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Items: 1 to 50 of 93

1.

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

Boot E, Butcher NJ, Udow S, Marras C, Mok KY, Kaneko S, Barrett MJ, Prontera P, Berman BD, Masellis M, Dufournet B, Nguyen K, Charles P, Mutez E, Danaila T, Jacquette A, Colin O, Drapier S, Borg M, Fiksinski AM, Vergaelen E, Swillen A, Vogels A, Plate A, Perandones C, Gasser T, Clerinx K, Bourdain F, Mills K, Williams NM, Wood NW, Booij J, Lang AE, Bassett AS; International Research Group on 22q11.2DS-associated Parkinson's Disease.

Neurology. 2018 May 11. pii: 10.1212/WNL.0000000000005660. doi: 10.1212/WNL.0000000000005660. [Epub ahead of print]

PMID:
29752303
2.

Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.

Thygesen JH, Wolfe K, McQuillin A, Viñas-Jornet M, Baena N, Brison N, D'Haenens G, Esteba-Castillo S, Gabau E, Ribas-Vidal N, Ruiz A, Vermeesch J, Weyts E, Novell R, Buggenhout GV, Strydom A, Bass N, Guitart M, Vogels A.

Br J Psychiatry. 2018 May;212(5):287-294. doi: 10.1192/bjp.2017.65.

PMID:
29693535
3.

Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

Guissart C, Latypova X, Rollier P, Khan TN, Stamberger H, McWalter K, Cho MT, Kjaergaard S, Weckhuysen S, Lesca G, Besnard T, Õunap K, Schema L, Chiocchetti AG, McDonald M, de Bellescize J, Vincent M, Van Esch H, Sattler S, Forghani I, Thiffault I, Freitag CM, Barbouth DS, Cadieux-Dion M, Willaert R, Guillen Sacoto MJ, Safina NP, Dubourg C, Grote L, Carré W, Saunders C, Pajusalu S, Farrow E, Boland A, Karlowicz DH, Deleuze JF, Wojcik MH, Pressman R, Isidor B, Vogels A, Van Paesschen W, Al-Gazali L, Al Shamsi AM, Claustres M, Pujol A, Sanders SJ, Rivier F, Leboucq N, Cogné B, Sasorith S, Sanlaville D, Retterer K, Odent S, Katsanis N, Bézieau S, Koenig M, Davis EE, Pasquier L, Küry S.

Am J Hum Genet. 2018 May 3;102(5):744-759. doi: 10.1016/j.ajhg.2018.02.021. Epub 2018 Apr 12.

PMID:
29656859
4.

Low-Dose Aripiprazole and Risperidone for Treating Problem Behavior in Children With Pitt-Hopkins Syndrome.

Lambrechts S, Devriendt K, Vogels A.

J Clin Psychopharmacol. 2018 Jun;38(3):260-261. doi: 10.1097/JCP.0000000000000871. No abstract available.

PMID:
29596149
5.

Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.

Brison N, Neofytou M, Dehaspe L, Bayindir B, Van Den Bogaert K, Dardour L, Peeters H, Van Esch H, Van Buggenhout G, Vogels A, de Ravel T, Legius E, Devriendt K, Vermeesch JR.

Prenat Diagn. 2018 Mar;38(4):258-266. doi: 10.1002/pd.5223. Epub 2018 Feb 19.

PMID:
29388226
6.

Iodixanol versus Iopromide at Coronary CT Angiography: Lumen Opacification and Effect on Heart Rhythm-the Randomized IsoCOR Trial.

Lubbers MM, Kock M, Niezen A, Galema T, Kofflard M, Bruning T, Kooij HS, van Valen H, Dijkshoorn M, Booij R, Padmos A, Vogels A, Budde RPJ, Nieman K.

Radiology. 2018 Jan;286(1):71-80. doi: 10.1148/radiol.2017162779. Epub 2017 Aug 15.

PMID:
28809582
7.

Prevalence and comorbidities of autism among children referred to the outpatient clinics for neurodevelopmental disorders.

Mpaka DM, Okitundu DL, Ndjukendi AO, N'situ AM, Kinsala SY, Mukau JE, Ngoma VM, Kashala-Abotnes E, Ma-Miezi-Mampunza S, Vogels A, Steyaert J.

Pan Afr Med J. 2016 Oct 17;25:82. doi: 10.11604/pamj.2016.25.82.4151. eCollection 2016.

8.

Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies.

Brison N, Van Den Bogaert K, Dehaspe L, van den Oever JM, Janssens K, Blaumeiser B, Peeters H, Van Esch H, Van Buggenhout G, Vogels A, de Ravel T, Legius E, Devriendt K, Vermeesch JR.

