Neudle.com: ocular muscular dystrophy

Differential
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abdominal distention

abducens nerve paralysis, bilateral

abiotrophy

acanthocytosis

advances in neurology

agammaglobulinemia

akinesia of eyelid function

ANA

apraxia of eyelid opening

aqueduct of Sylvius, stenosis

auditory evoked brainstem potentials

basal ganglia, calcification of

Bassen-Kornzweig syndrome

brainstem, tuberculoma of

cachexia

calcification, intracranial

CAT scan, false negative

cataracts

cataracts, congenital

cause of death

celiac disease, childhood

central core disease

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebral cortical atrophy

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot's sign

chemosis

children

chromosomal abnormality

chromosome 14

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

cogwheel rigidty

collagen vascular disease

coma

congenital myopathy

conjunctival injection

cranial neuropathy, multiple

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

cytochrome c oxidase

cytochrome c oxidase, deficiency

digitalis intoxication

diplopia

distal muscle weakness

dysthyroid ocularmyopathy

dystonia

dystrophin

edema, periorbital

electroencephalogram, abnormalities of

electromyogram

electronystagmography

electronystagmography, abnormal

electroretinograph

encephalocele

encephalopathy

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

evoked potentials

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, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fistula, arterio-venous, carotid-cavernous

Friedreich's ataxia

gait disorder

gargoylism

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

gaze palsy

gaze palsy, horizontal

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glabellar sign

glaucoma

Graves ophthalmopathy

hemianopia, homonymous

hepatic failure

hepatomegaly

heralding manifestation

hippus

Hispanics

histochemistry of muscle

Hurler's syndrome

hydrocephalus

hydrocephalus, congenital

immunosuppressive agents

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

intestinal pseudoobstruction

jaw jerk, abnormal

joint hypermobility

Kearns-Sayre syndrome

keratoconus

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

Leber's hereditary optic neuropathy

Leigh's disease

leukodystrophy

leukoencephalopathy

lid closure, weakness of

lissencephaly

malformation, CNS, congenital

masked facies

medial rectus palsy

medulla oblongata, lesion of

MELAS syndrome

Melkersson's syndrome

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mucopolysaccharidoses

muscle atrophy, progressive

muscle biopsy

muscle biopsy, extraocular

muscle pain

muscle weakness

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, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myopathy, centronuclear

myopathy, distal

myopathy, mitochondrial

myopathy, steroid induced

nemaline rod myopathy

neuritis

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

obicularis oculi, weakness of

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

oculovestibular reflex

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

orbicularis oculi muscle

Parkinsonism syndrome

photophobia

photophobia, central

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

POLG1 gene

polydactyly

polymerase chain reaction

progressive infantile poliodystrophy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

proptosis, bilateral

proptosis, unilateral

prostigmine

pseudobulbar palsy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

saccadic eye movements

saccadic eye movements, abnormal

schizophrenia

scintillations

scleroderma

scleroderma, neurologic involvement with

screening

sedimentation rate

seizure

sensorineural hearing loss

seronegative

short stature

skin, tight

Southern immunoblot test

spasticity

Spielmeyer Vogt syndrome

standing difficulty

Stephens syndrome

steroid therapy, CNS treatment and complications with

strokelike episodes

symmetric brain lesions

systemic illness

tongue, fasciculations of

treatment of neurologic disorder

trinucleotide repeats

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

visual fields, constricted

visual loss

Walker-Warburg syndrome

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Showing articles 1650 to 1700 of 1880 << Previous Next >>

Functional Paralysis of Horizontal Gaze
Neurol 29:82-85, Troost,B.T.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Craniopharyngioma with Midbrain Involvement
Arch Neurol 36:319-320, Waga,S.,et al, 1979

The Syndrome of Painful Ophthalmoplegia
Arch Neurol 36:41-43, Rosenbaum,D.H.,et al, 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Central Vestibular Involvement in Peroneal Muscle Atrophy:A Preliminary Report
Ann Neurol 5:118-120, Melgaard,B.,et al, 1979

Eye Movement Fatigue in Myasthenia Gravis
Neurol 29:29-33, Spooner,J.W.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Bilateral Rhinocerebral Phycomycosis
Ann Neurol 6:131-133, Kasper,L.H.,et al, 1979

Neurologic Abnormalities of Lyme Disease
Medicine 58:281-294, Reik,L.,et al, 1979

Interobserver Agreement in Assessment of Ocular Signs in Coma
JNNP 42:1163-1168, van den Berge,J.H.,et al, 1979

Neuromuscular Diseases that Affect the Eye
International Ophthal Clx 18:103, Black,J., 1978

Myasthenia, In Neuroophthalmology
1978, Harper & Row, P. 268., Glaser,J.S., 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Painful Ophthalmoplegia in Systemic Lupus Erythematosus
Ann Neurol 4:584-585, Evans,O.B.,et al, 1978

Superior Branch Palsy of the Oculomotor Nerve with Spontaneous Recovery
Ann Neurol 4:478-479, Derakhshan,I., 1978

Recovery from Primary Pontine Hemorrhage
Ann Neurol 4:557-558, Payne,H.A.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Asymptomatic Carotid Bruit
Ann Surg 188:308, Thompson,J.E.,et al, 1978

Noninvasive Techniques for Diagnosis of Carotid Artery Disease
Stroke 9:427-429, Sandok,B.A., 1978

Eye Movements in Ataxia-telangiectasia
Neurol 28:1099-1104, Baloh,R.W.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Human Pneumatic Tourniquet Paralysis
Neurol 28:787-793, Bolton,C.F.,et al, 1978

Total Blindness after Trivial Frontal Head Trauma:Bilateral Indirect Optic Nerve Injury
Neurol 28:1066-1068, Venable,H.P.,et al, 1978

Pseudocaloric Nystagmus
Arch Neurol 35:93, Becker,G.D.,et al, 1978

Migraine Presenting as Acute Confusion & Delirium:A Case Report
Neurol 28:1201, Finelli,P.F., 1978

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Penicillamine-induced Myasthenia Gravis Associated with Antibodies to Acetylcholine Receptor
Neurol 28:847-849, Russell,A.S.,et al, 1978

Tolosa-Hunt Syndrome
Arch Neurol 35:219, 1978, Takeoka,T.,et al, 1978

Neurologic Manifestations of Cogan Syndrome
Neurol 28:278, Bicknell,J.M.,et al, 1978

Forced Downward Ocular Deviation
Arch Neurol 35:456, Simon,R.P., 1978

Bilateral Oculomotor Paralysis Due to Neurosyphilis
Ann Neurol 3:90, Jordan,K.,et al, 1978

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

Alternating Proptosis
Arch Neurol 34:642, Keane,J.R., 1977

Inferior Branch Palsy of the Oculomotor Nerve
Ann Neurol 2:336, Susac,J.O.,et al, 1977

Gaze-induced Laughter
JNNP 40:815, Leopold,N.A., 1977

Showing articles 1650 to 1700 of 1880 << Previous Next >>