Torthaí cuardaigh - Richard G. Weleber

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  1. 1
    The dystrophic retina in multisystem disorders: The electroretinogram in neuronal ceroid lipofuscinoses

    The dystrophic retina in multisystem disorders: The electroretinogram in neuronal ceroid lipofuscinoses de réir Richard G. Weleber

    Foilsithe / Cruthaithe 1998
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  2. 2
    Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy

    Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy de réir Grazyna Adamus, Gaoying Ren, Richard G. Weleber

    Foilsithe / Cruthaithe 2004
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  3. 3
    Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions

    Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions de réir Neruban Kumaran, Anthony T. Moore, Richard G. Weleber, Michel Michaelides

    Foilsithe / Cruthaithe 2017
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  4. 4
    Randomized Trial of Ciliary Neurotrophic Factor Delivered by Encapsulated Cell Intraocular Implants for Retinitis Pigmentosa

    Randomized Trial of Ciliary Neurotrophic Factor Delivered by Encapsulated Cell Intraocular Implants for Retinitis Pigmentosa de réir David G. Birch, Richard G. Weleber, Jacque L. Duncan, Glenn J. Jaffe, Weng Tao

    Foilsithe / Cruthaithe 2013
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  5. 5
    Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies

    Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies de réir A. L. Fletcher, Mark E. Pennesi, Cary O. Harding, Richard G. Weleber, Melanie B. Gillingham

    Foilsithe / Cruthaithe 2012
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  6. 6
    Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

    Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2 de réir Petra Jakobs, John F. Hess, Paul G. Fitzgerald, Patricia Kramer, Richard G. Weleber, M. Litt

    Foilsithe / Cruthaithe 2000
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  7. 7
    Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa

    Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa de réir Travis Smith, Maria A. Parker, Peter Steinkamp, Richard G. Weleber, Ning Smith, David J. Wilson

    Foilsithe / Cruthaithe 2016
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  8. 8
    Long-term Follow-up of Patients With Retinitis Pigmentosa Receiving Intraocular Ciliary Neurotrophic Factor Implants

    Long-term Follow-up of Patients With Retinitis Pigmentosa Receiving Intraocular Ciliary Neurotrophic Factor Implants de réir David G. Birch, Lea D. Bennett, Jacque L. Duncan, Richard G. Weleber, Mark E. Pennesi

    Foilsithe / Cruthaithe 2016
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  9. 9
    Haplotypes in the Complement Factor H (CFH) Gene: Associations with Drusen and Advanced Age-Related Macular Degeneration

    Haplotypes in the Complement Factor H (CFH) Gene: Associations with Drusen and Advanced Age-Related Macular Degeneration de réir Peter J. Francis, Dennis W. Schultz, Sara Hamon, Jürg Ott, Richard G. Weleber, Michael L. Klein

    Foilsithe / Cruthaithe 2007
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  10. 10
    Optical Coherence Tomography Angiography in Choroideremia

    Optical Coherence Tomography Angiography in Choroideremia de réir Nieraj Jain, Yali Jia, Simon S. Gao, Xinbo Zhang, Richard G. Weleber, David Huang, Mark E. Pennesi

    Foilsithe / Cruthaithe 2016
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  11. 11
    Clinical and Electrophysiologic Characterization of Paraneoplastic and Autoimmune Retinopathies Associated With Antienolase Antibodies

    Clinical and Electrophysiologic Characterization of Paraneoplastic and Autoimmune Retinopathies Associated With Antienolase Antibodies de réir Richard G. Weleber, Robert C. Watzke, William T. Shults, Karmen M Trzupek, John R. Heckenlively, Robert A. Egan, Grazyna Adamus

    Foilsithe / Cruthaithe 2005
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  12. 12
    Variable expressivity of <i>BEST1</i>-associated autosomal dominant vitreoretinochoroidopathy (ADVIRC) in a three-generation pedigree

    Variable expressivity of <i>BEST1</i>-associated autosomal dominant vitreoretinochoroidopathy (ADVIRC) in a three-generation pedigree de réir Mariana Matioli da Palma, Mauricio E. Vargas, Amanda Burr, Rui Chen, Mark E. Pennesi, Richard G. Weleber, Paul Yang

