Neudle.com: hereditary diffuse leukoencephalopathy

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Differential
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abdominal distention

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

affect, inappropriate

Aicardi-Goutieres syndrome

Alexanders disease

Alexanders disease, adult onset

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anti MAG antibodies

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, paroxysmal

ataxia, progressive

ataxia, sensory

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autonomic dysfunction

autosomal dominant leukodystrophy

axonal degeneration

axonal spheroid

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Binswanger disease

biologic markers

bladder dysfunction

bone marrow transplantation

brainstem, atrophy

brainstem, lesion of

brucellosis, nervous system involvement with

calcification, intracranial

calcification, intracranial, rim

calcifications, intracranial, punctate

Canavan's disease

CAT scan, abnormal

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, 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

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

compression fracture

compression neuropathy

contractures, joint

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cyst, benign intracranial

cyst, cortical parenchyma

cyst, parenchymal

cystic infarction

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delayed dentition

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

diplopia, transient

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dystonia, children

dystroglycanopathies

electron microscopy

emotional lability

enzyme, muscle disease

epicanthal folds

episodic disorders

episodic neurologic deficits

evoked potentials

exome sequencing

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

failure to thrive

fatty acid dehydrogenase deficiency

feeding disorder

fever, recurrent

flow study, carotid artery

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

galactocerebrosidase

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

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

growth retardation

gyrus, abnormal

head circumference

hemiparesis, transient

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

hormone replacement

human immunodeficiency virus type 1

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

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic intracranial pachymeningitis

hypomyelination

hypoparathyroidism

hypotension, systemic

hypotonia, infants

immunodeficiency

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

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles, wasting of

Kearns-Sayre syndrome

Krabbe's disease

lacunar infarction

laughing, pathologic

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukodystrophy, pigmented orthochromatic

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

life expectancy

lysosomes, abnoral

manic-depressive

maple syrup urine disease

Marinesco-Sjogren 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

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine with aura

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

movement disorder

MRI, black holes on

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, gradient-echo

MRI, high signal foci on

MRI, spinal cord

MRI, susceptibility weighted

MRI, target sign

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

myelination of nervous system

myelitis, longitudinal

myelitis, transverse

myeloneuropathy

myelopathy, chronic progressive

nausea and vomiting

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, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

nystagmus, rotary

ocular dysmetria

oculodentodigital dysplasia

old age, neurology of

ophthalmoplegia

optic atrophy, bilateral

optic neuritis, bilateral

optic neuropathy

orthostatic hypotension

overlap syndrome

owl's eye sign of spinal cord

pain, abdominal

palatal myoclonus

palmoplantar keratoderma

paralysis, recurrent

paraparesis, familial spastic

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive material in the brain

Pelizaeus Merzbacher

peroxisomal disease

personality change

phenylketonuria

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polyglucosan body

polyglucosan body disease

polymerase chain reaction

pons, lesion of

posterior fossa, lesion of

posterior leukoencephalopathy syndrome

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary familial brain calcification

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

psychotic behavior

pupil, dilated, bilateral

pupil, dilated, episodic

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriplegia, transient

ragged-red fibers

release phenomena

retina, abnormal

retinal degeneration

reversible neurologic disorder

Rosenthal fibers

saccadic eye movements, abnormal

Schilder's disease

sedimentation rate, elevated

seizure, drug resistance

self-mutilation

sensorineural hearing loss

Sjogren-Larsson syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

small vessel disease

small vessel disease, cerebral

somatosensory evoked potentials

spastic diplegia

speech disorder, childhood

spinal cord, lesion of

spinocerebellar ataxia

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

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

symmetric brain lesions

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

telangiectases, retinal

temporal lobe, lesion, bilateral

testicular biopsy

thalamus, lesion of

thalamus, lesion of-bilateral

tomaculous neuropathy

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

treatment resistant

tremor, cerebellar

tremor, intention

trichopoliodystrophy

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

very long chain fatty acids

vibratory sensation, abnormal

visceral neuropathy

vision loss, sequential

visual acuity, decreased

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin E deficiency

walking, difficulty with

water channel antibodies

weakness, generalized

weakness, progressive

weaning from respirator, failure to

white matter disease

white matter disease, location

white matter disease, pattern

white matter disease, subcortical

white matter disease, unilateral

wide based gait

X-linked neuropathy

Showing articles 1250 to 1300 of 2965 << Previous Next >>

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

Electrocardiogram in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients Without Any Clinical Evidence of Coronary Artery Disease
Stroke 37:1100-1102, Cumurciuc,R.,et al, 2006

