successful Thrombolysis
Stroke 35:2128, Audebert,H.J.,et al, 2004

The Metabolic Syndrome, Inflammation, and Risk of Cognitive Decline
JAMA 292:2237-2242, Yaffe,K.,et al, 2004

CJD--A Case of Mistaken Identity
Lancet 364:2068, Campbell,S.,et al, 2004

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Transmissible Spongiform Encephalopathies
Lancet 363:51-61, Collins,S.J.,et al, 2004

Tissue Distribution of Bovine Spongiform Encephalopathy Agent in Primates after Intravenous or Oral Infection
Lancet 363:422-428,411, Herzog,C.,et al, 2004

Possible Transmission of Variant Creutzfeldt-Jakob Disease by Blood Transfusion
Lancet 363:417-421,411, Llewelyn,C.A.,et al, 2004

Prion Deposition in Olfactory Biopsy of Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 55:294-296, Tabaton,M.,et al, 2004

Cognitive Functions in Survivors of Primary Central Nervous System Lymphoma
Neurol 62:548-555,532, Correa,D.D.,et al, 2004

Cognitive Status and Quality of Life After Treatment for Primary CNS Lymphoma
Neurol 62:544-547,532, Harder,H.,et al, 2004

Susac Syndrome:Report of Four Cases and Review of the Literature
AJNR 25:382-388,351, Do,T.H.,et al, 2004

Progressive Binasal Hemianopia
Lancet 363:1606, Pringle,E.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

An Organic Cause of Neuropsychiatric Illness in Adolescence
Lancet 361:572, Taylor,S.E.,et al, 2003

Bilateral Striatal Necrosis Associated with Mycoplasma pneumoniae Infection
NEJM 348:720, van Vuiren,M. &Uhl,M., 2003

Showing articles 400 to 450 of 1005 << Previous Next >>