Benedikt Schoser (B Schoser, Angela Abicht)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 55

Top Venues

Journal of neurology

Brain : a journal of neurology

European journal of neurology

Orphanet journal of rare diseases

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

Publications

Benedikt Schoser, Nadine A M E van der Beek, Alexander Broomfield, Esther Brusse, Jordi Díaz-Manera, Andreas Hahn, Thomas Hundsberger, Cornelia Kornblum, Michelle Kruijshaar, Pascal Laforêt, Eugen Mengel, Tiziana Mongini, David Orlikowski, Giancarlo Parenti, W W M Pim Pijnappel, Mark Roberts, Thomas Scherer, Antonio Toscano, John Vissing, Johanna M P van den Hout, Pieter A van Doorn, Stephan Wenninger, Ans T van der Ploeg
Start, switch and stop (triple-S) criteria for enzyme replacement therapy of late-onset Pompe disease: European Pompe Consortium recommendation update 2024. European journal of neurology (2024)
Kristl G Claeys, Hani Kushlaf, Syed Raza, Noemi Hummel, Simon Shohet, Ian Keyzor, Agnieszka Kopiec, Ryan Graham, Brian Fox, Benedikt Schoser
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease. Orphanet journal of rare diseases 19 (1) (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology (2024)
Harmke A van Kooten, Mike C Horton, Stephan Wenninger, Haris Babačić, Benedikt Schoser, Claire Lefeuvre, Najib Taouagh, Pascal Laforêt, Sonia Segovia, Jordi Díaz-Manera, Kristl G Claeys, Tiziana Mongini, Olimpia Musumeci, Antonio Toscano, Thomas Hundsberger, Esther Brusse, Pieter A van Doorn, Ans T van der Ploeg, Nadine A M E van der Beek, null null
Improving outcome measures in late onset Pompe disease: Modified Rasch-Built Pompe-Specific Activity scale. European journal of neurology (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology 271 (5) (2024)
Kristl G Claeys, Hani Kushlaf, Syed Raza, Noemi Hummel, Simon Shohet, Ian Keyzor, Agnieszka Kopiec, Ryan Graham, Brian Fox, Benedikt Schoser
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease. Orphanet journal of rare diseases 19 (1) (2024)
Benedikt Schoser, Nadine A M E van der Beek, Alexander Broomfield, Esther Brusse, Jordi Díaz-Manera, Andreas Hahn, Thomas Hundsberger, Cornelia Kornblum, Michelle Kruijshaar, Pascal Laforêt, Eugen Mengel, Tiziana Mongini, David Orlikowski, Giancarlo Parenti, W W M Pim Pijnappel, Mark Roberts, Thomas Scherer, Antonio Toscano, John Vissing, Johanna M P van den Hout, Pieter A van Doorn, Stephan Wenninger, Ans T van der Ploeg
Start, switch and stop (triple-S) criteria for enzyme replacement therapy of late-onset Pompe disease: European Pompe Consortium recommendation update 2024. European journal of neurology 31 (9) (2024)
Kristl G Claeys, Hani Kushlaf, Syed Raza, Noemi Hummel, Simon Shohet, Ian Keyzor, Agnieszka Kopiec, Ryan Graham, Brian Fox, Benedikt Schoser
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease. Orphanet journal of rare diseases 19 (1) (2024)
Benedikt Schoser, Nadine A M E van der Beek, Alexander Broomfield, Esther Brusse, Jordi Díaz-Manera, Andreas Hahn, Thomas Hundsberger, Cornelia Kornblum, Michelle Kruijshaar, Pascal Laforêt, Eugen Mengel, Tiziana Mongini, David Orlikowski, Giancarlo Parenti, W W M Pim Pijnappel, Mark Roberts, Thomas Scherer, Antonio Toscano, John Vissing, Johanna M P van den Hout, Pieter A van Doorn, Stephan Wenninger, Ans T van der Ploeg
