Search Results - Schöls, Ludger

Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3 by Elter, Tim (Author) , Sturm, Daniel (Author) , Santana, Magda M. (Author) , Schaprian, Tamara (Author) , Raposo, Mafalda (Author) , Melo, Ana Rosa Vieira (Author) , Lima, Manuela (Author) , Koyak, Berkan (Author) , Oender, Demet (Author) , Grobe-Einsler, Marcus (Author) , Lopes, Sara (Author) , Silva, Patrick (Author) , de Almeida, Luís Pereira (Author) , Giunti, Paola (Author) , Garcia-Moreno, Hector (Author) , Nethisinhe, Suran (Author) , de Vries, Jeroen (Author) , van de Warrenburg, Bart P. (Author) , van Gaalen, Judith (Author) , Synofzik, Matthis (Author) , Schöls, Ludger (Author) , Reetz, Kathrin (Author) , Erdlenbruch, Friedrich (Author) , Jacobi, Heike (Author) , Infante, Jon (Author) , Rieß, Olaf (Author) , Klockgether, Thomas (Author) , Timmann, Dagmar (Author) , Thieme, Andreas (Author) , Faber, Jennifer (Author) , Hübener-Schmid, Jeannette (Author) ,

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Stage-dependent biomarker changes in spinocerebellar ataxia type 3 by Faber, Jennifer (Author) , Berger, Moritz (Author) , Wilke, Carlo (Author) , Hubener-Schmid, Jeannette (Author) , Schaprian, Tamara (Author) , Santana, Magda M. (Author) , Grobe-Einsler, Marcus (Author) , Onder, Demet (Author) , Koyak, Berkan (Author) , Giunti, Paola (Author) , Garcia-Moreno, Hector (Author) , Gonzalez-Robles, Cristina (Author) , Lima, Manuela (Author) , Raposo, Mafalda (Author) , Melo, Ana Rosa Vieira (Author) , de Almeida, Luis Pereira (Author) , Silva, Patrick (Author) , Pinto, Maria M. (Author) , van de Warrenburg, Bart P. (Author) , van Gaalen, Judith (Author) , de Vries, Jeroen (Author) , Oz, Gulin (Author) , Joers, James M. (Author) , Synofzik, Matthis (Author) , Schols, Ludger (Author) , Riess, Olaf (Author) , Infante, Jon (Author) , Manrique, Leire (Author) , Timmann, Dagmar (Author) , Thieme, Andreas (Author) , Jacobi, Heike (Author) , Reetz, Kathrin (Author) , Dogan, Imis (Author) , Onyike, Chiadikaobi (Author) , Povazan, Michal (Author) , Schmahmann, Jeremy (Author) , Ratai, Eva-Maria (Author) , Schmid, Matthias (Author) , Klockgether, Thomas (Author) ,

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Recommendations for optimal interdisciplinary management and healthcare settings for patients with rare neurological diseases by Graessner, Holm (Author) , Reinhard, Carola (Author) , Bäumer, Tobias (Author) , Baumgärtner, Annette (Author) , Brockmann, Knut (Author) , Brüggemann, Norbert (Author) , Bültmann, Eva (Author) , Erdmann, Jeanette (Author) , Heise, Kirstin (Author) , Höglinger, Günter (Author) , Hüning, Irina (Author) , Kaiser, Frank J. (Author) , Klein, Christine (Author) , Klopstock, Thomas (Author) , Krägeloh-Mann, Ingeborg (Author) , Kraemer, Markus (Author) , Luedtke, Kerstin (Author) , Mücke, Martin (Author) , Musacchio, Thomas (Author) , Nadke, Andreas (Author) , Osmanovic, Alma (Author) , Ritter, Gabriele (Author) , Röse, Katharina (Author) , Schippers, Christopher (Author) , Schöls, Ludger (Author) , Schüle-Freyer, Rebecca (Author) , Schulz, Jörg B. (Author) , Sproß, Joachim (Author) , Stasch, Eveline (Author) , Wunderlich, Gilbert (Author) , Münchau, Alexander (Author) ,

