Vogels A - Search Results

1

Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial.

van der Vaart T, Plasschaert E, Rietman AB, Renard M, Oostenbrink R, Vogels A, de Wit MC, Descheemaeker MJ, Vergouwe Y, Catsman-Berrevoets CE, Legius E, Elgersma Y, Moll HA. van der Vaart T, et al. Among authors: vogels a. Lancet Neurol. 2013 Nov;12(11):1076-83. doi: 10.1016/S1474-4422(13)70227-8. Epub 2013 Oct 1. Lancet Neurol. 2013. PMID: 24090588 Clinical Trial.

2

Behavioral Changes in Patients With Prader-Willi Syndrome Can Mask Severe Physical Illness.

Van Loo L, Vogels A, Rochtus A. Van Loo L, et al. Among authors: vogels a. JCEM Case Rep. 2023 Feb 3;1(1):luac034. doi: 10.1210/jcemcr/luac034. eCollection 2023 Jan. JCEM Case Rep. 2023. PMID: 37908247 Free PMC article.

3

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: vogels 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

4

Atypical presentation of the Prader-Willi syndrome. Mosaic trisomy 15?

Vogels A, Holvoet M, Descheemaeker MJ, Fryns JP, Devriendt K. Vogels A, et al. Ann Genet. 2002 Jan-Mar;45(1):1-3. doi: 10.1016/s0003-3995(02)01107-3. Ann Genet. 2002. PMID: 11934381

5

Personality profiles of children and adolescents with neurofibromatosis type 1.

Prinzie P, Descheemaeker MJ, Vogels A, Cleymans T, Haselager GJ, Curfs LM, Hellinckx W, Onghena P, Legius E, van Lieshout CF, Fryns JP. Prinzie P, et al. Among authors: vogels a. Am J Med Genet A. 2003 Apr 1;118A(1):1-7. doi: 10.1002/ajmg.a.10003. Am J Med Genet A. 2003. PMID: 12605433

6

Psychotic disorders in Prader-Willi syndrome.

Vogels A, De Hert M, Descheemaeker MJ, Govers V, Devriendt K, Legius E, Prinzie P, Fryns JP. Vogels A, et al. Am J Med Genet A. 2004 Jun 15;127A(3):238-43. doi: 10.1002/ajmg.a.30004. Am J Med Genet A. 2004. PMID: 15150773

7

Autism spectrum disorder profile in neurofibromatosis type I.

Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, Evans DG, Legius E, Green J. Garg S, et al. Among authors: vogels a. J Autism Dev Disord. 2015 Jun;45(6):1649-57. doi: 10.1007/s10803-014-2321-5. J Autism Dev Disord. 2015. PMID: 25475362

8

Behavioral and cognitive outcomes for clinical trials in children with neurofibromatosis type 1.

van der Vaart T, Rietman AB, Plasschaert E, Legius E, Elgersma Y, Moll HA; NF1-SIMCODA Study Group. van der Vaart T, et al. Neurology. 2016 Jan 12;86(2):154-60. doi: 10.1212/WNL.0000000000002118. Epub 2015 Oct 30. Neurology. 2016. PMID: 26519538 Free PMC article. Clinical Trial.

9

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. Among authors: vogels a. Genet Couns. 1999;10(1):79-88. Genet Couns. 1999. PMID: 10191433 Review.

10

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

Vogels A, Van Den Ende J, Keymolen K, Mortier G, Devriendt K, Legius E, Fryns JP. Vogels A, et al. Eur J Hum Genet. 2004 Mar;12(3):238-40. doi: 10.1038/sj.ejhg.5201135. Eur J Hum Genet. 2004. PMID: 14679397

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