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H Fingert

Showing results (41-50 of 159) with videos related to

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Ophthalmic Genetics|May 11, 2010
Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmusJohn H Fingert, Ben Roos, Mari E Eyestone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cellsA R Shepard, N Jacobson, J H Fingert, et al.
Journal of Glaucoma|March 8, 2016
The Utility of Diaton Tonometer Measurements in Patients With Ocular Hypertension, Glaucoma, and Glaucoma Tube Shunts: A Preliminary Study for its Potential Use in Keratoprosthesis PatientsJustin M Risma, Shandiz Tehrani, Kai Wang, et al.
Journal of Glaucoma|April 25, 2012
Circumferential iris transillumination defects in exfoliation syndromeJohn H Fingert, James H Burden, Kai Wang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 10, 2006
Case of Stargardt disease caused by uniparental isodisomyJohn H Fingert, David A Eliason, Nicole C Phillips, et al.
Ophthalmology|December 24, 2023
The Effect of Insurance Coverage Laws on Glaucoma Eyedrop Medication UsageNicole Hehr, Patrick B Barlow, Wisam Najdawi, et al.
Eye (London, England)|January 20, 2018
A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigreeM J Schnieders, W Goar, M Griess, et al.
Current Eye Research|July 31, 2019
Novel Intragenic <i>PAX6</i> Deletion in a Pedigree with Aniridia, Morbid Obesity, and DiabetesErin A Boese, Mallory R Tollefson, Michael J Schnieders, et al.
Human Molecular Genetics|May 27, 2017
Primary congenital and developmental glaucomasCarly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, et al.
Pageof 16

Showing results (41-50 of 159) with videos related to

Sort By:
Pageof 16
Ophthalmic Genetics|May 11, 2010
Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmusJohn H Fingert, Ben Roos, Mari E Eyestone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1997
Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)J Brown, J H Fingert, C M Taylor, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cellsA R Shepard, N Jacobson, J H Fingert, et al.
Journal of Glaucoma|March 8, 2016
The Utility of Diaton Tonometer Measurements in Patients With Ocular Hypertension, Glaucoma, and Glaucoma Tube Shunts: A Preliminary Study for its Potential Use in Keratoprosthesis PatientsJustin M Risma, Shandiz Tehrani, Kai Wang, et al.
Journal of Glaucoma|April 25, 2012
Circumferential iris transillumination defects in exfoliation syndromeJohn H Fingert, James H Burden, Kai Wang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 10, 2006
Case of Stargardt disease caused by uniparental isodisomyJohn H Fingert, David A Eliason, Nicole C Phillips, et al.
Ophthalmology|December 24, 2023
The Effect of Insurance Coverage Laws on Glaucoma Eyedrop Medication UsageNicole Hehr, Patrick B Barlow, Wisam Najdawi, et al.
Eye (London, England)|January 20, 2018
A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigreeM J Schnieders, W Goar, M Griess, et al.
Current Eye Research|July 31, 2019
Novel Intragenic <i>PAX6</i> Deletion in a Pedigree with Aniridia, Morbid Obesity, and DiabetesErin A Boese, Mallory R Tollefson, Michael J Schnieders, et al.
Human Molecular Genetics|May 27, 2017
Primary congenital and developmental glaucomasCarly J Lewis, Adam Hedberg-Buenz, Adam P DeLuca, et al.
Pageof 16