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abducens nerve paralysis

abstract reasoning

accomodation, abnormal

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

advances in neurology

adverse drug reaction

affective disorders

alcohol intolerance

alien hand syndrome

alkalosis, respiratory

alkylating agents

alpha-synuclein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, misdiagnosis

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

amnesia, concussion

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

angiography, cerebral

anticholinergic drugs

anticholinergic drugs, side effects of

anticholinesterase

aphasia, progressive, primary

apolipoprotein E

apraxia of eye movements

apraxia of eyelid opening

apraxia, constructional

apraxia, speech

arm swing, reduced

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

atlanto axial dislocation, congenital

attention deficit disorder with hyperactivity

auditory and vestibular pathways

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

Binswanger disease

biologic markers

black box warning

bladder dysfunction

blinking, reduced

blood dyscrasias, neurologic findings with

brain transplantation

burst suppression pattern, electroencephalogram

calcification, intracranial

carbon monoxide poisoning

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, venography

cavernous sinus, syndrome

cavum septi pellucidi

central hypoventilation

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar lesion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral infarction, subcortical

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, MHPG(3-methoxy 4-hydroxyphenyl glycol)

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, recurrent

ceruloplasmin, serum

Charcot-Marie-Tooth

Charles Bonnet's syndrome

chemotherapy, CNS treatment and complications with

choline acetyltransferase

cholinergic drug

choreoathetosis

cigarette smoking

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coat-hanger pain

cogwheel rigidty

comprehension, impaired

conjunctival biopsy

contractures, joint

controversies in neurology

convergence, impaired

conversion reaction

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cranial neuropathy, multiple

cultured skin fibroblasts

cycad seed flour

dantrolene sodium

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, clinical diagnosis

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, posttraumatic

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, thalamic

dementia, treatment of

depression, psychotic

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

disability, neurological

dopamine agonist

downward gaze, paralysis of

drug induced neurologic disorders

drug withdrawal

dural arteriovenous malformation

dysdiadochokinesia

dysexecutive syndrome

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, post traumatic

dystonia, treatment of

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electron microscopy

emotional lability

encephalitis, viral

encephalopathy, delayed

enzyme inhibition

epidemiology of neurology

erectile dysfunction

ethics in neurology

evidence-based research

executive dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

Fabry's disease

facial nerve palsy, bilateral

fine motor function, impaired

fingerprint bodies

fistula, arterio-venous, dural

fracture, long bone

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait, festinating

gamma amino butyric acid

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

Gilles de la Tourette syndrome

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granulovacuolar degeneration

gyrus, abnormal

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

hallucination, visual, benign

head injury, severe

hemifacial spasm

hemorrhage, thalamic

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

herpes virus infection

homovanillic acid

hormone replacement

Huntington's chorea

hydrocephalus, normal pressure

hyperventilation

hypocalcemia, causes of

hypometric saccades

hypoparathyroidism

hypotension, neurologic causes of

hypotension, systemic

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunosuppression

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, location of

incontinence, fecal

infantile tremor syndrome

inflexibility, mental

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

intracerebral hemorrhage

intracranial hypotension

Isaacs syndrome

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

jaw contractures

jaw jerk, abnormal

judgement, impaired

Kayser-Fleischer ring

kinesia paradoxica

Korsakoff's psychosis

lactic acidemia

lacunar infarction

language disorder in adults

laryngismus stridulus

L-dopa, drug interactions with and side effects of

Leigh's disease

Lesch-Nyhan syndrome

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

life expectancy

lipid storage disorder of CNS

liver function enzymes

liver transplantation

locus ceruleus, lesion of

loss of sympathy

lumbar puncture, complications of

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

manganese intoxication

marche a petits pas

medical-legal aspects of neurology

memory enhancement

memory, defect of recent

memory, impairment of

meningitis, carcinomatous

meningoencephalopathy

methylhydrazine derivatives

microangiopathy, brain

microhemorrhage, intracerebral

midbrain, atrophy

migraine with aura

mild cognitive impairment

Mini Mental Status Examination

mitochondrial disease

molecular genetics

monoamine oxidase inhibitors

motor neuron disease

motor neuron disease, juvenile form

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, angiography, false negative

