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1.

[Behavioral phenotypes and recent developments in genetic technologies]. / Gedragsfenotypes en recente ontwikkelingen in het genetisch onderzoek.

Vermeulen, K; Vogels, A.

Tijdschr Psychiatr ; 61(11): 779-785, 2019.

Artículo en Holandés | MEDLINE | ID: mdl-31907888

2.

[Patients with ARHGEF9-mutation: a case report and implications of genetic disorders in child psychiatry]. / Patiënten met ARHGEF9-mutatie: rol van genetica in de psychiatrische praktijk.

van Roey, W; Vogels, A; Emmery, P.

Tijdschr Psychiatr ; 61(12): 891-896, 2019.

Artículo en Holandés | MEDLINE | ID: mdl-31907904

3.

[Intellectual developmental disorder and child psychiatry]. / Verstandelijke beperking en kinder- en jeugdpsychiatrie.

Vogels, A.

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

Artículo en Holandés | MEDLINE | ID: mdl-26727568

4.

[Psychiatry and low intelligence]. / Psychiatrie en lage intelligentie.

van Amelsvoort, T A M J; Zinkstok, J R; Vogels, A; Wieland, J.

Tijdschr Psychiatr ; 61(11): 746-747, 2019.

Artículo en Holandés | MEDLINE | ID: mdl-31907882

5.

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

Geysenbergh, B; De Catte, L; Vogels, A.

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

Artículo en Inglés | MEDLINE | ID: mdl-21848014

6.

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, F D; Sharp, A J; Mefford, H C; de Ravel, T; Ruivenkamp, C A; Breuning, M H; Fryns, J-P; Devriendt, K; Van Buggenhout, G; Vogels, A; Stewart, H; Hennekam, R C; Cooper, G M; Regan, R; Knight, S J L; Eichler, E E; Vermeesch, J R.

J Med Genet ; 46(4): 223-32, 2009 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-18550696

7.

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, A-C; Nourissier, C; Sharma, N; Vogels, A.

J Intellect Disabil Res ; 53(6): 538-47, 2009 Jun.

Artículo en Inglés | MEDLINE | ID: mdl-19457156

8.

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 ; 52(Pt 5): 426-36, 2008 May.

Artículo en Inglés | MEDLINE | ID: mdl-18298478

9.

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, Dominique; Salden, I; Matthijs, G; Fryns, J-P; Vermeesch, J R.

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

Artículo en Inglés | MEDLINE | ID: mdl-16179223

10.

Is attrition bias a problem in neonatal follow-up?

Hille, E T M; den Ouden, A L; Stuifbergen, M C; Verrips, G H W; Vogels, A G C; Brand, R; Gravenhorst, J Bennebroek; Verloove-Vanhorick, S P.

Early Hum Dev ; 81(11): 901-8, 2005 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-16150560

11.

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

Swillen, A; Vogels, A; Devriendt, K; Fryns, J P.

Am J Med Genet ; 97(2): 128-35, 2000.

Artículo en Inglés | MEDLINE | ID: mdl-11180220

12.

Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).

Claes, S; Vogels, A; Holvoet, M; Devriendt, K; Raeymaekers, P; Cassiman, J J; Fryns, J P.

Am J Med Genet ; 73(4): 474-9, 1997 Dec 31.

Artículo en Inglés | MEDLINE | ID: mdl-9415477

13.

Clinical cariostatic effectiveness of a NaF rinse in a low prevalence child population.

Ruiken, R; Truin, G J; König, K; Vogels, A; van 't Hof, M.

Community Dent Oral Epidemiol ; 15(2): 57-9, 1987 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-3471376

14.

Dental caries in 5-, 7-, 9- and 11-year-old schoolchildren during a 9-year dental health campaign in The Hague.

Truin, G J; Plasschaert, A J; König, K G; Vogels, A L.

Community Dent Oral Epidemiol ; 9(2): 55-60, 1981 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-6946882

15.

Dental caries and gingivitis in second grade schoolchildren in The Hague over the period 1969-1981.

Truin, G J; König, K G; Ruiken, R M; Plasschaert, F J; Vogels, A L.

Community Dent Oral Epidemiol ; 13(6): 319-22, 1985 Dec.

Artículo en Inglés | MEDLINE | ID: mdl-3866651

16.

Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndrome.

Vogels, A; Fryns, J P.

Genet Couns ; 15(4): 397-404, 2004.

Artículo en Inglés | MEDLINE | ID: mdl-15658614

17.

The velocardiofacial syndrome: a review.

Vogels, A; Fryns, J P.

Genet Couns ; 13(2): 105-13, 2002.

Artículo en Inglés | MEDLINE | ID: mdl-12150209

18.

The Prader-Willi syndrome and the Angelman syndrome.

Vogels, A; Fryns, J P.

Genet Couns ; 13(4): 385-96, 2002.

Artículo en Inglés | MEDLINE | ID: mdl-12558108

19.

Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)).

Vogels, A; Haegeman, J; Fryns, J P.

Genet Couns ; 8(3): 249-52, 1997.

Artículo en Inglés | MEDLINE | ID: mdl-9327270

20.

Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?

Fryns, J P; Vogels, A; van den Berghe, H.

Genet Couns ; 1(1): 63-6, 1990.

Artículo en Inglés | MEDLINE | ID: mdl-2222924

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[Behavioral phenotypes and recent developments in genetic technologies]. / Gedragsfenotypes en recente ontwikkelingen in het genetisch onderzoek.

[Patients with ARHGEF9-mutation: a case report and implications of genetic disorders in child psychiatry]. / Patiënten met ARHGEF9-mutatie: rol van genetica in de psychiatrische praktijk.

[Intellectual developmental disorder and child psychiatry]. / Verstandelijke beperking en kinder- en jeugdpsychiatrie.

[Psychiatry and low intelligence]. / Psychiatrie en lage intelligentie.

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

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.

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

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

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

Is attrition bias a problem in neonatal follow-up?

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

Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).

Clinical cariostatic effectiveness of a NaF rinse in a low prevalence child population.

Dental caries in 5-, 7-, 9- and 11-year-old schoolchildren during a 9-year dental health campaign in The Hague.

Dental caries and gingivitis in second grade schoolchildren in The Hague over the period 1969-1981.

Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndrome.

The velocardiofacial syndrome: a review.

The Prader-Willi syndrome and the Angelman syndrome.

Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)).

Craniosynostosis and low middle frequency perceptive deafness in mother and son. A distinct entity?