Start, switch and stop (triple-S) criteria for enzyme replacement therapy of late-onset Pompe disease: European Pompe Consortium recommendation update 2024. European journal of neurology 31 (9) (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology 271 (5) (2024)
Kristl G Claeys, Hani Kushlaf, Syed Raza, Noemi Hummel, Simon Shohet, Ian Keyzor, Agnieszka Kopiec, Ryan Graham, Brian Fox, Benedikt Schoser
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease. Orphanet journal of rare diseases 19 (1) (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology 271 (5) (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology 271 (5) (2024)
Kristl G Claeys, Hani Kushlaf, Syed Raza, Noemi Hummel, Simon Shohet, Ian Keyzor, Agnieszka Kopiec, Ryan Graham, Brian Fox, Benedikt Schoser
Minimal clinically important differences in six-minute walking distance in late-onset Pompe disease. Orphanet journal of rare diseases 19 (1) (2024)
Benedikt Schoser, Nadine A M E van der Beek, Alexander Broomfield, Esther Brusse, Jordi Díaz-Manera, Andreas Hahn, Thomas Hundsberger, Cornelia Kornblum, Michelle Kruijshaar, Pascal Laforêt, Eugen Mengel, Tiziana Mongini, David Orlikowski, Giancarlo Parenti, W W M Pim Pijnappel, Mark Roberts, Thomas Scherer, Antonio Toscano, John Vissing, Johanna M P van den Hout, Pieter A van Doorn, Stephan Wenninger, Ans T van der Ploeg
Start, switch and stop (triple-S) criteria for enzyme replacement therapy of late-onset Pompe disease: European Pompe Consortium recommendation update 2024. European journal of neurology 31 (9) (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology 271 (5) (2024)
Benedikt Schoser, Priya S Kishnani, Drago Bratkovic, Barry J Byrne, Kristl G Claeys, Jordi Díaz-Manera, Pascal Laforêt, Mark Roberts, Antonio Toscano, Ans T van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Yasmine Wasfi, Tahseen Mozaffar, null null
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07). Journal of neurology 271 (5) (2024)
Katharina Lukas, Kristina Gutschmidt, Benedikt Schoser, Stephan Wenninger
Evaluation of myotonometry for myotonia, muscle stiffness and elasticity in neuromuscular disorders. Journal of neurology (2023)
Afshin Saffari, Tracy Lau, Homa Tajsharghi, Ehsan Ghayoor Karimiani, Ariana Kariminejad, Stephanie Efthymiou, Giovanni Zifarelli, Tipu Sultan, Mehran Beiraghi Toosi, Sahar Sedighzadeh, Victoria Mok Siu, Juan Darío Ortigoza-Escobar, Aisha M AlShamsi, Shahnaz Ibrahim, Nouriya Abbas Al-Sannaa, Walla Al-Hertani, Sandra Whalen, Mark Tarnopolsky, Shahryar Alavi, Chumei Li, Debra-Lynn Day-Salvatore, Maria Jesús Martínez-González, Kristin M Levandoski, Emma Bedoukian, Suneeta Madan-Khetarpal, Michaela J Idleburg, Minal Juliet Menezes, Aishwarya Siddharth, Konrad Platzer, Henry Oppermann, Martin Smitka, Felicity Collins, Monkol Lek, Mohmmad Shahrooei, Maryam Ghavideldarestani, Isabella Herman, John Rendu, Julien Faure, Janice Baker, Vikas Bhambhani, Laurel Calderwood, Javad Akhondian, Shima Imannezhad, Hanieh Sadat Mirzadeh, Narges Hashemi, Mohammad Doosti, Mojtaba