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Number of items: 5.

Hasselmann, O; Blau, N; Ramaekers, V T; Quadros, E V; Sequeira, J M; Weissert, M (2010). Cerebral folate deficiency and CNS inflammatory markers in Alpers disease. Molecular Genetics and Metabolism, 99(1):58-61.

Grunt, S; Wingeier, K; Wehrli, E; Boltshauser, E; Capone, A; Fluss, J; Gubser-Mercati, D; Jeannet, P Y; Keller, E; Marcoz, J P; Schmitt-Mechelke, T; Weber, P; Weissert, M; Steinlin, M (2010). Cerebral sinus venous thrombosis in Swiss children. Developmental Medicine and Child Neurology, 52(12):1145-1150.

Buerki, S; Roellin, K; Remonda, L; Mercati, D G; Jeannet, P Y; Keller, E; Luetschg, J; Menache, C; Ramelli, G P; Schmitt-Mechelke, T; Weissert, M; Boltshauser, E; Steinlin, M (2010). Neuroimaging in childhood arterial ischaemic stroke: evaluation of imaging modalities and aetiologies. Developmental Medicine and Child Neurology, 52(11):1033-1037.

Poretti, A; Limperopoulos, C; Roulet-Perez, E; Wolf, N I; Rauscher, C; Prayer, D; Müller, A; Weissert, M; Kotzaeridou, U; Du Plessis, A J; Huisman, T A G M; Boltshauser, E (2010). Outcome of severe unilateral cerebellar hypoplasia. Developmental Medicine and Child Neurology, 52(8):718-724.

Bartholdi, D; Klein, A; Weissert, M; Koenig, N; Baumer, A; Boltshauser, E; Schinzel, A; Berger, W; Mátyás, G (2006). Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene. Clinical Genetics, 69(4):319-326.

This list was generated on Wed Jul 26 19:58:38 2017 CEST.