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The New England Journal of Medicine
|
May 20, 2011
Genomics and the eye
Val C Sheffield, Edwin M Stone
Ophthalmology
|
June 5, 2002
Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations
Sandeep Grover, Gerald A Fishman, Edwin M Stone
Ophthalmic Genetics
|
December 7, 2006
Lumpers or splitters? The role of molecular diagnosis in Leber congenital amaurosis
Elias I Traboulsi, Robert Koenekoop, Edwin M Stone
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
October 21, 2009
Which Leber congenital amaurosis patients are eligible for gene therapy trials?
Arlene V Drack, Rebecca Johnston, Edwin M Stone
Ophthalmology
|
October 7, 2004
A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa
Sandeep Grover, Gerald A Fishman, Edwin M Stone
Vision Research
|
September 11, 2007
Visual function testing: a quantifiable visually guided behavior in mice
Stewart Thompson, Alisdair R Philp, Edwin M Stone
JAMA Ophthalmology
|
March 17, 2021
Hyperlipofuscinosis With Subretinal Fibrosis and Choroidal Vascular Remodeling in Stargardt Disease
Ian C Han, Meghan C Menzel, Edwin M Stone
Human Molecular Genetics
|
March 21, 2014
Stem cells for investigation and treatment of inherited retinal disease
Budd A Tucker, Robert F Mullins, Edwin M Stone
Ophthalmology. Retina
|
November 2, 2020
Subliminal Message Outer Retinal Tubulations Resembling Mitochondria in Maternally Inherited Diabetes and Deafness
Ian C Han, D Brice Critser, Edwin M Stone
JAMA Ophthalmology
|
September 12, 2014
Outer segment length in different best disease genotypes
Michael D Abràmoff, Robert F Mullins, Edwin M Stone
Page
of 39
Search research articles
Search
Showing results (11-20 of 384) with videos related to
Sort By:
Page
of 39
The New England Journal of Medicine
|
May 20, 2011
Genomics and the eye
Val C Sheffield, Edwin M Stone
Ophthalmology
|
June 5, 2002
Atypical presentation of pattern dystrophy in two families with peripherin/RDS mutations
Sandeep Grover, Gerald A Fishman, Edwin M Stone
Ophthalmic Genetics
|
December 7, 2006
Lumpers or splitters? The role of molecular diagnosis in Leber congenital amaurosis
Elias I Traboulsi, Robert Koenekoop, Edwin M Stone
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
October 21, 2009
Which Leber congenital amaurosis patients are eligible for gene therapy trials?
Arlene V Drack, Rebecca Johnston, Edwin M Stone
Ophthalmology
|
October 7, 2004
A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa
Sandeep Grover, Gerald A Fishman, Edwin M Stone
Vision Research
|
September 11, 2007
Visual function testing: a quantifiable visually guided behavior in mice
Stewart Thompson, Alisdair R Philp, Edwin M Stone
JAMA Ophthalmology
|
March 17, 2021
Hyperlipofuscinosis With Subretinal Fibrosis and Choroidal Vascular Remodeling in Stargardt Disease
Ian C Han, Meghan C Menzel, Edwin M Stone
Human Molecular Genetics
|
March 21, 2014
Stem cells for investigation and treatment of inherited retinal disease
Budd A Tucker, Robert F Mullins, Edwin M Stone
Ophthalmology. Retina
|
November 2, 2020
Subliminal Message Outer Retinal Tubulations Resembling Mitochondria in Maternally Inherited Diabetes and Deafness
Ian C Han, D Brice Critser, Edwin M Stone
JAMA Ophthalmology
|
September 12, 2014
Outer segment length in different best disease genotypes
Michael D Abràmoff, Robert F Mullins, Edwin M Stone
Page
of 39