Neudle.com: mitochondrial encephalomyopathy

Differential
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abdominal distention

acanthocytosis

adrenoleukodystrophy

adverse drug reaction

aneurysm, intracranial, familial

anorexia

anticonvulsants

anticonvulsants, selection of

aphasia

areflexia

arginine

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, xenon-enhanced

cataracts

caudate nucleus

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cause of death

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 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

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

congestive heart failure

consanguinity

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

crying

cultured skin fibroblasts

cyanide poison

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

degenerative diseases of CNS

dementia

dementia, rapidly progressive

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diarrhea

differential diagnosis

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electroretinograph

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalomyopathy

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

enkephalins

enzyme, defect

epilepsia partialis continua

exercise

exercise intolerance

exome sequencing

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

fourth ventricle, enlargement of

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

hypoparathyroidism, idiopathic

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance

impulsivity

inborn errors of metabolism

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

intraventricular hemorrhage

iron, brain

irritability

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

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

lid closure, weakness of

lipid storage disorder of CNS

liver disease

macular degeneration

magnetic susceptibility

malformation, CNS, congenital

manic-depressive

maple syrup urine disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

MELAS syndrome

Melkersson's syndrome

memory, impairment of

meningioma

mental retardation

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methanol intoxication

metronidazole

microangiopathy, brain

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, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

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

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle pain

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic syndrome

myelitis

myelitis, longitudinal

myopathy, mitochondrial

neoplasm, primary of CNS

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

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

neuroradiology

neurotoxin

next-generation sequencing

night blindness

normal

nutritional deficiency

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

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, nutritional

optic neuropathy, toxic

optic tract, lesion of

orbicularis oculi muscle

osmotic demyelination syndrome

overlap syndrome

owl's eye sign of spinal cord

Parkinsonism syndrome

peroxisomal disease

personality change

pes cavus

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

polyneuropathy

pons, lesion of

posterior cerebral artery territory infarction

prevention of neurologic disorders

prognosis

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

prostigmine

proteinuria

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

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

respiratory failure

respiratory tract infection

restless leg syndrome

retina, abnormal

retinal degeneration

retinal lesion

retinal nerve fiber layer

retinitis pigmentosa

retinopathy

reversible neurologic disorder

seizure, treatment of

sensorineural hearing loss

sensory loss

seronegative

short stature

single photon emission computed tomography

small vessel disease

Southern immunoblot test

spasticity

speech, loss of

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

standing difficulty

status epilepticus

Stephens syndrome

steroid therapy, CNS treatment and complications with

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subependymal nodules

substantia nigra

succinate dehydrogenase deficiency

suck, poor

sudden death

sumatriptan

symmetric brain lesions

systemic illness

tapetoretinal degeneration

temporal lobe, lesion

term infant

tetany

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

titubation

tonic spasms

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

triptans

tuberous sclerosis

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

white matter disease

white matter disease, pattern

white matter disease, periventricular

wide based gait

workup

Showing articles 150 to 195 of 195 << Previous

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Epilepsy in Adults with Mitochondrial Disease: A Cohort Study
Ann Neurol 78:949-957, Whittaker, R.G.,et al, 2015

Rapidly Progressive Leukoencephalopathy in Mitochondrial Complex I Deficiency
Neurol 81:e10-e11, Baertling, F.,et al, 2013

Clinico-Radiological Spectrum of Bilateral Temporal Lobe Hyperintensity: A Retrospective Review
Br J Radiol 85:e782-e792, Sureka, J. & Jakkani, R.K., 2012

Alzheimers Disease
NEJM 362:329-344, Querfurth,H.W. &LaFerla,F.M., 2010

Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
Clin Radiol 63:1245-1253, Sheerin,F.,et al, 2008

Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine
AJNR 26:695-701,687, Tardieu,M.,et al, 2005

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Proton MR Spectroscopy in the Diagnostic Evaluation of Suspected Mitochondrial Disease
AJNR 24:33-41, Lin,D.D.M.,et al, 2003

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

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

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

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

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

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

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

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

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

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

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

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

Mitochondrial Involvement in Parkinson's Disease:The Controversy Continues
Neurol 43:2170-2172, DiMauro,S., 1993

Evidence for Mitochondrial Dysfunction in Patients with Alternating Hemiplegia of Childhood
Ann Neurol 33:604-607, Arnold,D.L.,et al, 1993

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
Am J Med 92:167-172, Harle,J.,et al, 1992

Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
Neurol 42:128-130, Riggs,J.E.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Adult Reye's Syndrome:A Review with New Evidence for a Generalized Defect in Intramitochondrial Enzyme Processing
Neurol 41:1815-1821, VanCoster,R.N.,et al, 1991

Mitochondrial Oxidative Phosphorylation Defects in Parkinson's Disease
Ann Neurol 30:332-339, 3301991., Shoffner,J.M.,et al, 1991

Mitochondrial Dysfunction in Multiple Symmetrical Lipomatosis
Ann Neurol 29:566-569, Berkovic,S.F.,et al, 1991

Depletion of Muscle Mitochondrial DNA in AIDS Patients with Zidovudine-Induced Myopathy
Lancet 337:508-510, Arnaudo,E.,et al, 1991

Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction
Ann Neurol 29:606-614, Mhiri,C.,et al, 1991

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Peripheral Neuropathy Associated with Mitochondrial Myopathy
Ann Neurol 20:249-257, Yiannikas,C.,et al, 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Showing articles 150 to 195 of 195 << Previous