Ludger Schöls (L Schöls, Ludger Schoels)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 15

Top Topics

Traumatic Brain Injury

Intellectual Disability

Top Venues

Journal of neurology

Acta neuropathologica

Disease models & mechanisms

This page only lists publications with an associated author ORCID identifier.

Publications

Jonasz Jeremiasz Weber, Leah Czisch, Priscila Pereira Sena, Florian Fath, Chrisovalantou Huridou, Natasa Schwarz, Rana Dilara Incebacak Eltemur, Anna Würth, Daniel Weishäupl, Miriam Döcker, Gunnar Blumenstock, Sandra Martins, Leonor Correia Guedes, Guy A Rouleau, Laura Bannach Jardim, Maria-Luiza Saraiva-Pereira, Marcondes Cavalcante de França Junior, Carlos R Gordon, Roy Zaltzman, Mario R Cornejo-Olivas, Bart P C van de Warrenburg, Alexandra Dürr, Alexis Brice, Peter Bauer, Thomas Klockgether, Ludger Schöls, Olaf H Rieß, null null, Thorsten Schmidt
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Acta neuropathologica 148 (1) (2024)
Jonasz Jeremiasz Weber, Leah Czisch, Priscila Pereira Sena, Florian Fath, Chrisovalantou Huridou, Natasa Schwarz, Rana Dilara Incebacak Eltemur, Anna Würth, Daniel Weishäupl, Miriam Döcker, Gunnar Blumenstock, Sandra Martins, Leonor Correia Guedes, Guy A Rouleau, Laura Bannach Jardim, Maria-Luiza Saraiva-Pereira, Marcondes Cavalcante de França Junior, Carlos R Gordon, Roy Zaltzman, Mario R Cornejo-Olivas, Bart P C van de Warrenburg, Alexandra Dürr, Alexis Brice, Peter Bauer, Thomas Klockgether, Ludger Schöls, Olaf H Rieß, null null, Thorsten Schmidt
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Acta neuropathologica 148 (1) (2024)
Andreas Riedel, Christoph Faul, Kristina Reuss, Jan Christian Schroeder, Peter J Lang, Claudia Lengerke, Nadine Weissert, Holger Hengel, Samuel Gröschel, Ludger Schöls, Wolfgang Andreas Bethge
Allogeneic hematopoietic cell transplantation for adult metachromatic leukodystrophy: a case series. Blood advances 8 (6) (2024)
Andreas Riedel, Christoph Faul, Kristina Reuss, Jan Christian Schroeder, Peter J Lang, Claudia Lengerke, Nadine Weissert, Holger Hengel, Samuel Gröschel, Ludger Schöls, Wolfgang Andreas Bethge
Allogeneic hematopoietic cell transplantation for adult metachromatic leukodystrophy: a case series. Blood advances 8 (6) (2024)
Andreas Riedel, Christoph Faul, Kristina Reuss, Jan Christian Schroeder, Peter Lang, Claudia Lengerke, Nadine Weissert, Holger Hengel, Samuel Gröschel, Ludger Schöls, Wolfgang Andreas Bethge
Allogeneic Hematopoietic Stem Cell Transplantation for Adult Metachromatic Leukodystrophy (MLD): A Case Series. Blood advances (2024)
Theresa Kagermeier, Stefan Hauser, Kseniia Sarieva, Lucia Laugwitz, Samuel Groeschel, Wibke G Janzarik, Zeynep Yentür, Katharina Becker, Ludger Schöls, Ingeborg Kraegeloh-Mann, Simone Mayer
Human organoid model of pontocerebellar hypoplasia 2a recapitulates brain region-specific size differences. Disease models & mechanisms 17 (7) (2024)
Jonasz Jeremiasz Weber, Leah Czisch, Priscila Pereira Sena, Florian Fath, Chrisovalantou Huridou, Natasa Schwarz, Rana Dilara Incebacak Eltemur, Anna Würth, Daniel Weishäupl, Miriam Döcker, Gunnar Blumenstock, Sandra Martins, Leonor Correia Guedes, Guy A Rouleau, Laura Bannach Jardim, Maria-Luiza Saraiva-Pereira, Marcondes Cavalcante de França Junior, Carlos R Gordon, Roy Zaltzman, Mario R Cornejo-Olivas, Bart P C van de Warrenburg, Alexandra Dürr, Alexis Brice, Peter Bauer, Thomas Klockgether, Ludger Schöls, Olaf H Rieß, null null, Thorsten Schmidt
