Neudle.com: "macular degeneration"

Differential
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acoustic nerve

adrenoleukodystrophy

adverse drug reaction

anticoagulant, complications of

antiretinal antibodies

apraxia of eye movements

basal ganglia, calcification of

basilar impression

Bassen-Kornzweig syndrome

battered child syndrome

brainstem, hypoplasia

brainstem, lesion of

calcification, intracranial

carotid artery occlusion, neck

cat exposure

CAT scan

CAT scan, abnormal

CAT scan, false negative

cataracts

cat-scratch disease

cerebellar ataxia, children

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebro hepato renal syndrome

cerebrospinal fluid, elevated protein of

cerebrovascular accident

Charles Bonnet's syndrome

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

children

chorioretinitis

chromosomal abnormality

chromosome 17

Clinical Pathologic Conference(C.P.C.)

cluster, geographic

Cockayne's syndrome

color vision

color vision, impaired

corpus callosum, hypoplastic

cranial nerve palsies

cranial neuropathy, multiple

cytochrome c oxidase, deficiency

deafness

degenerative diseases of CNS

dementia

developmental abnormality of brain

developmental milestones, loss of

developmental retardation

diarrhea

differential diagnosis

diplopia

DNA probes

drug induced neurologic disorders

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

endophthlamitis

enzyme, defect

epidermal nevus syndrome

exercise

exophthalmus

eye injury

eye movement, disorders of

facial nerve palsy

falling

familial

fatty acid dehydrogenase deficiency

fingolimod

fluorescein angiography

fourth ventricle, enlargement of

fundus, abnormality of

gait disorder

gastrointestinal motility

gaze palsy

gaze palsy, supranuclear

gene

gene mutation

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

glare, light-induced

glaucoma

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

Hallgren's syndrome

hallucination

hallucination, visual

hallucination, visual, benign

iatrogenic neurologic disorders

imbalance

immunomodulation

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inclusion bodies, intracytopasmic

incoordination

infection

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

intestinal pseudoobstruction

Jehovah's witness

Joubert syndrome

Kearns-Sayre syndrome

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leber's idiopathic stellate retinopathy

lymphadenopathy, hilar

lymphocyte fingerprint profiles

lysosomal storage disease

macular degeneration

macular degeneration, senile

macular degeneration, senile disciform

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

medial longitudinal fasciculus(MLF)

mental retardation

microcephaly

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, treatment of

multiple sclerosis, tumefactive

myopathy, mitochondrial

myopia

nausea and vomiting

neuraminidase deficiency

neurocutaneous disease

neuroendocrinology

neuroichthyosis

neurolipidosis IV

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic atrophy, hereditary

optic atrophy, unilateral

optic disc edema

optic glioma

optic nerve

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis

optic neuropathy

optic neuropathy, hereditary

optical coherence tomography

orbit, cellulitis of

Paget's disease

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

Parkinsonism syndrome

photosensitivity, eye

pigmentary retinopathy

platelet inhibiting drugs

polyneuropathy

Poretti-Boltshauser syndrome

pre-retinal hemorrhage

prognosis

progressive neurologic disorder

psychomotor retardation

ptosis

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

remote effect of cancer on the nervous system

respiratory tract infection

retina, abnormal

retinal arteriole attenuation

retinal artery occlusion

scotoma, paracentral-homonymous

seizure

seizure, children

seizure, neonatal

sensorineural hearing loss

short stature

Sjogren-Larsson syndrome

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

spastic diplegia

spinal cord, compression of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

sports medicine, neurology of

steroid

steroid therapy, CNS treatment and complications with

superior orbital fissure syndrome

tapetoretinal degeneration

third nerve palsy

titubation

trauma

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

Usher's syndrome

uveitis

valsalva maneuver

ventricular enlargement

vertebral-basilar insufficiency

viral infection

vision, blurred

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

visual loss, sudden-unilateral

white matter disease

wide based gait

Showing articles 0 to 40 of 40

Decreased Visual Acuity After a Cat Scratch
BMJ 372:n552, Zhou, L. & Kong, X., 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

Sudden Loss of Vision at the Gym
BMJ 375:e067964, Ng, J.K.Y.,et al, 2021

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

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Profound Anemia and Acute Blindness in a Jehovahs Witness
Lancet 382:998, Bretagnol, A.,et al, 2013

Fingolimod-Associated Macular Edema
Neurol 78:672-680, Jain,N. and Bhatti,M.T., 2012

Tumefactive Multiple Sclerosis Lesions under Fingolimod Treatment
Neurol 79:2000-2002,1942, Visser, F.,et al, 2012

"Retinal Diplopia" Associated with Macular Wrinkling
Neurol 63:925-927, Barton,J.J.S., 2004

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Ocular Involvement in Sarcoidosis
Br J Ophthalmol 84:110-116, Rothova, A., 2000

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Visual Hallucinations in Psychologically Normal People:Charles Bonnet's Syndrome
Lancet 347:794-797, Teunisse,R.J.,et al, 1996

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

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Macular Hemorrhage in the Aging Eye:The Effects of Anticoagulants
NEJM 318:1126-1127, Kingham,J.D.,et al, 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Does Neuroretinitis Rule Out Multiple Sclerosis
CPT, et al, Arch Neurol 44:1045-1048987., Parmley,V.C., 1987

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

Leber's Idiopathic Stellate Retinopathy
Am J Ophthalmol 93:96-101, Carroll,D.M.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

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

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Senile Disciform Macular Degeneration
Editioral, BMJ 1:1444-14451979., , 1979

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

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

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

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972

Showing articles 0 to 40 of 40