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Jesse, Christopher Marvin; Bushuven, E; Tripathi, P; Chandrasekar, A; Simon, C M; Drepper, C; Yamoah, A; Dreser, A; Katona, I; Johann, S; Beyer, C; Wagner, S; Grond, M; Nikolin, S; Anink, J; Troost, D; Sendtner, M; Goswami, A; Weis, J (2017). ALS-Associated Endoplasmic Reticulum Proteins in Denervated Skeletal Muscle: Implications for Motor Neuron Disease Pathology. Brain pathology, 27(6), pp. 781-794. Blackwell 10.1111/bpa.12453
Steinbach, Sarah; Weis, J; Schweighauser, Ariane; Francey, Thierry; Neiger, Reto (2014). Plasma and urine neutrophil gelatinase-associated lipocalin (NGAL) in dogs with acute kidney injury or chronic kidney disease. Journal of veterinary internal medicine, 28(2), pp. 264-269. Wiley-Blackwell 10.1111/jvim.12282
Andres, R H; Guzman, R; Weis, J; Brekenfeld, C; Fandino, J; Seiler, R W (2009). Lhermitte-Duclos disease with atypical vascularization--case report and review of the literature. Clinical neuropathology, 28(2), pp. 83-90. München-Deisenhofen: Dustri-Verlag
Guzman, R; Altrichter, S; El-Koussy, M; Gralla, J; Weis, J; Barth, A; Seiler, R W; Schroth, G; Lövblad, K O (2008). Contribution of the apparent diffusion coefficient in perilesional edema for the assessment of brain tumors. Journal of neuroradiology, 35(4), pp. 224-229. Issy-les-Moulineaux (F): Elsevier Masson 10.1016/j.neurad.2008.02.003
Andres, RH; Guzman, R; Weis, J; Schroth, G; Barth, A (2007). Granuloma formation and occlusion of an unruptured aneurysm after wrapping. Acta neurochirurgica, 9(149), 953-8.. Wien: Springer 10.1007/s00701-007-1260-8
Hergersberg, M; Mariani, L; Vassella, E; Murtin, C; Weis, J; Moschopulos, M; Laeng, H; Landolt, H; Huber, A; Roelcke, U (2006). Age at diagnosis and loss of heterozygosity on chromosome 1p and 19q in oligodendroglial tumors. Journal of neuro-oncology, 80(2), pp. 215-7. Boston, Mass.: Springer 10.1007/s11060-006-9177-2
Landolt, H-P; Glatzel, M; Blättler, T; Achermann, P; Roth, C; Mathis, J; Weis, J; Tobler, I; Aguzzi, A; Bassetti, C L (2006). Sleep-wake disturbances in sporadic Creutzfeldt-Jakob disease. Neurology, 66(9), pp. 1418-24. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1212/01.wnl.0000210445.16135.56
Yen, K; Weis, J; Kreis, R; Aghayev, E; Jackowski, C; Thali, M; Boesch, C; Maier, S E; Dirnhofer, R; Lövblad, K O (2006). Line-scan diffusion tensor imaging of the posttraumatic brain stem: changes with neuropathologic correlation. American journal of neuroradiology AJNR, 27(1), pp. 70-3. Oak Brook, Ill.: American Society of Neuroradiology
Ramelli, G P; Joncourt, F; Luetschg, J; Weis, J; Tolnay, M; Burgunder, J M (2006). Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series. Swiss medical weekly, 136(11-12), pp. 189-93. Muttenz: EMH Schweizerischer Ärzteverlag
Brun, C; Suter, D; Pauli, C; Dunant, P; Lochmüller, H; Burgunder, J M; Schümperli, Daniel; Weis, J (2003). U7 snRNAs induce correction of mutated dystrophin pre-mRNA by exon skipping. Cellular and molecular life sciences, 60(3), pp. 557-566. Springer
