Neudle.com: "akinesia"

Differential
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accommodation

accomodation, abnormal

addiction, heroin

addiction, heroin-neurologic complications with

advances in neurology

adverse drug reaction

affect, flat

agitation

akinesia

akinesia of eyelid function

angiography, cerebral

anti IgLON5

anticholinergic drugs

antihistamines

aphasia

aphasia, progressive, primary

apraxia

apraxia of eye movements

apraxia of eyelid opening

autonomic dysfunction

axonal spheroid

Babinski sign

basal ganglia

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brainstem, deformity of

brainstem, dysfunction

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, venography

catatonia

caudate nucleus, lesion of, bilateral

cerebellar atrophy, primary

cerebellar lesion

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral palsy

cerebrovascular accident

Clinical Pathologic Conference(C.P.C.)

convergence, impaired

cortical-basal ganglionic degeneration

cyanide poison

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dementia, rapidly progressive

dementia, thalamic

depression

developmental milestones, loss of

diabetes dialysis basal ganglia syndrome

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

dialysis

differential diagnosis

disability, neurological

distal muscle atrophy

dopa responsive dystonia

drug abuse, inhalation

drug abuse, neurologic complications of

dural arteriovenous malformation

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, face

dystonia, focal

dystonia, treatment of

efficacy

electroencephalogram, abnormalities of

encephalitis

encephalitis, autoimmune

encephalitis, episodic

executive dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

eyelid opening, difficulty with

facial appearance, abnormal

facial expression abnormality

fine motor function, impaired

fistula, arterio-venous, dural

fracture, long bone

frontal behavioral spatial syndrome

frontal lobe, anatomy and physiology

gait disorder

gait, festinating

gaze palsy

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

genetic neurologic disorders

glabellar sign

globus pallidus, lesion of

glutamate dehydrogenase deficiency

granular osmiphilic material

grimacing

gyrus, abnormal

Hallervorden Spatz disease

hemorrhage, putamenal

hemorrhage, thalamic

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes virus infection

hip fracture

HLA

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

iatrogenic neurologic disorders

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

infection

intellectual deficit

intellectual deterioration

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, young adult

jaw jerk, abnormal

Kayser-Fleischer ring

kinesia paradoxica

L-dopa

L-dopa, drug interactions with and side effects of

L-dopa, potentiators of

leg dragging

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

lumbar puncture, complications of

manganese intoxication

marche a petits pas

masked facies

memory, impairment of

meningitis

metabolic acidosis

metabolic disorder, primary

micrographia

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

midbrain, compression

Mini Mental Status Examination

misdiagnosis

monoamine oxidase inhibitors

mood change

mortality

movement disorder

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, angiography, false negative