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, functional

MRI, susceptibility weighted

MRI, venography

multiple sclerosis

multiple sclerosis, diet in

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, static

muscle spasm, face

muscle stiffness

muscle twitching

muscle weakness

muscular dystrophy

myasthenia gravis

myasthenic syndrome

myasthenic syndrome, treatment of

myoclonic jerks

myoclonus, action

myoclonus, epilepsy

myoclonus, stimulus sensitive

nausea and vomiting

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-treatment of

nerve growth factor

neurofibrillary degeneration

neuroleptic sensitivity

neuroleptic, atypical

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic practice

neurologic signs

neurologic symptoms

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neuroprotective agents

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

nuclear medicine

nucleus basalis of Meynert

nystagmus, monocular

nystagmus, rotary

obsessive-compulsive disorder

ocular motility, disorders of

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, total

optokinetic nystagmus, abnormal

orthostatic hypotension

pain, increased response

palliative care

paraplegia, in flexion

parietal lobe, atrophy

parietal lobe, lesion of

Parkinson disease

Parkinson disease, akinetic form

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, early symptoms

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, motor neuron disease with

Parkinson disease, nonmotor problems of

Parkinson disease, pathogenesis of

Parkinson disease, postencephalitic

Parkinson disease, presymptomatic detection

Parkinson disease, prognosis of

Parkinson disease, rapid progression

Parkinson disease, sensory symptoms in

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism plus syndrome

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathologic reflex

peduncular hallucinosis

penguin silhouette sign

peptides, brain

perceptual-motor dysfunction

periodic paralysis

periodic paralysis, thyrotoxic

personality change

personality disorder

phenylketonuria

pleocytosis of cerebrospinal fluid

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postural abnormality

practice guidelines

precipitating factors

prevention of neurologic disorders

primary intracranial hypotension

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

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

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosomatic disease

psychotic behavior

ptosis, bilateral

punch-drunk syndrome

pure autonomic failure

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quality of life

radiation therapy, CNS treatment and complications with

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reflex sympathetic dystrophy

release phenomena

REM sleep behavior disorder

repetition, impaired

respirations in CNS disease

restless leg syndrome

retina, abnormal

retinal degeneration

retinitis pigmentosa

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rigidity, axial

Riley-Day syndrome

saccadic eye movements, abnormal

sagging of the brain

salivation, excessive

seborrheic dermatitis

seizure, children

seizure, neonatal

seizure, treatment of

seizure, treatment of, first

selective serotonin reuptake inhibitors

sensorineural hearing loss

sensory loss, cortical

sequencing difficulty

sexual dysfunction in neurologic disease

shoulder, pain in

single photon emission computed tomography

sleep apnea, obstructive

sleep pathology and physiology

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

Smell Identification Test

SNCA duplication

sodium-glucoe cotransporter-2 inhibitors

speech disorder

speech, loss of

spinal cord, injury of

spinal muscular atrophy

spinocerebellar ataxia

spongy degeneration of brain

sports medicine, neurology of

startle reaction

status epilepticus

status tetanicus

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subacute myelo-opticoneuropathy(S.M.O.N.)complex

