Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Malattia Leventinese

Known as: MLVT 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2007
Highly Cited
2007
Malattia leventinese (ML) is a dominantly inherited macular degenerative disease characterized by the presence of sub-retinal… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2006
2006
PURPOSE Malattia leventinese (ML) is an inherited macular degeneration characterized by the presence of large paracentral and… Expand
Is this relevant?
Highly Cited
2004
Highly Cited
2004
Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a matrix-bound inhibitor of matrix metalloproteinases. Mutations in the Timp… Expand
Is this relevant?
Review
2003
Review
2003
Age-related macular degeneration (ARM) is a progressive, chronic condition that results when the macula degenerates and central… Expand
Is this relevant?
Highly Cited
2002
Highly Cited
2002
Malattia Leventinese (ML), an inherited macular degenerative disease, is closely reminiscent of age-related macular degeneration… Expand
Is this relevant?
2001
2001
PURPOSE To report a case of malattia leventinese involving subretinal hemorrhage. METHODS Case report. RESULTS Two weeks… Expand
Is this relevant?
Highly Cited
1999
Highly Cited
1999
Malattia Leventinese (ML) and Doyne honeycomb retinal dystrophy (DHRD) refer to two autosomal dominant diseases characterized by… Expand
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
1998
1998
Purpose The lack of histopathological material has placed limitation on our knowledge on the composition of focal deposits in… Expand
Is this relevant?
1998
1998
PURPOSE To study the phenotypic variability in patients inheriting the disease gene for malattia leventinese (dominant macular… Expand
Is this relevant?
1996
1996
OBJECTIVE To identify the chromosomal location of the gene involved in the pathogenesis of autosomal dominant radial drusen… Expand
Is this relevant?