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abdominal distention

acanthocytosis

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

adrenoleukodystrophy

advances in neurology

adverse drug reaction

alternating hemiplegia

Alzheimer's disease

Alzheimer's disease, pathogenesis

amyloid angiopathy, cerebral

amyloid beta protein

anatomy of

aneurysm, intracranial, familial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anorexia

anterior tibial muscle weakness

anticonvulsants

anticonvulsants, selection of

Arnold Chiari malformation

ataxia telangiectasia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

Bassen-Kornzweig syndrome

bitemporal visual field defect

blindness

blindness, sudden

blood dyscrasias, neurologic findings with

calcification, intracranial

Canavan's disease

carbon monoxide poisoning

CAT scan, contrast enhanced

CAT scan, dense artery sign

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

CAT scan, xenon-enhanced

cataracts

cataracts, congenital

caudate nucleus

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cause of death

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral infarction, small, deep

cerebral palsy

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

children

chorea

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10

coenzyme Q10 deficiency

cognition

color vision

color vision, impaired

coma

congenital birth defects

congenital myopathy

congestive heart failure

consanguinity

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

crying

cultured skin fibroblasts

cyanide poison

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalovirus infection

degenerative diseases of CNS

dementia

dementia, rapidly progressive

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diarrhea

differential diagnosis

diplegia, brachial

diplopia

distal muscle weakness

dizziness

DNA probes

drug induced neurologic disorders

drug induced neurologic disorders in children

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electroretinograph

encephalitis

encephalitis, human immunodeficiency virus type 1

encephalitis, Japanese

encephalitis, viral

encephalomyopathy

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

enkephalins

enzyme, defect

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

extraocular muscle atrophy

extraocular muscle lesion

eye closure

eye movement, disorders of

Fabry's disease

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fine motor function, impaired

foot ulcer, neuropathic

fourth ventricle, enlargement of

frataxin

free radical

Friedreich's ataxia

fundus, abnormality of

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic neurologic disorders

Hallervorden Spatz disease

headache, sudden onset of

headache, treatment of

hearing loss

hearing loss, bilateral

heart block

hemianopia

hemianopia, alternating

hemianopia, homonymous

hemianopia, recurrent

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

hiccoughs

hirsutism

histochemistry

histochemistry of muscle

HLA

human immunodeficiency virus type 1

Huntington's chorea

Hurler's syndrome

hydrocephalus

hydrocephalus, viral induced

hyperglycemia

hyperphagia

hyperreflexia

hypertensive encephalopathy

hypoparathyroidism, idiopathic

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance

impulsivity

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

infant and newborn with distress, neurologic prognosis in

infant, evaluation of

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intestinal pseudoobstruction

intracranial hypertension, benign

intrauterine

intraventricular hemorrhage

iron, brain

irritability

ischemic exercise test

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

L-dopa, drug interactions with and side effects of

Leber's hereditary optic neuropathy

leg numbness

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lethargy

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lewy body

lid closure, weakness of

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lipoma of skin

lipomatosis

lipomatosis, multiple symmetrical

liver disease

locus ceruleus, lesion of

lordosis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macular degeneration

magnetic susceptibility

malaise

malformation, CNS, congenital

manic-depressive

maple syrup urine disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

MELAS syndrome

Melkersson's syndrome

memory, impairment of

meningioma

meningitis

meningitis, CSF cell count-normal

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal lobe

mesial temporal sclerosis

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

methanol intoxication

metronidazole

microangiopathy, brain

microcephaly

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

movement disorder, extrapyramidal

MRI

MRI pattern

MRI, abnormal

MRI, abnormal, seizure causing

MRI, ADC maps

MRI, artifacts

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, muscle

MRI, optic nerve

MRI, paramagnetic effect

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

MRI, target sign

MRS

MRS, false negative

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle pain

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic syndrome

myelitis

myelitis, longitudinal

myopathy, centronuclear

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

nemaline rod myopathy

neoplasm, primary of CNS

nephrotic syndrome

neuritis

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

neuroradiology

neurotoxic

neurotoxin

next-generation sequencing

night blindness

nigrostriatal pathway

normal

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, rotary

obesity

occipital lobe

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic chiasm

optic chiasm, enlarged

optic chiasm, lesion of

optic disc edema

optic glioma

optic nerve

optic nerve, compression of

optic nerve, enhancement

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis

optic neuritis, bilateral

optic neuritis, treatment of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optic neuropathy, ischemic

