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Cachemaille, M; Laedermann, C J; Pertin, M; Abriel, H; Gosselin, R-D; Decosterd, I (2012). Neuronal expression of the ubiquitin ligase Nedd4-2 in rat dorsal root ganglia: modulation in the spared nerve injury model of neuropathic pain. Neuroscience, 227, pp. 370-380. Oxford: Elsevier 10.1016/j.neuroscience.2012.09.044
Pignier, C; Rougier, JS; Vié, B; Culié, C; Verscheure, Y; Vacher, B; Abriel, H; Le Grand, B (2010). Selective inhibition of persistent sodium current by F 15845 prevents ischaemia-induced arrhythmias. British journal of pharmacology, 161(1), pp. 79-91. Oxford: Wiley-Blackwell 10.1111/j.1476-5381.2010.00884.x
Tfelt-Hansen, J; Jespersen, T; Hofman-Bang, J; Rasmussen, H Borger; Cedergreen, P; Skovby, F; Abriel, H; Svendsen, J Hastrup; Olesen, Soren-Peter; Christiansen, M; Haunso, S (2009). Ventricular tachycardia in a Brugada syndrome patient caused by a novel deletion in SCN5A. Canadian journal of cardiology, 25(3), pp. 156-60. Oakville (Canada): Canadian Cardiology Publications 10.1016/S0828-282X(09)70043-1
Michaud, K; Fellmann, F; Abriel, H; Beckmann, JS; Mangin, P; Elger, BS (2009). Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration. Swiss medical weekly, 2009(139 (49-50)), pp. 712-8. Muttenz: EMH Schweizerischer Ärzteverlag
Petitprez, S; Jespersen, T; Pruvot, E; Keller, D I; Corbaz, C; Schläpfer, J; Abriel, H; Kucera, J P (2008). Analysis of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome. Cardiovascular research, 78(3), pp. 494-504. Oxford: Oxford University Press 10.1093/cvr/cvn023
Keller, D; Rougier, J; Kucera, J; Benammar, N; Fressart, V; Guicheney, P; Madle, A; Fromer, M; Schläpfer, J; Abriel, H (2005). Brugada syndrome and fever: Genetic and molecular characterization of patients carrying mutations. Cardiovascular research, 67(3), pp. 510-519. Oxford University Press 10.1016/j.cardiores.2005.03.024
