Resultados da pesquisa - Alexandra Götz

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  1. 1
    Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome

    Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome Por Alexandra Götz, Pirjo Isohanni, Helena Pihko, Anders Paetau, Riitta Herva, Outi Saarenpää‐Heikkilä, Leena Valanne, Sanna Marjavaara, Anu Suomalainen

    Publicado em 2008
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  2. 2
    Stigmatization experience, coping and sense of coherence in vitiligo patients

    Stigmatization experience, coping and sense of coherence in vitiligo patients Por Gerhard Schmid‐Ott, H‐W Künsebeck, E. W. Jecht, R Shimshoni, Ilya Lazaroff, Sabine Schallmayer, IT Calliess, Peter Malewski, Friedhelm Lamprecht, Alexandra Götz

    Publicado em 2007
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  3. 3
    Global Transcript Profiles of Fat in Monozygotic Twins Discordant for BMI: Pathways behind Acquired Obesity

    Global Transcript Profiles of Fat in Monozygotic Twins Discordant for BMI: Pathways behind Acquired Obesity Por Kirsi H. Pietiläinen, Jussi Naukkarinen, Aila Rissanen, Juha Saharinen, Pekka Ellonen, Heli Keränen, Anu Suomalainen, Alexandra Götz, Tapani Suortti, Hannele Yki‐Järvinen, Matej Orešič, Jaakko Kaprio, Leena Peltonen

    Publicado em 2008
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  4. 4
    Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy

    Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy Por Jenni M. Elo, Srujana S. Yadavalli, Liliya Euro, Pirjo Isohanni, Alexandra Götz, Christopher J. Carroll, Leena Valanne, Fowzan S. Alkuraya, Johanna Uusimaa, Anders Paetau, Eric M. Caruso, Helena Pihko, Michael Ibba, Henna Tyynismaa, Anu Suomalainen

    Publicado em 2012
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  5. 5
    Exome Sequencing Identifies Mitochondrial Alanyl-tRNA Synthetase Mutations in Infantile Mitochondrial Cardiomyopathy

    Exome Sequencing Identifies Mitochondrial Alanyl-tRNA Synthetase Mutations in Infantile Mitochondrial Cardiomyopathy Por Alexandra Götz, Henna Tyynismaa, Liliya Euro, Pekka Ellonen, Tuulia Hyötyläinen, Tiina Ojala, Riikka H. Hämäläinen, Johanna Tommiska, Taneli Raivio, Matej Orešič, Riitta Karikoski, Outi Tammela, K. O. J. Simola, Anders Paetau, Tiina Tyni, Anu Suomalainen

    Publicado em 2011
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  6. 6
    A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation

    A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantation Por Mikal Jacob Hole, Kristin Kaasen Jørgensen, Kristian Holm, Peder R. Braadland, Malin Holm Meyer‐Myklestad, Asle W. Medhus, Dag Henrik Reikvam, Alexandra Götz, Krzysztof Grzyb, Kirsten Muri Boberg, Tom H. Karlsen, Martin Kummen, Johannes R. Hov

    Publicado em 2022
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  7. 7
    Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice

    Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice Por Kati J. Ahlqvist, Riikka H. Hämäläinen, Shuichi Yatsuga, Marko Uutela, Mügen Terzioglu, Alexandra Götz, Saara Forsström, Petri Salvén, Alexandre Angers‐Loustau, Outi Kopra, Henna Tyynismaa, Nils‐Göran Larsson, Kirmo Wartiovaara, Tomas A. Prolla, Aleksandra Trifunović, Anu Suomalainen

    Publicado em 2012
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  8. 8
    Rifaximin or Saccharomyces boulardii in heart failure with reduced ejection fraction: Results from the randomized GutHeart trial

    Rifaximin or Saccharomyces boulardii in heart failure with reduced ejection fraction: Results from the randomized GutHeart trial Por Ayodeji Awoyemi, Cristiane C.K. Mayerhofer, Alex S. Felix, Johannes R. Hov, Samuel Datum Moscavitch, Knut Tore Lappegård, Anders Hovland, Sigrun Halvorsen, Bente Halvorsen, Ida Gregersen, Asbjørn Svardal, Rolf K. Berge, Simen H. Hansen, Alexandra Götz, Kristian Holm, Pål Aukrust, Sissel Åkra, Ingebjørg Seljeflot, Svein Solheim, Andrea De Lorenzo, Lars Gullestad, Marius Trøseid, Kaspar Broch

    Publicado em 2021
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