Centre of Expertise Applied Artificial Intelligence
L.E. de Koning (Lisanne)
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Somatic symptoms, pain, catastrophizing and the association with disability among children with heritable connective tissue disorders
de Koning, L. E., Warnink-Kavelaars, J., van Rossum, M. A., Bosman, D., Menke, L. A., Malfait, F., de Boer, R., Oosterlaan, J., Engelbert, R. H. H., & Rombaut, L. (2023). Somatic symptoms, pain, catastrophizing and the association with disability among children with heritable connective tissue disorders. American Journal of Medical Genetics, Part A, 191(7), 1792-1803. https://doi.org/10.1002/ajmg.a.63204
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An exploratory study of clinical characteristics and gait features of adolescents with hypermobility disorders
de Koning, L. E., Scheper, M. C., Ploeger, H. E., Warnink-Kavelaars, J., Oosterlaan, J., Bus, S. A., & Engelbert, R. H. H. (2023). An exploratory study of clinical characteristics and gait features of adolescents with hypermobility disorders. Gait & Posture, 100, 222-229. https://doi.org/10.1016/j.gaitpost.2023.01.001
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Physical activity and physical fitness in children with heritable connective tissue disorders
de Koning, L., Warnink-Kavelaars, J., van Rossum, M., Limmen, S., Van der Looven, R., Muiño-Mosquera, L., van der Hulst, A., Oosterlaan, J., Rombaut, L., & Engelbert, R. (2023). Physical activity and physical fitness in children with heritable connective tissue disorders. Frontiers in Pediatrics, 11, Article 1057070. https://doi.org/10.3389/fped.2023.1057070
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Heritable connective tissue disorders in childhood: Decreased health-related quality of life and mental health
Warnink-Kavelaars, J., de Koning, L. E., Rombaut, L., Menke, L. A., Alsem, M. W., van Oers, H. A., Buizer, A. I., Engelbert, R. H. H., Oosterlaan, J., & Pediatric Heritable Connective Tissue Disorder study group (2022). Heritable connective tissue disorders in childhood: Decreased health-related quality of life and mental health. American Journal of Medical Genetics - Part A, 188(7), 2096-2109. https://doi.org/10.1002/ajmg.a.62750
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Heritable connective tissue disorders in childhood
Warnink-Kavelaars, J., de Koning, L. E., Rombaut, L., Alsem, M. W., Menke, L. A., Oosterlaan, J., Buizer, A. I., Engelbert, R. H. H., & On Behalf Of The Pediatric Heritable Connective Tissue Disorders Study Group (2021). Heritable connective tissue disorders in childhood: increased fatigue, pain, disability and decreased general health. Genes, 12(6). https://doi.org/10.3390/genes12060831
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Marfan syndrome in adolescence: adolescents' perspectives on (physical) functioning, disability, contextual factors and support needs
Warnink-Kavelaars, J., Beelen, A., Goedhart, T. M. H. J., de Koning, L. E., Nollet, F., Alsem, M. W., Menke, L. A., & Engelbert, R. H. H. (2019). Marfan syndrome in adolescence: adolescents' perspectives on (physical) functioning, disability, contextual factors and support needs. European Journal of Pediatrics, 178, 1883-1892. https://doi.org/10.1007%2Fs00431-019-03469-7
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Children and adolescents with Marfan Syndrome
de Koning, L., Warnink, J., Scheper, M., de Vries, J., Menke, L., Rombaut, L., & Engelbert, R. (2019). Children and adolescents with Marfan Syndrome: lessons learned from Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders regarding chronic pain and fatigue. Poster session presented at European Pediatric Physiotherapy Congress, Utrecht, Netherlands.