نتائج البحث - Stuart Douglas

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  1. 1
    A physician's story of his own illness: Aphasia from possible stroke but more likely from encephalitis

    A physician's story of his own illness: Aphasia from possible stroke but more likely from encephalitis حسب Lathan, S. Robert, Stuart, Douglas

    منشور في 2018
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  2. 2
    The beginning of intracellular recording in spinal neurons: Facts, reflections, and speculations(, )

    The beginning of intracellular recording in spinal neurons: Facts, reflections, and speculations(, ) حسب Stuart, Douglas G., Brownstone, Robert M.

    منشور في 2011
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  3. 3
    Thomas Graham Brown (1882–1965): Behind the Scenes at the Cardiff Institute of Physiology

    Thomas Graham Brown (1882–1965): Behind the Scenes at the Cardiff Institute of Physiology حسب Jones, J. Gareth, Tansey, E.M. (Tilli), Stuart, Douglas G.

    منشور في 2011
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  4. 4
    Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia

    Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia حسب Lijia Huang, Jodi Warman‐Chardon, Melissa T. Carter, K. Friend, Tracy Dudding, Jeremy Schwartzentruber, Ruobing Zou, Peter W. Schofield, Stuart Douglas, Dennis E. Bulman, Kym M. Boycott

    منشور في 2012
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  5. 5
    Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly

    Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly حسب Matthew A. Lines, Lijia Huang, Jeremy Schwartzentruber, Stuart Douglas, Danielle C. Lynch, Chandree L. Beaulieu, Maria Leine Guion‐Almeida, Roseli Maria Zechi‐Ceide, Blanca Gener, Gabriele Gillessen‐Kaesbach, Caroline Nava, Geneviève Baujat, Denise Horn, Usha Kini, Almuth Caliebe, Yasemin Alanay, Gülen Eda Ütine, Dorit Lev, Jürgen Kohlhase, Arthur W. Grix, Dietmar Lohmann, Ute Hehr, Detlef Böhm, Jacek Majewski, Dennis E. Bulman, Dagmar Wieczorek, Kym M. Boycott

    منشور في 2012
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  6. 6
    TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone

    TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone حسب Lijia Huang, Katarzyna Szymańska, Victor L. Jensen, Andreas Janecke, A. Micheil Innes, Erica E. Davis, Patrick Frosk, Chunmei Li, Jason R. Willer, Bernard N. Chodirker, Cheryl R. Greenberg, D. Ross McLeod, François Bernier, Albert E. Chudley, Andreas Th. Müller, Mohammad Shboul, Clare V. Logan, Catrina M. Loucks, Chandree L. Beaulieu, Rachel V. Bowie, Sandra Bell, Jonathan Adkins, Freddi I. Zuniga, Kevin D. Ross, Jian Wang, Matthew R. Ban, Christian Becker, Peter Nürnberg, Stuart Douglas, Cheryl M. Craft, Marie-Andree Akimenko, Robert A. Hegele, Carole Ober, Gerd Utermann, Hanno J. Bolz, Dennis E. Bulman, Nicholas Katsanis, Oliver E. Blacque, Dan Doherty, Jillian S. Parboosingh, Michel R. Leroux, Colin A. Johnson, Kym M. Boycott

    منشور في 2011
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