Neudle.com: "cerebral palsy adults"

Differential
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abscess, intracerebral

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

affect, inappropriate

agnosia

agnosia, visual

alcoholism

altered states of consciousness

amaurosis fugax

anemia

aneurysm

aneurysm, intracranial

angiography, cerebral

anomic aphasia

antibiotic prophylaxis

antibiotics

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

aphasia

aphasia, progressive, primary

attention deficit disorder with hyperactivity

Babinski sign

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, hemorrhage

basal ganglia, hemorrhage, bilateral

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bone marrow transplantation

bradykinesia

brain biopsy

brain biopsy, stereotaxic

brain scan, abnormal

brainstem

brainstem, glioma

brainstem, glioma, adult

brainstem, lesion of

brainstem, neoplasms of

bruit

bruit, asymptomatic

calcification, intracranial

carotid artery disease

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, gray matter enhancement

cataracts

central nervous system, infection of

central retinal artery occlusion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral infarction

cerebral infarction, subcortical

cerebral palsy

cerebral palsy, adults

cerebral palsy, associated problems with

cerebral palsy, risk factors

cerebral venous infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, leak

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, delayed onset

cerebrovascular accident, familial occurrence

cerebrovascular accident, incidence of

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

children

chorea

chromosomal abnormality

chromosome 19

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

coccidioidomycosis

cognition

collagen vascular disease

coma

complications

comprehension, impaired

confusion

congenital bilateral perisylvian syndrome

controversies in neurology

conversion reaction

cornea, abnormal

cortical blindness

cortical-basal ganglionic degeneration

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crying, pathologic

cultured skin fibroblasts

deafness

decerebrate posture

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, cerebrovascular disease causing

dementia, frontotemporal

dementia, presenile

dementia, subcortical

depression

diabetes insipidus

diabetes mellitus

differential diagnosis

diplopia

disability, neurological

doppler

drooling

drug abuse

drug induced neurologic disorders

dural sinus thrombosis

Ehlers-Danlos syndrome

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electromyogram

embolism

emergencies, neurologic

encephalopathy, progressive

endocarditis

endocarditis, neurologic manifestations with

endocarditis, subacute bacterial

endocarditis, treatment of

episodic disorders

episodic neurologic deficits

executive dysfunction

exercise intolerance

external capsule

eye movement, disorders of

facial weakness, bilateral

falling

familial

familial hemiplegic migraine

fever

fibromuscular dysplasia

frontal lobe, atrophy

frontal lobe, pathologic signs of

fundus, abnormality of

gadolinium

gait disorder

gaze palsy

gaze palsy, horizontal

genetic neurologic disorders

hallucination, visual

hematuria, microscopic

hemianopia, homonymous

hemiparesis

hemiplegia

hemoglobinuria

hemorrhage, putamenal

heparin

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herniation syndromes, intracranial