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

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

subdural hematoma, acute

substantia nigra

swallow tail sign

sweating, abnormality of

synucleinopathy

syphilis, diagnosis and treatment

syphilis, neurologic complications with

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tardive dyskinesia

temporal lobe, atrophy

tetany, normocalcemic

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

Tolosa Hunt syndrome

torticollis, post traumatic

treatment of neurologic disorder

tremor, intention

tremor, post traumatic

tremor, resting

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

tricyclic antidepressant

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

upgaze, paralysis of

urinary incontinence

urine test for metabolic disorders

vasospasm, cerebral

venous hypertension

venous ischemia

vertigo, cervical

vertigo, treatment of

vincristine neurotoxicity

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual impairment

visual loss, progressive

visual loss, slow

visual symptoms

visuospatial disturbance

vocal cord paralysis

voice, abnormality of

von Bonsdorff's sign

walking, difficulty with

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

Showing articles 150 to 200 of 3566 << Previous Next >>

Mental Disorders in Parkinson's Disease
RI Med Jour 69:323-326, Rafal,R., 1986

Alzheimer's Disease, Parkinson's Disease, & Motoneurone Disease:Abiotropic Interaction Between Ageing & Environment
Lancet 2:1067-1068, Calne,D.B.,et al, 1986

Neuropeptides in Neurological Disease
Ann Neurol 20:547-565, Beal,M.F.&Martin,J.B., 1986

Pathologic Correlates of Dementia in Parkinson's Disease
Arch Neurol 43:991-995, Chui,H.C.,et al, 1986

Subcortical Dementia
BMJ 292:1035-1036, Foster,J.B., 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Parkinson's Disease in Patients with Alzheimer's Disease
Arch Neurol 43:662-664, Leverenz,J.&Sumi,S.M., 1986

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
Neurol 36:1005-1006, Maher,E.R.,et al, 1986

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

The Heterogeneity of Parkinson's Disease:Clinical & Prognostic Implications
Neurol 35:522-526, Zetusky,W.J.,et al, 1985

Atypical Presentation of Progressive Supranuclear Palsy
Ann Neurol 17:334-343, Davis,P.H.,et al, 1985

The Nucleus Basalis of Meynert in Neurological Disease:A Quantitative Morphological Study
Ann Neurol 17:163-170, Rogers,J.D.,et al, 1985

Olfactory Dysfunction in Alzheimer's Disease & Parkinson's Disease
Am J Psychiatry 142:781-782, Serby,M.,et al, 1985

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

How Common is Dementia In Parkinson's Disease
Lancet 2:1262-1265, Brown,R.G.,et al, 1984

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Parkinsonism Secondary to Neurosyphillis. A Case Report.
S Afr Med J 63:665-666, Sandy,R., 1983

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Parkinson Disease, Dementia, & Alzheimer Disease:Clinicopathological Correlations
Ann Neurol 7:329-335, Boller,F.,et al, 1980

The Effect of Symptom Duration on Cognitive & Motor Performance in Parkinsonism
Neurol 29:951-956, Matthews,C.G.,et al, 1979

Dementia in Parkinson Disease:A Neuropathologic Study
Neurol 29:1209-1214, Hakim,A.M.,et al, 1979

Dementia in Parkinson Disease
Ann Neurol 6:355-359, Lieberman,A.,et al, 1979

Lewy Bodies in the Presence of Alzheimer's Disease
Arch Neurol 36:170-171, Rosenblum,W.I.,et al, 1979

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Considerations in the Management of Parkinsonism
Neurol 28:5, Fahn,S.,et al, 1978

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

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Important Advances in Clinical Medicine
West J Med 123:128, Mosier,J.M.,et al, 1975

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Oculogyric Crisis
In Ocular Differential Diagnosis, Lea & Febiger, Phila. 1975 p. 133, Roy,F.H., 1975

Subcortical Dementia of Progressive Supranuclear Palsy
JNNP 37:121, Albert,M.,et al, 1974

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Occult Normal Pressure Hydrocephalus Manifested by Parkinsonism-dementia Complex
Neurol 23:234-238, Sypert,G.W.,et al, 1973

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

Diseases of the Extrapyramidal System
Disease-a-month-Jan 1970., Klawans,H.,et al, 1970

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

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

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

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

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

Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
Ann Neurol 97:435-448, Berthet,E.,et al, 2025

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

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Showing articles 150 to 200 of 3566 << Previous Next >>