leucine and Choroid Diseases

leucine has been researched along with Choroid Diseases in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kurotaki, J; Miyagawa, Y; Nakazawa, M; Ohguro, H; Sato, M; Yanagihashi, S	1
Keilhauer, CN; Meigen, T; Weber, BH	1

Other Studies

2 other study(ies) available for leucine and Choroid Diseases

Article	Year
Autosomal dominant central areolar choroidal dystrophy and a novel Arg195Leu mutation in the peripherin/RDS gene. Archives of ophthalmology (Chicago, Ill. : 1960), 2003, Volume: 121, Issue:10 Topics: Aged; Amino Acid Substitution; Arginine; Choroid Diseases; Codon; Electroretinography; Fluorescein Angiography; Genes, Dominant; Humans; Intermediate Filament Proteins; Leucine; Male; Membrane Glycoproteins; Middle Aged; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation	2003
Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene. Archives of ophthalmology (Chicago, Ill. : 1960), 2006, Volume: 124, Issue:7 Topics: Adolescent; Adult; Age of Onset; Arginine; Choroid Diseases; Codon; Disease Progression; DNA Mutational Analysis; Electroretinography; Female; Fluorescein Angiography; Genes, Dominant; Humans; Intermediate Filament Proteins; Leucine; Male; Membrane Glycoproteins; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation; Visual Acuity	2006

Article

Year

Autosomal dominant central areolar choroidal dystrophy and a novel Arg195Leu mutation in the peripherin/RDS gene.

Archives of ophthalmology (Chicago, Ill. : 1960), 2003, Volume: 121, Issue:10

Topics: Aged; Amino Acid Substitution; Arginine; Choroid Diseases; Codon; Electroretinography; Fluorescein Angiography; Genes, Dominant; Humans; Intermediate Filament Proteins; Leucine; Male; Membrane Glycoproteins; Middle Aged; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation

2003

Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene.

Archives of ophthalmology (Chicago, Ill. : 1960), 2006, Volume: 124, Issue:7

Topics: Adolescent; Adult; Age of Onset; Arginine; Choroid Diseases; Codon; Disease Progression; DNA Mutational Analysis; Electroretinography; Female; Fluorescein Angiography; Genes, Dominant; Humans; Intermediate Filament Proteins; Leucine; Male; Membrane Glycoproteins; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation; Visual Acuity

2006