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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 AC, Nourissier C, Sharma N, Vogels A. Holland A, et al. Among authors: curfs l. J Intellect Disabil Res. 2009 Jun;53(6):538-47. doi: 10.1111/j.1365-2788.2009.01172.x. Epub 2009 Apr 23. J Intellect Disabil Res. 2009. PMID: 19457156
Attentional set-shifting in fragile X syndrome.
Van der Molen MJ, Van der Molen MW, Ridderinkhof KR, Hamel BC, Curfs LM, Ramakers GJ. Van der Molen MJ, et al. Among authors: curfs lm. Brain Cogn. 2012 Apr;78(3):206-17. doi: 10.1016/j.bandc.2011.12.008. Epub 2012 Jan 18. Brain Cogn. 2012. PMID: 22261226
Burden of illness in Rett syndrome: initial evaluation of a disorder-specific caregiver survey.
Kaufmann WE, Percy AK, Neul JL, Downs J, Leonard H, Nues P, Sharma GD, Bartolotta TE, Townend GS, Curfs LMG, Mariotti O, Buda C, O'Leary HM, Oberman LM, Vogel-Farley V, Barnes KV, Missling CU. Kaufmann WE, et al. Among authors: curfs lmg. Orphanet J Rare Dis. 2024 Aug 13;19(1):296. doi: 10.1186/s13023-024-03313-8. Orphanet J Rare Dis. 2024. PMID: 39138481 Free PMC article.
205 results