Neudle.com: subcortical white matter disease

Differential
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abulia

aciduria

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

addiction, heroin

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

anemia

aneurysm

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

antibodies to measles

autoimmune basal ganglia encephalitis

autonomic dysfunction

B 12 deficiency

basal ganglia

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

border zone hypoperfusion

border zone infarct

border zone infarct, internal

calcification, intracranial

calcification, intraventricular

calcification, periventricular

Canavan's disease

carbon monoxide poisoning

carcinoma

carotid angiogram

carotid artery

carotid artery disease

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, cerebrovascular disease

catatonia

central nervous system, infection of

central pontine myelinolysis

centrum semiovale

cerebellar hypoplasia

cerebellar infarction

cerebellar infarction, bilateral

cerebellar lesion

cerebellar peduncle

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, familial occurrence

cerebrovascular accident, genetic

cerebrovascular accident, location of

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, pathophysiology

cerebrovascular accident, recurrent

cerebrovascular accident, silent

cerebrovascular accident, topographic pattern

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, rapidly progressive

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 19

circle of Willis

Clinical Pathologic Conference(C.P.C.)

cognition

collapsin response mediator protein 5 IgG

coma

complications

confusion

confusional state, acute

congenital infection, CNS

congenital infection, viral

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deafness

deep gray nuclei

dementia

dementia, cerebrovascular disease causing

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

differential diagnosis

digital subtraction angiography

disability rating scale, neurological

disability, neurological

disseminated intravascular coagulation(DIC)

DPPX, antibodies, encephalitis

drug abuse

drug abuse, neurologic complications of

electrical fields, alternating

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electron microscopy

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy

encephalopathy, delayed

exercise

external capsule

Fabry's disease

faciobrachial dystonic seizure

falling

false negative

familial

familial hemiplegic migraine

ferritinemia

fever

finger nose finger test

fluorescein angiography

fundus, abnormality of

gamma amino butyric acid receptor antibody

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

gliomatosis cerebri

granular osmiphilic material

hemianopia, homonymous

hemiparesis

hemophagocytic lymphohistiocytosis

hemophagocytosis

hemosiderosis of CNS, superficial

herpes simplex encephalitis

HTRA1 gene

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hyperekplexia

hyperglycemia

hyperglycemia, neurologic dysfunction associated with

hyperglycemia, nonketotic

hyperglycemic hemianopia

hyperreflexia

hypersomnia

hypertension

hypertension, cerebrovascular disease with

hypertensive encephalopathy

hypomyelination

hyponatremia

hypoxic encephalopathy

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

immunosuppression

immunosuppressive agents

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

insomnia

intellectual deficit

intellectual deterioration

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, lobar

iron, serum

iron, serum, elevated

leg weakness, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leuko-araiosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, toxic

level of consciousness, decreased

life expectancy

limbic encephalitis

liver function enzymes

low back pain

lupus anticoagulant

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macrocephaly

magnetic susceptibility

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, noninfectious

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metachromatic leukodystrophy

methylmalonic aciduria

microangiopathy, brain

microangiopathy, retina

microcephaly

microemboli

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

monoclonal antibodies

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, FLAIR

MRI, gradient-echo

MRI, gray matter enhancement

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, negative

MRI, punctate pattern

MRI, ring sign

MRI, susceptibility weighted

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

myelitis, transverse, recurrent

myelopathy

myoclonus

neoplasm, primary of CNS

neoplastic angioendotheliosis

neurexin-3 alpha antibodies

neurologic disease, diagnoses of

neurologic examination, focal

neurologic symptoms

neuronal cell surface antigen

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuroradiology

neurotoxic

next-generation sequencing

NMDA antagonists

Notch3 gene

nystagmus

old age, neurology of

opportunistic infection, CNS

Parkinson disease, arteriosclerotic

Parkinson disease, L-dopa nonresponsive

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

Pelizaeus Merzbacher

persistent vegetative state

personality change

pes cavus

phenylketonuria

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymerase chain reaction, false negative

