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Number of items: 11.

Servais, L; Montus, M; Le Guiner, C; Ben Yaou, R; Annoussamya, M; Moraux, A; Hogrel, J-Y; Seferian, A M; Zehrouni, K; Lo Moing, A-G; Gidaro, T; Vanhulle, C; Laugel, V; Butoianu, N; Cuisset, J-M; Sabouraud, P; Cances, C; Klein, A; Leturcq, F; Moullier, P; Voit, T (2015). Non-ambulant duchenne patients theoretically treatable by exon 53 skipping have severe phenotype. Journal of Neuromuscular Diseases, 2(3):269-279.

Maggi, L; Scoto, M; Cirak, S; Robb, S A; Klein, A; Lillis, S; Cullup, T; Feng, L; Manzur, A Y; Sewry, C A; Abbs, S; Jungbluth, H; Muntoni, F (2013). Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom. Neuromuscular Disorders : NMD, 23(3):195-205.

Goetti, R; Wille, D; Kretzschmar, U; Klein, A; Scheer, I (2013). Idiopathic spinal cord herniation: first reported case in a child. JAMA Neurology, 70(1):125-126.

von Klitzing, K; Perren, S; Klein, A; Stadelmann, S; White, L O; Groeben, M; Holsboer-Trachsler, E; Brand, S; Hatzinger, M (2012). The interaction of social risk factors and HPA axis dysregulation in predicting emotional symptoms of five- and six-year-old children. Journal of Psychiatric Research, 46(3):290-297.

Klein, A; Jetzer, P (2010). Spin effects in the phasing of gravitational waves from binaries on eccentric orbits. Physical Review D, 81(12):124001.

Rohrbach, M; Klein, A; Köhli-Wiesner, A; Veraguth, D; Scheer, I; Balmer, C; Lauener, R; Baumgartner, M R (2010). CRIM-negative infantile Pompe disease: 42-month treatment outcome. Journal of Inherited Metabolic Disease, 33(6):751-757.

Klein, A; Jetzer, P; Sereno, M (2009). Parameter estimation for coalescing massive binary black holes with LISA using the full 2-post-Newtonian gravitational waveform and spin-orbit precession. Physical Review D, 80(6):064027.

Clement, E; Mercuri, E; Godfrey, C; Smith, J; Robb, S; Kinali, M; Straub, V; Bushby, K; Manzur, A; Talim, B; Cowan, F; Quinlivan, R; Klein, A; Longman, C; McWilliam, R; Topaloglu, H; Mein, R; Abbs, S; North, K; Barkovich, A J; Rutherford, M; Muntoni, F (2008). Brain involvement in muscular dystrophies with defective dystroglycan glycosylation. Annals of Neurology, 64(5):573-582.

Poretti, A; Leventer, R J; Cowan, F M; Rutherford, M A; Steinlin, M; Klein, A; Scheer, I; Huisman, T A G M; Boltshauser, E (2008). Cerebellar cleft: a form of prenatal cerebellar disruption. Neuropediatrics, 39(2):106-112.

Klein, A; Clement, E; Mercuri, E; Muntoni, F (2008). Differential diagnosis of congenital muscular dystrophies. European Journal of Paediatric Neurology, 12(5):371-377.

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 Fri Nov 24 03:58:07 2017 CET.