Genet Med. 2017 Mar;19(3):306-313. doi: 10.1038/gim.2016.113. Epub 2016 Sep 1.

PMID:
27584908
9.

Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor.

Breckpot J, Vercruyssen M, Weyts E, Vandevoort S, D'Haenens G, Van Buggenhout G, Leempoels L, Brischoux-Boucher E, Van Maldergem L, Renieri A, Mencarelli MA, D'Angelo C, Mericq V, Hoffer MJ, Tauber M, Molinas C, Castiglioni C, Brison N, Vermeesch JR, Danckaerts M, Sienaert P, Devriendt K, Vogels A.

Eur J Med Genet. 2016 Sep;59(9):436-43. doi: 10.1016/j.ejmg.2016.08.003. Epub 2016 Aug 9.

PMID:
27519580
10.

[Intellectual developmental disorder and child psychiatry].

Vogels A.

Tijdschr Psychiatr. 2015;57(12):907-11. Review. Dutch.

11.

Comparing three short questionnaires to detect psychosocial problems among 3 to 4-year olds.

Theunissen MH, Vogels AG, de Wolff MS, Crone MR, Reijneveld SA.

BMC Pediatr. 2015 Jul 16;15:84. doi: 10.1186/s12887-015-0391-y.

12.

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.

Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, Vogels A, van Amelsvoort T, Gothelf D, Weinberger R, Weizman A, Klaassen PW, Koops S, Kates WR, Antshel KM, Simon TJ, Ousley OY, Swillen A, Gur RE, Bearden CE, Kahn RS, Bassett AS; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

JAMA Psychiatry. 2015 Apr;72(4):377-85. doi: 10.1001/jamapsychiatry.2014.2671.

13.

Punishment and reward in parental discipline for children aged 5 to 6 years: prevalence and groups at risk.

Theunissen MH, Vogels AG, Reijneveld SA.

Acad Pediatr. 2015 Jan-Feb;15(1):96-102. doi: 10.1016/j.acap.2014.06.024.

PMID:
25528127
14.

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.

J Autism Dev Disord. 2015 Jun;45(6):1649-57. doi: 10.1007/s10803-014-2321-5.

PMID:
25475362
15.

Presenting symptoms in adults with the 22q11 deletion syndrome.

Vogels A, Schevenels S, Cayenberghs R, Weyts E, Van Buggenhout G, Swillen A, Van Esch H, de Ravel T, Corveleyn P, Devriendt K.

Eur J Med Genet. 2014 Mar;57(4):157-62. doi: 10.1016/j.ejmg.2014.02.008. Epub 2014 Feb 24.

PMID:
24576609
16.

Increased dosage of RAB39B affects neuronal development and could explain the cognitive impairment in male patients with distal Xq28 copy number gains.

Vanmarsenille L, Giannandrea M, Fieremans N, Verbeeck J, Belet S, Raynaud M, Vogels A, Männik K, Õunap K, Jacqueline V, Briault S, Van Esch H, D'Adamo P, Froyen G.

Hum Mutat. 2014 Mar;35(3):377-83.

PMID:
24357492
17.

Three questionnaires to detect psychosocial problems in toddlers: a comparison of the BITSEA, ASQ:SE, and KIPPPI.

de Wolff MS, Theunissen MH, Vogels AG, Reijneveld SA.

Acad Pediatr. 2013 Nov-Dec;13(6):587-92. doi: 10.1016/j.acap.2013.07.007.

PMID:
24238686
18.

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.

Lancet Neurol. 2013 Nov;12(11):1076-83. doi: 10.1016/S1474-4422(13)70227-8. Epub 2013 Oct 1.

PMID:
24090588
19.

Reproductive value, sensitivity, and nonlinearity: population-management heuristics derived from classical demography.

Karsten R, Teismann H, Vogels A.

Theor Popul Biol. 2013 May;85:20-5. doi: 10.1016/j.tpb.2013.01.002. Epub 2013 Jan 18.

PMID:
23337316
20.

Characteristics of the strengths and difficulties questionnaire in preschool children.

Theunissen MH, Vogels AG, de Wolff MS, Reijneveld SA.

Pediatrics. 2013 Feb;131(2):e446-54. doi: 10.1542/peds.2012-0089. Epub 2013 Jan 6.

PMID:
23296429
21.

Work experience and style explain variation among pediatricians in the detection of children with psychosocial problems.

Theunissen MH, Vogels AG, Reijneveld SA.