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Correction to: The frequency of non‑motor symptoms in SCA3 and their association with disease severity and lifestyle factors by Hengel, Holger (Author) , Martus, Peter (Author) , Faber, Jennifer (Author) , Giunti, Paola (Author) , Garcia-Moreno, Hector (Author) , Solanky, Nita (Author) , Klockgether, Thomas (Author) , Reetz, Kathrin (Author) , van de Warrenburg, Bart P. (Author) , Santana, Magda M. (Author) , Silva, Patrick (Author) , Cunha, Inês (Author) , de Almeida, Luís Pereira (Author) , Timmann-Braun, Dagmar (Author) , Infante, Jon (Author) , de Vries, Jeroen (Author) , Lima, Manuela (Author) , Pires, Paula (Author) , Bushara, Khalaf (Author) , Jacobi, Heike (Author) , Onyike, Chiadi (Author) , Schmahmann, Jeremy D. (Author) , Hübener-Schmid, Jeannette (Author) , Synofzik, Matthis (Author) , Schöls, Ludger (Author) ,

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Levels of neurofilament light at the preataxic and ataxic stages of spinocerebellar ataxia type 1 by Wilke, Carlo (Author) , Mengel, David (Author) , Schöls, Ludger (Author) , Hengel, Holger (Author) , Rakowicz, Maria (Author) , Klockgether, Thomas (Author) , Durr, Alexandra (Author) , Filla, Alessandro (Author) , Melegh, Bela (Author) , Schüle-Freyer, Rebecca (Author) , Reetz, Kathrin (Author) , Jacobi, Heike (Author) , Synofzik, Matthis (Author) ,

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Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy by Park, Joohyun (Author) , Tucci, Arianna (Author) , Cipriani, Valentina (Author) , Demidov, German (Author) , Rocca, Clarissa (Author) , Senderek, Jan (Author) , Butryn, Michaela (Author) , Velic, Ana (Author) , Lam, Tanya (Author) , Galanaki, Evangelia (Author) , Cali, Elisa (Author) , Vestito, Letizia (Author) , Maroofian, Reza (Author) , Deininger, Natalie (Author) , Rautenberg, Maren (Author) , Admard, Jakob (Author) , Hahn, Gesa-Astrid (Author) , Bartels, Claudius (Author) , Os, Nienke J. H. van (Author) , Horvath, Rita (Author) , Chinnery, Patrick F. (Author) , Tiet, May Yung (Author) , Hewamadduma, Channa (Author) , Hadjivassiliou, Marios (Author) , Tofaris, George K. (Author) , Wood, Nicholas (Author) , Hayer, Stefanie Nicole (Author) , Bender, Friedemann (Author) , Menden, Benita (Author) , Cordts, Isabell (Author) , Klein, Katrin (Author) , Nguyen, Huu Phuc (Author) , Krauss, Joachim K. (Author) , Blahak, Christian (Author) , Strom, Tim M. (Author) , Sturm, Marc (Author) , Warrenburg, Bart Petrus Christoffel van de (Author) , Lerche, Holger (Author) , Maček, Boris (Author) , Synofzik, Matthis (Author) , Ossowski, Stephan (Author) , Timmann-Braun, Dagmar (Author) , Wolf, Marc (Author) , Smedley, Damian (Author) , Rieß, Olaf (Author) , Schöls, Ludger (Author) , Houlden, Henry (Author) , Haack, Tobias (Author) , Hengel, Holger (Author) ,

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Differential temporal dynamics of axial and appendicular ataxia in SCA3 by Maas, Roderick (Author) , Teerenstra, Steven (Author) , Lima, Manuela (Author) , Pires, Paula (Author) , Pereira de Almeida, Luís (Author) , Gaalen, Judith van (Author) , Timmann, Dagmar (Author) , Infante, Jon (Author) , Onyike, Chiadi (Author) , Bushara, Khalaf (Author) , Jacobi, Heike (Author) , Reetz, Kathrin (Author) , Santana, Magda M. (Author) , Afonso Ribeiro, Joana (Author) , Hübener-Schmid, Jeannette (Author) , Vries, Jeroen J. de (Author) , Synofzik, Matthis (Author) , Schöls, Ludger (Author) , Garcia-Moreno, Hector (Author) , Giunti, Paola (Author) , Faber, Jennifer (Author) , Klockgether, Thomas (Author) , Warrenburg, Bart P. C. van de (Author) ,

