Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy
Li, Shouling, Tiab, Leila, Jiao, Xiaodong, Munier, Francis L., Zografos, Leonidas, Frueh, Béatrice E., Sergeev, Yuri, Smith, Janine, Rubin, Benjamin, Meallet, Mario A., Forster, Richard K., Hejtmancik, J. Fielding, Schorderet, Daniel F.
Published in American journal of human genetics (01.07.2005)
Published in American journal of human genetics (01.07.2005)
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Thomas A. Swift's Electric Rifle Injuries to the Eye and Ocular Adnexa: The Management of Complex Trauma
Moysidis, Stavros N, Koulisis, Nicole, Rodger, Damien C, Chao, Jennifer R, Leng, Theodore, de Carlo, Talisa, Burkemper, Bruce, Ediriwickrema, Lilangi S, George, Meena S, Jiang, Yi, Bohm, Kelley J, Gulati, Shilpa, Torres, Rodrigo J, Meallet, Mario A, Moshfeghi, Andrew A, Flynn, Jr, Harry W, Mieler, William F, Williams, George A, Humayun, Mark S, Eliott, Dean
Published in Ophthalmology retina (01.03.2019)
Published in Ophthalmology retina (01.03.2019)
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Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene
Aldave, Anthony J., Gutmark, Julie G., Yellore, Vivek S., Affeldt, John A., Meallet, Mario A., Udar, Nitin, Rao, Narsing A., Small, Kent W., Klintworth, Gordon K.
Published in American journal of ophthalmology (01.11.2004)
Published in American journal of ophthalmology (01.11.2004)
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Journal Article
No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition
Aldave, Anthony J, Rayner, Sylvia A, King, Julie A, Salem, Andrew K, Prechanond, Apiradi, Hashida, Setsuko, Affeldt, John C, Meallet, Mario A, Glasgow, Ben J, Small, Kent W, Yellore, Vivek S
Published in Cornea (01.05.2006)
Published in Cornea (01.05.2006)
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An extreme case of retinal avascularity in a female neonate with incontinentia pigmenti
Meallet, Mario A, Song, Jonathan, Stout, J Timothy
Published in Retina (Philadelphia, Pa.) (01.08.2004)
Published in Retina (Philadelphia, Pa.) (01.08.2004)
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An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His βig H3 mutation in an African-American woman
MEALLET, Mario A, AFFELDT, John A, MCFARLAND, Trevor J, APPUKUTTAN, Binoy, READ, Rusell, STOUT, J. Timothy, RAO, Narsing A
Published in American journal of ophthalmology (01.04.2004)
Published in American journal of ophthalmology (01.04.2004)
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Journal Article
An unusual clinical phenotype of avellino corneal dystrophy associated with an Arg124His [beta]iG-H3 mutation in an African-American woman
Meallet, Mario A, Affeldt, John A, McFarland, Trevor J, Appukuttan, Binoy, Read, Rusell, Stout, JTimothy, Rao, Narsing A
Published in American journal of ophthalmology (01.04.2004)
Published in American journal of ophthalmology (01.04.2004)
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Journal Article
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in theTGFBIgene
Aldave, Anthony J, Gutmark, Julie G, Yellore, Vivek S, Affeldt, John A, Meallet, Mario A, Udar, Nitin, Rao, Narsing A, Small, Kent W, Klintworth, Gordon K
Published in American journal of ophthalmology (01.11.2004)
Published in American journal of ophthalmology (01.11.2004)
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Journal Article
An unusual clinical phenotype of avellino corneal dystrophy associated with an Arg124His βiG-H3 mutation in an African-American woman
Meallet, Mario A., Affeldt, John A., McFarland, Trevor J., Appukuttan, Binoy, Read, Rusell, Stout, J.Timothy, Rao, Narsing A.
Published in American journal of ophthalmology (01.04.2004)
Published in American journal of ophthalmology (01.04.2004)
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Journal Article