Neudle.com: "cataracts"

Differential
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acanthocytosis

achilles tendon, enlarged

acoustic nerve, vestibular division of

acoustic neurinoma, bilateral

acute necrotizing encephalitis

adrenoleukodystrophy

advances in neurology

adverse drug reaction

alopecia

altered states of consciousness

alveolar hypoventilation

angiography, cerebral

angiography, posterior fossa

anticoagulant, complications of

anticoagulant, discontinuation

anticoagulant, restarting

anticoagulant, reversal of

anticoagulant, treatment

atherosclerosis, premature

atrial fibrillation

audiogram

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

baldness

band keratopathy

basal ganglia, calcification of

Bassen-Kornzweig syndrome

bruit, supraclavicular

calcification, intracranial

carcinoma of lung

carcinoma of uterus

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

caries

carotid artery occlusion, perioperative

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataract surgery

cataracts

cataracts, congenital

central nervous system, infection of

central retinal artery occlusion

central serous chorioretinitis

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebral cortical atrophy

cerebral ischemia

cerebral palsy

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, postoperative

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

chelation therapy

chemotherapy, CNS treatment and complications with

chondrodysplasia punctata

chorea

choreoathetosis

chorioretinitis

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cirrhosis

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

congenital infection, CNS

congenital infection, viral

congenital malformation

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corpus callosum, atrophy of

corpus callosum, hypoplastic

cough

coumarin

coumarin, stopping treatment

cranial nerve tumor

creatine phosphokinase(CPK)elevated

cry, weak

cryptorchidism

cultured skin fibroblasts

cyclosporine

cyst, porencephalic

cytomegalic inclusion disease

cytosine arabinoside

deafmute

deafness

degenerative diseases of CNS

delay in diagnosis

dementia

dental procedure, neurologic complications with

depression

depression, psychotic

dermatoglyphics

developmental retardation

differential diagnosis

digits, abnormal

dilantin

diplopia

disability, neurological

disseminated intravascular coagulation(DIC)

distal muscle weakness

dizziness

DNA probes

drooling

dropped head syndrome

drug induced neurologic disorders

ectatic basilar artery

edema, pedal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electroretinograph

embolism

encephalitis

encephalitis, brainstem

encephalopathy

endocarditis

endocarditis, marantic

episodic neurologic deficits

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

fatty acid, elevated plasma content

feeding disorder

fever

fluorescein angiography

fundus, abnormality of

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

Guillain Barre syndrome

gynecomastia

gyrate atrophy of choroid and retina

hair, loss

Hallervorden Spatz disease

Hallgren's syndrome

hallucination, visual

hearing loss, sudden, bilateral

heart block

heart murmur

hematuria, microscopic

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

hypercoagulable state

hypoparathyroidism, idiopathic

hypotonia

iatrogenic neurologic disorders

imbalance

immunofluorescent exam of CSF cells

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

infectious mononucleosis

intellectual deficit

intellectual deterioration

interferon

interferon inducer

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

Kayser-Fleischer ring

Kearns-Sayre syndrome

keratitis, interstitial

keratoconus

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg weakness, bilateral

level of consciousness, decreased

lid closure, weakness of

limbic encephalitis

limbic system

lipid storage disorder of CNS

lissencephaly

liver disease

liver function enzymes

liver transplantation

Lowe's syndrome

lymphadenopathy

lysosomal storage disease

macrocephaly

macular degeneration

malabsorption

malformation, CNS, congenital

Marinesco-Sjogren syndrome

MELAS syndrome

memory, impairment of

meningitis, noninfectious

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

microangiopathic hemolytic anemia

midbrain, infarction of

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve vegetation

mononeuritis multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, spinal cord

