Search Results - Santorelli, Filippo M.

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  1. 1
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    Integrated modeling of digital-motor and clinician-reported outcomes using item response theory: towards powerful trials for rare neurological diseases by Hamdan, Alzahra (Author) , Traschütz, Andreas (Author) , Beichert, Lukas (Author) , Chen, Xiaomei (Author) , Gagnon, Cynthia (Author) , van de Warrenburg, Bart P. (Author) , Santorelli, Filippo M. (Author) , Başak, Nazlı (Author) , Coarelli, Giulia (Author) , Horvath, Rita (Author) , Klebe, Stephan (Author) , Schüle-Freyer, Rebecca (Author) , Hooker, Andrew C. (Author) , Synofzik, Matthis (Author) , Karlsson, Mats O. (Author) ,


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  2. 2
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    Digital gait outcomes for autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): discriminative, convergent, and ecological validity in a multicenter study (PROSPAX) by Beichert, Lukas David (Author) , Ilg, Winfried (Author) , Kessler, Christoph (Author) , Traschütz, Andreas (Author) , Reich, Selina (Author) , Santorelli, Filippo M. (Author) , Başak, Ayşe Nazli (Author) , Gagnon, Cynthia (Author) , Schüle-Freyer, Rebecca (Author) , Synofzik, Matthis (Author) ,


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  3. 3
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    Sacsin levels in PBMCs: a diagnostic assay for SACS variants in peripheral blood cells : a PROSPAX study by Tunca, Ceren (Author) , İşlek Camadan, Eylül Ece (Author) , Smolina, Natalia (Author) , Palvadeau, Robin J. (Author) , Öztop Çakmak, Özgür (Author) , Vural, Atay (Author) , Traschütz, Andreas (Author) , Santorelli, Filippo M. (Author) , Brais, Bernard (Author) , Schüle-Freyer, Rebecca (Author) , Synofzik, Matthis (Author) , Başak, A. Nazlı (Author) ,


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  4. 4
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    The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15 by Saffari, Afshin (Author) , Kellner, Melanie (Author) , Jordan, Catherine (Author) , Rosengarten, Helena (Author) , Mo, Alisa (Author) , Zhang, Bo (Author) , Strelko, Oleksandr (Author) , Neuser, Sonja Anna (Author) , Davis, Marie Y (Author) , Yoshikura, Nobuaki (Author) , Futamura, Naonobu (Author) , Takeuchi, Tomoya (Author) , Nabatame, Shin (Author) , Ishiura, Hiroyuki (Author) , Tsuji, Shoji (Author) , Aldeen, Huda Shujaa (Author) , Cali, Elisa (Author) , Rocca, Clarissa (Author) , Houlden, Henry (Author) , Efthymiou, Stephanie (Author) , Assmann, Birgit (Author) , Yoon, Grace (Author) , Trombetta, Bianca A (Author) , Kivisäkk, Pia (Author) , Eichler, Florian (Author) , Nan, Haitian (Author) , Takiyama, Yoshihisa (Author) , Tessa, Alessandra (Author) , Santorelli, Filippo M (Author) , Sahin, Mustafa (Author) , Blackstone, Craig (Author) , Yang, Edward (Author) , Schüle-Freyer, Rebecca (Author) , Ebrahimi-Fakhari, Darius (Author) ,


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  5. 5
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    The ARCA Registry: a collaborative global platform for advancing trial readiness in autosomal recessive cerebellar ataxias by Traschütz, Andreas (Author) , Reich, Selina (Author) , Adarmes, Astrid D. (Author) , Anheim, Mathieu (Author) , Ashrafi, Mahmoud Reza (Author) , Baets, Jonathan (Author) , Basak, A. Nazli (Author) , Bertini, Enrico (Author) , Brais, Bernard (Author) , Gagnon, Cynthia (Author) , Gburek-Augustat, Janina (Author) , Hanagasi, Hasmet A. (Author) , Heinzmann, Anna Constanze (Author) , Horvath, Rita (Author) , Jonghe, Peter de (Author) , Kamm, Christoph (Author) , Klivenyi, Peter (Author) , Klopstock, Thomas (Author) , Minnerop, Martina (Author) , Münchau, Alexander (Author) , Renaud, Mathilde (Author) , Roxburgh, Richard H. (Author) , Santorelli, Filippo M. (Author) , Schirinzi, Tommaso (Author) , Sival, Deborah A. (Author) , Timmann-Braun, Dagmar (Author) , Vielhaber, Stefan (Author) , Wallner, Michael (Author) , Warrenburg, Bart Petrus Christoffel van de (Author) , Zanni, Ginevra (Author) , Züchner, Stephan (Author) , Klockgether, Thomas (Author) , Schüle-Freyer, Rebecca (Author) , Schöls, Ludger (Author) , Synofzik, Matthis (Author) ,


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