Neudle.com: ophthalmoplegia congenital

Differential
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abducens nerve palsy, evaluation of

abducens nerve paralysis

acanthocytosis

acoustic neurinoma

advances in neurology

alien hand syndrome

alpha-fetoprotein

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

anatomy of

aneurysm

aneurysm, berry

aneurysm, cavernous sinus

aneurysm, cavernous sinus-bilateral

aneurysm, fusiform

aneurysm, giant cerebral

aneurysm, infraclinoid

aneurysm, intracranial

aneurysm, intracranial, acute deterioration

aneurysm, intracranial, treatment of

aneurysm, posterior communicating artery

aneurysm, ruptured

aneurysm, supraclinoid

aneurysm, vertebral basilar system

angiography, cerebral

angiography, cerebral, indications

anisocoria

anterior tibial muscle weakness

apraxia

apraxia of eye movements

areflexia

arthrogryposis multiplex

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, truncal

atlanto axial dislocation, congenital

basal ganglia, calcification of

Bassen-Kornzweig syndrome

brainstem, hypoplasia

brainstem, lesion of

brainstem, malformation

calcification, intracranial

calcification, intracranial, rim

carcinoembryonic antigen

carcinoma

carotid angiogram

carotid artery calcification

case studies

CAT scan

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, false negative

CAT scan, muscle

CAT scan, ring sign

cataracts

cataracts, congenital

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, meningioma

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar peduncle

cerebral vasculature, calcification

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

chromosomal abnormality

chromosome 11

chronic progressive external ophthalmoplegia

Cockayne's syndrome

congenital malformation

congenital myasthenic syndromes

congenital myopathy

congenital ocular motor apraxia

conjunctival injection

consanguinity

convergence, impaired

cornea, abnormal

corneal reflex, abnormal

cortical blindness

cortical-basal ganglionic degeneration

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

deafmute

deafness

dementia

developmental retardation

diabetes mellitus

diabetes mellitus, congenital and infectious disease with

diabetes mellitus, neurologic manifestations of

diabetes mellitus, ocular complications in

diabetic amyotrophy

diabetic cranialneuropathies

diabetic mononeuropathy

diabetic ophthalmoplegia

diabetic radiculopathy

diabetic spinal syndromes

diabetic visceral neuropathy

diplopia

diplopia, transient

diplopia, vertical

distal muscle weakness

drooling

drug induced neurologic disorders

dwarfism

dysarthria

dyskinesia, buccal lingual facial

Ehlers-Danlos syndrome

electroencephalogram, abnormalities of

electromyogram

embolization, therapeutic, coils

empyema, epidural-spinal

encephalocele

encephalopathy

endovascular therapy

epidemiology of neurology

epistaxis

exome sequencing

exophthalmus

exophthalmus, bilateral

exophthalmus, pulsatile

exophthalmus, unilateral

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, lesion of

facial pain

facial weakness

facioscapulohumeral syndrome

familial

fasciculation

fatigue

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fluctuate

foot drop

fourth ventricle, enlargement of

Friedreich's ataxia

fundus, abnormality of

fungal infection, CNS

gargoylism

gaze palsy

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

hallucination, visual

headache, sudden onset of

heralding manifestation

HGPPS

high arched palate

histochemistry of muscle

inclusion body myositis

infantile tremor syndrome

internuclear ophthalmoplegia

ipsilateral hemiplegia

jaw pain

joint hypermobility

Kearns-Sayre syndrome

keratoconus

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

leukemia

levitation

lid abnormalities

lid closure, weakness of

lordosis

lymphoma

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

MELAS syndrome

Melkersson's syndrome

mitochondrial disease

mitochondrial encephalomyopathy

motor neuron disease, juvenile form

