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Thaddeus P Dryja

Showing results (31-40 of 75) with videos related to

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Human Mutation|February 16, 2005
Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseasesKoji M Nishiguchi, Michael A Sandberg, Nasim Gorji, et al.
The New England Journal of Medicine|February 17, 2006
Case records of the Massachusetts General Hospital. Case 5-2006. An 11-year-old girl with loss of vision in the right eyeDavid S Walton, Shizuo Mukai, Eric F Grabowski, et al.
Investigative Ophthalmology & Visual Science|August 31, 2002
Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutationsEliot L Berson, Bernard Rosner, Carol Weigel-DiFranco, et al.
Experimental Eye Research|August 25, 2004
Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosaBabak Jian Seyedahmadi, Carlo Rivolta, Julia A Keene, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 4, 2007
Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 geneAlessandro Iannaccone, Salvatore A Tedesco, Kevin T Gallaher, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosaMargaret M DeAngelis, Jonna L Grimsby, Michael A Sandberg, et al.
Journal of Medical Genetics|May 29, 2010
Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosaTerri L McGee, Babak Jian Seyedahmadi, Meredith O Sweeney, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 13, 2019
Isolated orbital amyloidosis causing internal and external ophthalmoplegiaMary-Magdalene Ugo Dodd, Natalie Wolkow, Mary Elizabeth Cunnane, et al.
American Journal of Human Genetics|October 18, 2003
RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosaDror Sharon, Michael A Sandberg, Vivian W Rabe, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2003
Clinicopathologic reports, case reports, and small case series: surgical removal and histopathologic findings of a subfoveal neovascular membrane associated with choroidal osteomaBradley S Foster, Jessica P Fernandez-Suntay, Thaddeus P Dryja, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Human Mutation|February 16, 2005
Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseasesKoji M Nishiguchi, Michael A Sandberg, Nasim Gorji, et al.
The New England Journal of Medicine|February 17, 2006
Case records of the Massachusetts General Hospital. Case 5-2006. An 11-year-old girl with loss of vision in the right eyeDavid S Walton, Shizuo Mukai, Eric F Grabowski, et al.
Investigative Ophthalmology & Visual Science|August 31, 2002
Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutationsEliot L Berson, Bernard Rosner, Carol Weigel-DiFranco, et al.
Experimental Eye Research|August 25, 2004
Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosaBabak Jian Seyedahmadi, Carlo Rivolta, Julia A Keene, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 4, 2007
Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 geneAlessandro Iannaccone, Salvatore A Tedesco, Kevin T Gallaher, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosaMargaret M DeAngelis, Jonna L Grimsby, Michael A Sandberg, et al.
Journal of Medical Genetics|May 29, 2010
Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosaTerri L McGee, Babak Jian Seyedahmadi, Meredith O Sweeney, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 13, 2019
Isolated orbital amyloidosis causing internal and external ophthalmoplegiaMary-Magdalene Ugo Dodd, Natalie Wolkow, Mary Elizabeth Cunnane, et al.
American Journal of Human Genetics|October 18, 2003
RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosaDror Sharon, Michael A Sandberg, Vivian W Rabe, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2003
Clinicopathologic reports, case reports, and small case series: surgical removal and histopathologic findings of a subfoveal neovascular membrane associated with choroidal osteomaBradley S Foster, Jessica P Fernandez-Suntay, Thaddeus P Dryja, et al.
Pageof 8