Neudle.com: leukodystrophy

Differential
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abdominal distention

abscess, intracerebral

abulia

acrocyanosis

acute disseminated encephalomyelitis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, inappropriate

Aicardi-Goutieres syndrome

akinetic mute

Alexanders disease

Alexanders disease, adult onset

anterior tibial muscle weakness

arylsulfatase A pseudodeficiency

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autonomic dysfunction

axonal spheroid

Babinski sign

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bone marrow transplantation

calcification, intracranial

calcifications, intracranial, punctate

Canavan's disease

carcinoma of pancreas

CAT scan

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

celiac disease, adult

centrum semiovale

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral edema, cytotoxic

cerebral edema, vasogenic

cerebral venous infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

chemotherapy, CNS treatment and complications with

chilbran skin lesions

children

cholelithiasis

chorea

chromosomal abnormality

chronic graft versus host disease

Clinical Pathologic Conference(C.P.C.)

color vision, impaired

controversies in neurology

cornea, abnormal

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve enhancement

cranial nerve enlargement

creatine phosphokinase(CPK)elevated

cry, abnormal

crying

crying, pathologic

cultured skin fibroblasts

cytochrome c oxidase, deficiency

deafness

decerebrate posture

deep gray nuclei

degenerative diseases of CNS

delayed dentition

dementia

dementia, childhood

dementia, frontal lobe type

dementia, presenile

dementia, subcortical

dementia, thalamic

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

diarrhea

diet

differential diagnosis

difficulty going down stairs

distal muscle weakness

DNA probes

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

dysarthria

dysarthria-clumsy hand syndrome

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

emergencies, ocular

empyema, subdural

encephalitis

encephalitis, diagnosis of

encephalitis, viral

encephalopathy

encephalopathy, progressive

enzyme treatment

enzyme, defect

epicanthal folds

epidemiology of neurology

episodic neurologic deficits

extraocular muscle lesion

Fabry's disease

facial appearance, abnormal

fatty acid, elevated plasma content

feeding disorder

fever

flow study, carotid artery

fluorescein angiography

fracture, pathologic

frontal lobe, anatomy and physiology

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

gangliosidosis, generalized

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

GFAP gene

glioma

globoid cells

growth hormone deficiency

Hallervorden Spatz disease

hallucination

hallucination, auditory

hearing problems in children

hemiparesis

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hydrocephalus, exvacuo

hyperadrenalism

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunofluorescent exam of CSF cells

immunosuppressive agents

inattention

inborn errors of metabolism

inclusion bodies, intracytopasmic

incoordination

intellectual deficit

intellectual deterioration

intelligence testing in children

interferon alpha

internal capsule

intestinal pseudoobstruction

intrathecal chemotherapy

intrauterine

irritability

Kearns-Sayre syndrome

Krabbe's disease

lactic acidemia

lacunar infarction

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukodystrophy, 4H

leukodystrophy, pigmented orthochromatic

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

level of consciousness, decreased

lipid storage disorder of CNS

lipomembranous polycystic osteodysplasia

liver transplantation

Lorenzo's oil

lysosomal storage disease

lysosomes, abnoral

macrocephaly

meconium staining

medulla oblongata, lesion of

MELAS syndrome

memory, impairment of

meningitis

meningitis, aseptic

meningitis, leptospira

meningitis, noninfectious

meningoencephalitis

meningoencephalitis, diagnosis of

mental retardation

mental status, abnormal

merosin

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

methotrexate

microcephaly

microdontia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, spinal cord

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

mumps virus

muscle biopsy

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, Duchenne

myelin basic protein

myelinolysis, extrapontine

myopathy, mitochondrial

myopia

N-acetyl-L-aspartic acid

nausea and vomiting

neoplasm, intracranial

nerve biopsy

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic testing

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

neuropsychiatry

neurotoxic

neurotoxin

next-generation sequencing

Niemann-Pick disease

nystagmus

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

occupational neurologic disorders

oculodentodigital dysplasia

oleic acid therapy

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

organ transplantation

ovarian dysgenesis

pain, abdominal

palatal myoclonus

palmoplantar keratoderma

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paroxysmal neurologic deficits