Acad Pediatr. 2012 Nov-Dec;12(6):495-501. doi: 10.1016/j.acap.2012.07.004. Epub 2012 Sep 12.

PMID:
22980728
22.

Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills.

Denayer A, Van Esch H, de Ravel T, Frijns JP, Van Buggenhout G, Vogels A, Devriendt K, Geutjens J, Thiry P, Swillen A.

Mol Syndromol. 2012 Jun;3(1):14-20. Epub 2012 May 16.

23.

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.

Van Houdt JK, Nowakowska BA, Sousa SB, van Schaik BD, Seuntjens E, Avonce N, Sifrim A, Abdul-Rahman OA, van den Boogaard MJ, Bottani A, Castori M, Cormier-Daire V, Deardorff MA, Filges I, Fryer A, Fryns JP, Gana S, Garavelli L, Gillessen-Kaesbach G, Hall BD, Horn D, Huylebroeck D, Klapecki J, Krajewska-Walasek M, Kuechler A, Lines MA, Maas S, Macdermot KD, McKee S, Magee A, de Man SA, Moreau Y, Morice-Picard F, Obersztyn E, Pilch J, Rosser E, Shannon N, Stolte-Dijkstra I, Van Dijck P, Vilain C, Vogels A, Wakeling E, Wieczorek D, Wilson L, Zuffardi O, van Kampen AH, Devriendt K, Hennekam R, Vermeesch JR.

Nat Genet. 2012 Feb 26;44(4):445-9, S1. doi: 10.1038/ng.1105.

PMID:
22366787
24.

Early detection of psychosocial problems in children aged 5 to 6 years by preventive child healthcare: has it improved?

Theunissen MH, Vogels AG, Reijneveld SA.

J Pediatr. 2012 Mar;160(3):500-4. doi: 10.1016/j.jpeds.2011.08.038. Epub 2011 Oct 13.

PMID:
22000303
25.

Can fetal ultrasound result in prenatal diagnosis of Prader-Willi syndrome?

Geysenbergh B, De Catte L, Vogels A.

Genet Couns. 2011;22(2):207-16.

PMID:
21848014
26.

An accurate and efficient identification of children with psychosocial problems by means of computerized adaptive testing.

Vogels AG, Jacobusse GW, Reijneveld SA.

BMC Med Res Methodol. 2011 Aug 4;11:111. doi: 10.1186/1471-2288-11-111.

27.

Comparing three short questionnaires to detect psychosocial dysfunction among primary school children: a randomized method.

Vogels AG, Crone MR, Hoekstra F, Reijneveld SA.

BMC Public Health. 2009 Dec 28;9:489. doi: 10.1186/1471-2458-9-489.

28.

The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder.

Holland A, Whittington J, Cohen O, Curfs L, Delahaye F, Dudley O, Horsthemke B, Lindgren AC, Nourissier C, Sharma N, Vogels A.

J Intellect Disabil Res. 2009 Jun;53(6):538-47. doi: 10.1111/j.1365-2788.2009.01172.x. Epub 2009 Apr 23.

PMID:
19457156
29.

Testicular histology in boys with Prader-Willi syndrome: fertile or infertile?

Vogels A, Moerman P, Frijns JP, Bogaert GA.

J Urol. 2008 Oct;180(4 Suppl):1800-4. doi: 10.1016/j.juro.2008.03.113. Epub 2008 Aug 21.

PMID:
18721940
30.

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

Hannes FD, Sharp AJ, Mefford HC, de Ravel T, Ruivenkamp CA, Breuning MH, Fryns JP, Devriendt K, Van Buggenhout G, Vogels A, Stewart H, Hennekam RC, Cooper GM, Regan R, Knight SJ, Eichler EE, Vermeesch JR.

J Med Genet. 2009 Apr;46(4):223-32. doi: 10.1136/jmg.2007.055202. Epub 2008 Jun 11.

31.

Identification of children with psychosocial problems differed between preventive child health care professionals.

Vogels AG, Jacobusse GW, Hoekstra F, Brugman E, Crone M, Reijneveld SA.

J Clin Epidemiol. 2008 Nov;61(11):1144-51. doi: 10.1016/j.jclinepi.2007.12.005. Epub 2008 Jun 6.

PMID:
18538994
32.

A comparison of four scoring methods based on the parent-rated Strengths and Difficulties Questionnaire as used in the Dutch preventive child health care system.

Crone MR, Vogels AG, Hoekstra F, Treffers PD, Reijneveld SA.

BMC Public Health. 2008 Apr 4;8:106. doi: 10.1186/1471-2458-8-106.