Safi, Najmeh Ahangari, Paria Najarzadeh Torbati, Soheila Abedini, Vincenzo Salpietro, Elif Yilmaz Gulec, Safieh Eshaghian, Mohammadreza Ghazavi, Michael T Pascher, Marina Vogel, Benedikt Schoser, Sebastien Moutton, Ange-Line Bruel, Claudine Rieubland, Sabina Gallati, Tim M Strom, Hanns Lochmüller, Mohammad Hasan Mohammadi, Javeria Raza Alvi, Elaine H Zackai, Beth A Keena, Cara M Skraban, Seth I Berger, Hallie E Andrew, Elham Rahimian, Michelle M Morrow, Ingrid M Wentzensen, Francisca Millan, Lindsay B Henderson, Hormos Salimi Dafsari, Heinz Jungbluth, Natalia Gomez-Ospina, Anne McRae, Merlene Peter, Danai Veltra, Nikolaos M Marinakis, Christalena Sofocleous, Farah Ashrafzadeh, Davut Pehlivan, Johannes R Lemke, Judith Melki, Audrey Benezit, Peter Bauer, Denisa Weis, James R Lupski, Jan Senderek, John Chrisodoulou, Wendy K Chung, Rose E Goodchild, Amaka C Offiah, Andres Moreno-De-Luca, Suri Mohnish, Darius Ebrahimi-Fakhari, Henry Houlden, Reza Maroofian
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders. Brain : a journal of neurology (2023)
Tina Donandt, Vanessa Todorow, Stefan Hintze, Alexandra Graupner, Benedikt Schoser, Maggie C Walter, Peter Meinke
Nuclear Small Dystrophin Isoforms during Muscle Differentiation. Life (Basel, Switzerland) 13 (6) (2023)
Heinz Wiendl, Angela Abicht, Andrew Chan, Adela Della Marina, Tim Hagenacker, Khosro Hekmat, Sarah Hoffmann, Hans-Stefan Hoffmann, Sebastian Jander, Christian Keller, Alexander Marx, Arthur Melms, Nico Melzer, Wolfgang Müller-Felber, Marc Pawlitzki, Jens-Carsten Rückert, Christiane Schneider-Gold, Benedikt Schoser, Bettina Schreiner, Michael Schroeter, Bettina Schubert, Jörn-Peter Sieb, Fritz Zimprich, Andreas Meisel
Guideline for the management of myasthenic syndromes. Therapeutic advances in neurological disorders 16 (2023)
Afshin Saffari, Tracy Lau, Homa Tajsharghi, Ehsan Ghayoor Karimiani, Ariana Kariminejad, Stephanie Efthymiou, Giovanni Zifarelli, Tipu Sultan, Mehran Beiraghi Toosi, Sahar Sedighzadeh, Victoria Mok Siu, Juan Darío Ortigoza-Escobar, Aisha M AlShamsi, Shahnaz Ibrahim, Nouriya Abbas Al-Sannaa, Walla Al-Hertani, Sandra Whalen, Mark Tarnopolsky, Shahryar Alavi, Chumei Li, Debra-Lynn Day-Salvatore, Maria Jesús Martínez-González, Kristin M Levandoski, Emma Bedoukian, Suneeta Madan-Khetarpal, Michaela J Idleburg, Minal Juliet Menezes, Aishwarya Siddharth, Konrad Platzer, Henry Oppermann, Martin Smitka, Felicity Collins, Monkol Lek, Mohmmad Shahrooei, Maryam Ghavideldarestani, Isabella Herman, John Rendu, Julien Faure, Janice Baker, Vikas Bhambhani, Laurel Calderwood, Javad Akhondian, Shima Imannezhad, Hanieh Sadat Mirzadeh, Narges Hashemi, Mohammad Doosti, Mojtaba Safi, Najmeh Ahangari, Paria Najarzadeh Torbati, Soheila Abedini, Vincenzo Salpietro, Elif Yilmaz Gulec, Safieh Eshaghian, Mohammadreza Ghazavi, Michael T Pascher, Marina Vogel, Benedikt Schoser, Sebastien Moutton, Ange-Line Bruel, Claudine Rieubland, Sabina Gallati, Tim M Strom, Hanns Lochmüller, Mohammad Hasan Mohammadi, Javeria Raza Alvi, Elaine H Zackai, Beth A Keena, Cara M Skraban, Seth I Berger, Hallie E Andrew, Elham Rahimian, Michelle M Morrow, Ingrid M Wentzensen, Francisca Millan, Lindsay B Henderson, Hormos Salimi Dafsari, Heinz Jungbluth, Natalia Gomez-Ospina, Anne McRae, Merlene Peter, Danai Veltra, Nikolaos M Marinakis, Christalena Sofocleous, Farah Ashrafzadeh, Davut Pehlivan, Johannes R Lemke, Judith Melki, Audrey Benezit, Peter Bauer, Denisa Weis, James R Lupski, Jan Senderek, John Chrisodoulou, Wendy K Chung, Rose E Goodchild, Amaka C Offiah, Andres Moreno-De-Luca, Suri Mohnish, Darius Ebrahimi-Fakhari, Henry Houlden, Reza Maroofian
