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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, intracranial-fungal

abscess, sphenoid sinus

acetylcholine receptor

acetylcholine receptor antibody

acquired immunodeficiency syndrome

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

akinesia of eyelid function

alcohol, neurologic complications with

alpha-fetoprotein

altered states of consciousness

aminoacidopathies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

aneurysm, cavernous sinus

aneurysm, cavernous sinus-bilateral

aneurysm, intracranial

aneurysm, intracranial, acute deterioration

aneurysm, intracranial, treatment of

aneurysm, ruptured

angiography, cerebral

antecedent illness

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti Hu antibody

anti Ri antibody

anti Yo antibody

anticonvulsants, untoward effects of

antiganglioside antibodies

apraxia of eye movements

apraxia of eyelid opening

Argyll Robertson pupil

arm swing, reduced

arrhythmia, cardiac

arteritis, temporal

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

atheromatous branch disease, intracranial

atlanto axial dislocation, congenital

atrial fibrillation

autoimmune disease

autonomic dysfunction

autonomic dysfunction, acute

autonomic neuropathy

axonal degeneration

azidodeoxythymidine

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavioral disorder

Bickerstaff's brainstem encephalitis

bilirubin encephalopathy

bitemporal visual field defect

blindness, monocular

blindness, sudden

blinking, reduced

botulism antitoxin

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, tuberculoma of

bruit, pulsatile

bulbar dysfunction

bulbar palsy, acute

calcification, intracranial

caloric testing

caloric testing, unconscious patient

campylobacter infection

capsular warning syndrome

carbamazepine, toxicity

carcinoembryonic antigen

carcinoma of bladder

carcinoma of lung

carcinoma of ovary

carcinoma of prostate

carcinoma of testis

carcinoma of tongue

carotid angiogram

carotid artery disease

carotid artery occlusion, neck

carpo-pedal spasm

CAT scan, abnormal

CAT scan, base of skull

CAT scan, dense artery sign

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

CAT scan, orbits

cataracts, congenital

cauda equina, enhancement

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, metastasis to

cavernous sinus, syndrome

celiac disease, childhood

central artery of Percheron

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebro hepato renal syndrome

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, postoperative

cerebrovascular accident, recurrent

cerebrovascular accident, stuttering

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chlorotrianisine

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 engorgement

conjunctival injection

cornea, abnormal

corneal reflex, abnormal

corpus callosum, lesion of

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial nerve palsies, unilateral

cranial nerves, toxins effecting

cranial neuropathy

cranial neuropathy, multiple

cranial neuropathy, progressive

craniopharyngioma

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cricopharyngeal bar

critical care unit

cry, high-pitched

crying, pathologic

Cushing's syndrome

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dental procedure, neurologic complications with

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

digitalis intoxication

dilantin, serum level

dilantin, toxicity

diplopia, transient

diplopia, vertical

distal muscle atrophy

distal muscle weakness

doll's head maneuver

down-beat nystagmus

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dysthyroid ocularmyopathy

dystonia, cervical

edema, periorbital

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electron microscopy

electronystagmography

electroretinograph

embolization, therapeutic, coils

emergencies, neurologic

emotional lability

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalopathy, neonatal

encephalopathy, progressive

endovascular therapy

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

exercise intolerance

exophthalmus, bilateral

exophthalmus, pulsatile

exophthalmus, unilateral

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 swelling

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fine motor function, impaired

Fisher's syndrome

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption/false positive

Friedreich's ataxia

fundus, abnormality of

fungal infection

fungal infection, CNS

fungal infection, CNS, treatment 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

geographic location

giant cell arteritis

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

gonadal dysgenesis

granulomatosis with polyangiitis

granulomatous disease

Graves ophthalmopathy

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, auditory

Hand-Schuller-Christian disease

headache, bifrontal

headache, frontal

headache, severe

headache, sudden onset of

headache, unilateral

hemianopia, homonymous

hemianopia, transient

hemifacial atrophy

hepatic failure

hepatosplenomegaly

heralding manifestation

herpes zoster, ophthalmicus

heterochromia iridis

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

hummingbird sign

Hurler's syndrome

hyperadrenalism

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperinsulinism

hyperparathyroidism

hyperthyroidism

hypoglycorrhachia

hypokalemic periodic paralysis

hypometric saccades

hypoparathyroidism

hypoparathyroidism, idiopathic

hypothalamus, disturbance of

iatrogenic neurologic disorders

ideomotor apraxia

idiopathic inflammatory orbital disease

imbalance, postural

immunodeficiency

immunohistochemistry

immunosuppression

immunosuppressive agents

inclusion body myositis

infantile tremor syndrome

inferior rectus palsy

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intrinsic hand muscles, wasting of

