Works matching IS 00068950 AND DT 2013 AND VI 136 AND IP 10

Results: 38
    1
    2
    3
    4
    5

    Anterior temporal lobe degeneration produces widespread network-driven dysfunction.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 2979, doi. 10.1093/brain/awt222
    By:
    • Guo, Christine C.;
    • Gorno-Tempini, Maria Luisa;
    • Gesierich, Benno;
    • Henry, Maya;
    • Trujillo, Andrew;
    • Shany-Ur, Tal;
    • Jovicich, Jorge;
    • Robinson, Simon D.;
    • Kramer, Joel H.;
    • Rankin, Katherine P.;
    • Miller, Bruce L.;
    • Seeley, William W.
    Publication type:
    Article
    6

    DNA methylation map of mouse and human brain identifies target genes in Alzheimer’s disease.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3018, doi. 10.1093/brain/awt237
    By:
    • Sanchez-Mut, Jose V.;
    • Aso, Ester;
    • Panayotis, Nicolas;
    • Lott, Ira;
    • Dierssen, Mara;
    • Rabano, Alberto;
    • Urdinguio, Rocio G.;
    • Fernandez, Agustin F.;
    • Astudillo, Aurora;
    • Martin-Subero, Jose I.;
    • Balint, Balazs;
    • Fraga, Mario F.;
    • Gomez, Antonio;
    • Gurnot, Cecile;
    • Roux, Jean-Christophe;
    • Avila, Jesus;
    • Hensch, Takao K.;
    • Ferrer, Isidre;
    • Esteller, Manel
    Publication type:
    Article
    7
    8

    The lifelong course of chronic epilepsy: the Chalfont experience.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3187, doi. 10.1093/brain/awt117
    By:
    • Novy, Jan;
    • Belluzzo, Marco;
    • Caboclo, Luís Otávio;
    • Catarino, Claudia B.;
    • Yogarajah, Mahinda;
    • Martinian, Lillian;
    • Peacock, Janet L.;
    • Bell, Gail S.;
    • Koepp, Matthias J.;
    • Thom, Maria;
    • Sander, Josemir W.;
    • Sisodiya, Sanjay M.
    Publication type:
    Article
    9
    10
    11

    The reel of consciousness.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3200, doi. 10.1093/brain/awt245
    By:
    • Cornwell, John
    Publication type:
    Article
    12
    13
    14

    Correlation of dopaminergic terminal dysfunction and microstructural abnormalities of the basal ganglia and the olfactory tract in Parkinson’s disease.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3028, doi. 10.1093/brain/awt234
    By:
    • Scherfler, Christoph;
    • Esterhammer, Regina;
    • Nocker, Michael;
    • Mahlknecht, Philipp;
    • Stockner, Heike;
    • Warwitz, Boris;
    • Spielberger, Sabine;
    • Pinter, Bernadette;
    • Donnemiller, Eveline;
    • Decristoforo, Clemens;
    • Virgolini, Irene;
    • Schocke, Michael;
    • Poewe, Werner;
    • Seppi, Klaus
    Publication type:
    Article
    15

    Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3151, doi. 10.1093/brain/awt212
    By:
    • Irani, Sarosh R.;
    • Stagg, Charlotte J.;
    • Schott, Jonathan M.;
    • Rosenthal, Clive R.;
    • Schneider, Susanne A.;
    • Pettingill, Philippa;
    • Pettingill, Rosemary;
    • Waters, Patrick;
    • Thomas, Adam;
    • Voets, Natalie L.;
    • Cardoso, Manuel J.;
    • Cash, David M.;
    • Manning, Emily N.;
    • Lang, Bethan;
    • Smith, Shelagh J. M.;
    • Vincent, Angela;
    • Johnson, Michael R.
    Publication type:
    Article
    16
    17
    18

    From The Archives.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 2928, doi. 10.1093/brain/awt260
    By:
    • Compston, Alastair
    Publication type:
    Article
    19

    Erratum.

    Published in:
    2013
    Publication type:
    Erratum
    20
    21

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

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3106, doi. 10.1093/brain/awt236
    By:
    • Németh, Andrea H.;
    • Kwasniewska, Alexandra C.;
    • Lise, Stefano;
    • Parolin Schnekenberg, Ricardo;
    • Becker, Esther B. E.;
    • Bera, Katarzyna D.;
    • Shanks, Morag E.;
    • Gregory, Lorna;
    • Buck, David;
    • Zameel Cader, M.;
    • Talbot, Kevin;
    • de Silva, Rajith;
    • Fletcher, Nicholas;
    • Hastings, Rob;
    • Jayawant, Sandeep;
    • Morrison, Patrick J.;
    • Worth, Paul;
    • Taylor, Malcolm;
    • Tolmie, John;
    • O’Regan, Mary
    Publication type:
    Article
    22

    ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3096, doi. 10.1093/brain/awt218
    By:
    • Webb, Emma A.;
    • AlMutair, Angham;
    • Kelberman, Daniel;
    • Bacchelli, Chiara;
    • Chanudet, Estelle;
    • Lescai, Francesco;
    • Andoniadou, Cynthia L.;
    • Banyan, Abdul;
    • Alsawaid, Al;
    • Alrifai, Muhammad T.;
    • Alahmesh, Mohammed A.;
    • Balwi, M.;
    • Mousavy-Gharavy, Seyedeh N.;
    • Lukovic, Biljana;
    • Burke, Derek;
    • McCabe, Mark J.;
    • Kasia, Tessa;
    • Kleta, Robert;
    • Stupka, Elia;
    • Beales, Philip L.
    Publication type:
    Article
    23

    Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3140, doi. 10.1093/brain/awt233
    By:
    • Kasperavičiūtė, Dalia;
    • Catarino, Claudia B.;
    • Matarin, Mar;
    • Leu, Costin;
    • Novy, Jan;
    • Tostevin, Anna;
    • Leal, Bárbara;
    • Hessel, Ellen V. S.;
    • Hallmann, Kerstin;
    • Hildebrand, Michael S.;
    • Dahl, Hans-Henrik M.;
    • Ryten, Mina;
    • Trabzuni, Daniah;
    • Ramasamy, Adaikalavan;
    • Alhusaini, Saud;
    • Doherty, Colin P.;
    • Dorn, Thomas;
    • Hansen, Jörg;
    • Krämer, Günter;
    • Steinhoff, Bernhard J.
    Publication type:
    Article
    24
    25

    Erratum.

    Published in:
    2013
    Publication type:
    Erratum
    26
    27
    28
    29

    Erratum.

    Published in:
    2013
    Publication type:
    Erratum
    30
    31
    32
    33

    Editorial.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 2925, doi. 10.1093/brain/awt261
    By:
    • Compston, Alastair
    Publication type:
    Article
    34
    35
    36

    Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3119, doi. 10.1093/brain/awt227
    By:
    • Vantaggiato, Chiara;
    • Crimella, Claudia;
    • Airoldi, Giovanni;
    • Polishchuk, Roman;
    • Bonato, Sara;
    • Brighina, Erika;
    • Scarlato, Marina;
    • Musumeci, Olimpia;
    • Toscano, Antonio;
    • Martinuzzi, Andrea;
    • Santorelli, Filippo Maria;
    • Ballabio, Andrea;
    • Bresolin, Nereo;
    • Clementi, Emilio;
    • Bassi, Maria Teresa
    Publication type:
    Article
    37
    38