Works matching IS 00068950 AND DT 2022 AND VI 145 AND IP 5

Results: 35
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    Alemtuzumab-induced immune phenotype and repertoire changes: implications for secondary autoimmunity.

    Published in:
    2022
    By:
    • Ruck, Tobias;
    • Barman, Sumanta;
    • Schulte-Mecklenbeck, Andreas;
    • Pfeuffer, Steffen;
    • Steffen, Falk;
    • Nelke, Christopher;
    • Schroeter, Christina B.;
    • Willison, Alice;
    • Heming, Michael;
    • Müntefering, Thomas;
    • Melzer, Nico;
    • Krämer, Julia;
    • Lindner, Maren;
    • Riepenhausen, Marianne;
    • Gross, Catharina C.;
    • Klotz, Luisa;
    • Bittner, Stefan;
    • Muraro, Paolo A.;
    • Schneider-Hohendorf, Tilman;
    • Schwab, Nicholas
    Publication type:
    journal article
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    18F-MK-6240 tau-PET in genetic frontotemporal dementia.

    Published in:
    2022
    By:
    • Levy, Jake P;
    • Bezgin, Gleb;
    • Savard, Melissa;
    • Pascoal, Tharick A;
    • Finger, Elizabeth;
    • Laforce, Robert;
    • Sonnen, Joshua A;
    • Soucy, Jean-Paul;
    • Gauthier, Serge;
    • Rosa-Neto, Pedro;
    • Ducharme, Simon
    Publication type:
    journal article
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    All manner of ingenuity and industry.

    Published in:
    Brain: A Journal of Neurology, 2022, v. 145, n. 5, p. 1866, doi. 10.1093/brain/awac056
    By:
    • Molnár, Zoltán;
    • Coles, Alasdair
    Publication type:
    Article
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    Withdrawal of intravenous immunoglobulin in chronic inflammatory demyelinating polyradiculoneuropathy.

    Published in:
    2022
    By:
    • Adrichem, Max E.;
    • Lucke, Ilse M.;
    • Vrancken, Alexander F. J. E.;
    • Goedee, H. Stephan;
    • Wieske, Luuk;
    • Dijkgraaf, Marcel G. W.;
    • Voermans, Nicol C.;
    • Notermans, Nicolette C.;
    • Faber, Catharina G.;
    • Visser, Leo H.;
    • Kuitwaard, Krista;
    • Doorn, Pieter A. van;
    • Merkies, Ingemar S. J.;
    • Haan, Rob J. de;
    • Schaik, Ivo N. van;
    • Eftimov, Filip;
    • van Doorn, Pieter A;
    • de Haan, Rob J;
    • van Schaik, Ivo N
    Publication type:
    journal article
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    DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome.

    Published in:
    2022
    By:
    • Stenton, Sarah L.;
    • Tesarova, Marketa;
    • Sheremet, Natalia L.;
    • Catarino, Claudia B.;
    • Carelli, Valerio;
    • Ciara, Elżbieta;
    • Curry, Kathryn;
    • Engvall, Martin;
    • Fleming, Leah R.;
    • Freisinger, Peter;
    • Iwanicka-Pronicka, Katarzyna;
    • Jurkiewicz, Elżbieta;
    • Klopstock, Thomas;
    • Koenig, Mary K.;
    • Kolářová, Hana;
    • Kousal, Bohdan;
    • Krylova, Tatiana;
    • Morgia, Chiara La;
    • Nosková, Lenka;
    • Piekutowska-Abramczuk, Dorota
    Publication type:
    journal article
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    A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia.

    Published in:
    2022
    By:
    • Ende, Emma L van der;
    • Bron, Esther E;
    • Poos, Jackie M;
    • Jiskoot, Lize C;
    • Panman, Jessica L;
    • Papma, Janne M;
    • Meeter, Lieke H;
    • Dopper, Elise G P;
    • Wilke, Carlo;
    • Synofzik, Matthis;
    • Heller, Carolin;
    • Swift, Imogen J;
    • Sogorb-Esteve, Aitana;
    • Bouzigues, Arabella;
    • Borroni, Barbara;
    • Sanchez-Valle, Raquel;
    • Moreno, Fermin;
    • Graff, Caroline;
    • Laforce, Robert;
    • Galimberti, Daniela
    Publication type:
    journal article
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    A multi-pronged investigation of option generation using depression, PET and modafinil.

    Published in:
    2022
    By:
    • Ang, Yuen-Siang;
    • Cusin, Cristina;
    • Petibon, Yoann;
    • Dillon, Daniel G;
    • Breiger, Micah;
    • Belleau, Emily L;
    • Normandin, Marc;
    • Schroder, Hans;
    • Boyden, Sean;
    • Hayden, Emma;
    • Levine, M Taylor;
    • Jahan, Aava;
    • Meyer, Ashley K;
    • Kang, Min Su;
    • Brunner, Devon;
    • Gelda, Steven E;
    • Hooker, Jacob;
    • Fakhri, Georges El;
    • Fava, Maurizio;
    • Pizzagalli, Diego A
    Publication type:
    journal article
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    De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.

    Published in:
    2022
    By:
    • Manivannan, Sathiya N;
    • Roovers, Jolien;
    • Smal, Noor;
    • Myers, Candace T;
    • Turkdogan, Dilsad;
    • Roelens, Filip;
    • Kanca, Oguz;
    • Chung, Hyung-Lok;
    • Scholz, Tasja;
    • Hermann, Katharina;
    • Bierhals, Tatjana;
    • Caglayan, Hande S;
    • Stamberger, Hannah;
    • Consortium, MAE Working Group of EuroEPINOMICS RES;
    • Mefford, Heather;
    • Jonghe, Peter de;
    • Yamamoto, Shinya;
    • Weckhuysen, Sarah;
    • Bellen, Hugo J;
    • MAE Working Group of EuroEPINOMICS RES Consortium
    Publication type:
    journal article
    32

    A brain atlas of axonal and synaptic delays based on modelling of cortico-cortical evoked potentials.

    Published in:
    2022
    By:
    • Lemaréchal, Jean-Didier;
    • Jedynak, Maciej;
    • Trebaul, Lena;
    • Boyer, Anthony;
    • Tadel, François;
    • Bhattacharjee, Manik;
    • Deman, Pierre;
    • Tuyisenge, Viateur;
    • Ayoubian, Leila;
    • Hugues, Etienne;
    • Chanteloup-Forêt, Blandine;
    • Saubat, Carole;
    • Zouglech, Raouf;
    • Mejia, Gina Catalina Reyes;
    • Tourbier, Sébastien;
    • Hagmann, Patric;
    • Adam, Claude;
    • Barba, Carmen;
    • Bartolomei, Fabrice;
    • Blauwblomme, Thomas
    Publication type:
    journal article
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    Assessing the landscape of STXBP1-related disorders in 534 individuals.

    Published in:
    2022
    By:
    • Xian, Julie;
    • Parthasarathy, Shridhar;
    • Ruggiero, Sarah M;
    • Balagura, Ganna;
    • Fitch, Eryn;
    • Helbig, Katherine;
    • Gan, Jing;
    • Ganesan, Shiva;
    • Kaufman, Michael C;
    • Ellis, Colin A;
    • Lewis-Smith, David;
    • Galer, Peter;
    • Cunningham, Kristin;
    • O'Brien, Margaret;
    • Cosico, Mahgenn;
    • Baker, Kate;
    • Darling, Alejandra;
    • Goes, Fernanda Veiga de;
    • Achkar, Christelle M El;
    • Doering, Jan Henje
    Publication type:
    journal article
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