33.

Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome.

Dudley O, McManus B, Vogels A, Whittington J, Muscatelli F.

J Intellect Disabil Res. 2008 May;52(Pt 5):426-36. doi: 10.1111/j.1365-2788.2008.01044.x. Epub 2008 Feb 20.

PMID:
18298478
34.

Mental health problems in children with intellectual disability: use of the Strengths and Difficulties Questionnaire.

Kaptein S, Jansen DE, Vogels AG, Reijneveld SA.

J Intellect Disabil Res. 2008 Feb;52(Pt 2):125-31. doi: 10.1111/j.1365-2788.2007.00978.x.

PMID:
18197951
35.

The oro-dental phenotype in Prader-Willi syndrome: a survey of 15 patients.

Bailleul-Forestier I, Verhaeghe V, Fryns JP, Vinckier F, Declerck D, Vogels A.

Int J Paediatr Dent. 2008 Jan;18(1):40-7.

PMID:
18086025
36.

Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation.

Denayer E, Parret A, Chmara M, Schubbert S, Vogels A, Devriendt K, Frijns JP, Rybin V, de Ravel TJ, Shannon K, Cools J, Scheffzek K, Legius E.

Hum Mutat. 2008 Feb;29(2):232-9.

PMID:
17979197
37.

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.

J Intellect Disabil Res. 2007 Sep;51(Pt 9):666-70.

PMID:
17845235
38.

ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.

Demily C, Legallic S, Bou J, Houy-Durand E, Van Amelsvoort T, Zinkstok J, Manouvrier-Hanue S, Vogels A, Drouin-Garraud V, Philip N, Philippe A, Héron D, Sarda P, Petit M, Thibaut F, Frébourg T, Campion D.

Psychiatr Genet. 2007 Oct;17(5):311-2. No abstract available.

PMID:
17728672
39.

Health-related quality of life problems of children aged 8-11 years with a chronic disease.

Grootenhuis MA, Koopman HM, Verrips EG, Vogels AG, Last BF.

Dev Neurorehabil. 2007 Jan-Mar;10(1):27-33.

PMID:
17608324
40.

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.

Hum Mol Genet. 2007 Jan 1;16(1):83-91. Epub 2006 Nov 29.

PMID:
17135275
41.

Use of the Pediatric Symptom Checklist for the detection of psychosocial problems in preventive child healthcare.

Reijneveld SA, Vogels AG, Hoekstra F, Crone MR.

BMC Public Health. 2006 Jul 27;6:197.

42.

Pfeiffer syndrome.

Vogels A, Fryns JP.

Orphanet J Rare Dis. 2006 Jun 1;1:19. Review.

43.

The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients.

Van Buggenhout G, Van Ravenswaaij-Arts C, Mc Maas N, Thoelen R, Vogels A, Smeets D, Salden I, Matthijs G, Fryns JP, Vermeesch JR.

Eur J Med Genet. 2005 Jul-Sep;48(3):276-89.

PMID:
16179223
44.

Is attrition bias a problem in neonatal follow-up?

Hille ET, den Ouden AL, Stuifbergen MC, Verrips GH, Vogels AG, Brand R, Gravenhorst JB, Verloove-Vanhorick SP.

Early Hum Dev. 2005 Nov;81(11):901-8. Epub 2005 Sep 16.

PMID:
16150560
45.

Terminal 2q37 deletion and autistic behaviour.

Lukusa T, Smeets E, Vogels A, Vermeesch JR, Fryns JP.

Genet Couns. 2005;16(2):179-80. No abstract available.

PMID:
16080299
46.
47.

Parenting, family contexts, and personality characteristics in youngsters with VCFS.

Prinzie P, Swillen A, Maes B, Onghena P, Vogels A, Van Hooste A, Devriendt K, Van Lieshout CF, Fryns JP.

Genet Couns. 2004;15(2):141-57.

PMID:
15287414
48.

Psychotic disorders in Prader-Willi syndrome.

Vogels A, De Hert M, Descheemaeker MJ, Govers V, Devriendt K, Legius E, Prinzie P, Fryns JP.

Am J Med Genet A. 2004 Jun 15;127A(3):238-43.

PMID:
15150773
49.

Second polar body inclusion results in diploid/triploid mixoploidy.

Brems H, Vogels A, Ribai P, De Raedt T, Fryns JP, Legius E.

Genet Couns. 2003;14(4):425-9.

PMID:
14738117
50.

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.

Eur J Hum Genet. 2004 Mar;12(3):238-40.

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