Smeets E - Search Results

1

Rett Syndrome as a Rare Disease: A European Perspective.

Townend GS, van Kranen HJ, van der Stel R, van den Berg M, Smeets E, van Waardenburg D, Curfs LM. Townend GS, et al. Among authors: smeets e. Public Health Genomics. 2015;18(4):233-6. doi: 10.1159/000381139. Epub 2015 Apr 14. Public Health Genomics. 2015. PMID: 25895605 No abstract available.

2

Rett syndrome and developmental regression.

Smeets EE, Townend GS, Curfs LMG. Smeets EE, et al. Neurosci Biobehav Rev. 2019 Sep;104:100-101. doi: 10.1016/j.neubiorev.2019.06.038. Epub 2019 Jul 5. Neurosci Biobehav Rev. 2019. PMID: 31283952 No abstract available.

3

Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands.

Townend GS, Marschik PB, Smeets E, van de Berg R, van den Berg M, Curfs LM. Townend GS, et al. Among authors: smeets e. J Dev Phys Disabil. 2016;28:101-112. doi: 10.1007/s10882-015-9455-z. Epub 2015 Oct 19. J Dev Phys Disabil. 2016. PMID: 27069348 Free PMC article.

4

Abnormal Foot Position and Standing and Walking Ability in Rett Syndrome: an Exploratory Study.

Borst HE, Townend GS, van Eck M, Smeets E, van den Berg M, Laan A, Curfs LMG. Borst HE, et al. Among authors: smeets e. J Dev Phys Disabil. 2018;30(2):281-295. doi: 10.1007/s10882-017-9585-6. Epub 2018 Jan 2. J Dev Phys Disabil. 2018. PMID: 29563764 Free PMC article.

5

Oculomotor Function in Individuals With Rett Syndrome.

Townend GS, van de Berg R, de Breet LHM, Hiemstra M, Wagter L, Smeets E, Widdershoven J, Kingma H, Curfs LMG. Townend GS, et al. Among authors: smeets e. Pediatr Neurol. 2018 Nov;88:48-58. doi: 10.1016/j.pediatrneurol.2018.08.022. Epub 2018 Aug 30. Pediatr Neurol. 2018. PMID: 30340908 Free article.

6

Challenges in evaluating the oculomotor function in individuals with Rett syndrome using electronystagmography.

de Breet LHM, Townend GS, Curfs LMG, Kingma H, Smeets EEJ, Lucieer F, Widdershoven J, van de Berg R. de Breet LHM, et al. Among authors: smeets eej. Eur J Paediatr Neurol. 2019 Mar;23(2):262-269. doi: 10.1016/j.ejpn.2018.12.003. Epub 2018 Dec 18. Eur J Paediatr Neurol. 2019. PMID: 30635145

7

Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes.

Ehrhart F, Coort SL, Eijssen L, Cirillo E, Smeets EE, Bahram Sangani N, Evelo CT, Curfs LMG. Ehrhart F, et al. Among authors: smeets ee. World J Biol Psychiatry. 2020 Dec;21(10):712-725. doi: 10.1080/15622975.2019.1593501. Epub 2019 Apr 29. World J Biol Psychiatry. 2020. PMID: 30907210 Free article.

8

New insights in Rett syndrome using pathway analysis for transcriptomics data.

Ehrhart F, Coort SL, Cirillo E, Smeets E, Evelo CT, Curfs L. Ehrhart F, et al. Among authors: smeets e. Wien Med Wochenschr. 2016 Sep;166(11-12):346-52. doi: 10.1007/s10354-016-0488-4. Epub 2016 Aug 12. Wien Med Wochenschr. 2016. PMID: 27517371 Free PMC article.

9

Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes.

Ehrhart F, Coort SL, Cirillo E, Smeets E, Evelo CT, Curfs LM. Ehrhart F, et al. Among authors: smeets e. Orphanet J Rare Dis. 2016 Nov 25;11(1):158. doi: 10.1186/s13023-016-0545-5. Orphanet J Rare Dis. 2016. PMID: 27884167 Free PMC article. Review.

10

Aging in Rett syndrome: a longitudinal study.

Halbach NS, Smeets EE, Steinbusch C, Maaskant MA, van Waardenburg D, Curfs LM. Halbach NS, et al. Among authors: smeets ee. Clin Genet. 2013 Sep;84(3):223-9. doi: 10.1111/cge.12063. Epub 2012 Dec 7. Clin Genet. 2013. PMID: 23167724

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