Neudle.com: dementia rapidly progressive

Differential
(Click to cross reference)

abdominal reflex, absent

abdominal x-ray

abscess, intracerebral

abulia

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

addiction, heroin

adenovirus infection

adenylate kinase 5 autoantibodies

adrenal lesion

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

advances in neurology

adverse drug reaction

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, rapidly progressive

Alzheimer's disease, rate of clinical decline

ammonia

amnesia

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

animal exposure

anorexia

anti citrullinated antibody

anti GQ1b IgG antibody

anti Hu antibody

anti Tr antibodies

antibodies to voltage-gated calcium channels

anticonvulsants

antiganglioside antibodies

antithyroid antibodies

arteriovenous malformation

arteriovenous malformation, cerebral

arteritides

arthralgia

arthritis

artificial intelligence

autoimmune cerebellar ataxia

autoimmune disease

autoimmune encephalopathy

autoimmune meningitis

automobile accidents

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bovine spongiform encephalopathy

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brainstem, lesion of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

calcification, intracranial, miliary

carbon monoxide poisoning

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, venography

cauda equina

cauda equina, enhancement

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cavernous sinus, syndrome

CD4 counts

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral edema, vasogenic

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral palsy, work up

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, culture negative

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, three territory involvement

cerebrovascular accident, topographic pattern

cerebrovascular accident, women

cerebrovascular accident, young adult

choroid plexus, enhancement

chromosomal abnormality

chromosome 17

chromosome 20

climate change

Clinical Pathologic Conference(C.P.C.)

concentration, impaired

corpus callosum, lesion of

cortical blindness

cortical infarction

cortical infarction, small

cortical-basal ganglionic degeneration

COVID-19

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

degenerative diseases of CNS

dementia, cerebrovascular disease causing

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, thalamic

dementia, transmissible

dementia, treatment of

demyelinating disease

denervation of muscle

denervation potentials

denial of blindness(Antons syndrome)

dentate nuclei, lesion of

depression

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

diplopia

disorientation

down-beat nystagmus

down-beat nystagmus, primary position of gaze

driving

drug abuse

dural arteriovenous malformation

dural sinus thrombosis

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electromyogram

electron microscopy

electrophoretic pattern, CSF

ELISA

emergencies, neurologic

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalitis, bornavirus

encephalitis, brainstem

encephalitis, human immunodeficiency virus type 1

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

epidemiology of neurology

executive dysfunction

exercise intolerance

extralimbic encephalitis

eye movement, disorders of

Fabry's disease

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

fatal familial insomnia

fatigue

fever

fibrillations

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fourth ventricle, floor

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

frozen section

Fukuda step test

fundus, abnormality of

funduscopic exam

fungal infection

fungal infection, CNS

gadolinium

gait disorder

gait, apraxic

gammaglobulin therapy, intravenous

gastric partitioning

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

GM1 ganglioside antibodies

Guillain Barre syndrome

Guillain Barre syndrome, variant forms of

gyrus, abnormal

hallucination

hallucination, visual

headache, sudden onset of

hearing loss

hearing loss, bilateral

hearing loss, rapidly progressive

hearing loss, sudden, bilateral

hearing loss, unilateral

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemimyoclonic jerks

hemiparesis

hemiparesis, recurrent

hemiplegia

hemorrhage, thalamic

hemosiderosis of CNS, superficial

heralding manifestation

herniation syndromes, intracranial

hiccoughs

hiccoughs, intractable

highly active antiretroviral therapy

hippocampal atrophy

hippocampus

hippocampus, hyperintense

HIV CSF viral escape syndrome

hoarseness

human immunodeficiency virus type 1

hydrocephalus

hyperammonemic encephalopathy

hyperreflexia

hypersomnia

hypertensive encephalopathy

hypertensive encephalopathy, venous

hyperthyroidism

hypertrophic intracranial pachymeningitis

iatrogenic neurologic disorders

immunosuppressive agents

inclusion bodies, intracytopasmic

intellectual deterioration

internal auditory canal

intracerebral hemorrhage

intracerebral hemorrhage, lobar

intracranial pressure, increased

intravenous drug abuse

intubation

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

lactic dehydrogenase(LDH)