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The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors by Hengel, Holger (Author) , Martus, Peter (Author) , Faber, Jennifer (Author) , Giunti, Paola (Author) , Garcia-Moreno, Hector (Author) , Solanky, Nita (Author) , Klockgether, Thomas (Author) , Reetz, Kathrin (Author) , van de Warrenburg, Bart P. (Author) , Santana, Magda M. (Author) , Silva, Patrick (Author) , Cunha, Inês (Author) , de Almeida, Luís Pereira (Author) , Timmann-Braun, Dagmar (Author) , Infante, Jon (Author) , de Vries, Jeroen (Author) , Lima, Manuela (Author) , Pires, Paula (Author) , Bushara, Khalaf (Author) , Jacobi, Heike (Author) , Onyike, Chiadi (Author) , Schmahmann, Jeremy D. (Author) , Hübener-Schmid, Jeannette (Author) , Synofzik, Matthis (Author) , Schöls, Ludger (Author) ,

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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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Bi-allelic truncating mutations in VWA1 cause neuromyopathy by Deschauer, Marcus (Author) , Hengel, Holger (Author) , Rupprich, Katrin (Author) , Kreiß, Martina (Author) , Schlotter-Weigel, Beate (Author) , Grimmel, Mona (Author) , Admard, Jakob (Author) , Schneider, Ilka (Author) , Alhaddad, Bader (Author) , Gazou, Anastasia (Author) , Sturm, Marc (Author) , Vorgerd, Matthias (Author) , Balousha, Ghassan (Author) , Balousha, Osama (Author) , Falna, Mohammed (Author) , Kirschke, Jan S. (Author) , Kornblum, Cornelia (Author) , Jordan, Berit (Author) , Kraya, Torsten (Author) , Strom, Tim M. (Author) , Weis, Joachim (Author) , Schöls, Ludger (Author) , Schara, Ulrike (Author) , Zierz, Stephan (Author) , Riess, Olaf (Author) , Meitinger, Thomas (Author) , Haack, Tobias B. (Author) ,

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Safety and efficacy of Acetyl-DL-Leucine in certain types of Cerebellar Ataxia: the ALCAT randomized clinical crossover trial by Feil, Katharina (Author) , Adrion, Christine (Author) , Boesch, Sylvia (Author) , Doss, Sarah (Author) , Giordano, Ilaria (Author) , Hengel, Holger (Author) , Jacobi, Heike (Author) , Klockgether, Thomas (Author) , Klopstock, Thomas (Author) , Nachbauer, Wolfgang (Author) , Schöls, Ludger (Author) , Steiner, Katharina Marie (Author) , Stendel, Claudia (Author) , Timmann, Dagmar (Author) , Naumann, Ivonne (Author) , Mansmann, Ulrich (Author) , Strupp, Michael (Author) ,

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Conversion of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 to manifest ataxia (RISCA): a longitudinal cohort study by Jacobi, Heike (Author) , Du Montcel, Sophie Tezenas (Author) , Romanzetti, Sandro (Author) , Harmuth, Florian (Author) , Mariotti, Caterina (Author) , Nanetti, Lorenzo (Author) , Rakowicz, Maria (Author) , Makowicz, Grzegorz (Author) , Durr, Alexandra (Author) , Monin, Marie-Lorraine (Author) , Filla, Alessandro (Author) , Roca, Alessandro (Author) , Schöls, Ludger (Author) , Hengel, Holger (Author) , Infante, Jon (Author) , Kang, Jun-Suk (Author) , Timmann, Dagmar (Author) , Casali, Carlo (Author) , Masciullo, Marcella (Author) , Baliko, Laszlo (Author) , Melegh, Bela (Author) , Nachbauer, Wolfgang (Author) , Bürk-Gergs, Katrin (Author) , Schulz, Jörg B (Author) , Riess, Olaf (Author) , Reetz, Kathrin (Author) , Klockgether, Thomas (Author) ,

