Neudle.com: ocular myopathy

Differential
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abdominal distention

abducens nerve paralysis

abducens nerve paralysis, bilateral

abiotrophy

abortion, spontaneous

acanthocytosis

acquired immunodeficiency syndrome

Addison's disease

advances in neurology

adverse drug reaction

agammaglobulinemia

akinesia of eyelid function

anticardiolipin antibodies

anticonvulsants, untoward effects of

antiphospholipid antibodies

antiviral agents

aortic valve, insufficiency

aortitis

aphasia

apraxia of eyelid opening

arthrogryposis multiplex

aspartate aminotransferase

atrioventricular block

attention span

atypical

audiogram

auditory evoked brainstem potentials

autoimmune disease

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

Beau's lines

Behcet's syndrome

biological warfare

bitemporal visual field defect

bovine spongiform encephalopathy

brachial plexus neuropathy

brain biopsy

brain biopsy, negative

brainstem

brainstem, infarction of

brainstem, lesion of

brainstem, tuberculoma of

bulbar palsy

cachexia

CAG repeats

calcification, intracranial

carpal tunnel syndrome

CAT scan, false negative

cataplexy

cataracts

cauda equina

cauda equina, lesion of

cause of death

CD4 counts

celiac disease, childhood

central core disease

central nervous system, infection of

central retinal artery occlusion

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

Charcot's sign

chemical weapons

chemosis

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

chromosomal abnormality

chromosome 14

chronic progressive external ophthalmoplegia

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

collagen vascular disease

coma

complications

confusion

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

conjunctival injection

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

critical care unit

Cuba

cultured skin fibroblasts

Cushing's syndrome

cytochrome c oxidase

cytochrome c oxidase, deficiency

degenerative diseases of CNS

delirium

dementia

dementia, rapidly progressive

dementia, transmissible

depression

dermatitis

dermatomyositis

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

dialysis

diarrhea

diarrhea, bloody

differential diagnosis

digitalis intoxication

diplegia, brachial

diplopia

distal muscle weakness

doxycycline

dropped head syndrome

dysthyroid ocularmyopathy

dystonia

dystrophin

echocardiogram

echocardiogram, transesophageal

edema, pedal

edema, periorbital

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalopathy, progressive

endemic area

endocarditis

endocarditis, acute bacterial

endophthalmitis

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

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 palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fistula, arterio-venous, carotid-cavernous

flea bite

fleas

floppy infant

fluorescent treponema antibody absorption/false positive

foam cells

Friedreich's ataxia

Fukuda step test

fundus, abnormality of

gait disorder

gammaglobulin therapy, intravenous

gargoylism

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

granulomatosis with polyangiitis

Graves ophthalmopathy

growth hormone

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

Gulf War syndrome

Hallgren's syndrome

hallucination

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

headache

headache, new onset

headache, persistent

headache, retro-orbital

hearing loss

hearing loss, bilateral

hearing loss, sudden, bilateral

hearing loss, unilateral

heart block

heart block, complete

heart murmur

heart wall motion dysfunction

helminthic infection of CNS

hematuria, microscopic

hemianopia, homonymous

hemiparesis

hemorrhagic diathesis

hepatic failure

hepatomegaly

hepatosplenomegaly

heralding manifestation

histochemistry of muscle

hoarseness

homosexual

Horner's syndrome

human immunodeficiency virus type 1

hypokalemic paralysis

hypokalemic periodic paralysis

hyponatremia

hypoparathyroidism

hypoparathyroidism, idiopathic

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypothyroidism

hypotonia

iatrogenic neurologic disorders

IFA

imbalance

imbalance, postural

immune checkpoint inhibitors

immune-related adverse events

immunohistochemistry

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

impulsivity

inattention

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

intellectual deterioration

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles, wasting of

ipilimumab

iritis

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

Kearns-Sayre syndrome

keratitis

keratitis, interstitial

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

Leber's hereditary optic neuropathy

leg weakness, bilateral

lid closure, weakness of

limb-girdle weakness

lipid storage disorder of CNS

liver disease

liver function enzymes

liver transplantation

Loa loa

loiasis

lumbosacral radiculopathy

lupus anticoagulant

Lyme disease

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphopenia

malabsorption

malabsorption syndrome

malaise

malformation, CNS, congenital

malignant hyperpyrexia

medulla oblongata, lesion of

melanoma, malignant

MELAS syndrome

Melkersson's syndrome

meningitis, leptospira

meningitis, neutrophilic

meningitis, noninfectious

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mixed connective tissue disease

