Swillen A - Search Results

1

Low prevalence of substance use in people with 22q11.2 deletion syndrome.

Vingerhoets C, van Oudenaren MJF, Bloemen OJN, Boot E, van Duin EDA, Evers LJM, Fiksinski AM, Breetvelt EJ, Palmer LD, Vergaelen E, Vogels A, Meijer C, Booij J; Genetic Risk and Outcome of Psychosis (GROUP) investigators; de Haan L, Swillen A, Vorstman JAS, Bassett AS, van Amelsvoort TAMJ. Vingerhoets C, et al. Among authors: swillen a. Br J Psychiatry. 2019 Nov;215(5):661-667. doi: 10.1192/bjp.2018.258. Br J Psychiatry. 2019. PMID: 30604657

2

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.

3

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

Swillen A, Devriendt K, Legius E, Prinzie P, Vogels A, Ghesquière P, Fryns JP. Swillen A, et al. Genet Couns. 1999;10(1):79-88. Genet Couns. 1999. PMID: 10191433 Review.

4

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.

5

Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.

Descheemaeker MJ, Vogels A, Govers V, Borghgraef M, Willekens D, Swillen A, Verhoeven W, Fryns JP. Descheemaeker MJ, et al. Among authors: swillen a. J Intellect Disabil Res. 2002 Jan;46(Pt 1):41-50. doi: 10.1046/j.1365-2788.2002.00354.x. J Intellect Disabil Res. 2002. PMID: 11851855

6

The psychopathological phenotype of velo-cardio-facial syndrome.

Vogels A, Verhoeven WM, Tuinier S, DeVriendt K, Swillen A, Curfs LM, Frijns JP. Vogels A, et al. Among authors: swillen a. Ann Genet. 2002 Apr-Jun;45(2):89-95. doi: 10.1016/s0003-3995(02)01114-0. Ann Genet. 2002. PMID: 12119217 Review.

7

Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome.

Stiers P, Swillen A, De Smedt B, Lagae L, Devriendt K, D'Agostino E, Sunaert S, Fryns AP. Stiers P, et al. Among authors: swillen a. Child Neuropsychol. 2005 Feb;11(1):87-108. doi: 10.1080/09297040590911220. Child Neuropsychol. 2005. PMID: 15823985

8

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D. Raux G, et al. Among authors: swillen a. Hum Mol Genet. 2007 Jan 1;16(1):83-91. doi: 10.1093/hmg/ddl443. Epub 2006 Nov 29. Hum Mol Genet. 2007. PMID: 17135275

9

Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an update.

De Smedt B, Devriendt K, Fryns JP, Vogels A, Gewillig M, Swillen A. De Smedt B, et al. Among authors: swillen a. J Intellect Disabil Res. 2007 Sep;51(Pt 9):666-70. doi: 10.1111/j.1365-2788.2007.00955.x. J Intellect Disabil Res. 2007. PMID: 17845235

10

Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.

De Smedt B, Swillen A, Verschaffel L, Ghesquière P. De Smedt B, et al. Among authors: swillen a. Dev Disabil Res Rev. 2009;15(1):4-10. doi: 10.1002/ddrr.44. Dev Disabil Res Rev. 2009. PMID: 19213009 Review.

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