Works matching IS 00016322 AND DT 2020 AND VI 139 AND IP 3

Results: 12
    1

    cIMPACT-NOW update 5: recommended grading criteria and terminologies for IDH-mutant astrocytomas.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 603, doi. 10.1007/s00401-020-02127-9
    By:
    • Brat, Daniel J.;
    • Aldape, Kenneth;
    • Colman, Howard;
    • Figrarella-Branger, Dominique;
    • Fuller, Gregory N.;
    • Giannini, Caterina;
    • Holland, Eric C.;
    • Jenkins, Robert B.;
    • Kleinschmidt-DeMasters, Bette;
    • Komori, Takashi;
    • Kros, Johan M.;
    • Louis, David N.;
    • McLean, Catriona;
    • Perry, Arie;
    • Reifenberger, Guido;
    • Sarkar, Chitra;
    • Stupp, Roger;
    • van den Bent, Martin J.;
    • von Deimling, Andreas;
    • Weller, Michael
    Publication type:
    Article
    2
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    4

    POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 565, doi. 10.1007/s00401-019-02117-6
    By:
    • Servián-Morilla, E.;
    • Cabrera-Serrano, M.;
    • Johnson, K.;
    • Pandey, A.;
    • Ito, A.;
    • Rivas, E.;
    • Chamova, T.;
    • Muelas, N.;
    • Mongini, T.;
    • Nafissi, S.;
    • Claeys, K. G.;
    • Grewal, R. P.;
    • Takeuchi, M.;
    • Hao, H.;
    • Bönnemann, C.;
    • Lopes Abath Neto, O.;
    • Medne, L.;
    • Brandsema, J.;
    • Töpf, A.;
    • Taneva, A.
    Publication type:
    Article
    5

    PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteins.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 503, doi. 10.1007/s00401-019-02114-9
    By:
    • Corbett, Grant T.;
    • Wang, Zemin;
    • Hong, Wei;
    • Colom-Cadena, Marti;
    • Rose, Jamie;
    • Liao, Meichen;
    • Asfaw, Adhana;
    • Hall, Tia C.;
    • Ding, Lai;
    • DeSousa, Alexandra;
    • Frosch, Matthew P.;
    • Collinge, John;
    • Harris, David A.;
    • Perkinton, Michael S.;
    • Spires-Jones, Tara L.;
    • Young-Pearse, Tracy L.;
    • Billinton, Andrew;
    • Walsh, Dominic M.
    Publication type:
    Article
    6
    7

    Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 415, doi. 10.1007/s00401-019-02109-6
    By:
    • Perenthaler, Elena;
    • Nikoncuk, Anita;
    • Yousefi, Soheil;
    • Berdowski, Woutje M.;
    • Alsagob, Maysoon;
    • Capo, Ivan;
    • van der Linde, Herma C.;
    • van den Berg, Paul;
    • Jacobs, Edwin H.;
    • Putar, Darija;
    • Ghazvini, Mehrnaz;
    • Aronica, Eleonora;
    • van IJcken, Wilfred F. J.;
    • de Valk, Walter G.;
    • Medici-van den Herik, Evita;
    • van Slegtenhorst, Marjon;
    • Brick, Lauren;
    • Kozenko, Mariya;
    • Kohler, Jennefer N.;
    • Bernstein, Jonathan A.
    Publication type:
    Article
    8

    Human subiculo-fornico-mamillary system in Alzheimer's disease: Tau seeding by the pillar of the fornix.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 443, doi. 10.1007/s00401-019-02108-7
    By:
    • Thierry, Manon;
    • Boluda, Susana;
    • Delatour, Benoît;
    • Marty, Serge;
    • Seilhean, Danielle;
    • Brainbank Neuro-CEB Neuropathology Network;
    • Letournel, Franck;
    • Martin-Négrier, Marie-Laure;
    • Chapon, Françoise;
    • Godfraind, Catherine;
    • Maurage, Claude-Alain;
    • Deramecourt, Vincent;
    • Meyronnet, David;
    • Streichenberger, Nathalie;
    • de Paula, André Maues;
    • Rigau, Valérie;
    • Vandenbos-Burel, Fanny;
    • Duyckaerts, Charles;
    • Plu, Isabelle;
    • Milin, Serge
    Publication type:
    Article
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    Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 527, doi. 10.1007/s00401-019-02085-x
    By:
    • Aguilar-Calvo, Patricia;
    • Sevillano, Alejandro M.;
    • Bapat, Jaidev;
    • Soldau, Katrin;
    • Sandoval, Daniel R.;
    • Altmeppen, Hermann C.;
    • Linsenmeier, Luise;
    • Pizzo, Donald P.;
    • Geschwind, Michael D.;
    • Sanchez, Henry;
    • Appleby, Brian S.;
    • Cohen, Mark L.;
    • Safar, Jiri G.;
    • Edland, Steven D.;
    • Glatzel, Markus;
    • Nilsson, K. Peter R.;
    • Esko, Jeffrey D.;
    • Sigurdson, Christina J.
    Publication type:
    Article
    12

    Transcriptional profiling of medulloblastoma with extensive nodularity (MBEN) reveals two clinically relevant tumor subsets with VSNL1 as potent prognostic marker.

    Published in:
    Acta Neuropathologica, 2020, v. 139, n. 3, p. 583, doi. 10.1007/s00401-019-02102-z
    By:
    • Korshunov, Andrey;
    • Okonechnikov, Konstantin;
    • Sahm, Felix;
    • Ryzhova, Marina;
    • Stichel, Damian;
    • Schrimpf, Daniel;
    • Ghasemi, David R.;
    • Pajtler, Kristian W.;
    • Antonelli, Manila;
    • Donofrio, Vittoria;
    • Mastronuzzi, Angela;
    • Rossi, Sabrina;
    • Camassei, Francesca Diomedi;
    • Buccoliero, Anna Maria;
    • Haberler, Christine;
    • Slavc, Irene;
    • Dahiya, Sonika;
    • Casalini, Belen;
    • Sievers, Philipp;
    • Meyer, Jochen
    Publication type:
    Article