Retinitis

Known as: Retinitis NOS, Retinitis [Disease/Finding], swelling of the retina 
Inflammation of the RETINA. It is rarely limited to the retina, but is commonly associated with diseases of the choroid (CHORIORETINITIS) and of the… (More)

Topic mentions per year

Topic mentions per year

1935-2018
010020030019352017

Papers overview

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Highly Cited
2006
Highly Cited
2006
Retinitis pigmentosa (RP) is a label for a group of diseases caused by a large number of mutations that result in rod… (More)
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Highly Cited
2000
Highly Cited
2000
Mutation of a receptor tyrosine kinase gene, Mertk, in the Royal College of Surgeons (RCS) rat results in defective phagocytosis… (More)
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Highly Cited
2000
Highly Cited
2000
The X-linked RP3 locus codes for retinitis pigmentosa GTPase regulator (RPGR), a protein of unknown function with sequence… (More)
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Highly Cited
2000
Highly Cited
2000
The gene RPGR was previously identified in the RP3 region of Xp21.1 and shown to be mutated in 10–20% of patients with the… (More)
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Highly Cited
1999
Highly Cited
1999
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5… (More)
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Highly Cited
1999
Highly Cited
1999
BACKGROUND The intraocular ganciclovir implant is effective for local treatment of cytomegalovirus retinitis in patients with the… (More)
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Highly Cited
1998
Highly Cited
1998
Ophthalmological and molecular genetic studies were performed in a consanguineous family with individuals showing either… (More)
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Highly Cited
1994
Highly Cited
1994
Retinitis pigmentosa (RP) is a group of inherited human diseases in which photoreceptor degeneration leads to visual loss and… (More)
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Highly Cited
1994
Highly Cited
1994
In spite of recent advances in identifying genes causing monogenic human disease, very little is known about the genes involved… (More)
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Highly Cited
1993
Highly Cited
1993
We have found four mutations in the human gene encoding the β–subunit of rod cGMP phosphodiesterase (PDE β) that cosegregate with… (More)
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