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FIG4 mutations leading to parkinsonism and a phenotypical continuum between CMT4J and Yunis Varón syndrome by Zimmermann, Milan Raoul (Author) , Schuster, Stefanie (Author) , Boesch, Sylvia (Author) , Korenke, Christoph (Author) , Mohr, Julia (Author) , Reichbauer, Jennifer (Author) , Kernstock, Christoph (Author) , Kotzot, Dieter (Author) , Spahlinger, Veronika (Author) , Schüle-Freyer, Rebecca (Author) , Schöls, Ludger (Author) ,

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Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study by Diallo, Alhassane (Author) , Jacobi, Heike (Author) , Cook, Arron (Author) , Labrum, Robyn (Author) , Durr, Alexandra (Author) , Schmitz-Hübsch, Tanja (Author) , Schöls, Ludger (Author) , Hengel, Holger (Author) , Schulz, Jörg B. (Author) , Bauer, Peter (Author) , Kang, Jun-Suk (Author) , Tezenas du Montcel, Sophie (Author) ,

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Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients by Schüle-Freyer, Rebecca (Author) , Wiethoff, Sarah (Author) , Martus, Peter (Author) , Karle, Kathrin Nora (Author) , Otto, Susanne (Author) , Klebe, Stephan (Author) , Klimpe, Sven (Author) , Gallenmüller, Constanze (Author) , Kurzwelly, Delia (Author) , Henkel, Dorothea (Author) , Rimmele, Florian D. (Author) , Stolze, Henning Wolfgang (Author) , Kohl, Zacharias (Author) , Kassubek, Jan Rainer (Author) , Klockgether, Thomas (Author) , Vielhaber, Stefan (Author) , Kamm, Christoph (Author) , Klopstock, Thomas (Author) , Bauer, Peter (Author) , Züchner, Stephan (Author) , Liepelt-Scarfone, Inga (Author) , Schöls, Ludger (Author) ,

• Volltext

A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes

Depression comorbidity in spinocerebellar ataxia by Schmitz-Hübsch, Tanja (Author) , Coudert, Mathieu (Author) , Tezenas du Montcel, Sophie (Author) , Giunti, Paola (Author) , Labrum, Robyn (Author) , Dürr, Alexandra (Author) , Ribai, Pascale (Author) , Charles, Perrine (Author) , Linnemann, Christoph (Author) , Schöls, Ludger (Author) , Rakowicz, Maryla (Author) , Rola, Rafal (Author) , Zdzienicka, Elszbieta (Author) , Fancellu, Roberto (Author) , Mariotti, Caterina (Author) , Baliko, Lazlo (Author) , Melegh, Bela (Author) , Filla, Alessandro (Author) , Salvatore, Elena (Author) , van de Warrenburg, Bart P.C. (Author) , Szymanski, Sandra (Author) , Infante, Jon (Author) , Timmann, Dagmar (Author) , Boesch, Sylvia (Author) , Depondt, Chantal (Author) , Kang, Jun-Suk (Author) , Schulz, Jörg B. (Author) , Klopstock, Thomas (Author) , Loßnitzer, Nicole (Author) , Löwe, Bernd (Author) , Frick, Caroline (Author) , Rottländer, Daniela (Author) , Schlaepfer, Thomas E. (Author) , Klockgether, Thomas (Author) ,

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A potential role for a genetic variation of AKAP5 in human aggression and anger control by Kruse, Sylvia (Author) , Gorny, Xenia (Author) , Marco-Pallarés, Josep (Author) ,

• Abstract

The effects of COMT (Val108/158Met) and DRD4 (SNP -521) dopamine genotypes on brain activations related to valence and magnitude of rewards by Càmara, Estela (Author) , Krämer, Ulrike M. (Author) , Cunillera, Toni (Author) ,