Works matching AU Marsden, C. David


Results: 77
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    Benign hereditary chorea-Entity or syndrome?

    Published in:
    Movement Disorders, 2000, v. 15, n. 2, p. 280, doi. 10.1002/1531-8257(200003)15:2<280::AID-MDS1011>3.0.CO;2-Q
    By:
    • Schrag, Anette;
    • Quinn, Niall P.;
    • Bhatia, Kailash P.;
    • Marsden, C. David
    Publication type:
    Article
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    Genetic aspects of Parkinson's disease.

    Published in:
    Movement Disorders, 1998, v. 13, n. 2, p. 203, doi. 10.1002/mds.870130203
    By:
    • Bandmann, Oliver;
    • David Marsden, C.;
    • Wood, Nicholas W.
    Publication type:
    Article
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    Spinal rigidity following acute myelitis.

    Published in:
    Movement Disorders, 1997, v. 12, n. 6, p. 1056, doi. 10.1002/mds.870120635
    By:
    • Brown, Peter;
    • Quinn, Niall P.;
    • Barnes, David;
    • Wren, Damien R.;
    • Marsden, C. David
    Publication type:
    Article
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    Focal task-specific tremors.

    Published in:
    Movement Disorders, 1996, v. 11, n. 6, p. 665, doi. 10.1002/mds.870110611
    By:
    • Soland, Valerie L.;
    • Bhatia, Kailash P.;
    • Volonte, Maria A.;
    • Marsden, C. David
    Publication type:
    Article
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    Hereditary geniospasm: Two new families.

    Published in:
    Movement Disorders, 1996, v. 11, n. 6, p. 744, doi. 10.1002/mds.870110626
    By:
    • Soland, Valerie L.;
    • Bhatia, Kailash P.;
    • Sheean, Geoffrey L.;
    • Marsden, C. David
    Publication type:
    Article
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    Farewell editorial.

    Published in:
    Movement Disorders, 1995, v. 10, n. 6, p. 707, doi. 10.1002/mds.870100602
    By:
    • Fahn, Stanley;
    • Marsden, C. David
    Publication type:
    Article
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    Editorial.

    Published in:
    Movement Disorders, 1995, v. 10, n. 1, p. 1, doi. 10.1002/mds.870100102
    By:
    • Fahn, Stanley;
    • Marsden, C. David
    Publication type:
    Article
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    Reply.

    Published in:
    Brain: A Journal of Neurology, 1996, v. 119, n. 3, p. 1046, doi. 10.1093/brain/119.3.1046
    By:
    • Jahanshtri, Marjan;
    • Jenkins, Harri;
    • Brown, Richard G.;
    • Marsden, C. David;
    • Passingham, Richard G.;
    • Brooks, David J.
    Publication type:
    Article
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    The basal ganglia and apraxia.

    Published in:
    Brain: A Journal of Neurology, 1996, v. 119, n. 1, p. 319, doi. 10.1093/brain/119.1.319
    By:
    • Pramstaller, Peter P.;
    • Marsden, C. David
    Publication type:
    Article
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    Sequencing of the α-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations.

    Published in:
    Human Molecular Genetics, 1998, v. 7, n. 4, p. 751, doi. 10.1093/hmg/7.4.751
    By:
    • Vaughan, Jenny R.;
    • Farrer, Matthew J.;
    • Wszolek, Zbigniew K.;
    • Gasser, Thomas;
    • Durr, Alexandra;
    • Agid, Yves;
    • Bonifati, Vincenzo;
    • DeMichele, Giuseppe;
    • Volpe, Gianpiero;
    • Lincoln, Sarah;
    • Breteler, Monique;
    • Meco, Giuseppe;
    • Brice, Alexis;
    • Marsden, C. David;
    • Hardy, John;
    • Wood, Nicholas W.
    Publication type:
    Article
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    The α-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases.

    Published in:
    Annals of Neurology, 1998, v. 44, n. 2, p. 270, doi. 10.1002/ana.410440221
    By:
    • Vaughan, Jenny;
    • Durr, Alexandra;
    • Tassin, Johann;
    • Bereznai, Benjamin;
    • Gasser, Thomas;
    • Bonifati, Vincenzo;
    • De Michele, Giuseppe;
    • Fabrizio, Edito;
    • Volpe, Gianpiero;
    • Bandmann, O.;
    • Johnson, William G.;
    • Golbe, Lawrence I.;
    • Breteler, Monique;
    • Meco, Giuseppe;
    • Agid, Yves;
    • Brice, Alexis;
    • Marsden, C. David;
    • Wood, Nicholas W.
    Publication type:
    Article
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    Dopa-responsive dystonia.

    Published in:
    1994
    By:
    • Sawle, Guy V.;
    • Marsden, C. David;
    • Sawle, G V;
    • Marsden, C D
    Publication type:
    commentary
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