Neudle.com: "chronic progressive external ophthalmoplegia"

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abdominal distention

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acetylcholine receptor

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anterior tibial muscle weakness

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arm swing, reduced

arrhythmia, cardiac

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cherry red spot-myoclonus syndrome

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

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conjunctival biopsy

conjunctival injection

cornea, abnormal

corpus callosum, lesion of

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creatine phosphokinase isoenzyme elevation

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deep gray nuclei

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digitalis intoxication

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distal muscle weakness

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dysthyroid ocularmyopathy

edema, periorbital

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

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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 movement, disorders of

face, elongated

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fine motor function, impaired

Fisher's syndrome

fistula, arterio-venous, carotid-cavernous

Friedreich's ataxia

fundus, abnormality of

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis, generalized

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gonadal dysgenesis

granulomatosis with polyangiitis

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome, ophthalmoplegia in

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Hallgren's syndrome

headache, sudden onset of

hemianopia, homonymous

hemianopia, transient

hepatic failure

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histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

Hurler's syndrome

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ideomotor apraxia

idiopathic inflammatory orbital disease

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immunohistochemistry

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immunosuppressive agents

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infantile tremor syndrome

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal pseudoobstruction

intracerebral hemorrhage

ischemic exercise test

jaw jerk, abnormal

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

lactic acidemia

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leigh's disease

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

lid closure, weakness of

life expectancy

lipoprotein receptor-related protein 4

locked-in syndrome

lymphadenopathy, hilar

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

medial rectus palsy

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, leukemic

mental retardation

mental status, abnormal

metabolic acidosis

metachromatic leukodystrophy

midbrain, atrophy

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

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mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

molecular genetics

monoclonal antibodies

mononeuropathy multiplex

motor neuron disease

motor neuron disease, juvenile form

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, extraocular muscle enhancement

mucopolysaccharidoses

multicore myopathy

multiple sclerosis

multiple sclerosis, acute

multiple system atrophy

muscle atrophy, progressive

muscle biopsy, extraocular

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

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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

myasthenic crisis

myasthenic syndrome

myoclonus, epilepsy

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myopathy, drug-induced

myopathy, mitochondrial

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myopathy, toxic

myositis, ocular

myotonia dystrophica

nasal stuffiness

nausea and vomiting

nemaline rod myopathy

nerve conduction studies

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neurogenic vs.myopathic atrophy

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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, sensory

neuroophthalmology

neuropathy, ataxia, retinitis pigmentosa

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

Niemann-Pick disease

night blindness

nystagmus, dissociated

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

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

optic disc edema

optic nerve, lesion of

optic neuropathy

orbicularis oculi muscle

orbit, inflammation in

orbit, lesions of

orbital apex syndrome

overlap syndrome

pain, abdominal

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, spastic

parasellar syndrome

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

peroxisomal disease

personality change

photophobia, central

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy, chronic relapsing

pons, lesion of

practice guidelines

pregnancy, neurologic complications in

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proptosis, bilateral

proptosis, unilateral

proximal muscle atrophy

pseudobulbar palsy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, bilateral

ptosis, familial

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

quality of life

radiation hypersensitivity

ragged-red fibers

rapidly progressing neurologic illness

Raynaud's phenomenon

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

reticular activating system

retina, abnormal

retinal degeneration

retinitis pigmentosa

rhomboencephalopathy

rigidity, axial

saccadic eye movements, abnormal

scleroderma, neurologic involvement with

sedimentation rate

sensorineural hearing loss

sequencing difficulty

serologic testing

skin, lesions in neurologic disorders

Southern immunoblot test

Spielmeyer Vogt syndrome

spinal muscular atrophy

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spongy degeneration of brain

squamous cell carcinoma of head and neck

standing difficulty

startle reaction

Stephens syndrome

steroid therapy, CNS treatment and complications with

strokelike episodes

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

subarachnoid hemorrhage

succinate dehydrogenase deficiency

symmetric brain lesions

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

temporal lobe, lesion

thalamus, lesion of-bilateral

thymic hyperplasia

Tolosa Hunt syndrome

tongue, fasciculations of

transverse smile

treatment of neurologic disorder

trigeminal nerve

trigeminal nerve, lesion of

trinucleotide repeats

tuberculoma of CNS

tuberculosis, miliary

ulcerative colitis

Unverricht-Lundborg disease

upgaze, paralysis of

Usher's syndrome

vision, blurred

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual loss, slow-unilateral

visual symptoms

vitamin deficiency

vitamin E deficiency

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

whistle, inability to

white matter disease

white matter disease, pattern

wide based gait

winging of scapula

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Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

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

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

A Dizzy Architect
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A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

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

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

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

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

Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
JAMA 286:2437-2440, Becher,M.W.,et al, 2001

GCG Genetic Expansions in Italian Patients with Oculopharyngeal Muscular Dystrophy
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Age and Cause of Death in Mitochondrial Diseases
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The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

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

Adult Botulism
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Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

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

Cerebral Infarction Associated with Kearns-Sayre Syndrome-Related Cardiomyopathy
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Clinicopath Study of Paraneoplastic Brainstem Encephalitis and Ophthalmoparesis
J Neuro-Ophthalmol 16:44-48, Crino,P.B.,et al, 1996

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

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

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
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Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Clinicopath Conf
B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Infilt of Orbital Muscle, Case 4, 193,NEJM 328:266-275,1993., 1993

Polymyalgia Rheumatica and Mitochondrial Myopathy:Clinicopathologic and Biochemical Studies in Five Cases
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Cardioskeletal Mitochondrial Myopathy Associated with Chronic Magnesium Deficiency
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Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
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