Neudle.com: Kiloh Nevin ocular dystrophy

Differential
(Click to cross reference)

abducens nerve paralysis, bilateral

abiotrophy

acanthocytosis

advances in neurology

agammaglobulinemia

akinesia of eyelid function

ANA

apraxia of eyelid opening

basal ganglia, calcification of

Bassen-Kornzweig syndrome

brainstem, tuberculoma of

calcification, intracranial

cardiomyopathy

CAT scan

CAT scan, abnormal

CAT scan, false negative

cataracts

cause of death

celiac disease, childhood

cerebellar ataxia, primary

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

conjunctival injection

consanguinity

cornea, abnormal

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

digitalis intoxication

dysthyroid ocularmyopathy

dystonia

dystrophin

edema, periorbital

electroencephalogram, abnormalities of

electromyogram

encephalopathy

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

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

fistula, arterio-venous, carotid-cavernous

gaze palsy, horizontal

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glabellar sign

glaucoma

Graves ophthalmopathy

hemianopia, homonymous

hepatic failure

hippus

Hispanics

histochemistry of muscle

intestinal pseudoobstruction

jaw jerk, abnormal

Kearns-Sayre syndrome

keratoconus

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

L-dopa

Leber's hereditary optic neuropathy

Leigh's disease

lid closure, weakness of

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, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myopathy, mitochondrial

neurologic complications of, systemic cancer

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

obicularis oculi, weakness of

occipital lobe, lesion of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

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

pons, lesion of

prognosis

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

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated and fixed, unilateral

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

tongue, fasciculations of

treatment of neurologic disorder

trinucleotide repeats

tuberculoma of CNS

tuberculosis

tuberculosis, miliary

upgaze, paralysis of

Usher's syndrome

visual field defect

visual fields, constricted

visual loss

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

Showing articles 1300 to 1350 of 1530 << Previous Next >>

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 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

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

Superior Branch Palsy of Oculomotor Nerve & Pupillary Constriction Caused by Intracranial Carotid Artery Aneurysm
Ann Neurol 5:493-495, Feder,R.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

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

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Periodic Alternating Gaze
Neurol 29:222-224, Stewart,J.D.,et al, 1979

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

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

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

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,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

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

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Deformed Erythrocytes in Muscular Dystrophies
Neurol 28:842-844, Grassi,E.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Alteration in Erythrocyte Membrane Structure in Duchenne Muscular Dystrophy
Ann Neurol 4:253-256, Wakayama,Y.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

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

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

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,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

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

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

Solitary Oculomotor Nerve Palsy In Childhood
Am J Ophthal 83:106-111, Miller,N.R., 1977

Pseudopalsy of the Abducens Nerve, In Neuro-Ophthalmology Update
(Ed) , 1977, P. 64-72., Smith,J.L., 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Bone Scanning & Diagnosis of Reflex Sympathetic Dystrophy Secondary to Herniated Lumbar Disks
Neurol 27:791, Carlson,D.H.,et al, 1977

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

Showing articles 1300 to 1350 of 1530 << Previous Next >>