Works matching AU Chang, Bernard


Results: 88
    1

    Living with an artificial eye: qualitative insights into patient and family member experiences.

    Published in:
    International Ophthalmology, 2024, v. 44, n. 1, p. 1, doi. 10.1007/s10792-024-02933-0
    By:
    • Boele, Florien W.;
    • Kawalek, Jessica Charlotte;
    • Nicklin, Emma;
    • Gout, Taras;
    • Watson, Judith M.;
    • Woodward, Amie;
    • Coleman, Elizabeth;
    • Ronaldson, Sarah;
    • Zoltie, Tim;
    • Bartlett, Paul;
    • Wilson, Laura;
    • Walshaw, Emma;
    • Archer, Tom;
    • Chang, Bernard;
    • Kalantzis, George;
    • El-Hindy, Nabil;
    • Theaker, Mike
    Publication type:
    Article
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    LANGERHANS CELL HISTIOCYTOSIS OF THE EYELID.

    Published in:
    Journal of Paediatrics & Child Health, 2011, v. 47, n. 4, p. 240, doi. 10.1111/j.1440-1754.2011.02053.x
    By:
    • El Hindy, Nabil;
    • Jong Min Ong;
    • Kalantzis, George;
    • Philips, Robert;
    • Chang, Bernard
    Publication type:
    Article
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    Mutations in PNKP cause microcephaly, seizures and defects in DNA repair.

    Published in:
    Nature Genetics, 2010, v. 42, n. 3, p. 245, doi. 10.1038/ng.526
    By:
    • Jun Shen;
    • Gilmore, Edward C.;
    • Marshall, Christine A.;
    • Haddadin, Mary;
    • Reynolds, John J.;
    • Eyaid, Wafaa;
    • Bodell, Adria;
    • Barry, Brenda;
    • Gleason, Danielle;
    • Allen, Kathryn;
    • Ganesh, Vijay S.;
    • Chang, Bernard S.;
    • Grix, Arthur;
    • Hill, R. Sean;
    • Topcu, Meral;
    • Caldecott, Keith W.;
    • Barkovich, A. James;
    • Walsh, Christopher A.
    Publication type:
    Article
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    Beware the empty curette!

    Published in:
    Orbit, 2002, v. 21, n. 2, p. 177, doi. 10.1076/orbi.21.2.177.7191
    By:
    • Cunniffe, Geraldine;
    • Chang, Bernard Y.P.;
    • Kennedy, Susan;
    • Moriarty, Paul
    Publication type:
    Article
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    Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East.

    Published in:
    Human Mutation, 2008, v. 29, n. 11, p. E231, doi. 10.1002/humu.20844
    By:
    • Chiara Manzini, M.;
    • Gleason, Danielle;
    • Chang, Bernard S.;
    • Sean Hill, R.;
    • Barry, Brenda J.;
    • Partlow, Jennifer N.;
    • Poduri, Annapurna;
    • Currier, Sophie;
    • Galvin-Parton, Patricia;
    • Shapiro, Lawrence R.;
    • Schmidt, Karen;
    • Davis, Jessica G.;
    • Basel-Vanagaite, Lina;
    • Seidahmed, Mohamed Z.;
    • Salih, Mustafa A. M.;
    • Dobyns, William B.;
    • Walsh, Christopher A.
    Publication type:
    Article