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, lesion burden

MRI, paramagnetic effect

MRI, punctate pattern

MRI, T1 weighted high signal foci

MRI, venography

MRS

multiple sclerosis

multiple sclerosis, relapsing

multiple sclerosis, treatment of

multiple system atrophy

neuroaxonal leukodystrophy

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic signs

neurologic symptoms

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neurotoxic

non-dominant hemisphere

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

old age, neurology of

ophthalmoplegia

orthostatic hypotension

pain, abdominal

pallidotomy

PANK2 mutation

parietal lobe, lesion of

Parkinson disease

Parkinson disease, akinetic form

Parkinson disease, asymmetric onset

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, etiology of

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

pleocytosis of cerebrospinal fluid

polycythemia, secondary

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

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

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

ptosis

pure akinesia

pyridoxine

rapidly progressing neurologic illness

reading disorder, acquired

reading problem, causes of

real-time quaking-induced conversion

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

renal failure

reserpine and reserpine like drugs

retinitis pigmentosa

retropulsion

reversible neurologic disorder

saccadic eye movements

saccadic eye movements, abnormal

safety

sagging of the brain

seizure

sensorineural hearing loss

sensory loss

sensory loss, cortical

seroconversion

shunt procedure, lumboperitoneal

shunt procedure, lumboperitoneal-complications of

sinemet

sleep pathology and physiology

slurred speech

spasticity

speech disorder

speech disorder, childhood

speech, soft

spinocerebellar ataxia type 1

spongy degeneration of brain

stare

startle reaction

stem cell transplantation

stereotaxic surgery

stimulation, deep brain

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

suck reflex

suicide

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

toe walking

tonic foot response

tonsillar herniation of cerebellum

toxins, nervous system

treatment of neurologic disorder

urinary tract infection

voice, abnormality of

walking, difficulty with

weakness

weakness, progressive

Showing articles 0 to 50 of 54 Next >>

Reversible Symmetric Basal Ganglia Lesions in a Patient with Diabetes Undergoing Dialysis
Neurol 98:773-774, Quigley, S., 2022

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

Wilson Disease Presenting with Catatonia
Neurol 96:e2781-e2782, Patel, R.A. & Bailey, M., 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Neurologic Signs and Symptoms Frequently Manifest in Acute HIV Infection
Neurol 87:148-154, Hellmuth, J.,et al, 2016

Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
Neurol 87:e239, Sgobbi de Souza, P.V.,et al, 2016

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Alemtuzumab for Multiples Sclerosis: Who and When to treat?
Lancet 380:1795-1797, 1792, Springer, T. & Kappos, L., 2012

Parkinsons Disease
Lancet 373:2055-2066, Lees,A.J.,et al, 2009

Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
Nephrology 13:68-72, Li, J.,et al, 2008

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Does This Patient Have Parkinson Disease?
JAMA 289:347-353, Rao,G.,et al, 2003

Progression of Parkinsonian Signs in Alzheimer's Disease
Neurol 54:1284-1289, Wilson,R.S.,et al, 2000

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Ptosis, Blepharospasm, and Apraxia of Eyelid Opening Secondary to Putaminal Hemorrhage
Neurol 53:652, Verghese,J.,et al, 1999

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Mortality from Parkinson Disease
Arch Neurol 54:260-264, Louis,E.D.,et al, 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Apraxia of Lid Opening
Neurol 48:1491-1503, Boghen,D., 1997

Prevalence of Parkinsonian Signs and Associated Mortality in a Community Population of Older People
NEJM 334:71-76, Bennett,D.A.,et al, 1996

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Reversal of Amphotericin-B-Related Encephalopathy
Neurol 44:1183-1184, Balmaceda,C.M.,et al, 1994

Levodopa-Nonresponsive Lewy Body Parkinsonism:Clinicopathologic Study of Two Cases
Neurol 42:1323-1327, Mark,M.H.,et al, 1992

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Clinical & PET Studies in the'Extrapyramidal Syndrome'of Dementia of the Alzheimer Type
Arch Neurol 47:1318-1323, Tyrrell,P.J.,et al, 1990

Apraxia of Eyelid Opening Secondary to Right Hemisphere Infarction
Ann Neurol 25:622-624, Kohnston,J.C.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Chronic Manganese Intoxication
Arch Neurol 46:1104-1106, Huang,C.C.,et al, 1989

Dystonic-Parkinsonian Syndrome after Cyanide Poisoning:Clinical and MRI Findings
JNNP 51:1345-1348, Carella,F.,et al, 1988

Isolated Deficiency of Vitamin E with Progressive Neurologic Deterioration
Neurol 37:538-540, Krendel,D.A.,et al, 1987

Update on Parkinson Disease
NY State J Med, 87:147-1531987., Lieberman,A.N., 1987

"Apraxia"of Eyelid Opening:An Involuntary Levator Inhibition
Neurol 35:423-427, Lepore,F.E.,et al, 1985

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

Apraxia of Eyelid Opening in Progressive Supranuclear Palsy
Ann Neurol 15:115-116, Dehaene,I., 1984

Showing articles 0 to 50 of 54 Next >>