Neudle.com: dementia early onset

Differential
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abstract reasoning

acrocyanosis

activities of daily living scale

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, flat

age associated memory impairment

Alzheimer's disease, age of onset

Alzheimer's disease, diagnosis of

Alzheimer's disease, driving with

Alzheimer's disease, early onset

Alzheimer's disease, early symptoms

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, heterogeneity of

Alzheimer's disease, noncognitive symptoms

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, staging

Alzheimer's disease, treatment of

amyloid

amyloid angiopathy, cerebral

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

aneurysm, intracranial, familial

angiitis, granulomatous of CNS

angiography, cerebral

anomic aphasia

anosmia

anticholinesterase

anticoagulant, treatment

antiphospholipid antibody syndrome

anxiety

aphasia

aphasia, logopenic, progressive

aphasia, progressive

aphasia, progressive, non-fluent

aphasia, progressive, primary

apolipoprotein E

apoliprotein E, plasma level

autonomic dysfunction

basal ganglia, calcification of

brain biopsy, negative

brain volume

C0ORF72

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus, lesion of, bilateral

celiac disease, adult

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar plaques, amyloid

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, young adult

chorea

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

controversies in neurology

corneal dystrophy

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

degenerative diseases of CNS

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, clinical diagnosis

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, early detection

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, subcortical

dementia, transmissible

dementia, treatment of

depression

diagnostic criteria

differential diagnosis

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electromyogram

electron microscopy

encephalopathy

encephalopathy, progressive

enzyme, defect

epidemiology of neurology

ethics in neurology

evidence-based research

executive dysfunction

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, lesion of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait disorder

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

hallucination, visual

hemosiderosis of CNS, superficial

heralding manifestation

hippocampal atrophy

hippocampus

Hodgkin's disease

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, exvacuo

hydrocephalus, normal pressure

hypotension, systemic

imbalance

impulsivity

inappropriate behavior

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incoordination

inflexibility, mental

intellectual deficit

intellectual deterioration

intestinal biopsy

intracerebral hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, young adult

Kluver-Bucy syndrome

Lafora body

Lafora's disease

language disorder in adults

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

lecanemab

leg weakness, bilateral

lethargy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

Lewy body

Lewy body disease, diffuse

life expectancy

lipomembranous polycystic osteodysplasia

manganese intoxication

memory

Memory Impairment Screen

memory, defect of recent

memory, evaluation of

memory, impairment of

memory, impairment of, subjective

mental status, abnormal

microangiopathy, brain

microhemorrhage, intracerebral

mild cognitive impairment

mild cognitive impairment converting to Alzheimer's disease

mimics

Mini Mental Status Examination

misdiagnosis

molecular genetics

monoclonal antibodies

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, functional

MRI, linear enhancement

MRI, serial

MRI, T1 weighted high signal foci

MRI, volumetry

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neurocutaneous melanosis

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuropathology

neuropathology, brain

neuroprotective agents

neurosyphilis

nonsteroidal anti-inflammatory drug

normal

nutritional deficiency

nystagmus

obsessive-compulsive disorder

old age, neurology of

orthostatic hypotension

pain, increased response

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, early symptoms

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, nonmotor problems of

Parkinson disease, presymptomatic detection

Parkinson disease, rapid progression

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

pathologic reflex

patient information and support

Pittsburgh Compound B

pleocytosis of cerebrospinal fluid

polycystic lipomembranous osteodysplasia

polymerase chain reaction

posterior cortical atrophy

prevention of neurologic disorders

prion disease

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive subcortical gliosis

protein 14-3-3, cerebrospinal fluid

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

real-time quaking-induced conversion

Red flags

release phenomena

REM sleep

REM sleep behavior disorder

reticulum antibodies

review article

risk factors

risk factors, modification

seizure, diagnosis of

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

smell

Smell Identification Test

Sneddon's syndrome

spasticity

speech disorder

spongy degeneration of brain

startle myoclonus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stuttering

stuttering following CVA

symmetric brain lesions

syncope

synucleinopathy

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic illness

tau protein

tauopathy

temporal lobe, atrophy

thalamus, lesion of

thalamus, lesion of-bilateral

tinnitus

tissue plasminogen activator, intravenous

tongue, fasciculations of

transient neurologic deficit

treatment of neurologic disorder

tremor, thalamic stimulation for suppression of

uremia

urinary incontinence

vanishing white matter

word-finding difficulty

workup

Showing articles 100 to 150 of 3694 << Previous Next >>

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990

Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
Neurol 40:395-403, Farrer,L.A.,et al, 1990

