Neudle.com: degenerative diseases of CNS

Differential
(Click to cross reference)

abiotrophy

abortion, spontaneous

acanthocytosis

acoustic neurinoma

acute disseminated encephalomyelitis

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcoholic polyneuropathy

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, incidence

Alzheimer's disease, prognosis of

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

ammonia

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anatomy of

aneurysm

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

angiitis, isolated of CNS

angiofibroma, facial

ankylosing spondylitis

anomic aphasia

anosmia

antibiotics

anticoagulant, complications of

anticoagulant, discontinuation

anticoagulant, treatment

anticoagulant, treatment in CVD

anxiety

aphasia

aphasia, progressive

aphasia, progressive, primary

apnea

apnea, primary central

apraxia of eye movements

arachnoiditis

areflexia

arm swing, reduced

Arnold Chiari malformation

arteriovenous malformation

arthrogryposis multiplex

aspartocyclase

aspiration

ataxia

ataxia telangiectasia

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

blood dyscrasias, neurologic findings with

bone marrow biopsy

bovine spongiform encephalopathy

brain transplantation

brainstem, atrophy

brainstem, infarction of

brainstem, neoplasms of

Brown Sequard syndrome

bruxism

bulbar palsy

bulbar palsy, childhood

bulbar palsy, progressive

cafe au lait spots

CAG repeats

calcification, intracranial

Canavan's disease

cane

carbon monoxide poisoning

CAT scan, emission, abnormal

cataplexy

cataracts

cataracts, congenital

cauda equina, lesion of

caudate nucleus, atrophy

celiac disease, adult

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular disease

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical spine

cervical spine abnormality

cervical spine disease

cervical spine injury

cervical spine injury, compression

cervical spine injury, flexion

cervical spondylosis

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

children

choline acetyltransferase

chromosomal abnormality

chromosome 14

chromosome 20

chromosome 5

chronic traumatic encephalopathy

claustrophobia

Clinical Pathologic Conference(C.P.C.)

color vision, impaired

congenital birth defects

congenital deformities

congenital malformation

congenital malformation, non CNS

consanguinity

contactin associated protein like 2 antibodies

controversies in neurology

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cost

cost effectiveness

CPAP

crossed straight leg raising test

crying, pathologic

cultured skin fibroblasts

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, cerebrovascular disease causing

dementia, diagnostic evaluation of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, prevention of

dementia, rapidly progressive

dementia, screening for

dementia, thalamic

dementia, transmissible

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diastematomyelia

diet

differential diagnosis

dopaminergic dysfunction

dopaminergic neurons

downward gaze

drooling

drug induced neurologic disorders

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

emergencies, neurologic

emotional lability

employment

empyema, epidural-spinal

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, post traumatic

endocarditis, subacute bacterial

enkephalins

enzyme activity

enzyme, defect

epidemiology of neurology

executive dysfunction

exercise intolerance

extension-flexion injury of cervical spine

eye movement, disorders of

familial periodic ataxia

fasciculation

Fazio-Londe's disease

feeding disorder

fetal tissue

fibrillations

fine motor function, impaired

football neurologic injuries

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

free radical

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann syndrome

Gerstmann-Straussler-Scheinker disease

glabellar sign

gliadin antibodies

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid

glutamic acid decarboxylase

glutaric acidemia

gluten sensitivity

gluten-free diet

glycogen storage disease

granular osmiphilic material

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

head injury, repetitive

heavy metal intoxication

hematoma, epidural-spinal

hematomyelia

hepatic encephalopathy

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, cervical

herniated disc, differential diagnosis of

herniated disc, lumbar

herniated disc, lumbar-conservative vs.surgical treat.of

herniated disc, lumbar-laminectomy

herniated disc, steroid treatment of

herniated disc, thoracic

herpes zoster

highly active antiretroviral therapy

human immunodeficiency virus type 1

human T-lymphotropic virus type II(HTLV-II)

