Хайлтын үр дүнгүүд - Franz Zimmermann

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  1. 1
    ORTHOTOPIC LIVER ALLOGRAFTS IN THE RAT

    ORTHOTOPIC LIVER ALLOGRAFTS IN THE RAT -н Franz Zimmermann, HUGH FF. S. DAVIES, PETER P. KNOLL, J. M. Gokel, Traudel Schmidt

    Хэвлэсэн 1984
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    Artigo
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  2. 2
    Lipoic Acid Synthetase Deficiency Causes Neonatal-Onset Epilepsy, Defective Mitochondrial Energy Metabolism, and Glycine Elevation

    Lipoic Acid Synthetase Deficiency Causes Neonatal-Onset Epilepsy, Defective Mitochondrial Energy Metabolism, and Glycine Elevation -н Johannes A. Mayr, Franz Zimmermann, Christine Fauth, Christa Bergheim, David Meierhofer, Doris Radmayr, Johannes Zschocke, Johannes Koch, Wolfgang Sperl

    Хэвлэсэн 2011
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    Artigo
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  3. 3
    Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma

    Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma -н Johannes A. Mayr, David Meierhofer, Franz Zimmermann, René G. Feichtinger, Christian Kögler, Manfred Ratschek, N. Schmeller, Wolfgang Sperl, Barbara Kofler

    Хэвлэсэн 2008
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    Artigo
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  4. 4
    Lack of complex I is associated with oncocytic thyroid tumours

    Lack of complex I is associated with oncocytic thyroid tumours -н Franz Zimmermann, Johannes A. Mayr, Daniel Neureiter, René G. Feichtinger, Beate Alinger, N. D. Jones, Waltraud Eder, Wolfgang Sperl, Barbara Kofler

    Хэвлэсэн 2009
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    Artigo
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  5. 5
    Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma

    Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma -н René G. Feichtinger, Franz Zimmermann, Johannes A. Mayr, Daniel Neureiter, Cornelia Hauser‐Kronberger, Freimut H. Schilling, Neil D. Jones, Wolfgang Sperl, Barbara Kofler

    Хэвлэсэн 2010
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    Artigo
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  6. 6
    Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway

    Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway -н Johannes A. Mayr, Peter Freisinger, Kurt Schlachter, Boris Rolinski, Franz Zimmermann, T Scheffner, Tobias B. Haack, Johannes Koch, Uwe Ahting, Holger Prokisch, Wolfgang Sperl

    Хэвлэсэн 2011
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    Artigo
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  7. 7
    Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit

    Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit -н Johannes A. Mayr, Vendula Havlíčková, Franz Zimmermann, I. Magler, Vilma Kaplanová, Pavel Ješina, Alena Pecinová, Hana Nůsková, Johannes Koch, Wolfgang Sperl, J Houštěk

    Хэвлэсэн 2010
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    Artigo
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  8. 8
    Spectrum of combined respiratory chain defects

    Spectrum of combined respiratory chain defects -н Johannes A. Mayr, Tobias B. Haack, Peter Freisinger, Daniela Karall, Christine Makowski, Johannes Koch, René G. Feichtinger, Franz Zimmermann, Boris Rolinski, Uwe Ahting, Thomas Meitinger, Holger Prokisch, Wolfgang Sperl

    Хэвлэсэн 2015
    Бүрэн текст авах
    Revisão
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  9. 9
    Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study

    Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study -н Barbara Kofler, Edith E. Mueller, Waltraud Eder, Olaf Stanger, Richard Maier, Martin Weger, Anton Haas, Robert Winker, O. Schmut, Bernhard Paulweber, Bernhard Iglseder, Wilfried Renner, Martina Wiesbauer, Irene Aigner, Danijela Šantić, Franz Zimmermann, Johannes A. Mayr, Wolfgang Sperl

    Хэвлэсэн 2009
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    Artigo
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  10. 10
    Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome

    Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome -н Johannes A. Mayr, Tobias B. Haack, Elisabeth Graf, Franz Zimmermann, Thomas Wieland, Birgit Haberberger, Andrea Superti‐Furga, Janbernd Kirschner, Beat Steinmann, Matthias R. Baumgartner, Isabella Moroni, Eleonora Lamantea, Massimo Zeviani, Richard J. Rodenburg, Jan Smeitink, Tim M. Strom, Thomas Meitinger, Wolfgang Sperl, Holger Prokisch

    Хэвлэсэн 2012
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    Artigo
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  11. 11
    ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy

    ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy -н Tobias B. Haack, Robert Kopajtich, Peter Freisinger, Thomas Wieland, Joanna Rorbach, Thomas J. Nicholls, Enrico Baruffini, Anett Walther, Katharina Danhauser, Franz Zimmermann, Ralf A. Husain, Jessica Schum, Helen Mundy, Ileana Ferrero, Tim M. Strom, Thomas Meitinger, Robert W. Taylor, Michal Minczuk, Johannes A. Mayr, Holger Prokisch

    Хэвлэсэн 2013
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    Artigo
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  12. 12
    Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency

    Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency -н Uwe Ahting, Johannes A. Mayr, Arnaud Vanlander, Steven Hardy, Saikat Santra, Christine Makowski, Charlotte L. Alston, Franz Zimmermann, Lucia Abela, Barbara Plecko, Marianne Rohrbach, Stephanie Spranger, Sara Seneca, Boris Rolinski, Angela Hagendorff, Maja Hempel, Wolfgang Sperl, Thomas Meitinger, Joél Smet, Robert W. Taylor, Rudy Van Coster, Peter Freisinger, Holger Prokisch, Tobias B. Haack

    Хэвлэсэн 2015
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    Artigo
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