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders. Brain : a journal of neurology (2023)
Hannes Erdmann, Florentine Scharf, Ariane Hallermayr, Hayk Barsegehyan, Maggie C Walter, Elke Holinski-Feder, Benedikt Schoser, Benedikt Schoser
Reply: An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1. Brain : a journal of neurology (2023)
Heinz Wiendl, Angela Abicht, Andrew Chan, Adela Della Marina, Tim Hagenacker, Khosro Hekmat, Sarah Hoffmann, Hans-Stefan Hoffmann, Sebastian Jander, Christian Keller, Alexander Marx, Arthur Melms, Nico Melzer, Wolfgang Müller-Felber, Marc Pawlitzki, Jens-Carsten Rückert, Christiane Schneider-Gold, Benedikt Schoser, Bettina Schreiner, Michael Schroeter, Bettina Schubert, Jörn-Peter Sieb, Fritz Zimprich, Andreas Meisel
Guideline for the management of myasthenic syndromes. Therapeutic advances in neurological disorders 16 (2023)
Heinz Wiendl, Angela Abicht, Andrew Chan, Adela Della Marina, Tim Hagenacker, Khosro Hekmat, Sarah Hoffmann, Hans-Stefan Hoffmann, Sebastian Jander, Christian Keller, Alexander Marx, Arthur Melms, Nico Melzer, Wolfgang Müller-Felber, Marc Pawlitzki, Jens-Carsten Rückert, Christiane Schneider-Gold, Benedikt Schoser, Bettina Schreiner, Michael Schroeter, Bettina Schubert, Jörn-Peter Sieb, Fritz Zimprich, Andreas Meisel
Guideline for the management of myasthenic syndromes. Therapeutic advances in neurological disorders 16 (2023)
Afshin Saffari, Tracy Lau, Homa Tajsharghi, Ehsan Ghayoor Karimiani, Ariana Kariminejad, Stephanie Efthymiou, Giovanni Zifarelli, Tipu Sultan, Mehran Beiraghi Toosi, Sahar Sedighzadeh, Victoria Mok Siu, Juan Darío Ortigoza-Escobar, Aisha M AlShamsi, Shahnaz Ibrahim, Nouriya Abbas Al-Sannaa, Walla Al-Hertani, Sandra Whalen, Mark Tarnopolsky, Shahryar Alavi, Chumei Li, Debra-Lynn Day-Salvatore, Maria Jesús Martínez-González, Kristin M Levandoski, Emma Bedoukian, Suneeta Madan-Khetarpal, Michaela J Idleburg, Minal Juliet Menezes, Aishwarya Siddharth, Konrad Platzer, Henry Oppermann, Martin Smitka, Felicity Collins, Monkol Lek, Mohmmad Shahrooei, Maryam Ghavideldarestani, Isabella Herman, John Rendu, Julien Faure, Janice Baker, Vikas Bhambhani, Laurel Calderwood, Javad Akhondian, Shima Imannezhad, Hanieh Sadat Mirzadeh, Narges Hashemi, Mohammad Doosti, Mojtaba Safi, Najmeh Ahangari, Paria Najarzadeh Torbati, Soheila Abedini, Vincenzo Salpietro, Elif Yilmaz Gulec, Safieh Eshaghian, Mohammadreza Ghazavi, Michael T Pascher, Marina Vogel, Benedikt Schoser, Sebastien Moutton, Ange-Line Bruel, Claudine Rieubland, Sabina Gallati, Tim M Strom, Hanns Lochmüller, Mohammad Hasan Mohammadi, Javeria Raza Alvi, Elaine H Zackai, Beth A Keena, Cara M Skraban, Seth I Berger, Hallie E Andrew, Elham Rahimian, Michelle M Morrow, Ingrid M Wentzensen, Francisca