huntingtin

Huntington's chorea

Huntington's chorea, genetic counselling

hydrocephalus

hyperextension injury

hyperglycemia

hyperreflexia

hypersensitivity reaction

hypotension, systemic

hypothermia

hypotonia

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

insular cortex, lesion

intellectual deficit

intellectual deterioration

internet

intrathecal medication

intrathecal steroid

intrinsic hand muscles, wasting of

inverse association

iron, brain

Jackson's syndrome

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

klippel feil syndrome

Krabbe's disease

Kugelberg-Welander syndrome

language disorder in adults

L-dopa, drug interactions with and side effects of

learning disability, in children

leg numbness

leg weakness, unilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic system

limbic-predominant age-related TDP-43 encephalopathy

liver disease

lobar atrophy

locus ceruleus, lesion of

logopenia

loss of sympathy

low back pain

low back pain, differential diagnosis of

lumbar puncture, complications of

lumbosacral radiculopathy

lymphoma

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

magnetic susceptibility

malformation, CNS, congenital

malingering

maple syrup urine disease

Marinesco-Sjogren syndrome

masked facies

memory, defect of recent

memory, impairment of

meningeal enhancement

microhemorrhage, intracerebral

midbrain

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Millard Gubler syndrome

mimics

minocycline

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, complications with

MRI, contraindications

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, field strength

MRI, field strength, high

MRI, FLAIR

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, indications for

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle wasting, diffuse

muscular dystrophy

mutism

myasthenia gravis

myelination of nervous system

myelitis

myelogram

myelogram, cervical

myelogram, complications of

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myoclonic jerks

myoclonus

myoclonus, epilepsy

myoclonus, orthostatic

myopathy

myopathy, mitochondrial

myotonia dystrophica

N-acetyl-L-aspartic acid

Native Americans

neck pain

negative

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, spine

nerve root compression

nerve root, lumbar, lesion of

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuronal cell death

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal loss

neuronal migration disorder

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuroprotective agents

neurotoxic

neurotoxin

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

NMDA antagonists

NMDA receptors

nucleus basalis of Meynert

nystagmus

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

odontoid process

odontoid process, fracture of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

