Exploring the Development of Existing Sex Education Programmes for People with Intellectual Disabilities: An Intervention Mapping Approach

Por Schaafsma, Dilana, Stoffelen, Joke M T, Kok, Gerjo, Curfs, Leopold M G
Publicado em 2013

Identifying Effective Methods for Teaching Sex Education to Individuals With Intellectual Disabilities: A Systematic Review

Por Schaafsma, Dilana, Kok, Gerjo, Stoffelen, Joke M. T., Curfs, Leopold M. G.
Publicado no J Sex Res (2015)

The psychiatric phenotype in triple X syndrome: New hypotheses illustrated in two cases

Por Otter, Maarten, Schrander-Stumpel, Constance T. R. M., Didden, Robert, Curfs, Leopold M. G.
Publicado em 2012

Identifying the important factors associated with teaching sex education to people with intellectual disability: A cross-sectional survey among paid care staff(†)

Por Schaafsma, Dilana, Kok, Gerjo, Stoffelen, Joke M. T., Van Doorn, Paulien, Curfs, Leopold M. G.
Publicado em 2014

Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes

Por Ehrhart, Friederike, Coort, Susan L. M., Cirillo, Elisa, Smeets, Eric, Evelo, Chris T., Curfs, Leopold M. G.
Publicado no Orphanet J Rare Dis (2016)

Incontinence in Individuals with Rett Syndrome: A Comparative Study

Por Giesbers, Sanne, Didden, Robert, Radstaake, Maartje, Korzilius, Hubert, von Gontard, Alexander, Lang, Russell, Smeets, Eric, Curfs, Leopold M. G.
Publicado em 2012

Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands

Por Townend, Gillian S., Marschik, Peter B., Smeets, Eric, van de Berg, Raymond, van den Berg, Mariёlle, Curfs, Leopold M.G.
Publicado no J Dev Phys Disabil (2015)

Glutamatergic markers, age, intellectual functioning and psychosis in 22q11 deletion syndrome

Por Evers, Laurens J. M., van Amelsvoort, Therese A. M. J., Bakker, Jaap A., de Koning, Mariken, Drukker, Marjan, Curfs, Leopold M. G.
Publicado no Psychopharmacology (Berl) (2015)

Different distribution of the genetic subtypes of the Prader–Willi syndrome in the elderly

Por Sinnema, Margje, van Roozendaal, Kees E P, Maaskant, Marian A, Smeets, Hubert J M, Engelen, John J M, Jonker-Houben, Nieke, Schrander-Stumpel, Constance T R M, Curfs, Leopold M G
Publicado em 2010

Altered Carbon Dioxide Metabolism and Creatine Abnormalities in Rett Syndrome

Por Halbach, Nicky S. J., Smeets, Eric E. J., Bierau, Jörgen, Keularts, Irene M. L. W., Plasqui, Guy, Julu, Peter O. O., Engerström, Ingegerd Witt, Bakker, Jaap A., Curfs, Leopold M. G.
Publicado em 2011