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, diffusion tensor

MRI, diffusion weighted

MRI, muscle

mucopolysaccharidoses

multicore myopathy

multiminicore disease

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle pain

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

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, nystagmus in

myasthenia gravis, ocular

myasthenia gravis, sensory loss with

myoclonic jerks

myoglobinuria

myopathy

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, mitochondrial

nemaline rod myopathy

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

neuritis

neurocutaneous disease

neuroendocrinology

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular junction

nystagmus, dissociated

nystagmus, monocular

nystagmus, vertical

obesity

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

one and a half syndrome

opened mouth

ophthalmoplegia

ophthalmoplegia, cause of

ophthalmoplegia, congenital

ophthalmoplegia, head injury causing

ophthalmoplegia, neonatal

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

ophthalmoplegic migraine

optic neuritis

optic neuropathy

orbicularis oculi muscle

pain

pain, periorbital

papilledema

paraspinal muscle weakness

Parkinson disease

pathology

periodic paralysis

periodic paralysis, thyrotoxic

proptosis, unilateral

pseudointernuclear ophthalmoplegia

pseudomyasthenia

pseudoretinitis pigmentosa

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

pupil, light reflex, abnormal

pyramidal tract, uncrossed

radiation hypersensitivity

ragged-red fibers

reading problem, causes of

scoliosis, neurologic association with

seizure

sensory loss

sensory loss, cortical

short stature

skin, lesions in neurologic disorders

Spielmeyer Vogt syndrome

spina bifida

spinal muscular atrophy

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

subarachnoid hemorrhage

superior oblique palsy

superior ophthalmic vein, dilated

third nerve misdirection

third nerve palsy

third nerve palsy, childhood

third nerve palsy, congenital

third nerve palsy, cyclic

third nerve palsy, partial

third nerve palsy, pupil sparing in

third nerve palsy, superior branch

treatment of neurologic disorder

tremor

trigeminal neuropathy

trochlear nerve palsy

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual loss

visual loss, sudden-unilateral

walking, difficulty with

whistle, inability to

winging of scapula

xerophthalmia

Showing articles 1050 to 1100 of 1766 << Previous Next >>

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Abnormality in the Cavernous Sinus in Three Patients with Tolosa-Hunt Syndrome:MRI and CT Findings
JNNP 53:231-234, Goto,Y.,et al, 1990

Abnormalities of Horizontal Gaze, Clinical, Oculographic and Magnetic Resonance Imaging Findings, II Gaze Palsy and INO
JNNP 53:200-207, Bronstein,A.M.,et al, 1990

Diabetic Autonomic Neuropathy
NEJM 322:1078-1079, Watkins,P.J., 1990

Clinicopath Conf
Churg-Strauss Phenomena with Mononeuritis Multiplex, Case Record 38-1990, NEJM 323:812-822990., , 1990

Effect of Calcitonin-Gene-Related Peptide on Postoperative Neurological Deficits after Subarachnoid Haemorrhage
Lancet 335:869-872, Johnston,F.G.,et al, 1990

Warning Leak in Subarachnoid Haemorrhage
BMJ 301:190-191, Ostergaard,J.R., 1990

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Major Congenital Neurologic Malformations
Am J Dis Child 144:61-67, Wiswell,T.E.,et al, 1990

The Infant with Anencephaly
Med Task Force on Anencephaly, NEJM 322:669-6741990., , 1990

Putaminal Hemorrhage:Clinical-Computed Tomographic Correlations
Neuroradiology 32:200-206, Weisberg,L.A.,et al, 1990

Cerebral Venous Thrombosis in a Child with Iron Deficiency Anemia and Thrombocytosis
Stroke 21:488-493, Belman,A.L.,et al, 1990

The Diagnosis and Treatment of Cerebral Myocotic Aneurysms
Ann Neurol 27:238-246, Brust,J.C.M.,et al, 1990

Stroke in Young Adults
Stroke 21:382-386, Bevan,H.,et al, 1990

Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
Stroke 21:291-294, Ryu,S.J., 1990

