Swillen A - Search Results

1

Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research.

White LK, Crowley TB, Finucane B, McClellan EJ, Donoghue S, Garcia-Minaur S, Repetto GM, Fischer M, Jacquemont S, Gur RE, Maillard AM, Donald KA, Bassett AS, Swillen A, McDonald-McGinn DM. White LK, et al. Among authors: swillen a. Genes (Basel). 2023 Jan 7;14(1):169. doi: 10.3390/genes14010169. Genes (Basel). 2023. PMID: 36672911 Free PMC article.

2

VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

Stalmans I, Lambrechts D, De Smet F, Jansen S, Wang J, Maity S, Kneer P, von der Ohe M, Swillen A, Maes C, Gewillig M, Molin DG, Hellings P, Boetel T, Haardt M, Compernolle V, Dewerchin M, Plaisance S, Vlietinck R, Emanuel B, Gittenberger-de Groot AC, Scambler P, Morrow B, Driscol DA, Moons L, Esguerra CV, Carmeliet G, Behn-Krappa A, Devriendt K, Collen D, Conway SJ, Carmeliet P. Stalmans I, et al. Among authors: swillen a. Nat Med. 2003 Feb;9(2):173-82. doi: 10.1038/nm819. Epub 2003 Jan 21. Nat Med. 2003. PMID: 12539040

3

Referential communication abilities in children with 22q11.2 deletion syndrome.

Van Den Heuvel E, ReuterskiöLd C, Solot C, Manders E, Swillen A, Zink I. Van Den Heuvel E, et al. Among authors: swillen a. Int J Speech Lang Pathol. 2017 Oct;19(5):490-502. doi: 10.1080/17549507.2016.1221456. Epub 2016 Oct 3. Int J Speech Lang Pathol. 2017. PMID: 27690637

4

Autism and genetics: high incidence of specific genetic syndromes in 21 autistic adolescents and adults living in two residential homes in Belgium.

Swillen A, Hellemans H, Steyaert J, Fryns JP. Swillen A, et al. Am J Med Genet. 1996 May 31;67(3):315-6. doi: 10.1002/(SICI)1096-8628(19960531)67:3<315::AID-AJMG9>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8725750 No abstract available.

5

Basic number processing and difficulties in single-digit arithmetic: evidence from Velo-Cardio-Facial Syndrome.

De Smedt B, Reynvoet B, Swillen A, Verschaffel L, Boets B, Ghesquière P. De Smedt B, et al. Among authors: swillen a. Cortex. 2009 Feb;45(2):177-88. doi: 10.1016/j.cortex.2007.06.003. Epub 2008 Feb 1. Cortex. 2009. PMID: 19150519 Clinical Trial.

6

Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.

Van Aken K, Swillen A, Beirinckx M, Janssens L, Caeyenberghs K, Smits-Engelsman B. Van Aken K, et al. Among authors: swillen a. Res Dev Disabil. 2010 May-Jun;31(3):634-41. doi: 10.1016/j.ridd.2010.01.002. Epub 2010 Feb 23. Res Dev Disabil. 2010. PMID: 20181458

7

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications.

Swillen A, Vogels A, Devriendt K, Fryns JP. Swillen A, et al. Am J Med Genet. 2000 Summer;97(2):128-35. doi: 10.1002/1096-8628(200022)97:2<128::aid-ajmg4>3.0.co;2-z. Am J Med Genet. 2000. PMID: 11180220 Review.

8

Presenting symptoms and clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.

Vantrappen G, Devriendt K, Swillen A, Rommel N, Vogels A, Eyskens B, Gewillig M, Feenstra L, Fryns JP. Vantrappen G, et al. Among authors: swillen a. Genet Couns. 1999;10(1):3-9. Genet Couns. 1999. PMID: 10191424 Review.

9

Psychotic disorder associated with 22q11.2 duplication syndrome.

Amelsvoort TV, Denayer A, Boermans J, Swillen A. Amelsvoort TV, et al. Among authors: swillen a. Psychiatry Res. 2016 Feb 28;236:206-207. doi: 10.1016/j.psychres.2015.12.019. Epub 2015 Dec 17. Psychiatry Res. 2016. PMID: 26763109 No abstract available.

10

Renal and urological tract malformations caused by a 22q11 deletion.

Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M. Devriendt K, et al. Among authors: swillen a. J Med Genet. 1996 Apr;33(4):349. doi: 10.1136/jmg.33.4.349. J Med Genet. 1996. PMID: 8730297 Free PMC article. No abstract available.

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