lacunar infarction

Lafora body

Lafora's disease

laminar necrosis, cortical

lateropulsion

leg numbness

leg swelling

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

lesions too numerous to count

lethargy

leucine rich glioma inactivated 1 antibodies

leuko-araiosis

leukocytosis

leukoencephalopathy

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

lid closure, weakness of

life expectancy

limbic encephalitis

linear lesion

listeria monocytogenes

listeriosis, CNS

lobar atrophy

logopenia

lumbar puncture, complications of

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatosis cerebri

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, treatment of

Marburg's disease

masked facies

masseter muscle wasting

medulla oblongata, lesion of

melanocytoma, meningeal

MELAS syndrome

memory, defect of recent

memory, impairment of

memory, recent

meningeal biopsy

meningeal enhancement

meningeal enhancement, nodular

meningismus

meningitis

meningitis, aseptic

meningitis, aspergillus

meningitis, bacterial

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, fungal

meningitis, fungal-negative CSF culture

meningitis, granulomatous

meningitis, helminthic

meningitis, listeria monocytogenes

meningitis, neutrophilic

meningitis, neutrophilic, persistent

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, spinal fluid smear and culture-negative

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral etiology in

meningitis-encephalitis PCR panel

meningoencephalitis

meningoencephalitis, amoebic

mental status, abnormal

mesial temporal lobe

microabscesses, cerebral

microangiopathy, brain

microangiopathy, retina

microcephaly

microhemorrhage, intracerebral

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

monoclonal gammopathy

mononeuritis multiplex

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography, false negative

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, flow void, blood

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lesion burden

MRI, linear enhancement

MRI, mass effect on

MRI, negative

MRI, nodular enhancement

MRI, orbit

MRI, proton density

MRI, punctate pattern

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, venography

MRI, vessel wall enhancement

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, acute

multiple sclerosis, aggressive

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myelitis, longitudinal

myoclonus, stimulus sensitive

myopathy

myopathy, mitochondrial

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-miliary

neoplasm, metastatic to eye

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve root enhancement

neurocutaneous disease

neurocutaneous melanosis

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination, focal

neurologic signs

neurologic testing

neurolymphomatosis

neuron specific enolase

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, vasculitic, systemic

neurosyphilis

neurotoxic

neurotoxin

next-generation sequencing

night sweats

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, primary position of gaze

occipital cortex

occipital lobe, lesion of

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic atrophy

organ transplantation

paralysis, acute areflexic

paraparesis

paraphasias

parasitic infection

parasitic infection, CNS

paresthesias

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, atypical

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathologic reflex

perseveration

personality change

pituitary, hormones of

plasmapheresis

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

potassium channel antibodies

practice guidelines

precipitating factors

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

prosopagnosia

protein 14-3-3, cerebrospinal fluid

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

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

proteinuria

protozoan infection

pseudobulbar palsy

pseudomonas aeruginosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, dilated and fixed, bilateral

pursuit eye movements, abnormal

radiation therapy, stereotactic

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

real-time quaking-induced conversion

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinopathy

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure, psychomotor-temporal lobe

seizure, teenager

sensorineural hearing loss

short stature

simultanagnosia

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

small vessel vasculitis

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical hemorrhage

suicide

Susac's syndrome

sweating

symmetric brain lesions

synovitis

synucleinopathy

syphilis, neurologic complications with

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, fasciculations of

tonsillar herniation of cerebellum

toxic encephalopathy

toxins, nervous system

transient ischemic attack

transient ischemic attack, differential diagnosis of

transient ischemic attack, normal angiogram with

transient neurologic deficit

transverse smile

treatment of neurologic disorder

tremor

tremor, postural

trigeminal neuropathy

trigeminal neuropathy, bilateral

Venereal Disease Research Laboratory test

very long chain fatty acids

visual acuity, decreased

visual field defect

visual loss

visual loss, progressive

visuospatial disturbance

vitamin deficiency

vitiligo

vocal cord paralysis

voice, abnormality of

voriconazole

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

white matter disease, subcortical

Showing articles 550 to 600 of 3977 << Previous Next >>

Viral Infections & Demylinating Diseases
NEJM 288:1103, Weiner,J.,et al, 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Case Records of MGH-NEJM 289:628
1973 Necrotizing Giant Cell Arteritis., , 1973

