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Journal of Neuromuscular Diseases|September 19, 2022
Perioperative Care for Patients with Neuromuscular Disorders in the Netherlands - A Questionnaire Study Among Anaesthesiologists, Neurologists and Clinical GeneticistsL R van den Bersselaar, M H M Gubbels, H Jungbluth, et al.Neuromuscular Disorders : NMD|December 23, 2018
Functional impairments, fatigue and quality of life in RYR1-related myopathies: A questionnaire studyE van Ruitenbeek, J A E Custers, C Verhaak, et al.Parkinsonism & Related Disorders|September 26, 2020
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL geneKarlien Mul, Meyke I Schouten, Erica van der Looij, et al.Neuromuscular Disorders : NMD|October 3, 2022
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataractI E A Karnebeek, H T M Boon, A M P Huis, et al.Plos One|July 31, 2024
Optimising primary molecular profiling in non-small cell lung cancerR D Schouten, I Schouten, M M F Schuurbiers, et al.European Journal of Human Genetics : EJHG|September 7, 2019
KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegiaMaartje Pennings, Meyke I Schouten, Judith van Gaalen, et al.Journal of Neuromuscular Diseases|May 26, 2019
Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic ServiceDineke Westra, Meyke I Schouten, Bas C Stunnenberg, et al.Pageof 2