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pro vyhledávání: '"Alnabi, WA"'
Autor:
Wangtiraumnuay, N, Alnabi, WA, Tsukikawa, M, Thau, A, Capasso, J, Sharony, R, Inglehearn, CF, Levin, AV
Background/Aims: Pigmentary retinal dystrophy and macular dystrophy have been previously reported in Heimler syndrome due to mutations in PEX1. Here we reported the ocular manifestations in Heimler syndrome due to mutations in PEX6. Materials and met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::ef9cc3ac134c84f0180a8215fb95a259
Autor:
Thau A; Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA., Dawodu O; Department of Ophthalmology, University of Benin Teaching Hospital, Benin City, Nigeria., Mireskandari K; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, ON, Canada., Ali A; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, ON, Canada., Tehrani N; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, ON, Canada., DeBenedictis C; Pediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, PA., Bhoiwala D; Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA., Aultman W; Pediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, PA., Alnabi WA; Pediatric Ophthalmology and Ocular Genetics, Wills Eye Hospital, Philadelphia, PA., Leiby BE; Department of Pharmacology and Experimental Therapeutics, Thomas Jefferson University, Philadelphia, PA., Levin AV; Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA.; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, ON, Canada.
Publikováno v:
Cornea [Cornea] 2019 Aug; Vol. 38 (8), pp. 1003-1005.
Autor:
Thau A, Tsukikawa M, Wangtiraumnuay N, Capasso J, Affel E, Alnabi WA, Adam M, Alsulaiman SM, Spirn M, Levin AV
Publikováno v:
Ophthalmic surgery, lasers & imaging retina [Ophthalmic Surg Lasers Imaging Retina] 2019 Aug 01; Vol. 50 (8), pp. e203-e210.
Autor:
Wangtiraumnuay N; a Wills Eye Hospital , Philadelphia , PA , USA.; b Department of Ophthalmology , Queen Sirikit National Institute of Child Health , Bangkok , Thailand., Alnabi WA; a Wills Eye Hospital , Philadelphia , PA , USA., Tsukikawa M; c Sidney Kimmel Medical College at Thomas Jefferson University , Philadelphia , PA , USA., Thau A; c Sidney Kimmel Medical College at Thomas Jefferson University , Philadelphia , PA , USA., Capasso J; a Wills Eye Hospital , Philadelphia , PA , USA., Sharony R; d The Genetic Institute and Obstetrics and Gynecology Department, Meir Medical Center affiliated with the Sackler Faculty of Medicine , Tel Aviv University , Kfar Saba , Israel., Inglehearn CF; e Leeds Institute of Biomedical and Clinical Sciences, St. James's University Hospital, University of Leeds , Leeds , UK., Levin AV; a Wills Eye Hospital , Philadelphia , PA , USA.; c Sidney Kimmel Medical College at Thomas Jefferson University , Philadelphia , PA , USA.
Publikováno v:
Ophthalmic genetics [Ophthalmic Genet] 2018 Jun; Vol. 39 (3), pp. 384-390.