    Foilsithe / Cruthaithe 2021
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  13. 13
    Neuro-Ophthalmologic and Electroretinographic Findings in Pantothenate Kinase-Associated Neurodegeneration (formerly Hallervorden-Spatz Syndrome)

    Neuro-Ophthalmologic and Electroretinographic Findings in Pantothenate Kinase-Associated Neurodegeneration (formerly Hallervorden-Spatz Syndrome) de réir Robert A. Egan, Richard G. Weleber, Penelope Hogarth, Allison Gregory, Jason Coryell, Shawn K. Westaway, Jane Gitschier, Soma Das, Susan J. Hayflick

    Foilsithe / Cruthaithe 2005
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  14. 14
    Age-Related Macular Degeneration—a Genome Scan in Extended Families

    Age-Related Macular Degeneration—a Genome Scan in Extended Families de réir Jacek Majewski, Dennis W. Schultz, Richard G. Weleber, Mitchell Schain, Albert O. Edwards, Tara C. Matise, Ted S. Acott, Jürg Ott, Michael L. Klein

    Foilsithe / Cruthaithe 2003
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  15. 15
    Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain–Optical Coherence Tomography

    Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain–Optical Coherence Tomography de réir Amir H Hariri, Hong Yang Zhang, Alexander Ho, Peter J. Francis, Richard G. Weleber, David G. Birch, Frederick L. Ferris, Srinivas R. Sadda

    Foilsithe / Cruthaithe 2016
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  16. 16
    Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children

    Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children de réir William J. Kimberling, Michael S. Hildebrand, A. Eliot Shearer, Maren Jensen, Jennifer A. Halder, Karmen M Trzupek, Edward Cohn, Richard G. Weleber, Edwin M. Stone, Richard J. Smith

    Foilsithe / Cruthaithe 2010
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  17. 17
    Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency

    Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency de réir Melanie B. Gillingham, Richard G. Weleber, Martha Neuringer, William E. Connor, Monte D. Mills, Sandy van Calcar, James N. Ver Hoeve, Jon A. Wolff, Cary O. Harding

    Foilsithe / Cruthaithe 2005
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  18. 18
    Improved Rod Sensitivity as Assessed by Two-Color Dark-Adapted Perimetry in Patients With <i>RPE65</i>-Related Retinopathy Treated With Voretigene Neparvovec-rzyl

    Improved Rod Sensitivity as Assessed by Two-Color Dark-Adapted Perimetry in Patients With <i>RPE65</i>-Related Retinopathy Treated With Voretigene Neparvovec-rzyl de réir Cristy A. Ku, Austin D. Igelman, Samuel J. Huang, Huber Vasconcelos, Mariana Matioli da Palma, Steven T. Bailey, Andreas Lauer, Richard G. Weleber, Paul Yang, Mark E. Pennesi

    Foilsithe / Cruthaithe 2023
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  19. 19
    VFMA: Topographic Analysis of Sensitivity Data From Full-Field Static Perimetry

    VFMA: Topographic Analysis of Sensitivity Data From Full-Field Static Perimetry de réir Richard G. Weleber, Travis Smith, Dawn Peters, Elvira N. Chegarnov, Scott P. Gillespie, Peter J. Francis, Stuart K. Gardiner, Jens Paetzold, Janko Dietzsch, Ulrich Schiefer, Chris A. Johnson

    Foilsithe / Cruthaithe 2015
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  20. 20
    Mutations in FLVCR1 Cause Posterior Column Ataxia and Retinitis Pigmentosa

    Mutations in FLVCR1 Cause Posterior Column Ataxia and Retinitis Pigmentosa de réir Anjali M. Rajadhyaksha, Olivier Elemento, Erik G. Puffenberger, Kathryn C. Schierberl, Jenny Xiang, Maria Lisa Putorti, José Berciano, Chantal Poulin, Bernard Brais, Michel Michaelides, Richard G. Weleber, Joseph Higgins

    Foilsithe / Cruthaithe 2010
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