Browsing Universitätsbibliographie by Author "Leo-Kottler, Beate"

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A novel heterozygous OPA3 mutation located in the mitochondrial target sequence results in altered steady-state levels and fragmented mitochondrial network

Grau, Tanja; Burbulla, Lena F.; Engl, Gertraud; Delettre, Cecile; Delprat, Benjamin; Oexle, Konrad; Leo-Kottler, Beate; Roscioli, Tony; Krueger, Rejko; Rapaport, Doron; Wissinger, Bernd; Schimpf-Linzenbold, Simone (2013)
Cataract as ‘initial symptom’ of Creutzfeld–Jacob disease

Leitritz, Martin; Leo-Kottler, Beate; Batra, Marion; Ostertag, Karoline; Bartz-Schmidt, Karl Ulrich; Spitzer, Martin Stephan (2012)
Encephalopathic Susac's Syndrome associated with livedo racemosa in a young woman before the completion of family planning

Engeholm, Maik; Leo-Kottler, Beate; Rempp, Hansjoerg; Lindig, Tobias; Lerche, Holger; Kleffner, Ilka; Henes, Melanie; Dihne, Marcel (2013)
Evaluation of Fixation Pattern and Reading Ability in Patients With Leber Hereditary Optic Neuropathy

Altpeter, Elke K.; Blanke, Bjorn R.; Leo-Kottler, Beate; Nguyen, Xuan N.; Trauzettel-Klosinski, Susanne (2013)
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy

Achilli, Alessandro; Iommarini, Luisa; Olivieri, Anna; Pala, Maria; Kashani, Baharak Hooshiar; Reynier, Pascal; La Morgia, Chiara; Valentino, Maria Lucia; Liguori, Rocco; Pizza, Fabio; Barboni, Piero; Sadun, Federico; De Negri, Anna Maria; Zeviani, Massimo; Dollfus, Helene; Moulignier, Antoine; Ducos, Ghislaine; Orssaud, Christophe; Bonneau, Dominique; Procaccio, Vincent; Leo-Kottler, Beate; Fauser, Sascha; Wissinger, Bernd; Amati-Bonneau, Patrizia; Torroni, Antonio; Carelli, Valerio (2012)

Now showing items 1-5 of 5

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