optic atrophy

optic atrophy, hereditary

orthostatic hypotension

osmotic demyelination syndrome

osteomyelitis

osteomyelitis, spinal

osteoporosis

oxidative phosphorylation

pain

pain, back

pain, leg

pain, management of chronic

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, familial

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism-dementia complex

PAS positive

PAS positive material in the brain

pathologic reflex

patient information and support

penguin silhouette sign

peptides, brain

perseveration

persistent vegetative state

persistent vegetative state, children

persistent vegetative state, etiology of

personality change

phakomatoses

phobias

physician assisted suicide

Pick bodies

Pick's disease

pigmentary retinopathy

piriformis muscle syndrome

platelet inhibiting drugs

platelet inhibiting drugs, discontinuation

pneumonia

poison, mercury

poison, neurologic problems with

poliomyelitis

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

pontocerebellar atrophy

posterior column disease

posterior cortical atrophy

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

postural abnormality

practice guidelines

pramipexole

pregnancy, neurologic complications in

pretectal syndrome

prevention of neurologic disorders

primary lateral sclerosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

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

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

Red flags

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

seizure, drug resistance

seizure, laughing as manifestation

semantic dementia

senile plaques

sensorineural hearing loss

sequencing difficulty

short neck

short stature

shunt procedure, ventricular

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

SMN1 gene

soccer

sodium-glucoe cotransporter-2 inhibitors

speech disorder, childhood

speech, loss of

spinal cord

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, neurofibroma

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal headache

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spine, infection of

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 10

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenomegaly

spondylosis

spongy degeneration of brain

sports medicine, neurology of

standing difficulty

startle myoclonus

status epilepticus

stem cell transplantation

steroid

steroid injection

steroid therapy, CNS treatment and complications with

stillbirth

storage disease of CNS

straight leg raising test

striatonigral degeneration

striatonigral degeneration, infantile

stridor

stuttering

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

subarachnoid hemorrhage

survival motor neuron gene

symmetric brain lesions

temporal lobe, atrophy

tetracycline

thalamus, lesion of

thalamus, lesion of-bilateral

treatment of neurologic disorder

trinucleotide repeats

ventricular enlargement

vestibular function, tests of

visual acuity, decreased

visual evoked response

visual fields, constricted

visual impairment

visual loss

visual symptoms

visuospatial disturbance

vitamin A

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

web sites

Weber's syndrome

weight loss

Werdnig-Hoffman disease

West disease

West Nile fever

Western immunoblot test

word-finding difficulty

workup

writing

X-linked bulbospinal neuronopathy

x-ray, cervical spine

Showing articles 150 to 200 of 24359 << Previous Next >>

Management of Lumbar Nerve-root Pain by Intrathecal & Epidural Injections of Depot Methylprednisolone Acetate
Med J Aust 2:532-534, Ryan,M.D.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Brain Peptides
(part I & II) NEJM 304:876-885, 944-951., Krieger,D.T.&Martin,J.G., 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Introduction to Symposium on Cervical Spine Injuries
Arch Surg 111:637, Babcock,J.L., 1976

Limitations & Complications of Myelography, in Myelography
3rd Year Book Med Publ Inc, Chicago, 1975, p. 455-462., Shapiro,R., 1975

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Olivopontocerebellar Atrophies:A Review
Medicine 49:227, Konigsmark,B., 1970

Dopamine & Disease
C M A Journ 103:824, Barbeau,A., 1970

Electrophoretic Morphology of Gamma Globulins in Cerebrospinal Fluid of MS & other Diseases of the CNS
Neurol 20:982, Laterre,E.C.,et al, 1970

Progressive Supranuclear Palsy Clinico-Pathological Study of Four Cases
Brain 92:663, Behrman,S.,et al, 1969

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

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Tuberous Sclerosis:Reappraisal of a Clinical Entity
Mayo Clin Proc 42:26, Lagos,J.,et al, 1967

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

A 41-Year-Old Man with Steroid-Responsive Hemiparesis
Neurol 106:e214088, Obaidi,Z.A.,et al, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
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Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Uncommon Faces of Disk Herniation: Atypical Imaging Presentations and Mimics
AJNR 47:244-251, Galante,M-J.,et al, 2026

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
NEJM 394:383-391, Case 3-2026, 2026

Mucormycosis
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Treatment for Brain Metastases with Stereotactic Radiation vs Hippocampal-Avoidance Whole Brain Radiation, A Randomzid Clinical Trial
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Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Brain CT for Diagnosis of Intracranial Disease in Ambulatory Patients with Cancer:Assessment of the Diagnostic Value of Scanning without Contrast Prior to With Contrast
AJNR 47:694-698, Wang,E.,et al, 2026

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

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Polymyalgia Rheumatica
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Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

Patterns and Factors Associated with Cerebral Infarction on MRi in Tuberculous Meningitis: Secondary Anlysis of the ACT-TBM Trial
Stroke 57:856-864, Chandu,M.,et al, 2026

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

Creutzfeldt-Jakob-Like Presentation in Anti-AMPAR Encephalitis
Ann Neurol 99:1466-1467, Durbano,K.et al, 2026

Cerebral Syphilitic Vasculitis Presenting with Recurrent Stroke
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Granulomatosis with Polyangiitis Presenting as Isolated Ear Involvement A Case Series and Literature Review
ACTA Otorhinolaryngol Italica 45:217-230, Zorzi,S.,et al, 2025

Wearable Technology and Its Role in Neurologic Care, Emerging Issues in Neurology
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Anti-NMDAR Encephalitis Triggered by EBV and HSV-1
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High-Grade Gliomas with Autoimmune Encephalitis-Like Presentation: Case Report and Systematic Review of the Literature
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Myelin Oligodendrocyte Glycoprotein Antibody - Associated Cerebral Cortical Encephalitis: A Case Report Highlighting Diagnostic Challenges and Therapeutic Implications
Front Immunol 16:1619807, Liu,M. & Li, D., 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
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Anticoagulant Usage and Risk of Thromboembolic Events After Ischemic Stroke in Adults with Cancer
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A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
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A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

Showing articles 150 to 200 of 24359 << Previous Next >>