MNGIE syndrome

molecular genetics

monoclonal antibodies

monomelic myositis

mononeuritis multiplex

mononeuropathy

mononeuropathy multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, orbit

mucopolysaccharidoses

multicore myopathy

multiminicore disease

multiple sclerosis

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle cramp

muscle pain

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic syndrome

myelitis

myelopathy

myelopathy, chronic progressive

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, drug-induced

myopathy, inflammatory

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, immune-mediated

myopathy, steroid induced

myopathy, steroid responsive

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

myxedema, neurologic manifestations of

nasal septum, perforation of

necrotizing vasculitis

negative

nemaline rod myopathy

neoplasm, metastatic

neoplasm, pituitary

nephritis

nerve conduction studies

neuritis

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronopathy

neuroophthalmology

neuropathology

neuropathology, peripheral nerves

neuropathy

neuropathy, peripheral

neuropathy, vasculitic, systemic

obicularis oculi, weakness of

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

oculovestibular reflex

one and a half syndrome

opened mouth

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, neonatal

ophthalmoplegia, painful

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

orbicularis oculi muscle

orbit

orbit, biopsy

orbit, inflammation in

orbit, lesions of

orbit, pseudotumor of

orbital apex

organ transplantation

otitis, neurologic complications with

parasitic infection, CNS

paraspinal muscle weakness

parathyroid adenoma

paresthesias

paresthesias, feet

Parkinsonism syndrome

parotitis

partial thromboplastin time, prolonged

periodic paralysis, thyrotoxic

pigmentary retinopathy

pituitary, hormones of

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymyositis

polyneuropathy

pons, lesion of

posterior inferior cerebellar artery syndrome

primary aldosteronism

prion disease

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

proptosis, alternating

proptosis, bilateral

proptosis, unilateral

prostigmine

protein 14-3-3, cerebrospinal fluid

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

rapidly progressing neurologic illness

respiratory paralysis, pharmacologic

respiratory tract infection

retina, abnormal

retinal artery occlusion

rheumatoid arthritis factor(R.A.factor)

