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Number of items: 18.

Walker, Ruth H; Miranda, Marcelo; Jung, Hans H; Danek, Adrian (2019). Life expectancy and mortality in chorea-acanthocytosis and McLeod syndrome. Parkinsonism & Related Disorders, 60:158-161.

Roulis, Eileen; Hyland, Catherine; Flower, Robert; Gassner, Christoph; Jung, Hans H; Frey, Beat M (2018). Molecular Basis and Clinical Overview of McLeod Syndrome Compared With Other Neuroacanthocytosis Syndromes: A Review. JAMA Neurology, 75(12):1554.

Sveinsson, Olafur; Udd, Bjarne; Svenningsson, Per; Gassner, Christoph; Engström, Charlotte; Laffita-Mesa, José Miguel; Solders, Göran; Hertegård, Stellan; Savitcheva, Irina; Jung, Hans H; Tolnay, Markus; Frey, Beat M; Paucar, Martin (2018). Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred. Parkinsonism & Related Disorders:Epub ahead of print.

Hornemann, Thorsten; Alecu, Irina; Hagenbuch, Niels; Zhakupova, Assem; Cremonesi, Alessio; Gautschi, Matthias; Jung, Hans H; Meienberg, Fabian; Bilz, Stefan; Christ, Emanuel; Baumgartner, Matthias R; Hochuli, Michel (2018). Disturbed sphingolipid metabolism with elevated 1-deoxysphingolipids in glycogen storage disease type I – A link to metabolic control. Molecular Genetics and Metabolism, 125(1/2):73-78.

Renaud, Mathilde; Moreira, Maria-Céu; et al; Ochsner, François; Jung, Hans H (2018). Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1. JAMA Neurology, 75(4):495-502.

Schreglmann, Sebastian R; Riederer, Franz; Galovic, Marian; Ganos, Christos; Kägi, Georg; Waldvogel, Daniel; Jaunmuktane, Zane; Schaller, Andre; Hidding, Ute; Krasemann, Ernst; Michels, Lars; Baumann, Christian R; Bhatia, Kailash; Jung, Hans H (2018). Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellum. Movement Disorders, 33(1):146-155.

Blanquet, Marisa; Petersen, Jens A; Palla, Antonella; Veraguth, Dorothe; Weber, Konrad P; Straumann, Dominik; Tarnutzer, Alexander A; Jung, Hans H (2018). Vestibulo-cochlear function in inflammatory neuropathies. Clinical Neurophysiology, 129(4):863-873.

Mueller, Sandro Manuel; Gehrig, Saskia Maria; Petersen, Jens A; Frese, Sebastian; Mihaylova, Violeta; Ligon-Auer, Maria; Khmara, Natalia; Nuoffer, Jean-Marc; Schaller, André; Lundby, Carsten; Toigo, Marco; Jung, Hans H (2017). Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients. Orphanet Journal of Rare Diseases, 12(1):184.

Gassner, Christoph; Brönnimann, Chantal; Merki, Yvonne; Mattle-Greminger, Maja Patricia; Sigurdardottir, Sonja; Meyer, Eduardo; Engström, Charlotte; O'Sullivan, John D; Jung, Hans H; Frey, Beat M (2017). Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome. Transfusion, 57(9):2125-2135.

Gehrig, Saskia Maria; Petersen, Jens A; Frese, Sebastian; Mueller, Sandro Manuel; Mihaylova, Violeta; Ligon-Auer, Maria; Lundby, Carsten; Toigo, Marco; Jung, Hans H (2017). Skeletal muscle characteristics and mitochondrial function in Huntington's disease patients. Movement Disorders, 32(8):1258-1259.

Frese, Sebastian; Petersen, Jens A; Ligon-Auer, Maria; Mueller, Sandro Manuel; Mihaylova, Violeta; Gehrig, Saskia M; Kana, Veronika; Rushing, Elisabeth J; Unterburger, Evelyn; Kägi, Georg; Burgunder, Jean-Marc; Toigo, Marco; Jung, Hans H (2017). Exercise effects in Huntington disease. Journal of Neurology, 264(1):32-39.

Gehrig, Saskia Maria; Mihaylova, Violeta; Frese, Sebastian; Mueller, Sandro Manuel; Ligon-Auer, Maria; Spengler, Christina M; Petersen, Jens A; Lundby, Carsten; Jung, Hans H (2016). Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy. Orphanet Journal of Rare Diseases, 11(1):105.

Valko, Yulla; Rosengren, Sally M; Jung, Hans H; Straumann, Dominik; Landau, Klara; Weber, Konrad P (2016). Ocular vestibular evoked myogenic potentials as a test for myasthenia gravis. Neurology, 86(7):660-668.

Petersen, Jens A; Kuntzer, Thierry; Fischer, Dirk; von der Hagen, Maja; Huebner, Angela; Kana, Veronika; Lobrinus, Johannes A; Kress, Wolfram; Rushing, Elisabeth J; Sinnreich, Michael; Jung, Hans H (2015). Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effects. BMC Neurology, 15(182):online.

Mueller, Sandro Manuel; Aguayo, David; Lunardi, Fabio; Ruoss, Severin; Boutellier, Urs; Frese, Sebastian; Petersen, Jens A; Jung, Hans H; Toigo, Marco (2014). High-load resistance exercise with superimposed vibration and vascular occlusion increases critical power, capillaries and lean mass in endurance-trained men. European Journal of Applied Physiology, 114(1):123-133.

Hothorn, Torsten; Jung, Hans H (2014). RandomForest4Life: A Random Forest for predicting ALS disease progression. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 15(5-6):444-452.

Vögeli, Isabelle; Jung, Hans H; Dick, Bernhard; Erickson, Sandra K; Escher, Robert; Funder, John W; Frey, Felix J; Escher, Geneviève (2013). Evidence for a role of sterol 27-hydroxylase in glucocorticoid metabolism in vivo. Journal of Endocrinology, 219(2):119-129.

Akhvlediani, Tamar; Sandor, Peter S; Henning, Anke; Schaller, André; Jauslin, Marco; Gallati, Sabina; Boesiger, Peter; Jung, Hans H (2007). Mitochondrial encephalopathy with CADASIL-Like MRI. European Neurology, 58(3):185-188.

This list was generated on Mon Jun 24 21:59:45 2019 CEST.