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Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
October 1, 2009
Jack Crawford Day 2009
Elise Héon
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
November 10, 2009
My child has Leber congenital amaurosis: why is he/she not eligible for gene therapy trials?
Elise Héon
Investigative Ophthalmology & Visual Science
|
April 23, 2019
Introducing Artur V. Cideciyan and Samuel G. Jacobson, the 2018 Recipients of the Proctor Medal
Elise Héon, Gustavo D Aguirre
Advances in Experimental Medicine and Biology
|
December 21, 2011
Caenorhabditis elegans as a model organism for ciliopathies and related forms of photoreceptor degeneration
Calvin A Mok, Elise Héon
Ophthalmic Genetics
|
April 6, 2011
BBS mutational analysis: a strategic approach
Gail Billingsley, Catherine Deveault, Elise Héon
Ophthalmic Genetics
|
April 23, 2014
In memoriam Maria Musarella
Elise Héon, Alex Levin, Ian M MacDonald
Ophthalmic Genetics
|
May 26, 2012
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly
Gail Billingsley, Ajoy Vincent, Catherine Deveault, et al.
Investigative Ophthalmology & Visual Science
|
February 28, 2007
Assessment of central retinal function in patients with advanced retinitis pigmentosa
Christina Gerth, Tom Wright, Elise Héon, et al.
Ophthalmic Genetics
|
January 28, 2011
Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders
Ajoy Vincent, Tom Wright, Gail Billingsley, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
January 5, 2006
Unusual ocular presentation of von Hippel-Lindau disease
Alejandra Valenzuela, Harriet Druker, David Malkin, et al.
Page
of 12
Search research articles
Search
Showing results (1-10 of 114) with videos related to
Sort By:
Page
of 12
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
October 1, 2009
Jack Crawford Day 2009
Elise Héon
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
November 10, 2009
My child has Leber congenital amaurosis: why is he/she not eligible for gene therapy trials?
Elise Héon
Investigative Ophthalmology & Visual Science
|
April 23, 2019
Introducing Artur V. Cideciyan and Samuel G. Jacobson, the 2018 Recipients of the Proctor Medal
Elise Héon, Gustavo D Aguirre
Advances in Experimental Medicine and Biology
|
December 21, 2011
Caenorhabditis elegans as a model organism for ciliopathies and related forms of photoreceptor degeneration
Calvin A Mok, Elise Héon
Ophthalmic Genetics
|
April 6, 2011
BBS mutational analysis: a strategic approach
Gail Billingsley, Catherine Deveault, Elise Héon
Ophthalmic Genetics
|
April 23, 2014
In memoriam Maria Musarella
Elise Héon, Alex Levin, Ian M MacDonald
Ophthalmic Genetics
|
May 26, 2012
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly
Gail Billingsley, Ajoy Vincent, Catherine Deveault, et al.
Investigative Ophthalmology & Visual Science
|
February 28, 2007
Assessment of central retinal function in patients with advanced retinitis pigmentosa
Christina Gerth, Tom Wright, Elise Héon, et al.
Ophthalmic Genetics
|
January 28, 2011
Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders
Ajoy Vincent, Tom Wright, Gail Billingsley, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
January 5, 2006
Unusual ocular presentation of von Hippel-Lindau disease
Alejandra Valenzuela, Harriet Druker, David Malkin, et al.
Page
of 12