PAS positive material in the brain

phenylketonuria, adult onset

pheochromocytoma

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

POLR3B

pons, lesion of

porphyria

posterior fossa, lesion of

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

pseudobulbar palsy

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

psychosis, cause of

pterygoid muscle weakness

ptosis

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyrimethamine

quadriparesis

radiation therapy, CNS treatment and complications with

radioimmunoassay

ragged-red fibers

renal failure

respiratory tract infection

retinal vasculopathy with cerebral leukodystrophy

sensorineural hearing loss

skin, lesions in neurologic disorders

solvent

somatosensory evoked potentials

somnolence

spasticity

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord

spinal cord, lesion of

spinal cord, pathologic exam of

spongy degeneration of brain

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

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

subcortical U fibers

succinate dehydrogenase deficiency

sudanophilic leukodystrophy

sural nerve

symmetric brain lesions

syndactyly

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

teeth, number of in infants

temporal lobe, lesion

temporal lobe, lesion, bilateral

testicular atrophy

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

top of the basilar syndrome

toxins, nervous system

transient neurologic deficit

transitional sclerosis

treatment of neurologic disorder

tremor

tremor, intention

tripping

umbilical-cord blood transplantation

uncal herniation

urea-cycle enzymopathies

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

uveitis

vanishing white matter

very long chain fatty acids

vibratory sensation, abnormal

viral infection, CNS

visual evoked response

walking, difficulty with

Wallerian degeneration

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Wernicke's encephalopathy

white matter disease

white matter disease, pattern

white matter disease, periventricular

white matter disease, unilateral

wide based gait

writing

Showing articles 50 to 100 of 146 << Previous Next >>

Clinicopath Conf,Acute Hemorrhagic Leukoencephalitis,Case 1-1999
NEJM 340:127-135, , 1999

A New Metabolite Contributing to N-Acetyl Signal in 1H MRS of the Brain in Salla Disease
Neurol 52:1668-1672, Varho,T.,et al, 1999

Optic Nerve Enlargement in Krabbe's Disease
AJNR 20:1228-1231, Jones,B.V.,et al, 1999

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Long-Term Stabilization After Bone Marrow Transplantation in Juvenile Metachromatic Leukodystrophy
Arch Neurol 55:98-99, Kidd,D.,et al, 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

MR of Childhood Metachromatic Leukodystrophy
AJNR 18:733-738, Kim,T.S.,et al, 1997

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Leukodystrophy in Patients with Ovarian Dysgenesis
Ann Neurol 41:654-661, Schiffman,R.,et al, 1997

Late Juvenile Metachromatic Leukodystrophy Treated with Bone Marrow Transplantation:A 4-Year Follow-up Study
Neurol 46:254-256, Navarro,C.,et al, 1996

Progressive Familial Leukodystrophy of Late Onset
Neurol 46:429-434, Knopman,D.,et al, 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Immunosuppression-Induced Leukoencephalopathy from Tacrolimus (FK506)
Ann Neurol 40:575-580, Small,S.L.,et al, 1996

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,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 Symptoms of Adult Metachromatic Leukodystrophy and Arylsulfatase A Pseudodeficiency
Arch Neurol 52:408-413, Hageman,A.T.M.,et al, 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, Lossos,A.,et al, 1995

Serial MR After Bone Marrow Transplantation in Two Patients with Metachromatic Leukodystrophy
AJNR 15:1929-1932, Stillman,A.E.,et al, 1994

Characteristics of the Dementia in Late-Onset Metachromatic Leukodystrophy
Neurol 44:662-665, Shapiro,E.G.,et al, 1994

Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
Arch Neurol 51:757-766, Schwankhaus,J.D.,et al, 1994

Diffuse Leukodystrophy with a Large-Scale Mitochondrial DNA Deletion
Lancet 343:1397-1398, Nakai,A.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

X-Linked Adrenoleukodystrophy:Adult Cerebral Variant
Neurol 43:1518-1522, Farrell,D.F.,et al, 1993

A Two-Year Trial of Oleic and Erucic Acids ("Lorenzo's Oil") as Treatment for Adrenomyeloneuropathy
NEJM 329:745-752, 8011993., Aubourg,P.,et al, 1993

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Adult-Onset Metachromatic Leukodystrophy Presenting as Isolated Peripheral Neuropathy
Neurol 42:1396-1398, Fressinaud,C.,et al, 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,et al, 1992

Longitudinal Neurophysiologic Studies in Pt with Metachromatic Leukodystrophy Following Bone Marrow Trnspl
Arch Neurol 49:1088-1092, Dhuna,A.,et al, 1992

Late Onset Globoid Cell Leukodystrophy
JNNP 54:1011-1012, Grewal,R.P.,et al, 1991

Nystagmus of Pelizaeus-Merzbacher Disease
Arch Neurol 48:87-91, Trobe,J.D.,et al, 1991

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Membranous Lipodystrophy:MR Imaging Appearance of the Brain
Radiology 180:793-797, Araki,T.,et al, 1991

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults
Neurol 41:794-798, Coker,S.B., 1991

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

Adrenomyeloneuropathy Presenting as Addison's Disease in Childhood
NEJM 322:13-16, 54-551990., Sadeghi-Nejad,A.&Senior,B., 1990

The Leukodystrophies
NEJM 322:54-55, Menkes,J.H., 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990

MR Findings in Globoid Cell Leucodystrophy
Neuroradiology 32:520-522, Demaerel,Ph.,et al, 1990

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

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

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Adult Metachromatic Leukodystrophy, Value of Computed Tomographic Scanning & Magnetic Resonance Imaging of the Brain
Arch Neurol 44:225-227, Waltz,G.,et al, 1987

Metachromatic Leukodystrophy:Conduct Disorder Progressing to Dementia
JNNP 50:488-510, Fisher,N.R.,et al, 1987

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Showing articles 50 to 100 of 146 << Previous Next >>