Common Misdiagnosis of a Common Neurological Disorder: How Are We Misdiagnosing Essential Tremor?
Arch Neurol 63:1100-1104, Jain,S.,et al, 2006

Collaborative Analysis of a-Synuclein Gene Promotor Variability and Parkinson Disease
JAMA 296:661-670, Maraganore,D.M.,et al, 2006

Restless Legs Syndrome: Is Treatable But Under-Recognised
BMJ 333:457-458, Medcalf,P. &Bhatia,K.P., 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

Postpartum Eclampsia of Late Onset
BMJ 331:1070-1071, Munjuluri,N.,et al, 2005

Sustained Recovery of Progressive Multifocal Leukoencephalopathy After Treatment with IL-2
Neurol 65:1510, Kunschner,L. &Scott,T.F., 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Neuroblastoma -- from Genetic Profiles to Clinical Challenge
NEJM 353:2215-2217, Kushner,B.H. &Cheung,N.-K.V., 2005

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 65:1863-1872, McKeith,I.G.,et al, 2005

The Role of Levodopa in the Management of Dementia With Lewy Bodies
JNNP 76:1200-1203, Moloy,S.,et al, 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Progressive Multifocal Leukoencephalopathy After Natalizumab Therapy for Crohns Disease
NEJM 353:362-368, Van Assche,G.,et al, 2005

Progressive Multifocal Leukoencephalopathy in a Patient Treated with Natalizumab
NEJM 353:375-381, Langer-Gould,A.,et al, 2005

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Practice Parameter:Therapies for Essential Tremor
Neurol 64:2008-2020, Zesiewicz,T.A.,et al, 2005

Quality of Life in Patients with Charcot-Marie-Tooth Disease
Neurol 65:922-924, Vinci,P.,et al, 2005

Large Cerebral Artery Involvement in CADASIL
Neurol 65:1322-1324, Choi,E.J.,et al, 2005

Intracerebral Haemorrhage in CADASIL
JNNP 76:1606-1607, Ragoschke-Schumm,A.,et al, 2005

NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
Neurol 65:681-689, 662, Sahenk,Z.,et al, 2005

Postcarotid Endarterectomy Hyperperfusion or Reperfusion Syndrome
Stroke 36:21-26, Karapanayiotides,T.,et al, 2005

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

Delusions and Hallucinations in Dementia with Lewy Bodies: Worsening with Memantine
Neurol 65:481-482, Ridha,B.H.,et al, 2005

Creutzfeldt-Jakob Disease Mimicking Radiologic Posterior Reversible Leukoencephalopathy
Neurol 65:329, Sibon,I.,et al, 2005

NOA-03 Trial of High-Dose Methotrexate in Primary Central Nervous System Lymphoma:Final Report
Ann Neurol 57:843-847, Herrlinger,W.,et al, 2005

Proton MR Spectroscopy in Wilson Disease: Analysis of 36 Cases
AJNR 26:1066-1071, Lucato,L.T.,et al, 2005

Proton MR Spectroscopic Imaging Depicts Diffuse Axonal Injury in Children with Traumatic Brain Injury
AJNR 26:1276-1285, Holshouser,B.A.,et al, 2005

Atypical PML Leading to a Diagnosis of Common Variable Immunodeficiency
Neurol 64:1661, Snyder,M.D.,et al, 2005

FDA Public Health advisory-Suspended Marketing of Tysabri (natalizumab)
www.fda.gov/cder/drug/advisory/natalizumab.htm.,(Feb 28), US Food and Drug Admin., 2005

Autonomic Peripheral Neuropathy
Lancet 365:1259-1270, Freeman,R., 2005

Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
NEJM 352:686-691, de Jong,M.D., et al, 2005

Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Spontaneous Lobar Haemorrhage in CADASIL
JNNP 76:456-457, MacLean,A.V.,et al, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

Neurologic Symptoms are Common During Gestation and Puerperium in CADASIL
Neurol 64:1441-1443, Roine,S.,et al, 2005

Genetic Factors in Alzheimer's Disease
NEJM 352: 862-863, 884, Bird, T., 2005

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Spontaneous Lobar Hemorrhage in CADASIL
JNNP 76:456-457, MacLean,A.V., et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
Arch Neurol 62:1091-1094, Peters,N.,et al, 2005

Showing articles 1250 to 1300 of 2965 << Previous Next >>