Neudle.com: leukoencephalopathy hereditary diffuse

Differential
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abdominal distention

abulia

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

affect, inappropriate

Aicardi-Goutieres syndrome

akinetic mute

Alexanders disease

Alexanders disease, adult onset

angiitis, granulomatous of CNS

angiitis, isolated of CNS

ataxia telangiectasia

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autonomic dysfunction

autosomal dominant leukodystrophy

bacterial infection, CNS

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bone marrow transplantation

brucellosis, nervous system involvement with

bulbar palsy

cachexia

CAG repeats

calcification, intracranial

calcification, intracranial, rim

calcifications, intracranial, punctate

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

CAT scan, serial

cataracts

cataracts, congenital

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral peduncle

cerebral vasculature

cerebral vasculature, calcification

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, genetic

cerebrovascular accident, location of

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot-Marie-Tooth

chilbran skin lesions

children

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, weak

crying, pathologic

cryopyrin-associated periodic syndrome

cryptorchidism

cultured skin fibroblasts

cyst

cyst, benign intracranial

cyst, cortical parenchyma

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones, loss of

developmental retardation

diagnostic criteria

diarrhea

diet

differential diagnosis

dysarthria-clumsy hand syndrome

enzyme, muscle disease

epicanthal folds

episodic disorders

episodic neurologic deficits

evoked potentials

exome sequencing

extraocular muscle lesion

eye movement, disorders of

eye, pain in

eyes, sunken

Fabry's disease

facial appearance, abnormal

fatty acid dehydrogenase deficiency

feeding disorder

fever

fever, recurrent

flow study, carotid artery

foot deformity

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal bossing

frontal lobe, anatomy and physiology

frontal lobe, lesion of

frontal lobe, pathologic signs of

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

globus pallidus, lesion of, bilateral

glycogen storage disease

glycosyltransferase

gram negative rod

granular osmiphilic material

hemiparesis, transient

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

hiccoughs

hormone replacement

HTRA1 gene

human immunodeficiency virus type 1

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

hyperactivity

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertrophic intracranial pachymeningitis

hypotension, systemic

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

incontinentia pigmenti

incoordination

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracerebral hemorrhage

intrauterine

intrinsic hand muscles, wasting of

irritability

Jewish

Kearns-Sayre syndrome

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukodystrophy

leukodystrophy, pigmented orthochromatic

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

maple syrup urine disease

Marinesco-Sjogren syndrome

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, brucellosis

mental retardation

metabolic acidosis

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylmalonic aciduria

microangiopathy, brain

microcephaly

microdontia

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, FLAIR

MRI, gradient-echo

MRI, high signal foci on

MRI, susceptibility weighted

MRI, target sign

MRS

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle biopsy

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

myelination of nervous system

myelitis, longitudinal

myelopathy, chronic progressive

nerve conduction studies

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neuroichthyosis

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neuromuscular disease, electrodiagnosis of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronal intranuclear inclusion disease

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

oculodentodigital dysplasia

old age, neurology of

ophthalmoplegia

optic ataxia

optic atrophy

optic atrophy, bilateral

optic neuritis

optic neuritis, bilateral

optic neuropathy

orthostatic hypotension

overlap syndrome

owl's eye sign of spinal cord

palmoplantar keratoderma

paralysis

paralysis, recurrent

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy

pons, lesion of

posterior fossa, lesion of

posterior leukoencephalopathy syndrome

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary familial brain calcification

