检索结果 - Nicholas Fletcher

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  1. 1
    The relationship between trauma and idiopathic torsion dystonia.

    The relationship between trauma and idiopathic torsion dystonia. 由 Nicholas Fletcher, A. E. Harding, C. D. Marsden

    出版 1991
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    Artigo
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  2. 2
    Variably protease-sensitive prionopathy in the UK: a retrospective review 1991–2008

    Variably protease-sensitive prionopathy in the UK: a retrospective review 1991–2008 由 Mark Head, Helen Yull, Diane Ritchie, Jan Langeveld, Nicholas Fletcher, Richard Knight, James W. Ironside

    出版 2013
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    Revisão
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  3. 3
    <i>SCP2</i> mutations and neurodegeneration with brain iron accumulation

    <i>SCP2</i> mutations and neurodegeneration with brain iron accumulation 由 Rita Horváth, David Lewis‐Smith, Konstantinos Douroudis, Jennifer Duff, Michael J. Keogh, Angela Pyle, Nicholas Fletcher, Patrick F. Chinnery

    出版 2015
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  4. 4
    Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation

    Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation 由 Patrick F. Chinnery, Douglas E. Crompton, D. Birchall, Margaret Jackson, Alan Coulthard, A. Lombès, N. Quinn, Andy J. Wills, Nicholas Fletcher, J. P. Mottershead, Paul R. Cooper, Mark Kellett, David Bates, John Burn

    出版 2006
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    Artigo
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  5. 5
    The absence of intrarenal ACE protects against hypertension

    The absence of intrarenal ACE protects against hypertension 由 Romer A. Gonzalez‐Villalobos, Tea Janjoulia, Nicholas Fletcher, Jorge F. Giani, Mien T.X. Nguyen, Anne Riquier‐Brison, Dale M. Seth, Sébastien Fuchs, Dominique Eladari, Nicolas Picard, Sebastian Bachmann, Eric Delpire, János Peti‐Peterdi, L. Gabriel Navar, Kenneth E. Bernstein, Alicia A. McDonough

    出版 2013
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  6. 6
    Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model

    Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model 由 Andrea H. Németh, Alexandra Kwasniewska, Stefano Lise, Ricardo Parolin Schnekenberg, Esther B. E. Becker, Katarzyna D. Bera, Morag Shanks, Lorna Gregory, David Buck, M. Zameel Cader, Kevin Talbot, Rajith de Silva, Nicholas Fletcher, Rob Hastings, Sandeep Jayawant, Patrick J. Morrison, Paul Worth, A. Malcolm R. Taylor, John Tolmie, Mary O’Regan, Ruth A. Valentine, Emily Packham, Julie Evans, A Seller, Jiannis Ragoussis

    出版 2013
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  7. 7
    Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

    Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts 由 Emma M. Jenkinson, Mathieu P. Rodero, Paul R. Kasher, Carolina Uggenti, Anthony Oojageer, Laurence Goosey, Y Rose, Christopher J. Kershaw, Jill Urquhart, Simon G. Williams, Sanjeev S. Bhaskar, James D.B. O’Sullivan, Gabriela M. Baerlocher, Monika Haubitz, Geraldine Aubert, Kristin Barañano, Angela Barnicoat, Roberta Battini, Andrea Berger, Edward Blair, Janice Brunstrom-Hernandez, Johannes Buckard, David Cassiman, Rosaline Caumes, Duccio Maria Cordelli, Liesbeth M De Waele, Alexander Fay, Patrick Ferreira, Nicholas Fletcher, Alan Fryer, Himanshu Goel, Cheryl Hemingway, Marco Henneke, Imelda Hughes, Rosalind J Jefferson, Ram Kumar, Lieven Lagae, P. Landrieu, Charles Marques Lourenço, Timothy J Malpas, Sarju Mehta, Imke Metz, SakkuBai Naidu, Katrin Õunap, Axel Panzer, Prab Prabhakar, Gerardine Quaghebeur, Raphael Schiffmann, Elliott H. Sherr, Kanaga R Sinnathuray, Calvin Soh, Helen Stewart, Jon Stone, Hilde Van Esch, Christine E G Van Mol, Adeline Vanderver, Emma Wakeling, Andrea Whitney, Graham D. Pavitt, Sam Griffiths‐Jones, Gillian Rice, Patrick Revy, Marjo S. van der Knaap, John H. Livingston, Raymond T. O’Keefe, Yanick J. Crow

    出版 2016
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