Neudle.com: ophthalmoplegia chronic progressive external

Differential
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abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

abiotrophy

acanthocytosis

acetylcholine receptor

acetylcholine receptor antibody

acquired immunodeficiency syndrome

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

akinesia of eyelid function

algorithm

alpha-fetoprotein

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

ANA

anterior tibial muscle weakness

anti GQ1b IgG antibody

apraxia of eye movements

apraxia of eyelid opening

ataxia telangiectasia

atlanto axial dislocation, congenital

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

azathioprine

azidodeoxythymidine

basal ganglia, calcification of

basal ganglia, lesion, bilateral

basilar artery stenosis

Bassen-Kornzweig syndrome

brainstem, dysfunction

brainstem, lesion of

brainstem, tuberculoma of

calcification, intracranial

carcinoembryonic antigen

CAT scan, dense artery sign

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

cataracts

cataracts, congenital

cause of death

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, syndrome

celiac disease, childhood

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebritis

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot's sign

chemosis

cherry red spot-myoclonus syndrome

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 11

chromosome 14

chronic progressive external ophthalmoplegia

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10 deficiency

cognition

cogwheel rigidty

collagen vascular disease

congestive heart failure

conjunctival biopsy

conjunctival injection

consanguinity

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cytochrome c oxidase, deficiency

deafmute

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, rapidly progressive

diabetes mellitus

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

digitalis intoxication

diplopia

disorientation

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dysthyroid ocularmyopathy

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electroretinograph

emtricitabine

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalocele

encephalopathy

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

exercise intolerance

extraocular muscle atrophy

extraocular muscle enlargement

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye closure

eye movement, disorders of

eye, pain in

face, elongated

face, numbness of

facial appearance, abnormal

facial nerve

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fine motor function, impaired

Fisher C.M.

Fisher's syndrome

fistula, arterio-venous, carotid-cavernous

foot drop

Friedreich's ataxia

fundus, abnormality of

gait disorder

gait, apraxic

gammaglobulin therapy, intravenous

gangliosides

gangliosidosis GM1

gangliosidosis, generalized

gargoylism

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

granulomatosis with polyangiitis

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome, ophthalmoplegia in

Hallervorden Spatz disease

Hallgren's syndrome

headache

headache, chronic

headache, progressive

headache, sudden onset of

hemianopia, homonymous

hemianopia, transient

hemiparesis

hepatic failure

hepatomegaly

heralding manifestation

hippus

Hispanics

histochemistry of muscle

HLA

Horner's syndrome

human immunodeficiency virus type 1

hypoparathyroidism, idiopathic

iatrogenic neurologic disorders

ideomotor apraxia

idiopathic inflammatory orbital disease

immunosuppressive agents

impulsivity

inattention

inclusion body myositis

infantile tremor syndrome

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal pseudoobstruction

intracerebral hemorrhage

iridoplegia

ischemic exercise test

jaw jerk, abnormal

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

keratoconus

lactic acidemia

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

Leber's hereditary optic neuropathy

Leigh's disease

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

lid closure, weakness of

life expectancy

lipoprotein receptor-related protein 4

locked-in syndrome

lordosis

lymphadenopathy, hilar

lymphoma

macular degeneration

malabsorption

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

medulla oblongata, lesion of

MELAS syndrome

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

mental status, abnormal

MERRF syndrome

metabolic acidosis

metachromatic leukodystrophy

midbrain

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

migraine

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

MNGIE syndrome

molecular genetics

monoclonal antibodies

mononeuropathy multiplex

mortality

motor neuron disease

motor neuron disease, juvenile form

movement disorder

movement disorder, extrapyramidal

MRI

MRI pattern

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, extraocular muscle enhancement

MRI, muscle

MRI, negative

mucopolysaccharidoses

multicore myopathy

multiple sclerosis

multiple sclerosis, acute

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle pain

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

MuSK antibodies

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

myasthenia gravis, variants

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, mitochondrial

nemaline rod myopathy

nerve conduction studies

neuritis

neuroaxonal dystrophy

neurocutaneous disease

neuroendocrinology

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 disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

