Neudle.com: chronic progressive external ophthalmoplegia

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abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

acetylcholine receptor

acetylcholine receptor antibody

acquired immunodeficiency syndrome

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

akinesia of eyelid function

alpha-fetoprotein

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti Hu antibody

anti Ri antibody

anti Yo antibody

antiviral agents

apraxia of eye movements

apraxia of eyelid opening

arm swing, reduced

arrhythmia, cardiac

arteritis, temporal

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

atlanto axial dislocation, congenital

atrial fibrillation

autoimmune disease

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

azidodeoxythymidine

basal ganglia, calcification of

basal ganglia, lesion, bilateral

basilar artery stenosis

Bassen-Kornzweig syndrome

blindness, sudden

botulism antitoxin

brainstem, dysfunction

brainstem, lesion of

brainstem, tuberculoma of

bulbar dysfunction

bulbar palsy, acute

calcification, intracranial

carcinoembryonic antigen

carcinoma of bladder

carcinoma of lung

carcinoma of ovary

carcinoma of testis

CAT scan, abnormal

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, congenital

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

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

cherry red spot-myoclonus syndrome

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10 deficiency

cogwheel rigidty

collagen vascular disease

congenital myopathy

congestive heart failure

conjunctival biopsy

conjunctival injection

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

cricopharyngeal bar

critical care unit

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, rapidly progressive

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

digitalis intoxication

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dysdiadochokinesia

dysthyroid ocularmyopathy

edema, periorbital

electrical sensation

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

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

Hallervorden Spatz disease

Hallgren's syndrome

headache, chronic

headache, progressive

headache, sudden onset of

hemianopia, homonymous

hemianopia, transient

hepatic failure

heralding manifestation

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

Hurler's syndrome

hyperthyroidism

hypoglycorrhachia

hypoparathyroidism

hypoparathyroidism, idiopathic

iatrogenic neurologic disorders

ideomotor apraxia

idiopathic inflammatory orbital disease

immunocompetent

immunodeficiency

immunohistochemistry

immunosuppression

immunosuppressive agents

inclusion body myositis

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 biopsy

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

mitochondrial disease

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

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

myasthenic crisis

myasthenic syndrome

myoclonus, epilepsy

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, mitochondrial

myopathy, proximal

myopathy, toxic

myositis, ocular

myotonia dystrophica

nasal stuffiness

nausea and vomiting

nemaline rod myopathy

nerve conduction studies

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, 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

ophthalmoplegia, unilateral

optic disc edema

optic nerve, lesion of

optic neuropathy

orbicularis oculi muscle

orbit, inflammation in

orbit, lesions of

orbital apex syndrome

overlap syndrome

pachymeningitis, cranial

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

ptosis, unilateral

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

sedimentation rate, elevated

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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Acute Vincristine Neurotoxicity
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Presentation & Management of Parasellar & Suprasellar Metastatic Mass Lesions
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McArdle's Disease in the 1980s
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Amyotrophic Lateral Sclerosis:A Double-Blind Crossover Trial of Thyrotropin-Releasing Hormone
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Inhibition of Terminal Axonal Sprouting by Serum From Patients with Amyotrophic Lateral Sclerosis
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Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
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Familial Multisystem Atrophy with Possible Thalamic Dementia
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Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
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