Millan, Lindsay B Henderson, Hormos Salimi Dafsari, Heinz Jungbluth, Natalia Gomez-Ospina, Anne McRae, Merlene Peter, Danai Veltra, Nikolaos M Marinakis, Christalena Sofocleous, Farah Ashrafzadeh, Davut Pehlivan, Johannes R Lemke, Judith Melki, Audrey Benezit, Peter Bauer, Denisa Weis, James R Lupski, Jan Senderek, John Chrisodoulou, Wendy K Chung, Rose E Goodchild, Amaka C Offiah, Andres Moreno-De-Luca, Suri Mohnish, Darius Ebrahimi-Fakhari, Henry Houlden, Reza Maroofian
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders. Brain : a journal of neurology (2023)
Tina Donandt, Vanessa Todorow, Stefan Hintze, Alexandra Graupner, Benedikt Schoser, Maggie C Walter, Peter Meinke
Nuclear Small Dystrophin Isoforms during Muscle Differentiation. Life (Basel, Switzerland) 13 (6) (2023)
Tina Donandt, Stefan Hintze, Sabine Krause, Eckhard Wolf, Benedikt Schoser, Maggie C Walter, Peter Meinke
Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy. Life (Basel, Switzerland) 12 (10) (2022)
Marko Mijic, Benedikt Schoser, Peter Young
Efficacy of functional electrical stimulation in rehabilitating patients with foot drop symptoms after stroke and its correlation with somatosensory evoked potentials-a crossover randomised controlled trial. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)
Mazen M Dimachkie, Richard J Barohn, Barry Byrne, Ozlem Goker-Alpan, Priya S Kishnani, Shafeeq Ladha, Pascal Laforêt, Karl Eugen Mengel, Loren D M Peña, Sabrina Sacconi, Volker Straub, Jaya Trivedi, Philip Van Damme, Ans T van der Ploeg, John Vissing, Peter Young, Kristina An Haack, Meredith Foster, Jane M Gilbert, Patrick Miossec, Olivier Vitse, Tianyue Zhou, Benedikt Schoser, null null
Long-term Safety and Efficacy of Avalglucosidase Alfa in Patients With Late-Onset Pompe Disease. Neurology (2022)
Anne-Katrin Guettsches, Nancy Meyer, René P Zahedi, Teresinha Evangelista, Thomas Muentefering, Tobias Ruck, Emmanuelle Lacene, Christoph Heute, Humberto Gonczarowska-Jorge, Benedikt Schoser, Sabine Krause, Andreas Hentschel, Matthias Vorgerd, Andreas Roos
FYCO1 Increase and Effect of Arimoclomol-Treatment in Human VCP -Pathology. Biomedicines 10 (10) (2022)
Hannes Erdmann, Florentine Scharf, Stefanie Gehling, Anna Benet-Pagès, Sibylle Jakubiczka, Kerstin Becker, Maria Seipelt, Felix Kleefeld, Karl Christian Knop, Eva Christina Prott, Miriam Hiebeler, Krisztina Einvag, Dieter Gläser, Matthias Vorgerd, Tim Hagenacker, Maggie C Walter, Peter Reilich, Teresa Neuhann, Martin Zenker, Elke Holinski-Feder, Benedikt Schoser, Benedikt Schoser
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophy. Brain : a journal of neurology (2022)
Marko Mijic, Benedikt Schoser, Peter Young
Efficacy of functional electrical stimulation in rehabilitating patients with foot drop symptoms after stroke and its correlation with somatosensory evoked potentials-a crossover randomised controlled trial. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)
Marko Mijic, Benedikt Schoser, Peter Young
Efficacy of functional electrical stimulation in rehabilitating patients with foot drop symptoms after stroke and its correlation with somatosensory evoked potentials-a crossover randomised controlled trial. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2022)