optic neuropathy, toxic

optic tract, lesion of

orbicularis oculi muscle

orbit, lesions of

osmotic demyelination syndrome

overlap syndrome

owl's eye sign of spinal cord

oxidative phosphorylation

oxidative phosphorylation defect

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, etiology of

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

pigmentary retinopathy

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

POLG1 gene

polydactyly

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyalgia rheumatica

polymyositis

polyneuropathy

pons, lesion of

posterior cerebral artery territory infarction

posterior leukoencephalopathy syndrome

postictal encephalopathy

prevention of neurologic disorders

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

prostigmine

proteinuria

proximal muscle atrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

raphe nuclei

rapidly progressing neurologic illness

recurrent

red free light

red free light, fundus exam with

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

research

respiratory failure

respiratory tract infection

restless leg syndrome

retina, abnormal

retinal degeneration

retinal lesion

retinal nerve fiber layer

retinitis pigmentosa

retinopathy

reversible neurologic disorder

review article

Reye's syndrome

Reye's syndrome, adult

seizure, treatment of

senile plaques

sensorineural hearing loss

sensory loss

seronegative

short stature

single photon emission computed tomography

small vessel disease

sore throat

Southern immunoblot test

spastic diplegia

spasticity

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

standing difficulty

status epilepticus

Stephens syndrome

steroid therapy, CNS treatment and complications with

stimulation, deep brain

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subthalamic nucleus deep brain stimulation

succinate dehydrogenase deficiency

suck, poor

sudden death

sumatriptan

symmetric brain lesions

systemic illness

tapetoretinal degeneration

tau protein

tauopathy

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

tetany

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, intention

tremor, thalamic stimulation for suppression of

trinucleotide repeats

triptans

tuberous sclerosis

undiagnosed

Unverricht-Lundborg disease

upgaze, paralysis of

uremic encephalopathy

urine test for metabolic disorders

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual fields, constricted

visual loss

visual loss, progressive

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weaning from respirator, failure to

web sites

weight loss

Wernicke's encephalopathy

wheelchair

Whipple's disease

whistle, inability to

white matter disease

white matter disease, pattern

white matter disease, periventricular

wide based gait

winging of scapula

workup

Showing articles 50 to 100 of 194 << Previous Next >>

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

Response to Sumatriptan in Headache of MELAS Syndrome
Neurol 61:577-578, Iizuka,T.,et al, 2003

Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003

A Forearm Exercise Screening Test for Mitochondrial Myopathy
Neurol 58:1533-1538, Jensen,T.D.,et al, 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Mitochondrial Therapy for Parkinson Disease
Arch Neurol 59:1523, Rosenberg,R.N., 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Diffusion-weighted MR Imaging in a Case of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes
AJNR 22:269-272, Yonemura,K.,et al, 2001

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

Advances in the Genetics of Cerebrovascular Disease and Stroke
Neurol 56:997-1008, Hademenos,G.J.,et al, 2001

Mitochondrial Disease and Stroke
Stroke 32:2507-2510, Martinez-Fernandez,E.,et al, 2001

Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up
AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000

Mitochondrial Dysfunction in Bipolar Disorder
Bipolar Disord 2:180-190, Kato,T., 2000

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
JNNP 65:233-240, Sue,C.M.,et al, 1998

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Recurrent Strokes in a 34-Year-Old Man
Lancet 350:560, Chinnery,P.F.,et al, 1997

MELAS Presenting as Migraine Complicated by Stroke:Case Report
Neuroradiology 39:781-784, Ohnok,IK.,et al, 1997

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Optic Neuropathy
Neurol 46:315-322, Newman,N.J., 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
Neurol 46:826-828, Provenzale,J.M.,et al, 1996

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,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

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

High Resolution MRI of Anterior Visual Pathway in Pts with Optic Neuropathies Using Fast Spin Echo & Phased Array Local Coils
JNNP 58:562-569, Gass,A.,et al, 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
Stroke 26:1950-1952, Kosinski,C.,et al, 1995

Generalized Mitochondrial Dysfunction in Parkinson's Disease Detected by Magnetic Resonance Spectroscopy of Muscle
Neurol 45:2097-2099, Penn,A.M.W.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

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

Ekbom's Syndrome:Lypomas, Ataxia, and Neuropathy with MERRF
Muscle & Nerve 17:943-945994., Calabresi,P.,et al, 1994

Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutations in Multiple Sclerosis
Ann Neurol 36:109-112, Kellar-Wood,H.,et al, 1994

Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
Neurol 44:843-845, Hirano,M.,et al, 1994

The Syndrome of MELAS Presenting without Stroke
Arch Neurol 50:275-278, Mosewich,R.K.,et al, 1993

Cerebral Blood Flow in Mitochondrial Myopathy, Encephalopathy, lactic Acidosis, & Strokelike episodes
Stroke 24:304-309, Ooiwa,Y.,et al, 1993

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Showing articles 50 to 100 of 194 << Previous Next >>