prognosis

progressive neurologic disorder

propionic aciduria

proximal myotonic myopathy

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

psychotic behavior

ptosis

pupil, dilated, bilateral

pupil, dilated, episodic

putamen, lesion of, bilateral

pyramidal

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

quadriplegia, transient

reversible neurologic disorder

saccadic eye movements, abnormal

sedimentation rate, elevated

seizure

seizure, drug resistance

self-mutilation

sensorineural hearing loss

sensory loss

short stature

Sjogren-Larsson syndrome

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

small vessel disease

small vessel disease, cerebral

somatosensory evoked potentials

spastic diplegia

spasticity

speech disorder, childhood

spinal cord, lesion of

spinocerebellar ataxia

splenium of corpus callosum

spondylolysis

spondylosis

spongy degeneration of brain

spontaneous remission

staggering

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

striatum, lesion of

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

subdural hematoma

substantia nigra

succinate dehydrogenase deficiency

sural nerve

symmetric brain lesions

teeth, number of in infants

telangiectases, retinal

temporal lobe, lesion, bilateral

testicular biopsy

thalamus, lesion of

thalamus, lesion of-bilateral

titubation

tomaculous neuropathy

tongue, biting

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

trinucleotide repeats

tumefactive lesion

umbilical-cord blood transplantation

unconsciousness

unconsciousness, transient

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

vanishing white matter

vasculitides

vasculopathy

very long chain fatty acids

vibratory sensation, abnormal

visceral neuropathy

vision loss, sequential

visual acuity, decreased

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin E deficiency

walking, difficulty with

water channel antibodies

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

wheelchair

white matter disease

white matter disease, location

white matter disease, pattern

white matter disease, subcortical

white matter disease, unilateral

Showing articles 600 to 650 of 2950 << Previous Next >>

Granulomatous Angiitis of the Central Nervous System:Protean Manifestations and Response to Treatment
JNNP 51:1126-1133, Koo,E.H.&Massey,E.W., 1988

Magnetic Resonance Imaging in Central Nervous System Sarcoidosis
Neurol 38:378-383, Miller,D.H.,et al, 1988

Toluene Abuse Causes Diffuse Central Nervous System White Matter Changes
Ann Neurol 23:611-614, Rosenberg,N.L.,et al, 1988

Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
Arch Neurol 45:1004-1008, Schwankhaus,J.D.,et al, 1988

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

Cranial MRI in Acute Disseminated Encephalomyelitis
Neurol 38:332-333, Epperson,L.W.,et al, 1988

Nuclear Magnetic Resonance Image White Matter Lesions & Risk Factors for Stroke in Normal Individuals
Stroke 19:263-265, Lechner,H.,et al, 1988

Magnetic Resonance Imaging of Cerebral Lesions in Pts with the Sjogren Syndrome
Ann Int Med 108:815-823, Alexander,E.L.,et al, 1988

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

White Matter Signal Abnormalities in Normal Individuals:Correlation with Cerebrovascular Risk Factors
Stroke 19:1285-1288, Fazekas,F.,et al, 1988

Magnetic Resonance Imaging of Periventricular Hyperintensity in a Veterans Administration Hospital Population
Arch Neurol 44:725-728, Sarpel,G.,et al, 1987

Leukoencephalopathy in Patients with Ischemic Stroke
Stroke 18:896-899, Bugousslavsky,J.,et al, 1987

MR Findings in Normal-Pressure Hydrocephalus:Significace & Comparison with Other Forms of Dementia
Jr. , et al, J Comput Assist Tomogr 11:923-93187., Jack,C.R., 1987

Evidence for Central Nervous System Demyelination in Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Neurol 37:1291-1294, Mendell,J.R.,et al, 1987

Clinicopath Conference
Progressive Multifocal Leukoencephalopathy & Malignant Thymoma, with Metastases to Pleura, Case 1-19, 7, NE6:35-42,1987., 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

Magnetic Resonance Imaging in Vascular Dementia
Neurol 37:29-36, Hershey,L.A.,et al, 1987

Leuko-Araiosis
Arch Neurol 44:21-23, Hachinski,V.C.,et al, 1987

Cognitive & Neurologic Findings in Subjects with Diffuse White Matter Lucencies on CT Scan (Leuko-Araiosis)
Arch Neurol 44:32-35, Steingart,A.,et al, 1987

