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

cerebellar vermis

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

delay in diagnosis

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, eosinophilic intranuclear

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

paroxysmal neurologic deficits

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 frequency

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 1800 to 1850 of 2976 << Previous Next >>

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Botulinum Toxin Treatment of Essential Head Tremor
Neurol 45:822-824, Pahwa,R.,et al, 1995

The Effect of Nimodipine on Essential Tremor
Neurol 45:1523-1525, Biary,N.,et al, 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
Neurol 45:2018-2023, Gouider,R.,et al, 1995

Acute Anterior Interosseous Neuropathy in Pt with Hereditary Neuropathy with Liability to Press Palsies:Clin & EMG Study
Muscle & Nerve 18:1329-1331995., Felice,K.J., 1995

Diagnostic Value of Detecting JC Virus DNA in Cerebropsinal Fluid of Patients with Progressive Multifocal Leukoencephalopathy
J Clin Microbiol 33:484-486, Fong,I.W.,et al, 1995

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Hypertensive Encephalopathy After Bilateral Carotid Endarterectomy
Stroke 26:488-491, Ille,O.,et al, 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Dysphagia Caused by an Anterior Cervical Osteophyte:Case Report
Neuroradiology 37:58-59, Kodama,M.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

Progressive Multifocal Leukoencephalopathy:Unusual MR Findings
J Comput Assist Tomogr 19:302-305, Ng,S.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

JC Virus DNA in CSF of HIV-Infected Pts:Predictive Value for Progressive Multifocal Leukoencephalopathy
Ann Neurol 37:395-399, McGuire,D.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Multifocal Inflammatory Leukoencephalopathy Associated with Levamisole Therapy
Neurol 45:374-376, Kimmel,D.W.,et al, 1995

Bilateral Simultaneous Optic Neuropathy in Adults:Clinical, Imaging, Serological, and Genetic Studies
JNNP 58:70-74, Morrissey,S.P.,et al, 1995

Zinc-Induced Deterior in Wilson's Disease Aborted by Trtm with Penicillamine, Dimercaprol, & A Novel Zero Copper Diet
Arch Neurol 52:10-11, Walshe,J.M.,et al, 1995

A Positron Emission Tomography Study of Cerebral Activation Associated with Essential and Writing Tremor
Arch Neurol 52:299-305, Wills,A.J.,et al, 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Lower Cognitive Performance in Normal Older Adult Male Twins Carrying the Apolipoprotein E-E4 Allele
Arch Neurol 51:1189-1192, Reed,T.,et al, 1994

Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
Neurol 44:2159-2164, DalPan,G.J.,et al, 1994

Neurological Complications of Organ Transplantation
Ann Neurol 36:688-703, Patchell,R.A., 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Neurologic Manifestations of HIV Infection
Ann Int Med 121:769-785, Simpson,D.M.&Tagliati,M., 1994

Isolated Motor Control Dysfunction Related to Progressive Multifocal Leukoencephalopathy During AIDS with Normal MRI
Neurol 44:2352-2355, deToffol,B.,et al, 1994

Worsening of Neurologic Syndrome in Patients with Wilson's Disease with Initial Penicillamine Therapy
Arch Neurol 44:490-493, Brewer,G.J.,et al, 1994

Increased Risk of Parkinson's Disease in Parents and Siblings of Patients
Ann Neurol 36:659-661, Payami,H.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

In Situ Polymerase Chain Reaction Demo of JC Virus in Progressive Multifocal Leukoencephalopathy, Incl Index Case
Ann Neurol 36:670-673, Ueki,K.,et al, 1994

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

The Neurogenetic Genie:Testing for Huntington's Disease Mutation
Neurol 44:1369-1373, 1533-15361994., Hersch,S.,et al, 1994

Showing articles 1800 to 1850 of 2976 << Previous Next >>