Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes von Ehrhart, Friederike, Coort, Susan L M, Cirillo, Elisa, Smeets, Eric, Evelo, Chris T, Curfs, Leopold M G

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Understanding the Social Stigma of Fetal Alcohol Spectrum Disorders: From Theory to Interventions von Roozen, Sylvia, Stutterheim, Sarah E., Bos, Arjan E. R., Kok, Gerjo, Curfs, Leopold M. G.

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A novel insight into neurological disorders through HDAC6 protein–protein interactions von Bahram Sangani, Nasim, Koetsier, Jarno, Mélius, Jonathan, Kutmon, Martina, Ehrhart, Friederike, Evelo, Chris T., Curfs, Leopold M. G., Reutelingsperger, Chris P., Eijssen, Lars M. T.

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Triple X syndrome: a review of the literature von Otter, Maarten, Schrander-Stumpel, Constance TRM, Curfs, Leopold MG

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Involvement of extracellular vesicle microRNA clusters in developing healthy and Rett syndrome brain organoids von Bahram Sangani, Nasim, Koetsier, Jarno, Gomes, Ana Rita, Diogo, Maria Margarida, Fernandes, Tiago G., Bouwman, Freek G., Mariman, Edwin C. M., Ghazvini, Mehrnaz, Gribnau, Joost, Curfs, Leopold M. G., Reutelingsperger, Chris P., Eijssen, Lars M. T.

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Current developments in the genetics of Rett and Rett-like syndrome von Ehrhart, Friederike, Sangani, Nasim B, Curfs, Leopold M.G

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Identifying Effective Methods for Teaching Sex Education to Individuals With Intellectual Disabilities: A Systematic Review von Schaafsma, Dilana, Kok, Gerjo, Stoffelen, Joke M. T., Curfs, Leopold M. G.

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Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey von Kaufmann, Walter E, Percy, Alan K, Neul, Jeffrey L, Downs, Jenny, Leonard, Helen, Nues, Paige, Sharma, Girish D, Bartolotta, Theresa E, Townend, Gillian S, Curfs, Leopold M G, Mariotti, Orietta, Buda, Claude, O'Leary, Heather M, Oberman, Lindsay M, Vogel-Farley, Vanessa, Barnes, Katherine V, Missling, Christopher U

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Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion von Correa-da-Silva, Felipe, Carter, Jenny, Wang, Xin-Yuan, Sun, Rui, Pathak, Ekta, Kuhn, José Manuel Monroy, Schriever, Sonja C., Maya-Monteiro, Clarissa M., Jiao, Han, Kalsbeek, Martin J., Moraes-Vieira, Pedro M. M., Gille, Johan J. P., Sinnema, Margje, Stumpel, Constance T. R. M., Curfs, Leopold M. G., Stenvers, Dirk Jan, Pfluger, Paul T., Lutter, Dominik, Pereira, Alberto M., Kalsbeek, Andries, Fliers, Eric, Swaab, Dick F., Wilkinson, Lawrence, Gao, Yuanqing, Yi, Chun-Xia

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Extracellular Vesicles in CNS Developmental Disorders von Gomes, Ana Rita, Sangani, Nasim Bahram, Fernandes, Tiago G, Diogo, M Margarida, Curfs, Leopold M G, Reutelingsperger, Chris P

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Exogenous melatonin for sleep problems in individuals with intellectual disability: a meta‐analysis von BRAAM, WIEBE, SMITS, MARCEL G, DIDDEN, ROBERT, KORZILIUS, HUBERT, GEIJLSWIJK, INGEBORG M VAN, CURFS, LEOPOLD M G

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A resource to explore the discovery of rare diseases and their causative genes von Ehrhart, Friederike, Willighagen, Egon L., Kutmon, Martina, van Hoften, Max, Curfs, Leopold M. G., Evelo, Chris T.

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Development of consensus-based guidelines for managing communication of individuals with Rett syndrome von Townend, Gillian S, Bartolotta, Theresa E, Urbanowicz, Anna, Wandin, Helena, Curfs, Leopold MG

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

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Glutamatergic markers, age, intellectual functioning and psychosis in 22q11 deletion syndrome von Evers, Laurens J. M., van Amelsvoort, Therese A. M. J., Bakker, Jaap A., de Koning, Mariken, Drukker, Marjan, Curfs, Leopold M. G.

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Exploring the Development of Existing Sex Education Programmes for People with Intellectual Disabilities: An Intervention Mapping Approach von Schaafsma, Dilana, Stoffelen, Joke M. T., Kok, Gerjo, Curfs, Leopold M. G.

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Loss of response to melatonin treatment is associated with slow melatonin metabolism von Braam, W., Van Geijlswijk, I., Keijzer, Henry, Smits, Marcel G., Didden, Robert, Curfs, Leopold M. G.

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Physical health problems in adults with Prader-Willi syndrome von Sinnema, Margje, Maaskant, Marian A., van Schrojenstein Lantman-de Valk, Henny M.J., Caroline van Nieuwpoort, I., Drent, Madeleine L., Curfs, Leopold M.G., Schrander-Stumpel, Constance T.R.M.

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The role of Extracellular Vesicles during CNS development von Bahram Sangani, Nasim, Gomes, Ana Rita, Curfs, Leopold M.G., Reutelingsperger, Chris P.

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Psychiatric illness in a cohort of adults with Prader-Willi syndrome von Sinnema, Margje, Boer, Harm, Collin, Philippe, Maaskant, Marian A., van Roozendaal, Kees E.P., Schrander-Stumpel, Constance T.R.M., Curfs, Leopold M.G.

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