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

di Schaafsma, Dilana, Stoffelen, Joke M T, Kok, Gerjo, Curfs, Leopold M G
Pubblicazione 2013

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

di Schaafsma, Dilana, Kok, Gerjo, Stoffelen, Joke M. T., Curfs, Leopold M. G.
Pubblicato in J Sex Res (2015)

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

di Otter, Maarten, Schrander-Stumpel, Constance T. R. M., Didden, Robert, Curfs, Leopold M. G.
Pubblicazione 2012

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

di Schaafsma, Dilana, Kok, Gerjo, Stoffelen, Joke M. T., Van Doorn, Paulien, Curfs, Leopold M. G.
Pubblicazione 2014

Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes

di Ehrhart, Friederike, Coort, Susan L. M., Cirillo, Elisa, Smeets, Eric, Evelo, Chris T., Curfs, Leopold M. G.
Pubblicato in Orphanet J Rare Dis (2016)

A resource to explore the discovery of rare diseases and their causative genes

di Ehrhart, Friederike, Willighagen, Egon L., Kutmon, Martina, van Hoften, Max, Curfs, Leopold M. G., Evelo, Chris T.
Pubblicato in Sci Data (2021)

Communication in Individuals with Rett Syndrome: an Assessment of Forms and Functions

di Didden, Robert, Korzilius, Hubert, Smeets, Eric, Green, Vanessa A., Lang, Russell, Lancioni, Giulio E., Curfs, Leopold M.
Pubblicazione 2009

Body composition, adipokines, bone mineral density and bone remodeling markers in relation to IGF-1 levels in adults with Prader-Willi syndrome

di van Nieuwpoort, I. Caroline, Twisk, Jos W. R., Curfs, Leopold M. G., Lips, Paul, Drent, Madeleine L.
Pubblicato in Int J Pediatr Endocrinol (2018)

Incontinence in Individuals with Rett Syndrome: A Comparative Study

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

Review and gap analysis: molecular pathways leading to fetal alcohol spectrum disorders

di Ehrhart, Friederike, Roozen, Sylvia, Verbeek, Jef, Koek, Ger, Kok, Gerjo, van Kranen, Henk, Evelo, Chris T., Curfs, Leopold M. G.
Pubblicato in Mol Psychiatry (2018)

Extracellular Vesicles in CNS Developmental Disorders

di Gomes, Ana Rita, Sangani, Nasim Bahram, Fernandes, Tiago G., Diogo, M. Margarida, Curfs, Leopold M. G., Reutelingsperger, Chris P.
Pubblicato in Int J Mol Sci (2020)

Abnormal Foot Position and Standing and Walking Ability in Rett Syndrome: an Exploratory Study

di Borst, Hanneke E., Townend, Gillian S., van Eck, Mirjam, Smeets, Eric, van den Berg, Mariëlle, Laan, Aleid, Curfs, Leopold M. G.
Pubblicato in J Dev Phys Disabil (2018)

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

di Townend, Gillian S., Marschik, Peter B., Smeets, Eric, van de Berg, Raymond, van den Berg, Mariёlle, Curfs, Leopold M.G.
Pubblicato in J Dev Phys Disabil (2015)

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

di Evers, Laurens J. M., van Amelsvoort, Therese A. M. J., Bakker, Jaap A., de Koning, Mariken, Drukker, Marjan, Curfs, Leopold M. G.
Pubblicato in Psychopharmacology (Berl) (2015)

Beyond Pathway Analysis: Identification of Active Subnetworks in Rett Syndrome

di Miller, Ryan A., Ehrhart, Friederike, Eijssen, Lars M. T., Slenter, Denise N., Curfs, Leopold M. G., Evelo, Chris T., Willighagen, Egon L., Kutmon, Martina
Pubblicato in Front Genet (2019)

MECP2 variation in Rett syndrome—An overview of current coverage of genetic and phenotype data within existing databases

di Townend, Gillian S., Ehrhart, Friederike, van Kranen, Henk J., Wilkinson, Mark, Jacobsen, Annika, Roos, Marco, Willighagen, Egon L., van Enckevort, David, Evelo, Chris T., Curfs, Leopold M. G.
Pubblicato in Hum Mutat (2018)

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

di 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
Pubblicazione 2010

Altered Carbon Dioxide Metabolism and Creatine Abnormalities in Rett Syndrome

di 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.
Pubblicazione 2011

A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration

di Ehrhart, Friederike, Jacobsen, Annika, Rigau, Maria, Bosio, Mattia, Kaliyaperumal, Rajaram, Laros, Jeroen F. J., Willighagen, Egon L., Valencia, Alfonso, Roos, Marco, Capella-Gutierrez, Salvador, Curfs, Leopold M. G., Evelo, Chris T.
Pubblicato in Sci Data (2021)