obesity

obicularis oculi, weakness of

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculocephalic reflex

oculopharyngeal muscular dystrophy

old age, neurology of

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, painful

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

ophthalmoplegia, unilateral

optic atrophy

optic disc edema

optic nerve

optic nerve, lesion of

optic neuritis

optic neuropathy

orbicularis oculi muscle

orbit

orbit, inflammation in

orbit, lesions of

orbital apex

orbital apex syndrome

pachymeningitis, cranial

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis

paraparesis, spastic

parasellar syndrome

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

pathology

penguin silhouette sign

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

pigmentary retinopathy

plasmapheresis

pleocytosis of cerebrospinal fluid

POLG1 gene

polydactyly

polymerase chain reaction

polymyalgia rheumatica

polymyositis

polyneuropathy

polyneuropathy, chronic relapsing

pons, lesion of

practice guidelines

pregnancy, neurologic complications in

progeria

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

proptosis, bilateral

proptosis, unilateral

prostigmine

proteinuria

proximal muscle atrophy

pseudobulbar palsy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

quality of life

radiation hypersensitivity

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

reticular activating system

saccadic eye movements, abnormal

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure

seminoma

sensorineural hearing loss

sequencing difficulty

skin, lesions in neurologic disorders

skin, tight

Southern immunoblot test

spasticity

Spielmeyer Vogt syndrome

spina bifida

spinal muscular atrophy

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

squamous cell carcinoma of head and neck

steroid therapy, CNS treatment and complications with

strabismus

strokelike episodes

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subarachnoid hemorrhage

succinate dehydrogenase deficiency

sudden death

symmetric brain lesions

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

tau protein

telangiectases

temporal lobe, lesion

tetany

thalamus, lesion of-bilateral

tongue, fasciculations of

transverse smile

treatment of neurologic disorder

tremor

trigeminal nerve

trigeminal nerve, lesion of

trinucleotide repeats

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

ulcerative colitis

undiagnosed

Unverricht-Lundborg disease

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual loss

visual loss, slow-unilateral

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

web sites

weight loss

wheelchair

whistle, inability to

white matter disease

white matter disease, pattern

wide based gait

winging of scapula

xanthopsia

Showing articles 950 to 1000 of 6084 << Previous Next >>

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

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

Non-Invasive Diagnosis of Internal Carotid Artery Dissections
JNNP 55:98-104, Mullges,W.,et al, 1992

Spinal Cord Syphilis Associated with Human Immunodeficiency Virus Infection:A Treatable Myelopathy
Am J Med 91:101-103, Berger,J.R., 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Presence of HTLV-I Proviral DNA in Central Nervous System of Patients with HTLV-I-Associated Myelopathy
Ann Neurol 31:39-45, Kira,J.,et al, 1992

Octreotide and Graves'Ophthalmopathy and Pretibial Myxoedema
BMJ 304:158, Chang,T.C.,et al, 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

Clinicopath Conf
Spinal Dural Arteriovenous Fistula, Case 12-1992, NEJM 326:816-824992., , 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Diagnosis and Treatment of Ossification of the Posterior Longitudinal Ligament of the Spine:8 Cases and Lit Review
Am J Med 92:296-306, Trojan,D.A.,et al, 1992

Paramedian Thalamopeduncular Infarction:Clinical Syndromes and Magnetic REsonance Imaging
Ann Neurol 32:162-171, Tatemichi,T.K.,et al, 1992

Early Clinical Differentiation of Cerebral Infarction from Severe Atherosclerotic Stenosis and Cardioembolism
Stroke 23:486-491, Timsit,S.G.,et al, 1992

Clinicopath Conf
Left Middle Cerebral Art Territory Infarct, Athero Stenosis of Cavernous Int Carotid Art, Case 26-19, 2, M 326:1762-1769,1992., 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Midbrain Myasthenia:Fatigable Ptosis, 'Lid Twitch'Sign, and Ophthalmoparesis From a Dorsal Midbrain Glioma
Neurol 42 917-919, Ragge,N.K.&Hoyt,W.F., 1992

Neuro-Ophthalmic Features of Carotid Cavernous Fistulas and Their Treatment by Endoarterial Balloon Embolisation
JNNP 55:553-556, Brosnahan,D.,et al, 1992

Evolution of Oculomotor Nerve palsies
J Clin Neuro-Ophthalmol 12:21-25, Capo,H.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Cervical Disc Herniation Presenting as a Mass Lesion Posterior to the Odontoid Process
J Neurosurg 75:954-959, Rosenberg,W.S.,et al, 1991

Neurological Paraneoplastic Syndromes in Patients with Small Cell Lung Cancer, A Prospective Survey of 150 Pts
JNNP 54:764-767, Elrington,G.M.,et al, 1991

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

Intense Immunosuppression in Chronic Progressive Multiple Sclerosis:The Kaiser Study
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Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

Radiation Myelopathy:Significance of Gadolinium-DTPA Enhancement in the Diagnosis
Neuroradiology 33:286-289, Michikawa,M.,et al, 1991

The Spectrum of Vertical Gaze Palsy Following Unilateral Brainstem Stroke
Neurol 41:1229-1234, Hommel,M.&Bogousslavsky,J., 1991

Ocular Motor Abnormalities in Human Immunodeficiency Virus Infection
Ann Neurol 30:130-138, Merrill,P.T.,et al, 1991

Neuro-Ophthalmologic Signs of AIDS:50 patients
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
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Prevalence and Incidence of Becker Muscular Dystrophy
Lancet 337:1022-1024, Bushby,K.M.D.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Plasma Exchange in Chronic Progressive Multiple Sclerosis:A Long-Term Study
Neurol 41:409-414, Khatri,B.O.,et al, 1991

HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis in the United States
Neurol 41:1355-1357, Janssen,R.S.,et al, 1991

HTLV-I-Associated Myelopathy Endemic in Texas-Born Residents and Isolation of Virus from CSF Cells
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Association Between Tumor Necrosis Factor-x and Disease Progression in Patients with Multiple Sclerosis
NEJM 325:467-472, Shareif,M.K.&Hentges,R., 1991

A Placebo-Controlled, Double-Blind, Randomized, Two-Center, Pilot Trial of Cop 1 in Chronic Progressive MS
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Cyclosporine-Assoc Seizures in Bone Marrow Transplant Given Busulfan & Cyclophosphamide Prep
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The Canadian Coop Trial of Cyclophosphamide and Plasma Exchange in Progr MS
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Showing articles 950 to 1000 of 6084 << Previous Next >>