Marko Mijic, Benedikt Schoser, Peter Young
Efficacy of functional electrical stimulation in rehabilitating patients with foot drop symptoms after stroke and its correlation with somatosensory evoked potentials-a crossover randomised controlled trial. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)
Elena Sagerer, Corinna Wirner, Benedikt Schoser, Stephan Wenninger
Nociceptive pain in adult patients with 5q-spinal muscular atrophy type 3: a cross-sectional clinical study. Journal of neurology (2022)
Marko Mijic, Benedikt Schoser, Peter Young
Efficacy of functional electrical stimulation in rehabilitating patients with foot drop symptoms after stroke and its correlation with somatosensory evoked potentials-a crossover randomised controlled trial. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)
Hannes Erdmann, Florian Schöberl, Mădălina Giurgiu, Rafaela Magalhaes Leal Silva, Veronika Scholz, Florentine Scharf, Martin Wendlandt, Stephanie Kleinle, Marcus Deschauer, Georg Nübling, Wolfgang Heide, Sait Seymen Babacan, Christine Schneider, Teresa Neuhann, Katrin Hahn, Benedikt Schoser, Elke Holinski-Feder, Dieter A Wolf, Benedikt Schoser
Parallel in-depth analysis of repeat expansions in ataxia patients by long-read sequencing. Brain : a journal of neurology (2022)
Vanessa Todorow, Stefan Hintze, Alastair R W Kerr, Andreas Hehr, Benedikt Schoser, Peter Meinke
Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1. International journal of molecular sciences 22 (16) (2021)
Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, Kees Okkersen, Aura Cecilia Jimenez-Moreno, Ferroudja Daidj, Hanns Lochmüller, Fiona Hogarth, Hans Knoop, Guillaume Bassez, Darren G Monckton, Baziel G M van Engelen, Benedikt Schoser
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1. Neurology. Genetics 7 (2) (2021)
Sarah Schlaeger, Nico Sollmann, Agnes Zoffl, Edoardo Aitala Becherucci, Dominik Weidlich, Elisabeth Kottmaier, Isabelle Riederer, Tobias Greve, Federica Montagnese, Marcus Deschauer, Benedikt Schoser, Claus Zimmer, Dimitrios C Karampinos, Jan Stefan Kirschke, Thomas Baum
Quantitative Muscle MRI in Patients with Neuromuscular Diseases-Association of Muscle Proton Density Fat Fraction with Semi-Quantitative Grading of Fatty Infiltration and Muscle Strength at the Thigh Region. Diagnostics (Basel, Switzerland) 11 (6) (2021)
Rudolf Korinthenberg, Regina Trollmann, Barbara Plecko, Georg M Stettner, Markus Blankenburg, Joachim Weis, Benedikt Schoser, Wolfgang Müller-Felber, Nina Lochbuehler, Gabriele Hahn, Sabine Rudnik-Schöneborn
Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents-Consensus-Based Practice Guidelines. Children (Basel, Switzerland) 8 (8) (2021)
Kristina Gutschmidt, Olimpia Musumeci, Jordi Díaz-Manera, Yin-Hsiu Chien, Karl Christian Knop, Stephan Wenninger, Federica Montagnese, Alessia Pugliese, Graziana Tavilla, Jorge Alonso-Pérez, Paul Wuh-Liang Hwu, Antonio Toscano, Benedikt Schoser
STIG study: real-world data of long-term outcomes of adults with Pompe disease under enzyme replacement therapy with alglucosidase alfa. Journal of neurology 268 (7) (2021)