ischemic exercise test

islet cell tumor

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, young adult

jaw jerk, abnormal

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

lactic acidemia

Lafora's disease

lateral rectus palsy

laughing, pathologic

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

level of consciousness, decreased

lid abnormalities

lid closure, weakness of

life expectancy

light-near dissociation, causes of

lipoprotein receptor-related protein 4

locked-in syndrome

lymphadenopathy, hilar

lymphoma, primary of CNS

macular degeneration

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

Marcus Gunn pupil

medial rectus palsy

mediastinum, mass of

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, eosinophilic

meningitis, leukemic

meningitis, lymphomatous

mental retardation

mental status, abnormal

metabolic acidosis

metachromatic leukodystrophy

midbrain, atrophy

midbrain, hemorrhage

midbrain, infarction of

midbrain, lesion of

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, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, extraocular muscle enhancement

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, skull bone changes

MRI, spinal cord

mucopolysaccharidoses

multicore myopathy

multiple sclerosis

multiple sclerosis, acute

multiple system atrophy

muscle atrophy, progressive

muscle biopsy, extraocular

muscle weakness

muscle weakness, causes of

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, presenting manifestations

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, acute

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, mitochondrial

myopathy, proximal

myopathy, toxic

myositis, ocular

myotonia dystrophica

myxedema, neurologic manifestations of

nasal stuffiness

nausea and vomiting

nemaline rod myopathy

neoplasm, metastatic to base of skull

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, pituitary

nerve conduction studies

nerve conduction studies, motor

neuroaxonal dystrophy

neurocutaneous disease

neuroendocrinology

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathology, peripheral nerves

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, recurrent

neuropathy, sensory

neuropathy, vasculitic, systemic

Niemann-Pick disease

night blindness

numbness, ascending

numbness, extremity

nystagmus, primary position of gaze

nystagmus, retractorius

nystagmus, rotary

nystagmus, vertical

obicularis oculi, weakness of

obsessive-compulsive disorder

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculocephalic reflex

oculogyric crisis

oculopharyngeal muscular dystrophy

oculovestibular reflex

old age, neurology of

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, internal

ophthalmoplegia, neonatal

ophthalmoplegia, painful

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, recurrent

ophthalmoplegia, total

ophthalmoplegia, unilateral

opportunistic infection

optic disc edema

optic nerve, lesion of

optic neuropathy

optokinetic nystagmus(O.K.N.)

orbicularis oculi muscle

orbit, compression

orbit, inflammation in

orbit, lesions of

orbit, pseudotumor of

orbital apex syndrome

orbital compartment syndrome

overlap syndrome

pain, abdominal

pain, periorbital

palate, paralysis

paralysis, acute

paralysis, acute areflexic

paraneoplastic brainstem encephalitis

paraneoplastic cerebellar degeneration

paraparesis, spastic

paraproteinemia

parasellar syndrome

parathyroid adenoma

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism syndrome

PAS positive material in the brain

penguin silhouette sign

periarteritis nodosa

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peroxisomal disease

personality change

pheochromocytoma

photophobia, central

pigmentary retinopathy

pituitary, adenoma

pituitary, apoplexy

pituitary, metastasis to

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy, chronic relapsing

pons, infarction of

pons, lesion of

pontine warning syndrome

post infectious polyneuropathy

posterior inferior cerebellar artery syndrome

postoperative neurologic complications

practice guidelines

pregnancy, neurologic complications in

premature infant

pretectal syndrome

prevention of neurologic disorders

primary aldosteronism

progressive encephalomyelitis with rigidity syndrome

progressive hemifacial atrophy

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proptosis, bilateral

proptosis, unilateral

proximal muscle atrophy

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, alternating

ptosis, bilateral

ptosis, familial

ptosis, unilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pupil, midposition 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