herpes zoster

herpes zoster, disseminated

hydrocephalus, normal pressure

hyperpigmentation of skin

inclusion bodies, intracytopasmic

inclusion body myositis

insular cortex

intellectual deficit

intellectual deterioration

internal carotid artery

internuclear ophthalmoplegia, unilateral

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, bilateral

intracerebral hemorrhage, multiple

intracerebral hemorrhage, young adult

intracranial pressure, increased

iritis

jaw claudication

jaw jerk, abnormal

Kayser-Fleischer ring

Kearns-Sayre syndrome

lactic acidemia

lacunar infarction

lacunar state

language disorder in adults

language disorders in children

laughing, pathologic

Leber's hereditary optic neuropathy

level of consciousness, decreased

lumbar puncture, indications for

mania

manic-depressive

MELAS syndrome

memory, impairment of

meningeal gliomatosis

meningitis, bacterial

meningitis, bacteriologic etiology of

meningitis, clinical features of

meningitis, CSF cell count-normal

meningitis, CSF findings in

meningitis, elderly

meningitis, factors influencing mortality in

meningitis, fungal

meningitis, hemophilus influenza

meningitis, listeria monocytogenes

meningitis, meningococcal

meningitis, neurologic aspects and complications of

meningitis, pneumococcal

meningitis, predisposing factors in

meningitis, prophylaxis against

meningitis, recurrent

meningitis, seizures with

meningitis, spinal fluid smear and culture of

meningitis, syphilitic

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

microangiopathy, brain

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, serial

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle biopsy

muscle weakness

muscle weakness, proximal

muscular dystrophy

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myopathy, mitochondrial

neoplasm, primary of CNS-classification

neuroendocrinology

neurofibromatosis 1

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic examination

neurologic examination, focal

neurologic history

neurologic signs

neurologic symptoms

neurological intensive care

neuroophthalmology

neuropathology

neuropathy

neuropathy, vasculitic, systemic

night sweats

nonverbal

normal

ocular motility, disorders of

old age, neurology of

opened mouth

operculum syndrome

operculum syndrome, bilateral

optic neuropathy, ischemic

Osler's nodes

otitis, neurologic complications with

paraplegia, in flexion

Parkinson disease

Parkinsonism syndrome

pathologic reflex

pathology

pediatric neurology

pediatric neurology, transition to adult care

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

pneumonia

pontine glioma

primary lateral sclerosis

prognosis

progressive neurologic disorder

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

pulmonary embolism

pupil, abnormality in neurologic disorders

pupil, tonic

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

renal artery stenosis

saccadic eye movements, abnormal

schizophrenia

scleritis

scleroderma

scleroderma, neurologic involvement with

sedimentation rate

sedimentation rate, elevated

seizure

seizure, children

seizure, recurrent

seizure, risk factors for

seizure, treatment of

semantic dementia

sensorineural hearing loss

short stature

sinusitis

skin, lesions in neurologic disorders

slit lamp examination

spinal cord, infarction of

spinal cord, lesion of

splenomegaly

splinter hemorrhages

startle reaction

stent, carotid artery

steroid

steroid therapy, CNS treatment and complications with

strokelike episodes

suck reflex

symmetric brain lesions

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tentorium cerebelli

thrombophlebitis

tinnitus

tongue, impaired movements of

toxic encephalopathy

transient ischemic attack

transient ischemic attack, recurrent

transient ischemic attack, venous

transient neurologic deficit

transluminal angioplasty, carotid artery

treatment of neurologic disorder

tremor

trigeminal neuropathy

ulcerative colitis

ultrasonography, carotid artery

upgaze

upgaze, paralysis of

urinary incontinence

varicella zoster virus

varicella zoster virus, encephalitis

very long chain fatty acids

visual loss

walking, difficulty with

word-finding difficulty

workup

wrist drop

Showing articles 0 to 50 of 14947 Next >>

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Performance of Bedside Stroke Recognition Tools in Discrimination Childhood Stroke from Mimics
Neurol 86:2154-2161, Mackay, M.T.,et al, 2016

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Stroke and NonStroke Brain Attacks in Children
Neurol 82:1434-1440, Mackay, M.T.,et al, 2014

MELAS
MedLink.com, August, Klopstock, T., 2012

Transition to Adult Care for Children with Chronic Neurological Disorders
Ann Neurol 69:437-444, Camfiled, P. & Camfield, C., 2011

Community-Acquired Bacterial Meningitis in Adults
NEJM 354:44-53, van de Beek,D.,et al, 2006

Maternal and Infant Characteristics Associated with Perinatal Arterial Stroke in the Infant
JAMA 293:723-729, Lee,J.,et al, 2005

Is This Patient Having a Stroke?
JAMA 293:2391-2402, Goldstein,L.B. &Simel,D.L., 2005

Fibromuscular Dysplasia
NEJM 350:1862-1871, Slovut,D.P. &Olin,J.W., 2004

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Discontinuation of Antiepileptic Drug Treatment after Two Seizure-Free Yrs in Children with Cerebral Palsy
Pediatr 97:192-197, Delgado,M.R.,et al, 1996

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

Acute Bacterial Meningitis in Adults, A Review of 493 Episodes
NEJM 328:21-28, Durand,M.L.,et al, 1993

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Putaminal Hemorrhage:Clinical-Computed Tomographic Correlations
Neuroradiology 32:200-206, Weisberg,L.A.,et al, 1990

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

Cerebral Venous Thrombosis-A Review of 38 Cases
Stroke 16:199-213, Bousser,M.,et al, 1985

Herpes Zoster-Associated Encephalitis:Clinicopathologic Report of 12 Cases and Review of the Literature
Medicine 62:81-95, Jemsek,J.,et al, 1983

Lacunar Strokes & Infarcts:A Review
Neurol 32:871-876, Fisher,C.M., 1982

Neuro-Behcet Disease:Two Cases & Neuroradiologic Findings
Neurol 27:1148, Kozin,F.,et al, 1977

Neurologic Manifest. of Infective Endocarditis:A Review
Stroke 4:958, Greenlee,J.E.,et al, 1973

Case Records of MGH-NEJM 285:621
1971., , 1971

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
Stroke:Vasc Inter Neurol doi.org/10.1161/svi 270000.138, Sardana,S.,et al, 2025

Stroke in the Young
Neurol 104:e213543, Gattu,A.K.,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

GLP-1RA-Associated Diabetic Lumbosacral Radiculoplexus and Common Fibular Neuropathies
Neurol 105:e213916, Triplett,J.D.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

Atypical Diabetic Neuropathies
BMJ 390:e081109, McCray,B.A.,et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

Clinicopathologic Conference, Diffuse Meningeal Melanomatosis
NEJM 393:2152-2162, Case 34-2025, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Efficacy and Safety of IV Thrombolysis for Acute Ischemic Stroke Patients with Moyamoya Disease
Neurol 104:e210243, Chen,H.,et al, 2025

Showing articles 0 to 50 of 14947 Next >>