Works by Schwake, Michael

Results: 56
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    The EANS Young Neurosurgeons Committee’s vision of the future of European Neurosurgery.

    Published in:
    Journal of Neurosurgical Sciences, 2022, v. 66, n. 6, p. 473, doi. 10.23736/S0390-5616.22.05802-7
    By:
    • ZOIA, Cesare;
    • RAFFA, Giovanni;
    • ALDEA, Cristina C.;
    • Jr, Jiri BARTEK;
    • BEN-SHALOM, Netanel;
    • BELO, Diogo;
    • DROSOS, Evangelos;
    • FREYSCHLAG, Christian F.;
    • KAPROVOY, Stanislav;
    • LEPIC, Milan;
    • LIPPA, Laura;
    • RABIEI, Katrin;
    • SCHWAKE, Michael;
    • SPIRIEV, Toma;
    • STIENEN, Martin N.;
    • GANDÍA-GONZÁLEZ, Maria L.
    Publication type:
    Article
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    Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia.

    Published in:
    2021
    By:
    • Mencacci, Niccolò E.;
    • Brockmann, Marisa M.;
    • Jinye Dai;
    • Pajusalu, Sander;
    • Atasu, Burcu;
    • Campos, Joaquin;
    • Pino, Gabriela;
    • Gonzalez-Latapi, Paulina;
    • Patzke, Christopher;
    • Schwake, Michael;
    • Tucci, Arianna;
    • Pittman, Alan;
    • Simon-Sanchez, Javier;
    • Carvill, Gemma L.;
    • Balint, Bettina;
    • Wiethoff, Sarah;
    • Warner, Thomas T.;
    • Papandreou, Apostolos;
    • Ker Shin Soo, Audrey;
    • Rein, Reet
    Publication type:
    journal article
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    Doxorubicin induces caspase-mediated proteolysis of KV7.1.

    Published in:
    Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0162-z
    By:
    • Strigli, Anne;
    • Raab, Christian;
    • Hessler, Sabine;
    • Huth, Tobias;
    • Schuldt, Adam J. T.;
    • Alzheimer, Christian;
    • Friedrich, Thomas;
    • Burridge, Paul W.;
    • Luedde, Mark;
    • Schwake, Michael
    Publication type:
    Article
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    Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1067, doi. 10.1038/ng.2728
    By:
    • Lemke, Johannes R;
    • Lal, Dennis;
    • Reinthaler, Eva M;
    • Steiner, Isabelle;
    • Nothnagel, Michael;
    • Alber, Michael;
    • Geider, Kirsten;
    • Laube, Bodo;
    • Schwake, Michael;
    • Finsterwalder, Katrin;
    • Franke, Andre;
    • Schilhabel, Markus;
    • Jähn, Johanna A;
    • Muhle, Hiltrud;
    • Boor, Rainer;
    • Van Paesschen, Wim;
    • Caraballo, Roberto;
    • Fejerman, Natalio;
    • Weckhuysen, Sarah;
    • De Jonghe, Peter
    Publication type:
    Article
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    neurosurgery: when is this warranted?

    Published in:
    Journal of Neurosurgery, 2023, v. 138, n. 5, p. 1188, doi. 10.3171/2022.7.JNS22691
    By:
    • Schipmann, Stephanie;
    • Spille, Dorothee Cäcilia;
    • Gallus, Marco;
    • Lohmann, Sebastian;
    • Schwake, Michael;
    • Warneke, Nils;
    • Molina, Eric Suero;
    • Stummer, Walter;
    • Holling, Markus
    Publication type:
    Article
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    GRIN2B mutations in west syndrome and intellectual disability with focal epilepsy.

    Published in:
    Annals of Neurology, 2014, v. 75, n. 1, p. 147, doi. 10.1002/ana.24073
    By:
    • Lemke, Johannes R.;
    • Hendrickx, Rik;
    • Geider, Kirsten;
    • Laube, Bodo;
    • Schwake, Michael;
    • Harvey, Robert J.;
    • James, Victoria M.;
    • Pepler, Alex;
    • Steiner, Isabelle;
    • Hörtnagel, Konstanze;
    • Neidhardt, John;
    • Ruf, Susanne;
    • Wolff, Markus;
    • Bartholdi, Deborah;
    • Caraballo, Roberto;
    • Platzer, Konrad;
    • Suls, Arvid;
    • Jonghe, Peter;
    • Biskup, Saskia;
    • Weckhuysen, Sarah
    Publication type:
    Article
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    Structure of LIMP-2 provides functional insights with implications for SR-BI and CD36.

    Published in:
    Nature, 2013, v. 504, n. 7478, p. 172, doi. 10.1038/nature12684
    By:
    • Neculai, Dante;
    • Schwake, Michael;
    • Ravichandran, Mani;
    • Zunke, Friederike;
    • Collins, Richard F.;
    • Peters, Judith;
    • Neculai, Mirela;
    • Plumb, Jonathan;
    • Loppnau, Peter;
    • Pizarro, Juan Carlos;
    • Seitova, Alma;
    • Trimble, William S.;
    • Saftig, Paul;
    • Grinstein, Sergio;
    • Dhe-Paganon, Sirano
    Publication type:
    Article
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    Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 7, p. 1417, doi. 10.1093/hmg/dds558
    By:
    • Smith, Katherine R.;
    • Dahl, Hans-Henrik M.;
    • Canafoglia, Laura;
    • Andermann, Eva;
    • Damiano, John;
    • Morbin, Michela;
    • Bruni, Amalia C.;
    • Giaccone, Giorgio;
    • Cossette, Patrick;
    • Saftig, Paul;
    • Grötzinger, Joachim;
    • Schwake, Michael;
    • Andermann, Frederick;
    • Staropoli, John F.;
    • Sims, Katherine B.;
    • Mole, Sara E.;
    • Franceschetti, Silvana;
    • Alexander, Noreen A.;
    • Cooper, Jonathan D.;
    • Chapman, Harold A.
    Publication type:
    Article