respiratory paralysis, pharmacologic

respiratory tract infection

reticular activating system

retina, abnormal

retinal branch artery occlusion

retinal degeneration

retinal infarction

retinal ischemia

retinitis pigmentosa

retinopathy, ischemic

retrobulbar neuritis

retro-orbital pain

rhinocerebral phycomycoses

rhomboencephalopathy

rigidity, axial

saccadic eye movements, abnormal

salivation, excessive

Saturday night retinopathy

scalp tenderness

scleroderma, neurologic involvement with

sedimentation rate

sedimentation rate, elevated

sensorineural hearing loss

sequencing difficulty

setting sun phenomena

shell fish poisoning

sinuses, diseases of

skin, lesions in neurologic disorders

Southern immunoblot test

sphenoid sinus biopsy

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

stiff man syndrome

strokelike episodes

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

subarachnoid hemorrhage

subthalamic nucleus

succinate dehydrogenase deficiency

superior ophthalmic vein, dilated

sweating, abnormality of

symmetric brain lesions

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tapetoretinal degeneration

temporal artery, biopsy

temporal lobe, lesion

tensilon tonography

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

third nerve palsy

third nerve palsy, bilateral

third nerve palsy, partial

third nerve palsy, pupil sparing in

thymic hyperplasia

tick-borne encephalitis

Tolosa Hunt syndrome

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

top of the basilar syndrome

treatment of neurologic disorder

treatment, empirical

trigeminal nerve

trigeminal nerve, lesion of

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

tuberculoma of CNS

tuberculosis, miliary

ulcerative colitis

Unverricht-Lundborg disease

upgaze, paralysis of

urinary incontinence

Usher's syndrome

vectors of infection

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual impairment

visual loss, slow

visual loss, slow-unilateral

visual loss, sudden

visual loss, sudden-unilateral

visual symptoms

vitamin deficiency

vitamin E deficiency

vocal cord paralysis

Waldenstrom's macroglobulinemia

walking, difficulty with

weakness, acute

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Wernicke's encephalopathy

Whipple's disease

whistle, inability to

white matter disease

white matter disease, pattern

wide based gait

winging of scapula

Showing articles 50 to 100 of 3399 << Previous Next >>

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

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

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

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Neuro-Ophthalmic Presentation of Non-Hodgkins Lymphoma
Neurol 48:784-785, Finelli,P.F.&Lesser,R.L., 1997

Cranial Nerve Enhancement on Three-Dimentional MRI in Miller Fisher Syndrome
Neurol 47:1601-1602, Nagaoka,U.,et al, 1996

Bilateral Total Ophthalmoplegia Due to Midbrain Hematoma
Neurol 46:1176-1177, Worthington,J.M.&Halmagyi,G.M., 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,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
Neurol 46:826-828, Provenzale,J.M.,et al, 1996

Clinicopath Study of Paraneoplastic Brainstem Encephalitis and Ophthalmoparesis
J Neuro-Ophthalmol 16:44-48, Crino,P.B.,et al, 1996

Progressive Encephalomyelitis with Rigidity Responsive to Plasmapheresis and Immunosuppression
Ann Neurol 40:451-453, Fogan,L., 1996

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

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

Acute Bilateral Ophthalmoplegia Secondary to Metastatic Prostatic Carcinoma:Demonstr of Magnetic Resonance Imaging
J Neuro-Ophthalmol 15:45-47, Agarwal,P.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Evidence for Cardioembolic Stroke in a Case of Kearns-Sayre Syndrome
Stroke 26:1950-1952, Kosinski,C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Prolonged Paralysis Due to Nondepolarizing Neuromuscular Blocking Agents and Corticosteroids
Muscle & Nerve 17:647-654994., Barohn,R.J.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

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

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

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

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

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

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

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

Complete Ophthalmoplegia as a Complication of Acute Corticosteroid-and Pancuronium-Associated Myopathy
Neurol 41:921-922, Sitwell,L.D.,et al, 1991

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

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Incomplete Unilateral Ophthalmoplegia as the Presenting Manifestation of Waldenstrom's Macroglobulinemia
Neurol 40:1801-1802, Lossos,A.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Kearns-Sayre Syndrome and Dilated Cardiomyopathy
Neurol 40:553-554, Tveskov,C.&Angelo-Nielsen,K., 1990

Perineural Spread of Cutaneous Head and Neck Cancer
Arch Neurol 47:73-77, Clouston,P.D.,et al, 1990

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

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

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Showing articles 50 to 100 of 3399 << Previous Next >>