Predisposing Locus for Alzheimer's Disease on Chromosome 21
Lancet 1:352-355, Goate,A.M.,et al, 1989

Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985

Left-handedness in Early & Late Onset Dementia
Neurol 34:367-369, Seltzer,B.,et al, 1984

Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
Neurol 33:81-86, Bird,T.D.,et al, 1983

Demonstration of CSF Gamma-globulin Banding in Presenile Dementia
Neurol 30:882-884, Williams,A.,et al, 1980

Decreased Computerized Tomography Numbers in Patients With Presenile Dementia
Arch Neurol 37:401-409, Naeser,M.A.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Huntington Disease Associated with Alzheimer Disease
Ann Neurol 3:545, McIntosh,G.C.,et al, 1978

Presenile Dementia with Lewy Bodies & Neurofibrillary Tangles
Arch Neurol 35:818-822, Forno,L.S.,et al, 1978

Granulomatous Angiitis of the Brain:A Successfully-treated Case
Neurol 27:588, Rajjoub,R.K.,et al, 1977

Presenile Dementia Presenting as Aphasia
JNNP 40:303, Wechsler,A.F., 1977

Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
Neurol 27:213, Banta,R.G.,et al, 1977

Neurological Stuttering-A Clinical Entity
et al. , JNNP 40:699977., Quinn,P.T., 1977

Myoclonus in Alzheimer Disease
Arch Neurol 33:278-280, Faden,A.I.,et al, 1976

Clinical Neuropathological Conference
(Ed) , Dis Ner Sys 34:124, 1973, Pick's Disease., Aronson,S.&Aronson,B., 1973

Alzheimer's disease, Diffuse Parenchymatous Diseases of the CNS, In Dementia
F. A. Davis Co. , Phila. , 1971, p. 165., Wells,C.E., 1971

Encephalopathy in Whipple's Disease
Neurol 12:65, Lampert,P.,et al, 1962

Long-Term Consumption of Ultraprocessed Foods and Prodromal Features of Parkinson Disease
Neurol 104:e213562, Wang,P.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
Ann Neurol 96:1086-1091, Fadda,G.,et al, 2024

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

Risk of Parkinson Disease Among Service Members at Marine Corps Base Camp Lejeune
JAMA Neurol 80:673-681, Goldman,S.M.,et al, 2023

Thrombectomy for Acute Ischaemic Stroke Without Advanced Imaging
Lancet 402:1724-1725, Kippel,D.W.J. & Roozenbeek, B, 2023

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Noncontrast Computed Tomography vs Computed Tomography Perfusion or Magnetic Resonance Imaging Selection in Late Presentation of Stroke with Large-Vessel Occlusion
JAMA Neurol 79:22-31, Nguyen, T.N.,et al, 2022

Thrombectomy for Anterior Circulation Stroke Beyond 6 h from Time Last Known Well (AURORA): A Systematic Review and Individual Patient Data Meta-Analysis
Lancet 399:249-258, Jovin, T.G.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021

Hashimoto Encephalopathy in the 21st Century
Neurol 94:e217-e224, Mattozzi, S.,et al, 2020

Machine Learning Approach to Identify Stroke Within 4.5 Hours
Stroke 51:860-866, Lee, H.,et al, 2020

Epilepsy in Older People
Lancet 395:735-748, Sen, A.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Diffusion-Weighted MRI in Transient Global Amnesia and its Diagnositc Implications
Neurol 95:e206-e212, Szabo, K.,et al, 2020

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Trial of Fingolimod Versus Interferon Beta-1a in Pediatric Multiple Sclerosis
NEJM 379:1017-1027, Chitnis, T.,et al, 2018

Use of Newer Disease-Modifying Therapies in Pediatric Multiple Sclerosis in the US
Neurol 91:e1778-e1787, Krysko, K.M.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Introduction of a Dedicated Emergency Department MR Imaging Scanner at the Barrow Neurological Institute
AJNR 38:1480-1485, Buller, M. & Karis, JP, 2017

Conversion to Parkinson Disease in the PARS Hyposmic and Dopamine Transporter-Deficit Prodromal Court
JAMA Neurol 74:933-940,901, Jennings, D.,et al, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Clinical Imaging Factors Associated with Infarct Progression in Patients with Ischemic Stroke During Transfer for Mechanical Thrombectomy
JAMA Neurol 74:1361-1367,1298, Boulouis, G.,et al, 2017

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

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Showing articles 100 to 150 of 3694 << Previous Next >>