Výsledky vyhledávání - Shery Thomas

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  1. 1
    The effects of gabapentin and memantine in acquired and congenital nystagmus: a retrospective study

    The effects of gabapentin and memantine in acquired and congenital nystagmus: a retrospective study Autor Shery Thomas, Frank A. Proudlock, Nagini Sarvananthan, Russell McLean, Irène Gottlob

    Vydáno 2006
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    Artigo
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  2. 2
    Structural Grading of Foveal Hypoplasia Using Spectral-Domain Optical Coherence Tomography

    Structural Grading of Foveal Hypoplasia Using Spectral-Domain Optical Coherence Tomography Autor Mervyn G. Thomas, Anil Kumar, Sarim Mohammad, Frank A. Proudlock, Elizabeth C. Engle, Caroline Andrews, Wai‐Man Chan, Shery Thomas, Irène Gottlob

    Vydáno 2011
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    Artigo
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  3. 3
    Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation

    Autosomal-dominant nystagmus, foveal hypoplasia and presenile cataract associated with a novel PAX6 mutation Autor Shery Thomas, Mervyn G. Thomas, Caroline Andrews, Wai‐Man Chan, Frank A. Proudlock, Rebecca J. McLean, Archana Pradeep, Elizabeth C. Engle, Irène Gottlob

    Vydáno 2013
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  4. 4
    Abnormal retinal development associated with FRMD7 mutations

    Abnormal retinal development associated with FRMD7 mutations Autor Mervyn G. Thomas, Moira Crosier, Susan Lindsay, Anil Kumar, Masasuke Araki, Bart P. Leroy, Rebecca J. McLean, Viral Sheth, Gail Maconachie, Shery Thomas, Anthony T. Moore, Irène Gottlob

    Vydáno 2014
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  5. 5
    The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus

    The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus Autor Mervyn G. Thomas, Moira Crosier, Susan Lindsay, Anil Kumar, Shery Thomas, Masasuke Araki, Chris J. Talbot, Russell McLean, M. Surendran, Kent D. Taylor, Bart P. Leroy, A. T. Moore, David G. Hunter, Richard W. Hertle, Patrick Tarpey, A. Langmann, S. Lindner, Martina Brandner, Irène Gottlob

    Vydáno 2011
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  6. 6
    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus Autor Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, Uma Mallya, Steven Lisgo, Chris J. Talbot, E.O. Roberts, Musarat Awan, Mylvaganam Surendran, Rebecca J. McLean, Robert Reinecke, Andrea Langmann, S. Lindner, Martina Koch, Sunila Jain, Geoffrey Woodruff, Richard Gale, Andrew Bastawrous, Chris Degg, Konstantinos Droutsas, Ioannis Asproudis, Alina A. Zubcov, Christina Pieh, Colin Veal, Rajiv D. Machado, O Backhouse, Laura Baumber, Cris S. Constantinescu, Michael C. Brodsky, David G. Hunter, Richard W. Hertle, Randy J. Read, Sarah Edkins, Sarah O’Meara, Adrian G. Parker, Claire Stevens, Jon W. Teague, Richard Wooster, P. Andrew Futreal, Richard C. Trembath, Michael R. Stratton, F. Lucy Raymond, Irène Gottlob

    Vydáno 2006
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  7. 7
    Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

    Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus Autor Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, Uma Mallya, Steven Lisgo, Chris J. Talbot, E.O. Roberts, Musarat Awan, Mylvaganam Surendran, Rebecca J. McLean, Robert Reinecke, Andrea Langmann, S. Lindner, Martina Koch, Sunila Jain, Geoffrey Woodruff, Richard Gale, Chris Degg, Konstantinos Droutsas, Ioannis Asproudis, Alina A. Zubcov, Christina Pieh, Colin Veal, Rajiv D. Machado, O Backhouse, Laura Baumber, Cris S. Constantinescu, Michael C. Brodsky, David G. Hunter, Richard W. Hertle, Randy J. Read, Sarah Edkins, Sarah O’Meara, Adrian G. Parker, Claire Stevens, Jon W. Teague, Richard Wooster, P. Andrew Futreal, Richard C. Trembath, Michael R. Stratton, F. Lucy Raymond, Irène Gottlob

    Vydáno 2011
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