pons, lesion of

posterior leukoencephalopathy syndrome

postpartum

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

propionic aciduria

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

psychotic behavior

pyramidal tract

pyramidal tract dysfunction

quadriparesis

radiation therapy, CNS treatment and complications with

retinal branch artery occlusion

sedimentation rate, elevated

seizure

seizure, children

seizure, complications following

seizure, febrile

seizure, hyperglycemia causing

seizure, prolonged

seizure, visual loss with

sensorineural hearing loss

serologic testing

serologic testing, false negative

single photon emission computed tomography

skin, biopsy

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

snout reflex

spinal cord, infarction of

splenomegaly

spondylolysis

spondylosis

steroid therapy, CNS treatment and complications with

Still's disease

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

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

subarachnoid hemorrhage

subcortical hemorrhage

subcortical U fibers

Susac's syndrome

symmetric brain lesions

syncope

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

transient ischemic attack

treatment of neurologic disorder

treatment resistant

tremor

urea-cycle enzymopathies

urinary incontinence

Van der Knaap disease

visual acuity, decreased

visual field defect

visual loss

walking, difficulty with

white matter disease, location

white matter disease, periventricular

white matter disease, subcortical

white matter disease, unilateral

wide based gait

workup

Showing articles 50 to 100 of 1992 << Previous Next >>

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
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Cerebral Hemispheric Low-Flow Infarcts in Arterial Occlusive Disease:Lesion Patterns and Angiomorphological Conditions
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Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
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Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
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Clinical Correlates of White Matter Findings on Cranial Magnetic Resonance Imaging of 3301 Elderly People
Stroke 27:1274-1282, 12691996., Longstreth,W.T.,et al, 1996

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

White Matter MR Hyperintensities in Adult Patients with Congenital Rubella
AJNR 17:99-103, Barton Lane,E.,et al, 1996

Binswanger's Disease-Revisited
Neurol 45:626-633, Caplan,L.R., 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Pontine Ischemic Rarefaction
Ann Neurol 37:460-466, Pullicino,P.,et al, 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

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

Progressive Multifocal Leukoencephalopathy in 47 HIV-Sero (+) Pts:Neuroimaging, Clin, Path Correl
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Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections
Neuroradiology 33:239-242, Sugita,K.,et al, 1991

Dementia Due to Vascular Disease-A Multifactorial Disorder
Stroke 19:1291-1299, Scheinberg,P., 1988

Periventricular White Matter Changes & Dementia, Clinical, Neuropsych, Radiology & Pathological Correl
Arch Neurol 45:637-641, Gupta,S.R.,et al, 1988

Senile Dementia of the Binswanger Type, A Vascular Form of Dementia in the Elderly
JAMA 258:1782-1788, Roman,G.C., 1987

Binswanger's Disease:A Review
Stroke 18:2-12, Babikian,V.&Ropper,A.H., 1987

White Matter Lucencies on CT, Subacute Arteriosclerotic Enceph (Binswanger's Disease) , & Blood Pressure
Stroke 18:900-905, McQuinn,B.A.&O'Leary,D.H., 1987

Subcortical Arteriosclerotic Encephalopathy, (Binswanger's Disease)
Arch Neurol 42:951-959, Kinkel,W.R.,et al, 1985

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

Subcortical Arteriosclerotic Encephalopathy (Binswanger) :Computerized Tomography
Neurol 29:1102-1106, Rosenberg,G.A.,et al, 1979

Clinical Features of Subcortical Arteriosclerotic Encephalopathy (Binswanger Disease)
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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Lentiviral Gene Therapy for Cerebral adrenoleukodystrophy
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Uncommon Causes of Nontraumatic Intracerebral Hemorrhage
Stroke 55:1416-1427, Tartarin,H.,et al, 2024

Brainstem Chipmunk Sign: A Diagnostic Imaging Clue Across All Subtypes of Alexander Disease
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Partially Reversible FLAIR Hyperintensity Along the Brainstem Surface in Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Monkeypox-Associated Central Nervous System Disease:A Case Series and Review
Ann Neurol 93:893-905, Money,K.M.,et al, 2023

Posterior Reversible Encephalopathy Syndrome
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Progressive Hemiparesis and White Matter Abnormalities in an HIV-Negative Patient
Neurol 100:1156-1163, Jabbari,E.,et al, 2023

Characteristics of Progressive Multifocal Leukoencephalopathy Associated with Sarcoidosis without Therapeutic Immune Suppression
JAMA Neurol 80:624-633, McEntire,C.R.S.,et al, 2023

A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
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Intracerebral Haemorrhage Caused by Iatrogenic Cerebral Amyloid Angiopathy in a Patient with a History of Neurosurgery 35 Years Earlier
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Opioid-Associated Amnestic Syndrome Progressing to Diffuse Leukoencephalopathy
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Severe Amyloid-Related Imaging Abnormalities After Anti-B-Amyloid Monoclonal Antibody Treatment
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Tuberous Sclerosis Complex:Clinical Features
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Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
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Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
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Showing articles 50 to 100 of 1992 << Previous Next >>