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Mancuso, M; Houlden, H; Molnar, M J; Filla, A; Breza, M; Graessner, H; Bassetti, CLA; Boesch, S (2022). How to approach a neurogenetics diagnosis in different European countries - The EAN Neurogenetics Panel survey. European journal of neurology, 29(7), pp. 1885-1891. Wiley 10.1111/ene.15320
Bersano, A; Kraemer, M; Burlina, A; Mancuso, M; Finsterer, J; Sacco, S; Salvarani, C; Caputi, L; Chabriat, H; Oberstein, S Lesnik; Federico, A; Lasserve, E Tournier; Hunt, D; Dichgans, M; Arnold, M; Debette, S; Markus, H S (2021). Heritable and non-heritable uncommon causes of stroke. Journal of neurology, 268(8), pp. 2780-2807. Springer-Medizin-Verlag 10.1007/s00415-020-09836-x
Mancuso, M; Arnold, M.; Bersano, A; Burlina, A; Chabriat, H; Debette, S; Enzinger, C; Federico, A; Filla, A; Finsterer, J; Hunt, D; Lesnik Oberstein, S; Tournier-Lasserve, E; Markus, H S (2020). Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology. European journal of neurology, 27(6), pp. 909-927. Wiley 10.1111/ene.14183