Stephan Wenninger, Kristina Gutschmidt, Corinna Wirner, Krisztina Einvag, Federica Montagnese, Benedikt Schoser
The impact of interrupting enzyme replacement therapy in late-onset Pompe disease. Journal of neurology 268 (8) (2021)
Noemi Vereb, Federica Montagnese, Dieter Gläser, Benedikt Schoser
Non-dystrophic myotonias: clinical and mutation spectrum of 70 German patients. Journal of neurology 268 (5) (2020)
Stefan Hintze, Sarah Limmer, Paulina Dabrowska-Schlepp, Birgit Berg, Nicola Krieghoff, Andreas Busch, Andreas Schaaf, Peter Meinke, Benedikt Schoser
Moss-Derived Human Recombinant GAA Provides an Optimized Enzyme Uptake in Differentiated Human Muscle Cells of Pompe Disease. International journal of molecular sciences 21 (7) (2020)
K Gutschmidt, S Wenninger, F Montagnese, Benedikt Schoser
Dyslexia and cognitive impairment in adult patients with myotonic dystrophy type 1: a clinical prospective analysis. Journal of neurology 268 (2) (2020)
Sarah A Cumming, Aura Cecilia Jimenez-Moreno, Kees Okkersen, Stephan Wenninger, Ferroudja Daidj, Fiona Hogarth, Roberta Littleford, Gráinne Siobhan Gorman, Guillaume Bassez, Benedikt Schoser, Hanns Lochmüller, Baziel G M van Engelen, Darren G Monckton, null null
Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort. Neurology 93 (10) (2019)
Sarah Schlaeger, Dominik Weidlich, Elisabeth Klupp, Federica Montagnese, Marcus Deschauer, Benedikt Schoser, Sarah Bublitz, Stefan Ruschke, Claus Zimmer, Ernst J Rummeny, Jan Stefan Kirschke, Dimitrios C Karampinos
Water T2 Mapping in Fatty Infiltrated Thigh Muscles of Patients With Neuromuscular Diseases Using a T2 -Prepared 3D Turbo Spin Echo With SPAIR. Journal of magnetic resonance imaging : JMRI 51 (6) (2019)
Benedikt Schoser
Novel Pompe disease phenotype: a treatment-related modified phenotype neglecting the brain. Developmental medicine and child neurology 60 (6) (2018)
Federica Montagnese, Molly White, Anke Klein, Kristina Stahl, Stephan Wenninger, Benedikt Schoser
Cannabis use in myotonic dystrophy patients in Germany and USA: a pilot survey. Journal of neurology 266 (2) (2018)
Benedikt Schoser, Bruno Eymard, Joe Datt, Renato Mantegazza
Lambert-Eaton myasthenic syndrome (LEMS): a rare autoimmune presynaptic disorder often associated with cancer. Journal of neurology 264 (9) (2017)
Benedikt Schoser, Deborah A Bilder, David Dimmock, Digant Gupta, Emma S James, Suyash Prasad
The humanistic burden of Pompe disease: are there still unmet needs? A systematic review. BMC neurology 17 (1) (2017)
Federica Montagnese, Stefania Mondello, Stephan Wenninger, Wolfram Kress, Benedikt Schoser
Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2. Journal of neurology 264 (12) (2017)
Benedikt Schoser, Andrew Stewart, Steve Kanters, Alaa Hamed, Jeroen Jansen, Keith Chan, Mohammad Karamouzian, Antonio Toscano
Survival and long-term outcomes in late-onset Pompe disease following alglucosidase alfa treatment: a systematic review and meta-analysis. Journal of neurology 264 (4) (2016)

Benedikt Schoser.css-eqlu8i{font-size:small;padding-left:4px;} (B Schoser, Angela Abicht)

Publication Activity (10 Years)

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Benedikt Schoser (B Schoser, Angela Abicht)