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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2019 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 1 |
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6 results
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Page 1
Physical fitness in children with Marfan and Loeys-Dietz syndrome: associations between cardiovascular parameters, systemic manifestations, fatigue, and pain.
Eur J Pediatr. 2024 May;183(5):2421-2429. doi: 10.1007/s00431-024-05456-z. Epub 2024 Mar 11.
Eur J Pediatr. 2024.
PMID: 38466415
Free PMC article.
Somatic symptoms, pain, catastrophizing and the association with disability among children with heritable connective tissue disorders.
de Koning LE, Warnink-Kavelaars J, van Rossum MA, Bosman D, Menke LA, Malfait F, de Boer R, Oosterlaan J, Engelbert RHH, Rombaut L; Pediatric Heritable Connective Tissue Disorders Study Group.
de Koning LE, et al.
Am J Med Genet A. 2023 Jul;191(7):1792-1803. doi: 10.1002/ajmg.a.63204. Epub 2023 Apr 26.
Am J Med Genet A. 2023.
PMID: 37186039
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An exploratory study of clinical characteristics and gait features of adolescents with hypermobility disorders.
de Koning LE, Scheper MC, Ploeger HE, Warnink-Kavelaars J, Oosterlaan J, Bus SA, Engelbert RHH.
de Koning LE, et al.
Gait Posture. 2023 Feb;100:222-229. doi: 10.1016/j.gaitpost.2023.01.001. Epub 2023 Jan 5.
Gait Posture. 2023.
PMID: 36638668
Free article.
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Heritable connective tissue disorders in childhood: Decreased health-related quality of life and mental health.
Warnink-Kavelaars J, de Koning LE, Rombaut L, Menke LA, Alsem MW, van Oers HA, Buizer AI, Engelbert RHH, Oosterlaan J; Pediatric Heritable Connective Tissue Disorder study group.
Warnink-Kavelaars J, et al. Among authors: de koning le.
Am J Med Genet A. 2022 Jul;188(7):2096-2109. doi: 10.1002/ajmg.a.62750. Epub 2022 Apr 8.
Am J Med Genet A. 2022.
PMID: 35393672
Free PMC article.
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Heritable Connective Tissue Disorders in Childhood: Increased Fatigue, Pain, Disability and Decreased General Health.
Warnink-Kavelaars J, de Koning LE, Rombaut L, Alsem MW, Menke LA, Oosterlaan J, Buizer AI, Engelbert RHH, On Behalf Of The Pediatric Heritable Connective Tissue Disorders Study Group.
Warnink-Kavelaars J, et al. Among authors: de koning le.
Genes (Basel). 2021 May 28;12(6):831. doi: 10.3390/genes12060831.
Genes (Basel). 2021.
PMID: 34071423
Free PMC article.
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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 TMHJ, de Koning LE, Nollet F, Alsem MW, Menke LA, Engelbert RHH.
Warnink-Kavelaars J, et al. Among authors: de koning le.
Eur J Pediatr. 2019 Dec;178(12):1883-1892. doi: 10.1007/s00431-019-03469-7. Epub 2019 Oct 16.
Eur J Pediatr. 2019.
PMID: 31620888
Free PMC article.
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