Why the dim light melatonin onset (DLMO) should be measured before treatment of patients with circadian rhythm sleep disorders von Keijzer, Henry, Smits, Marcel G, Duffy, Jeanne F, Curfs, Leopold M.G

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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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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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Non‐pharmacological management of problematic sleeping in children with developmental disabilities von Spruyt, Karen, Curfs, Leopold M G

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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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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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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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Review and gap analysis: molecular pathways leading to fetal alcohol spectrum disorders von Ehrhart, Friederike, Roozen, Sylvia, Verbeek, Jef, Koek, Ger, Kok, Gerjo, van Kranen, Henk, Evelo, Chris T., Curfs, Leopold M. G.

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Triple X syndrome: a review of the literature von OTTER, Maarten, SCHRANDER-STUMPEL, Constance T. R. M, CURFS, Leopold M. G

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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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Extracellular vesicles in CNS developmental disorders von Gomes, Ana Rita, Sangani, Nasim Bahram, Fernandes, Tiago, Diogo, Maria Margarida, Curfs, Leopold M. G., Reutelingsperger, Chris P.

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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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Sleep in Angelman syndrome: a review of evidence von Spruyt, Karen, PhD, Braam, Wiebe, Curfs, Leopold MG

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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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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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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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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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Rett syndrome and developmental regression von Smeets, Eric E., Townend, Gillian S., 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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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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