saccadic eye movements, abnormal

salivary gland enlargement

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure

sensorineural hearing loss

serum alanine aminotransferase

skin, lesions in neurologic disorders

skin, tight

somatosensory evoked potentials

sore throat

Southern immunoblot test

spasticity

Spielmeyer Vogt syndrome

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar degeneration

spirochete infection

splenomegaly

splinter hemorrhages

spongy degeneration of brain

squamous cell carcinoma of head and neck

steroid therapy, CNS treatment and complications with

streptococcus pneumoniae

strokelike episodes

subarachnoid hemorrhage

sweating

Sweet's syndrome

symmetric brain lesions

syncope

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tabes dorsalis

tachycardia

tandem gait, ataxic

temporal lobe, lesion

thyroid function tests

thyroid gland, enlarged

thyrotoxicosis

tinnitus

tongue, fasciculations of

toxic encephalopathy

toxic shock syndrome

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transverse smile

travel history

travel, foreign

treatment of neurologic disorder

tremor

trichinosis

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

tuberculosis, miliary

typhus, murine

ulcerative colitis

ultrasonography

ultrasonography, orbit

Venereal Disease Research Laboratory test

vertigo

vestibulopathy

vincristine neurotoxicity

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, sudden-unilateral

vitamin deficiency

vitamin E

vitamin E deficiency

Walker-Warburg syndrome

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

web sites

weight loss

Western immunoblot test

Showing articles 1100 to 1150 of 2003 << Previous Next >>

The Ocular Manifestations of Multiple Sclerosis, 2, Abnormalities of Eye Movements
JNNP 55:863-868, Barnes,D.&McDonald,W.I., 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Immunologic Aspects of Neurological and Neuromuscular Diseases
JAMA 268:2918-2922, Zweiman,B.&Levinson,A.I., 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Acute Quadriplegic Myopathy:A Complic of Treat with Steroids, Nondepolarizing Blocking Agents, or Both
Neurol 42:2082-2087, Hirano,M.,et al, 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

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

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Fibromyalgia:The Copenhagen Declaration
Lancet 340:663-664, Csillag,C., 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

Post-Irradation Neuromyotona Affecting Trigeminal Nerve Distribution:An Unusual Presentation
Neurol 42:1102-1104, Diaz,J.M.,et al, 1992

Episodic Paroxysmal Hemicrania:Two New Cases and A Literature Review
Neurol 42:964-966, Newman,L.C.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

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

Midbrain Syndromes of Benedikt, Claude, and Nothnagel:Setting the Record Straight
Neurol 42:1820-1822, Liu,G.T.,et al, 1992

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

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

A Chronic Illness of Fatigue, Neurologic and Immunologic Disorders, & Active Human Herpesvirus Type 6 Infection
Ann Int Med 116:103-113, Buchwald,D.,et al, 1992

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

Cluster Headache Syndrome
Postgrad Med 91:96-104, Marks,D.R.&Rapoport,A.M., 1992

Headaches in Children Younger than 7 Years of Age
Arch Neurol 49:79-82, Chu,M.L.&Chinnar,S., 1992

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

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
Arch Neurol 49:158-160, Kartsounis,L.D.,et al, 1992

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

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Ipecac Myopathy and Cardiomyopathy
JNNP 56:560-562, Dresser,L.P.,et al, 1992

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

Severe Phenytoin Hypersensitivity with Myopathy:A Case Report
Neurol 42:2303, Barclay,C.L.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Clinical Signs in Severe Guillain-Barre Syndrome: Analysis of 63 Patients
J Neurol Sci 104:143-150, De Jager, A.E.J.,et al, 1991

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
Arch Neurol 48:1130-1135, Barohn,R.J.,et al, 1991

Wegener's Granulomatosis Mimicking Temporal Arteritis
Neurol 41:1694-1695, Palaic,M.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Cyclosporin in the Management of Polymyositis and Dermatomyositis
JNNP 54:1007-1008, Lueck,C.J.,et al, 1991

Unilateral Oculomotor Palsy and Bilateral Ptosis from Paramedian Midbrain Infarction
Arch Neurol 48:983-986, Liu,G.T.,et al, 1991

Muscle Carnitine Deficiency in Patients Using Valproic Acid
J Pediatr 118:646-649, Shapira,Y.&Gutman,A., 1991

Ultrasound Findings in Spontaneous Carotid Artery Dissection, The Value of Duplex Sonography
Arch Neurol 48:1057-1063, Sturzenegger,M., 1991

Carotid Endarterectomy and Prevention of Cerebral Ischemia in Symptomatic Carotid Stenosis
JAMA 266:3289-3294, 33321991., Mayberg,M.R.,et al, 1991

Clinical Genetics and Genetic Counseling in Alzheimer Disease
Ann Int Med 115:601-606, Breitner,J.C.S., 1991

Fatigue and Myalgia in AIDS Patients
Neurol 41:1603-1607, Miller,R.G.,et al, 1991

Short-Lasting Unilateral Neuralgiform Headache Atacks with Tearing & Conjunctival Injection:First"Symptomatic"Case
Cephalalgia 11:123-127, Bussone,G.,et al, 1991

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

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,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

Showing articles 1100 to 1150 of 2003 << Previous Next >>