MRI, spine

mucopolysaccharidoses

multiple sclerosis

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

myelitis

myelomalacia

myelopathy

myelopathy, chronic progressive

myoclonus

myopathy

myopathy, mitochondrial

myopathy, necrotizing

myotonia dystrophica, classification

myotonia dystrophica, type 2

nasal bridge, wide

neck weakness

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

neurofibromatosis 2, presymptomatic

neurogenic vs.myopathic atrophy

neuroichthyosis

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neurologic testing

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

nystagmus, congenital

nystagmus, pendular

obesity

ocular myopathy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic glioma

optic nerve

optic nerve, hypoplasia of

optic nerve, neoplasm of

optic neuritis

optic neuropathy

optic neuropathy, ischemic

orbit, cellulitis of

orbit, lesions of

P300

pacemaker, cardiac-transvenous

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

patent ductus arteriosus

pathology

patient information and support

penicillamine

percussion induced muscle contraction

peripheral blood stem cell transplantation

peripheral pulse, absent

photosensitivity, skin

phytanic acid

pigmentary retinopathy

platelet inhibiting drugs

platelet inhibiting drugs, discontinuation

pleocytosis of cerebrospinal fluid

polycystic kidneys

polydactyly

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polyneuropathy

polyneuropathy, familial

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progeria

prognosis

proteinuria

proximal myotonic myopathy

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

ptosis

ptosis, bilateral

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, oval

pupil, tonic

pyramidal tract dysfunction

radiation therapy, CNS treatment and complications with

radiation therapy, total body

remote effect of cancer on the nervous system

scleroderma, neurologic involvement with

screening

sedimentation rate, elevated

seizure

seizure, psychomotor-temporal lobe

sensorineural hearing loss

sensory loss

serum protein, decreased

short stature

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

skull x-ray, bony defect on

slit lamp examination

small vessel disease

somatosensory evoked potentials

sore throat

spasticity

Spielmeyer Vogt syndrome

spinal cord

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

spinal xanthomatosis

spinocerebellar degeneration

splenomegaly

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

stooped posture

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

subclavian artery occlusion

subclavian artery stenosis

subclavian steal syndrome

subtemporal decompression

sudden death

sweating, abnormality of

tapetoretinal degeneration

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tendon, enlarged

testicular atrophy

thrombocytopenia

thrombotic microangiopathy

thrombotic thrombocytopenia purpura

tinnitus

transient ischemic attack

transluminal angioplasty, coronary artery

transplacental virus infections

transurethral prostatectomy

trauma

treatment of neurologic disorder

tremor

trientine dihydrochloride

trigeminal neuralgia

trinucleotide repeats

tubular aggregates, muscle

type 2 muscle fiber

undiagnosed

upgaze

urea-cycle enzymopathies

uremia

urinary urgency

urine test for metabolic disorders

Usher's syndrome

uterus, enlarged

uvea, lesion of

uveal melanocytic proliferation

uveitis

vaccination, neurologic complications with

vertebral-basilar insufficiency

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, slow-unilateral

visual loss, sudden

visual loss, sudden-unilateral

Walker-Warburg syndrome

weakness

weaning from respirator, failure to

x-linked mental retardation

zinc

Showing articles 0 to 50 of 79 Next >>

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Chorioretinopathy After Corticosteroid Treatment for Optic Neuritis
Neurol 96:e305-e306, Ling, J. and Micieli, J.A., 2021

Blurred Vision
BMJ 368:m569, Zhou, S.,et al, 2020

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Inherited Metabolic Diseases of the Nervous System, Galactosemia
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Summary of Evidence-Based Guideline: Periprocedural Management of Antithrombic Medications in Patients with Ischemic Cerebrovascular Disease
Neurol 80:2065-2069, Armstrong, M.,et al, 2013

Oval Pupil
Neurol 81:e124-e125, Mittal, M.K.,et al, 2013

Cogan Syndrome An Analysis of Reported Neurological Manifestations
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A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke
Neurol 78:e113-e114, Seixas,J.C.,et al, 2012

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
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Management of Anticoagulation Before and After Elective Surgery
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Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

Myotonic Dystrophy Type 2
Neurol 60:657-664, Day,J.W.,et al, 2003

Perioperative Management of Patients Receiving Oral Anticoagulants: A Systematic Review
Arch Int Med 163:901-908, Dunn,A.S. &Turpie,A.G.G., 2003

Risks and Benefits of Anticoagulant and Antiplatelet Medication Use Before Cataract Surgery
Ophthalmology 110:1784-1788, Katz,J.,et al, 2003

Clinicopath Conf, Bilateral, Diffuse Uveal Melanocytic Proliferation, Metastatic Endometrial Carcinoma
NEJM 346:189-195, Case 2-2002, 2002

Severe Neurologic Complications After Hematopoietic Stem Cell Transplantation in Children
Neurol 59:1895-1904,E13, Farci,M.,et al, 2002

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Turning a Blind Eye
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MR of Zellweger Syndrome
AJNR 18:1163-1170, Barkowich,A.J.&Peck,W.W., 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,et al, 1997

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Takayasu's Arteritis
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

Myotonic Dystrophy
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Visual Impairment in Patients with Neurofibromatosis 2
Neurol 43:622-623, Bouzas,E.A.,et al, 1993

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Wilson Disease
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Wilson's Disease:Current Status
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Accelerated Aging of the Brain in Werner's Syndrome
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A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

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

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

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Neurological and Developmental Findings in Children with Cataracts
Am J Dis Child 13:706-710, Pike,M.G.,et al, 1989

Refsum Disease
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Showing articles 0 to 50 of 79 Next >>