Cognitive & Neurologic Findings in Demented Patients with Diffuse White Matter Lucencies on CT Scan (Leuko-Araiosis)
Arch Neurol 44:36-39, Steingard,A.,et al, 1987

Vascular Risk Factors & Leuko-Araiosis
Arch Neurol 44:42-47, Inzitari,D.,et al, 1987

Central Nervous System Toxicity After Liver Transplantation, The Role of Cyclosporine & Cholesterol
NEJM 317:861-866, DeGroen,P.C.,et al, 1987

Incidental Subcortical Lesions Identified on MRI in the Elderly, I, Correlation with Age & Cerebrovascular Risk Factors
Stroke 17:1084-1089, Awad,I.A.,et al, 1986

Infantile Sudanophilic Leukodystrophy:Computed Tomography Demonstration
Neuroradiology 28:170-172, Sano,N.,et al, 1986

MRI Periventricular Lesions in Adults
Neurol 36:998-1001, Gerard,G.&Geisberg,L.A., 1986

Magnetic Resonance Imaging in Cerebrotendinous Xanthomatosis
Neurol 36:124-126, Swanson,P.D.&Cromwell,L.D., 1986

Hypodense White Matter Lesions in Computed Tomography of Neurosarcoidosis
J Comput Assist Tomogr 10:181-183, Ketonen,L.,et al, 1986

Meningovascular Syphilis: CT and MR Findings
Radiology 158:439-442, Holland,B.A.,et al, 1986

Leukoencephalopathy in Diffuse Hemorrhagic Cerebral Amyloid Angiopathy
Ann Neurol 18:54-59, Gray,F.,et al, 1985

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

Progressive Multifocal Leukoencephalopathy:Clinical & Radiographic Features
Ann Neurol 17:344-349, Krupp,L.B.,et al, 1985

Demyelinating Encephalopathy in Lyme Disease
Neurol 35:267-269, Reik,L.,et al, 1985

Computed Tomography in White Matter Diseases
Ann Neurol 17:314-315, Ferriero,D.,et al, 1985

Computed Tomographic Changes of Hypertensive Encephalopathy
AJNR 6:395-398, Weingarten,K.L.,et al, 1985

Brain Shrinkage in Chronic Alcoholics:A Pathological Study
BMJ 290:501-504, Harper,C.G.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Adrenoleukodystrophy:Early Frontal Lobe Involvement on Computed Tomography
J Comput Assist Tomogr 8:128-130, MacDonald,J.T.,et al, 1984

Computed Tomography in Late-Onset Metachromatic Leucodystrophy
Neuroradiology 26:39-44, Schipper,H.I.,et al, 1984

Hereditary Adult-Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis
NEJM 311:948-953, Eldridge,R.,et al, 1984

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

Computed Tomography in Krabbe's Disease:Comparison with Neuropathology
Neuroradiology 25:323-327, Ieshima,A.,et al, 1983

Metachromatic Leukodystrophy (MLD) , XV. Adult MLD with Focal Lesions by Computed Tomography
Arch Neurol 40:354-355, Skomer,C.,et al, 1983

Computed Tomography in Acute Disseminated Encephalomyelitis
Ann Neurol 13:567-572, Lukes,S.A.,et al, 1983

Computerized Tomography as a Diagnostic Aid in Acute Hemorrhagic Leukoencephalitis
Ann Neurol 13:331-333, Rothstein,T.L.,et al, 1983

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

Computed Cranial Tomography in Congenital Rubella Syndrome
Arch Neurol 39:420-421, Ishikawa,A.,et al, 1982

Adrenoleukodystrophy, Unusual Computed Tomographic Appearance
Arch Neurol 39:782-783, Young,R.S.K.,et al, 1982

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

The Adrenoleukomyeloneuropathy Complex:Expression in Four Generations
Neurol 31:151-156, O'Neill,B.P.,et al, 1981

Showing articles 600 to 650 of 2950 << Previous Next >>