Swillen A - Search Results

1

Pre-academic and early academic achievement in children with velocardiofacial syndrome (del22q11.2) of borderline or normal intelligence.

De Smedt B, Swillen A, Ghesquière P, Devriendt K, Fryns JP. De Smedt B, et al. Among authors: swillen a. Genet Couns. 2003;14(1):15-29. Genet Couns. 2003. PMID: 12725586

2

An online survey to understand the needs of caregivers of family members with 22q11 deletion syndrome.

Cosman T, Finless A, Rideout AL, Lingley-Pottie P, Palmer LD, Shugar A, McDonald-McGinn DM, Swillen A, McGrath PJ, Bassett AS, Cytrynbaum C, Orr M, Meier S. Cosman T, et al. Among authors: swillen a. J Intellect Disabil Res. 2023 Sep;67(9):860-868. doi: 10.1111/jir.13061. Epub 2023 Jul 14. J Intellect Disabil Res. 2023. PMID: 37449408

3

The relationship between oxidative stress and psychotic disorders in 22q11.2 deletion syndrome.

Matalon N, Vergaelen E, Shani S, Dar S, Mekori-Domachevsky E, Segal-Gavish H, Hochberg Y, Gothelf D, Swillen A, Taler M. Matalon N, et al. Among authors: swillen a. Brain Behav Immun. 2023 Nov;114:16-21. doi: 10.1016/j.bbi.2023.07.028. Epub 2023 Aug 2. Brain Behav Immun. 2023. PMID: 37541396

4

Neurodevelopmental profile and stages of regression in Phelan-McDermid syndrome.

Dille Y, Lagae L, Swillen A, Buggenhout GV. Dille Y, et al. Among authors: swillen a. Dev Med Child Neurol. 2023 Jul;65(7):917-925. doi: 10.1111/dmcn.15482. Epub 2022 Dec 7. Dev Med Child Neurol. 2023. PMID: 36477723 Free article.

5

Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt.

Pelgrims E, Lynch SA, Hannes L, Hoffer MJV, Melotte C, Van Haeringen A, Swillen A, Breckpot J. Pelgrims E, et al. Among authors: swillen a. Am J Med Genet A. 2023 Jul;191(7):1889-1899. doi: 10.1002/ajmg.a.63222. Epub 2023 May 2. Am J Med Genet A. 2023. PMID: 37129290

6

Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys.

Borghgraef M, Swillen A, Van den Berghe H, Fryns JP. Borghgraef M, et al. Among authors: swillen a. Genet Couns. 1995;6(2):97-101. Genet Couns. 1995. PMID: 7546457

7

The Prader-Willi syndrome: a self supporting program for children, youngsters and adults.

Descheemaeker MJ, Swillen A, Plissart L, Borghgraef M, Rasenberg S, Curfs LM, Fryns JP. Descheemaeker MJ, et al. Among authors: swillen a. Genet Couns. 1994;5(2):199-205. Genet Couns. 1994. PMID: 7917134

8

Turner syndrome patients as adults: a study of their cognitive profile, psychosocial functioning and psychopathological findings.

Delooz J, Van den Berghe H, Swillen A, Kleczkowska A, Fryns JP. Delooz J, et al. Among authors: swillen a. Genet Couns. 1993;4(3):169-79. Genet Couns. 1993. PMID: 8267923

9

Intelligence, behaviour and psychosocial development in Turner syndrome. A cross-sectional study of 50 pre-adolescent and adolescent girls (4-20 years).

Swillen A, Fryns JP, Kleczkowska A, Massa G, Vanderschueren-Lodeweyckx M, Van den Berghe H. Swillen A, et al. Genet Couns. 1993;4(1):7-18. Genet Couns. 1993. PMID: 8471226

10

The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in 12 children.

Swillen A, Glorieux N, Peeters M, Fryns JP. Swillen A, et al. Clin Genet. 1995 Oct;48(4):177-82. doi: 10.1111/j.1399-0004.1995.tb04084.x. Clin Genet. 1995. PMID: 8591667

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