Works in Annals of Neurology, 2000, Vol 48, Issue 2


Results: 34
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    News and comment.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 274, doi. 10.1002/1531-8249(200008)48:2<274::AID-ANA32>3.0.CO;2-1
    Publication type:
    Article
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    The nervous system and the heart.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 273, doi. 10.1002/1531-8249(200008)48:2<273::AID-ANA29>3.0.CO;2-J
    By:
    • Oppenheimer, Stephen
    Publication type:
    Article
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    Ramsay Hunt syndrome in children.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 254, doi. 10.1002/1531-8249(200008)48:2<254::AID-ANA17>3.0.CO;2-V
    By:
    • Hato, Naohito;
    • Kisaki, Hisanobu;
    • Honda, Nobumitsu;
    • Gyo, Kiyofumi;
    • Murakami, Shingo;
    • Yanagihara, Naoaki
    Publication type:
    Article
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    Reply.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 269, doi. 10.1002/1531-8249(200008)48:2<269::AID-ANA23>3.0.CO;2-Y
    By:
    • Inzitari, Domenico
    Publication type:
    Article
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    Alzheimer's disease cybrids replicate β-amyloid abnormalities through cell death pathways.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 148, doi. 10.1002/1531-8249(200008)48:2<148::AID-ANA3>3.0.CO;2-7
    By:
    • Khan, Shaharyar M.;
    • Cassarino, David S.;
    • Abramova, Nicole N.;
    • Keeney, Paula M.;
    • Borland, M. Kate;
    • Trimmer, Patricia A.;
    • Krebs, Clara T.;
    • Bennett, Jason C.;
    • Parks, Janice K.;
    • Swerdlow, Russell H.;
    • Parker, W. Davis;
    • Bennett, James P.
    Publication type:
    Article
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    Hypertension and white matter changes.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 268, doi. 10.1002/1531-8249(200008)48:2<268::AID-ANA22>3.0.CO;2-1
    By:
    • Turnbull, John
    Publication type:
    Article
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    Reply.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 271, doi. 10.1002/1531-8249(200008)48:2<271::AID-ANA26>3.0.CO;2-U
    By:
    • Greenlee, John E.
    Publication type:
    Article
    33

    Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.

    Published in:
    Annals of Neurology, 2000, v. 48, n. 2, p. 170, doi. 10.1002/1531-8249(200008)48:2<170::AID-ANA6>3.0.CO;2-J
    By:
    • Bonne, G.;
    • Mercuri, E.;
    • Muchir, A.;
    • Urtizberea, A.;
    • Bécane, H. M.;
    • Recan, D.;
    • Merlini, L.;
    • Wehnert, M.;
    • Boor, R.;
    • Reuner, U.;
    • Vorgerd, M.;
    • Wicklein, E. M.;
    • Eymard, B.;
    • Duboc, D.;
    • Penisson-Besnier, I.;
    • Cuisset, J. M.;
    • Ferrer, X.;
    • Desguerre, I.;
    • Lacombe, D.;
    • Bushby, K.
    Publication type:
    Article
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