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Kuijf, Hugo J; Biesbroek, J Matthijs; de Bresser, Jeroen; Heinen, Rutger; Andermatt, Simon; Bento, Mariana; Berseth, Matt; Belyaev, Mikhail; Cardoso, M Jorge; Casamitjana, Adria; Collins, D Louis; Dadar, Mahsa; Georgiou, Achilleas; Ghafoorian, Mohsen; Jin, Dakai; Khademi, April; Knight, Jesse; Li, Hongwei; Llado, Xavier; Luna, Miguel; ... (2019). Standardized Assessment of Automatic Segmentation of White Matter Hyperintensities; Results of the WMH Segmentation Challenge. IEEE transactions on medical imaging, 38(11), pp. 2556-2568. Institute of Electrical and Electronics Engineers IEEE 10.1109/TMI.2019.2905770
Bigoni, Stefania; Neri, Marcella; Scotton, Chiara; Farina, Roberto; Sabatelli, Patrizia; Jiang, Chongyi; Zhang, Jianguo; Falzarano, Maria Sofia; Rossi, Rachele; Ognibene, Davide; Selvatici, Rita; Gualandi, Francesca; Bosshardt, Dieter; Perri, Paolo; Campa, Claudio; Brancati, Francesco; Salvatore, Marco; De Stefano, Maria Chiara; Taruscio, Domenica; Trombelli, Leonardo; ... (2019). Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family. Frontiers in genetics, 9, p. 723. Frontiers Media SA 10.3389/fgene.2018.00723
Cassatella, Daniele; Howard, Sasha R; Acierno, James S; Xu, Cheng; Papadakis, Georgios E; Santoni, Federico A; Dwyer, Andrew A; Santini, Sara; Sykiotis, Gerasimos P; Chambion, Caroline; Meylan, Jenny; Marino, Laura; Favre, Lucie; Li, Jiankang; Liu, Xuanzhu; Zhang, Jianguo; Bouloux, Pierre-Marc; Geyter, Christian De; Paepe, Anne De; Dhillo, Waljit S; ... (2018). Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures. European journal of endocrinology, 178(4), pp. 377-388. BioScientifica Ltd. 10.1530/EJE-17-0568
