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Michael A Grassi

Showing results (21-30 of 43) with videos related to

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Human Molecular Genetics|March 29, 2011
Genome-wide meta-analysis for severe diabetic retinopathyMichael A Grassi, Anna Tikhomirov, Sudha Ramalingam, et al.
American Journal of Ophthalmology|April 3, 2004
Atypical pigment dispersion syndrome in a childMichael A Grassi, Wallace L M Alward, Randall L Verdick, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 3, 2017
A novel MERTK mutation causing retinitis pigmentosaHasenin Al-Khersan, Kaanan P Shah, Segun C Jung, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Complement factor H polymorphism p.Tyr402His and cuticular DrusenMichael A Grassi, James C Folk, Todd E Scheetz, et al.
Ophthalmology|February 12, 2011
Thirty-Year follow-up of an African American family with macular dystrophy of the retina, locus 1 (North Carolina macular dystrophy)Daniel F Kiernan, Rohan J Shah, Seenu M Hariprasad, et al.
Molecular Vision|September 16, 2014
Role of FAM18B in diabetic retinopathyAi Ling Wang, Vidhya R Rao, Judy J Chen, et al.
American Journal of Ophthalmology|December 5, 2008
Patient self-report of prior laser treatment reliably indicates presence of severe diabetic retinopathyMichael A Grassi, D Anthony Mazzulla, Michael D Knudtson, et al.
The Journal of Biological Chemistry|February 13, 2014
Cytochrome P450 2C epoxygenases mediate photochemical stress-induced death of photoreceptorsQing Chang, Evgeny Berdyshev, Dingcai Cao, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Pathognomonic macular ripples are revealed by polarized infrared retinal imagingDarius Ansari, Poulami P Borkar, Patricia L Davis, et al.
Investigative Ophthalmology & Visual Science|March 26, 2005
A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)Izabela Sokal, William J Dupps, Michael A Grassi, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|March 29, 2011
Genome-wide meta-analysis for severe diabetic retinopathyMichael A Grassi, Anna Tikhomirov, Sudha Ramalingam, et al.
American Journal of Ophthalmology|April 3, 2004
Atypical pigment dispersion syndrome in a childMichael A Grassi, Wallace L M Alward, Randall L Verdick, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 3, 2017
A novel MERTK mutation causing retinitis pigmentosaHasenin Al-Khersan, Kaanan P Shah, Segun C Jung, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Complement factor H polymorphism p.Tyr402His and cuticular DrusenMichael A Grassi, James C Folk, Todd E Scheetz, et al.
Ophthalmology|February 12, 2011
Thirty-Year follow-up of an African American family with macular dystrophy of the retina, locus 1 (North Carolina macular dystrophy)Daniel F Kiernan, Rohan J Shah, Seenu M Hariprasad, et al.
Molecular Vision|September 16, 2014
Role of FAM18B in diabetic retinopathyAi Ling Wang, Vidhya R Rao, Judy J Chen, et al.
American Journal of Ophthalmology|December 5, 2008
Patient self-report of prior laser treatment reliably indicates presence of severe diabetic retinopathyMichael A Grassi, D Anthony Mazzulla, Michael D Knudtson, et al.
The Journal of Biological Chemistry|February 13, 2014
Cytochrome P450 2C epoxygenases mediate photochemical stress-induced death of photoreceptorsQing Chang, Evgeny Berdyshev, Dingcai Cao, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Pathognomonic macular ripples are revealed by polarized infrared retinal imagingDarius Ansari, Poulami P Borkar, Patricia L Davis, et al.
Investigative Ophthalmology & Visual Science|March 26, 2005
A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)Izabela Sokal, William J Dupps, Michael A Grassi, et al.
Pageof 5