Auflistung nach Autor "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 Friederike; Engl, Gertraud; Leo-Kottler, Beate; Rapaport, Doron; Wissinger, Bernd; Schimpf-Linzenbold, Simone; Krüger, Rejko (2013)
Cataract as ‘initial symptom’ of Creutzfeld–Jacob disease

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

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

Leo-Kottler, Beate; Trauzettel-Klosinski, Susanne; Altpeter, Elke Karin; Blanke, Björn Rudolf; Nguyen, Xuan Nhung (2013)
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy

Wissinger, Bernd; Leo-Kottler, Beate (2012)

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