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy. Acta neuropathologica 148 (1) (2024)
Holger Hengel, Peter Martus, Jennifer Faber, Paola Giunti, Hector Garcia-Moreno, Nita Solanky, Thomas Klockgether, Kathrin Reetz, Bart P van de Warrenburg, Magda M Santana, Patrick Silva, Inês Cunha, Luís Pereira de Almeida, Dagmar Timmann, Jon Infante, Jeroen de Vries, Manuela Lima, Paula Pires, Khalaf Bushara, Heike Jacobi, Chiadi Onyike, Jeremy D Schmahmann, Jeannette Hübener-Schmid, Matthis Synofzik, null null, Ludger Schöls
Correction to: The frequency of non‑motor symptoms in SCA3 and their association with disease severity and lifestyle factors. Journal of neurology (2023)
Jessica Bux, Nesli Ece Sen, Isa-Maria Klink, Stefan Hauser, Matthis Synofzik, Ludger Schöls, Georg Auburger, Olaf H Rieß, Jeannette Hübener
TR-FRET-Based Immunoassay to Measure Ataxin-2 as a Target Engagement Marker in Spinocerebellar Ataxia Type 2. Molecular neurobiology (2023)
Hector Garcia-Moreno, Mercedes Prudencio, Gilbert Thomas-Black, Nita Solanky, Karen R Jansen-West, Rana Hanna Al-Shaikh, Amanda J Heslegrave, Henrik Zetterberg, Magda M Santana, Luis Pereira de Almeida, Ana Vasconcelos-Ferreira, Cristina Januário, Jon Infante, Jennifer Faber, Thomas Klockgether, Kathrin Reetz, Mafalda Raposo, Ana F Ferreira, Manuela Lima, Ludger Schöls, Matthis Synofzik, Jeannette Hübener, Andreas Puschmann, Sorina Gorcenco, Zbigniew K Wszolek, Leonard Petrucelli, Paola Giunti
Tau and neurofilament light-chain as fluid biomarkers in spinocerebellar ataxia type 3. European journal of neurology 29 (8) (2022)
Tim W Rattay, Ludger Schöls, Lena Zeltner, Wiltrud K Rohrschneider, Ulrike Ernemann, Tobias Lindig
"Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers. Journal of neurology 269 (11) (2022)
Winfried Ilg, Björn Müller, Jennifer Faber, Judith van Gaalen, Holger Hengel, Ina R Vogt, Guido Hennes, Bart P C Van De Warrenburg, Thomas Klockgether, Ludger Schöls, Matthis Synofzik, null null
Digital Gait Biomarkers Allow to Capture 1-Year Longitudinal Change in Spinocerebellar Ataxia Type 3. Movement disorders : official journal of the Movement Disorder Society 37 (11) (2022)
Christian Laßmann, Winfried Ilg, Marc Schneider, Maximilian Völker, Daniel F B Haeufle, Rebecca Schüle, Martin A Giese, Matthis Synofzik, Ludger Schöls, Tim W Rattay
Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 Study. Movement disorders : official journal of the Movement Disorder Society (2022)
Holger Hengel, Peter Martus, Jennifer Faber, Paola Giunit, Hector Garcia-Moreno, Nita Solanky, Thomas Klockgether, Kathrin Reetz, Bart P van de Warrenburg, Magda M Santana, Patrick Silva, Inês Cunha, Luís Pereira de Almeida, Dagmar Timmann, Jon Infante, Jeroen de Vries, Manuela Lima, Paula Pires, Khalaf Bushara, Heike Jacobi, Chiadi Onyike, Jeremy D Schmahmann, Jeannette Hübener-Schmid, Matthis Synofzik, null null, Ludger Schöls
The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors. Journal of neurology (2022)
S Schuster, E Heuten, A Velic, J Admard, M Synofzik, S Ossowski, B Macek, Stefan Hauser, Ludger Schöls
CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons. Disease models & mechanisms 13 (10) (2020)