Hypokalemic Periodic Paralysis withArrhythmia
NEJM 286:253, Levitt,L.,et al, 1972

Progressive Supranuclear Palsy:A Clinical, Pathological & Biochemical Study
Neurol 22:445, Antunes,J.L.,et al, 1972

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Whipple's Disease-Dementia
ed. by Charles G. Wells, Chap. 10 by Gunther Haas-Contemporary Neuro. Series 192, 1971 Published by, . A. Davila., 1971

Case Records of MGH-NEJM 284:1023
1971 Herpes Simplex Encephalitis., , 1971

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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Wildfire Smoke Exposure and Incident Dementia
JAMA Neurol 82:40-48, Elser,H.,et al, 2025

Amyloid-Related Imaging Abnormalities (ARIA) in Clinical Trials of Gantenerumab in Early Alzheimer Disease
JAMA Neurol 92:19-29, Salloway,S.,et al, 2025

Bilaterally Symmetrical Globus Pallidus Infarction
Ann Neurol 97:254-255, Chen,L.,et al, 2025

Progress Toward Mitigating Disability Progression in Multiple Sclerosis
NEJM 392:1966-1968, Calabresi,P.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

Progressive Headache and Diplopia in an 89-Year-Old Man
Neurol 104:e213660, Riand,M.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

Teaching NeuroImage: The House Soign in Behavioral Varianht Frontotemporal Dementia
Neurol 104:e213519, Ioannidis,S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
NEJM 392:699-709, Case 5-2025, 2025

Orbital Apex Syndrome Associated with Herpes Zoster Ophthalmicus
Neurol 104:e213387, Imamura,D.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

Revised Criteria for Diagnosis and Staging of Alzheimers Disease: Alzheimers Association Workgroup
Alzheimers Dement 20:5143-5169, Jack,Jr.,C.R.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Progressive Peripheral Neuropathy in a 66-Year-Old Woman with Sezary Syndrome
Neurol 103:e209983, Fanouraki,S.,et al, 2024

Isolated Primary Central Nervous System Lymphoma of the Optic Nerve, A Case Report and Review of the Literature
Neurologist 29:351-355, Keertana,J.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 63-Year-Old Man With Progressive Multicranial Neuropathy and Leptomeningeal Enhancement
Neurol 103:e210100, Taga,A.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

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

Clinicopathologic Conference, Cryptococcal Meningoencephalitis
NEJM 391:2361-2369, Case 40-2024, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

SGLT2 Inhibitor Use and Risk of Dementia and Parkinson Disease Among Patients With Type 2 Diabetes
Neurol 103:e209805, Kim,H.K.,et al, 2024

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
Neurol 103:e209883, Maya-Gonzalez,C.,et al, 2024

A 32-Year-Old Man with Painless Bilateral Shoulder Girdle Weakness and Atrophy
Neurol 103:e209915, Gutti,N.B.,et al, 2024

Tau Positron Emission Tomography for Predicting Dementia in Individuals with Mild Cognitive Impairment
JAMA Neurol 81:845-856, Groot,C.,et al, 2024

Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
NEJM 391:641-650, Gaier,E.D.,et al, 2024

Risk of Dementia After Initiation of Sodium-Glucose Cotransporter-2 Inhibitors Versus Dipeptidyl Peptidase-4 Inhibitors in Adults Aged 40-69 years with type 2 Diabetes:Population Based Cohort Study
BMJ doi:10.1136/BMJ-2024-07945, Shin,A., et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024

MOG-IgG-Associated Encephalitis with FLAIR Hyperintensity Along the Brainstem Surface
Ann Neurol 96:460-462, Yin,J.,et al, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Showing articles 550 to 600 of 3977 << Previous Next >>