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

Oculo-Facial-Skeletal Myorhythmia in Whipple Disease:Treatment with Ceftriazone
Ann Int Med 112:467-469, Adler,C.H.&Galetta,S.L., 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

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

MR Imaging of Tolosa-Hunt Syndrome
AJR 154:167-170, Yousem,D.M.,et al, 1990

Vertical One-And-A-Half Syndrome
Arch Neurol 46:1361-1363, Deleu,D.,et al, 1989

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

Pseudo One-and-a-half Syndrome with Ocular Myasthenia
Neurol 39:1553, Davis,T.L.&Lavin,P.J.M., 1989

Diabetic Truncal Neuropathy Presenting as Abdominal Hernia
Neurol 39:1488-1490, Parry,G.J.&Floberg,J., 1989

Origins of Cerebral Palsy
Am J Dis Child 143:1154-1160, Naeye,R.L.,et al, 1989

Perinatal Asphyxia and Cerebral Palsy
Am J Dis Child 143:1139-1140, Bedrick,A.D., 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Divisional Oculomotor Nerve Paresis Caused by Intrinsic Brainstem Disease
Ann Neurol 26:714-718, Ksiazek,S.M.,et al, 1989

Clinicopathological Correlation in a Case of Painful Ophthalmoplegia:Tolosa-Hunt Syndrome
JNNP 52:1290-1293, Goadsby,P.J.&Lance,J.W., 1989

Brain Stem Type Neuro-Behcet's Syndrome
Neuroradiology 31:258-262, Kataoka,S.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Bilateral Giant Intracavernous Carotid Aneurysms in a 16-Year Old Boy
Neuroradiology 31:284-286, Winter,R.K.,et al, 1989

Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
Neurol 39:847-848, Kolodny,E.H., 1989

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Cerebral Infarction and Ventricular Septal Defect
Stroke 20:957-958, Shuiab,A., 1989

Positive Platelet Scintigram of a Vertebral Aneurysm Presenting Thromboembolic Transient Ischemic Attacks
Stroke 20:687-690, Maruyama,M.,et al, 1989

Neurofibromatosis Type 1 (Recklinghausen's Disease) , Neurologic and Cognitive Assessment
Am J Dis Child 143:833-837, Eldridge,R.,et al, 1989

The Canadian American Ticlopidine Study (CATS) in Thromboembolic Stroke
Lancet 1:1215-1220, Gent,M.,et al, 1989

CT Characteristics of Orbital Pseudotumors and Other Orbital Inflammatory Processes
J Comput Assist Tomogr 13:40-47, Flanders,A.E.,et al, 1989

Ptosis and Supranuclear Downgaze Paralysis
Neurol 39:385-389, Buttner-Ennever,J.A.,et al, 1989

Diabetic Truncal Neuropathy:Topography of the Sensory Deficit
Ann Neurol 25:233-238, Stewart,J.D., 1989

Outcome After Posthemorrhagic Ventriculomegaly in Comparison with Mild Hemorrhage Without Ventriculomegaly
J Pediatr 114:109-114, Shankaran,S.,et al, 1989

Painful Oculomotor Nerve Palsy Due to Dural-Cavernous Sinus Shunt
Arch Neurol 46:1252-1255, Hawke,S.H.,et al, 1989

Magnetic Resonance Angiography of the Extracranial Carotid Arteries and Intracranial Vessels:A Review
Neurol 39:1369-1376, Ross,J.S.,et al, 1989

Teratogenic Effects of Carbamazepine
Letter, NEJM 321:1480-14811989., , 1989

Unilateral Moya-Moya Disease:MRI Findings
Neuroradiology 31:442, Wilms,G.,et al, 1989

Myasthenia Gravis
In Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, 697, Penn,A.S.&Rowland,L.P., 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Cerebrovascular Disease
Neurology of Pregnancy, W. B. Saunders Co, London, 2nd Ed, p. 137, Donaldson,J.O., 1989

Showing articles 1050 to 1100 of 1766 << Previous Next >>