| What's in a name? The clinical features of facioscapulohumeral muscular dystrophy K Mul, S Lassche, NC Voermans, GW Padberg, CGC Horlings, ... Practical neurology 16 (3), 201-207, 2016 | 126 | 2016 |
| Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophy S Lassche, GJM Stienen, TC Irving, SM van der Maarel, NC Voermans, ... Neurology 80 (8), 733-737, 2013 | 55 | 2013 |
| Correlation between quantitative MRI and muscle histopathology in muscle biopsies from healthy controls and patients with IBM, FSHD and OPMD S Lassche, B Küsters, A Heerschap, MVP Schyns, CAC Ottenheijm, ... Journal of Neuromuscular Diseases 7 (4), 495-504, 2020 | 36 | 2020 |
| KBTBD13 is an actin-binding protein that modulates muscle kinetics JM De Winter, JP Molenaar, M Yuen, R Van Der Pijl, S Shen, S Conijn, ... The Journal of clinical investigation 130 (2), 754-767, 2020 | 35 | 2020 |
| An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy AT Pagnamenta, R Kaiyrzhanov, Y Zou, SI Da'as, R Maroofian, ... Brain 144 (2), 584-600, 2021 | 28 | 2021 |
| MRI-guided biopsy as a tool for diagnosis and research of muscle disorders S Lassche, BH Janssen, T IJzermans, JJ Fütterer, NC Voermans, ... Journal of neuromuscular diseases 5 (3), 315-319, 2018 | 26 | 2018 |
| Involvement of pelvic girdle and proximal leg muscles in early oculopharyngeal muscular dystrophy BM Van der Sluijs, S Lassche, GJ Knuiman, B Kusters, A Heerschap, ... Neuromuscular Disorders 27 (12), 1099-1105, 2017 | 22 | 2017 |
| Ultrasound imaging of muscle contraction of the tibialis anterior in patients with facioscapulohumeral dystrophy K Gijsbertse, R Goselink, S Lassche, M Nillesen, A Sprengers, ... Ultrasound in medicine & biology 43 (11), 2537-2545, 2017 | 22 | 2017 |
| Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers A van den Heuvel, S Lassche, K Mul, A Greco, D San León Granado, ... Scientific Reports 12 (1), 1426, 2022 | 15 | 2022 |
| Specific muscle strength is reduced in facioscapulohumeral dystrophy: an MRI based musculoskeletal analysis MA Marra, L Heskamp, K Mul, S Lassche, BGM van Engelen, ... Neuromuscular disorders 28 (3), 238-245, 2018 | 14 | 2018 |
| A novel KCNA1 mutation causing episodic ataxia type I S Lassche, S Lainez, BR Bloem, BPC van de Warrenburg, J Hofmeijer, ... Muscle & nerve 50 (2), 289-291, 2014 | 14 | 2014 |
| Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol S Lassche, CAC Ottenheijm, NC Voermans, HJ Westeneng, BH Janssen, ... BMC neurology 13, 1-7, 2013 | 14 | 2013 |
| Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy F Roth, J Dhiab, A Boulinguiez, HR Mouigni, S Lassche, E Negroni, ... Acta Neuropathologica 144 (6), 1157-1170, 2022 | 10 | 2022 |
| Facioscapulohumeral muscular dystrophy—Reproductive counseling, pregnancy, and delivery in a complex multigenetic disease SCC Vincenten, N Van Der Stoep, ADC Paulussen, K Mul, UA Badrising, ... Clinical Genetics 101 (2), 149-160, 2022 | 10 | 2022 |
| Computer-aided detection of fasciculations and other movements in muscle with ultrasound: Development and clinical application K Gijsbertse, M Bakker, A Sprengers, J Wijntjes, S Lassche, ... Clinical Neurophysiology 129 (12), 2567-2576, 2018 | 10 | 2018 |
| Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy S Lassche, NC Voermans, T Schreuder, A Heerschap, B Küsters, ... Muscle & Nerve 63 (1), 60-67, 2021 | 9 | 2021 |
| Age-associated salivary microRNA biomarkers for oculopharyngeal muscular dystrophy V Raz, RH Kroon, H Mei, M Riaz, H Buermans, S Lassche, C Horlings, ... International Journal of Molecular Sciences 21 (17), 6059, 2020 | 9 | 2020 |
| Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy S Lassche, NC Voermans, R van der Pijl, M van den Berg, A Heerschap, ... Neurology 94 (11), e1157-e1170, 2020 | 8 | 2020 |
| Muscle fiber dysfunction contributes to weakness in inclusion body myositis S Lassche, A Rietveld, A Heerschap, HW van Hees, MTE Hopman, ... Neuromuscular Disorders 29 (6), 468-476, 2019 | 7 | 2019 |
| Monitoring creatine and phosphocreatine by 13C MR spectroscopic imaging during and after 13C4 creatine loading: a feasibility study BH Janssen, S Lassche, MT Hopman, RA Wevers, BGM van Engelen, ... Amino Acids 48 (8), 1857-1866, 2016 | 7 | 2016 |
Baziel van EngelenRadboud University Medical Centre, Nijmegen, The NetherlandsVerified email at radboudumc.nl
