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Thaddeus P Dryja

Showing results (21-30 of 75) with videos related to

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Cornea|September 30, 2015
Dry Eye Signs and Symptoms Persist During Systemic Neutralization of IL-1β by Canakinumab or IL-17A by SecukinumabCynthia L Grosskreutz, Hans-Ulrich Hockey, Denise Serra, et al.
Retinal Cases & Brief Reports|November 13, 2014
Response of choroidal leiomyoma to treatment with proton beam radiationSzilárd Kiss, Evangelos S Gragoudas, Thaddeus P Dryja, et al.
Ophthalmic Plastic and Reconstructive Surgery|January 11, 2018
Mild Complications or Unusual Persistence of Porcine Collagen and Hyaluronic Acid Gel Following Periocular Filler InjectionsNatalie Wolkow, Frederick A Jakobiec, Thaddeus P Dryja, et al.
Molecular Vision|December 15, 2006
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosaGeetha H Mylvaganam, Terri L McGee, Eliot L Berson, et al.
Molecular Vision|April 18, 2007
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosaMeredith O Sweeney, Terri L McGee, Eliot L Berson, et al.
Ophthalmic Plastic and Reconstructive Surgery|January 20, 2018
Multiple Eyelid Cysts (Apocrine and Eccrine Hidrocystomas, Trichilemmal Cyst, and Hybrid Cyst) in a Patient With a ProlactinomaLina Ma, Frederick A Jakobiec, Natalie Wolkow, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 25, 2008
Diagnosis in a patient with fundus albipunctatus and atypical fundus changesManal Hajali, Gerald A Fishman, Thaddeus P Dryja, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutationsMichael A Sandberg, Bernard Rosner, Carol Weigel-DiFranco, et al.
Ophthalmic Genetics|November 8, 2005
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 genePatrik Schatz, Vesna Ponjavic, Sten Andréasson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2003
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degenerationDror Sharon, Michael A Sandberg, Rafael C Caruso, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
Cornea|September 30, 2015
Dry Eye Signs and Symptoms Persist During Systemic Neutralization of IL-1β by Canakinumab or IL-17A by SecukinumabCynthia L Grosskreutz, Hans-Ulrich Hockey, Denise Serra, et al.
Retinal Cases & Brief Reports|November 13, 2014
Response of choroidal leiomyoma to treatment with proton beam radiationSzilárd Kiss, Evangelos S Gragoudas, Thaddeus P Dryja, et al.
Ophthalmic Plastic and Reconstructive Surgery|January 11, 2018
Mild Complications or Unusual Persistence of Porcine Collagen and Hyaluronic Acid Gel Following Periocular Filler InjectionsNatalie Wolkow, Frederick A Jakobiec, Thaddeus P Dryja, et al.
Molecular Vision|December 15, 2006
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosaGeetha H Mylvaganam, Terri L McGee, Eliot L Berson, et al.
Molecular Vision|April 18, 2007
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosaMeredith O Sweeney, Terri L McGee, Eliot L Berson, et al.
Ophthalmic Plastic and Reconstructive Surgery|January 20, 2018
Multiple Eyelid Cysts (Apocrine and Eccrine Hidrocystomas, Trichilemmal Cyst, and Hybrid Cyst) in a Patient With a ProlactinomaLina Ma, Frederick A Jakobiec, Natalie Wolkow, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 25, 2008
Diagnosis in a patient with fundus albipunctatus and atypical fundus changesManal Hajali, Gerald A Fishman, Thaddeus P Dryja, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutationsMichael A Sandberg, Bernard Rosner, Carol Weigel-DiFranco, et al.
Ophthalmic Genetics|November 8, 2005
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 genePatrik Schatz, Vesna Ponjavic, Sten Andréasson, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 10, 2003
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degenerationDror Sharon, Michael A Sandberg, Rafael C Caruso, et al.
Pageof 8