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LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)

Known as: Amaurosis congenita of Leber, type 2, AMAUROSIS CONGENITA OF LEBER II, Leber congenital amaurosis type 2 
National Institutes of Health

Related topics

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3 relations

Broader (1)

Leber Congenital Amaurosis
RPE65 geneRPE65, ARG234TER

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Amaurosis Fugax Captured During Fluorescein Angiography.
2015
2015
Amaurosis Fugax in Ocular Vascular Occlusive Disorders
Amaurosis fugax is a transient brief blindness, dimming, fogging, or blurring of vision, lasting from a few seconds to minutes or… 
Review
2012
Review
2012
AAV-mediated gene therapy in mouse models of recessive retinal degeneration.
In recent years, more and more mutant genes that cause retinal diseases have been detected. At the same time, many naturally… 
2010
2010
Valsalva Maneuver-induced Amaurosis Fugax
Purpose: To report the case of a patient with amaurosis fugax that occurred following a Valsalva maneuver. Case summary: A 40… 
2008
2008
Two Teams Report Progress in Reversing Loss of Sight
The first safety trials of gene therapy for a degenerative eye disease produced good results in adults; researchers now intend to… 
2000
2000
Gestieltes Adenom der Leber
1994
1994
Human cytomegalovirus DNA in cerebrospinal fluid.
To determine the involvement of human cytomegalovirus (CMV) in conditions of neurological impairment, detection of CMV DNA was… 
1990
1990
Rupturiertes kavernöses Hämangiom der Leber
1978
1978
[Amaurosis fugax and obliteration of the carotid artery (author's transl)].
Obliterative processes of the carotid bifurcation can be a starting point for cerebral and especially retinal microemboli. Early… 
1957
1957
Amaurosis fugax: a specific type of transient loss of vision.
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