Publications by authors named "Franz Zimmermann"

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Vaccine safety in children with genetically confirmed mitochondrial disease.
Annemarie de Vreugd, Franz A Zimmermann, Katja Steinbrücker, Maaike C de Vries, Lonneke de Boer

Immunol Lett· February 2025

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Role of Energy Metabolism and Mitochondrial Function in Inflammatory Bowel Disease.
Mihriban Özsoy, Nathalie Stummer, Franz A Zimmermann, René G Feichtinger, Wolfgang Sperl

Inflamm Bowel Dis· September 2022

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Expression of Oxidative Phosphorylation Complexes and Mitochondrial Mass in Pediatric and Adult Inflammatory Bowel Disease.
Anna M Schneider, Mihriban Özsoy, Franz A Zimmermann, Susanne M Brunner, René G Feichtinger

Oxid Med Cell Longev· March 2022

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Age-Related Deterioration of Mitochondrial Function in the Intestine.
Anna M Schneider, Mihriban Özsoy, Franz A Zimmermann, René G Feichtinger, Johannes A Mayr

Oxid Med Cell Longev· May 2021

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Austrian study shows that delays in accessing acute paediatric health care outweighed the risks of COVID-19.
Matthias Schaffert, Franz Zimmermann, Leopold Bauer, Simon Kastner, Astrid Schwarz

Acta Paediatr· November 2020

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Changes in the expression of oxidative phosphorylation complexes in the aging intestinal mucosa.
Mihriban Özsoy, Franz A Zimmermann, René G Feichtinger, Johannes A Mayr, Barbara Kofler

Exp Gerontol· July 2020

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Alterations of Oxidative Phosphorylation Complexes in Papillary Thyroid Carcinoma.
Franz A Zimmermann, Daniel Neureiter, Wolfgang Sperl, Johannes A Mayr, Barbara Kofler

Cells· May 2018

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Oxidative Phosphorylation System in Gastric Carcinomas and Gastritis.
René G Feichtinger, Daniel Neureiter, Tom Skaria, Silja Wessler, Timothy L Cover, Franz A Zimmermann

Oxid Med Cell Longev· April 2018

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Alterations of oxidative phosphorylation in meningiomas and peripheral nerve sheath tumors.
René G Feichtinger, Serge Weis, Johannes A Mayr, Franz A Zimmermann, Barbara Bogner

Neuro Oncol· February 2016

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Deficiency of respiratory chain complex I in Hashimoto thyroiditis.
Franz A Zimmermann, Daniel Neureiter, René G Feichtinger, Andrea Trost, Wolfgang Sperl

Mitochondrion· January 2016

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Spectrum of combined respiratory chain defects.
Johannes A Mayr, Tobias B Haack, Peter Freisinger, Daniela Karall, Christine Makowski, Franz A Zimmermann

J Inherit Metab Dis· July 2015

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The spectrum of pyruvate oxidation defects in the diagnosis of mitochondrial disorders.
Wolfgang Sperl, Leanne Fleuren, Peter Freisinger, Tobias B Haack, Antonia Ribes, Franz A Zimmermann

J Inherit Metab Dis· May 2015

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Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
Johannes Koch, Peter Freisinger, René G Feichtinger, Franz A Zimmermann, Christian Rauscher

Orphanet J Rare Dis· April 2015

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Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency.
Uwe Ahting, Johannes A Mayr, Arnaud V Vanlander, Steven A Hardy, Saikat Santra, Franz A Zimmermann

Front Genet· April 2015

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From ventriculomegaly to severe muscular atrophy: expansion of the clinical spectrum related to mutations in AIFM1.
Matthias Kettwig, Max Schubach, Franz A Zimmermann, Lars Klinge, Johannes A Mayr

Mitochondrion· March 2015

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Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.
Siddharth Banka, Christian de Goede, Wyatt W Yue, Andrew A M Morris, Beate von Bremen, Franz A Zimmermann

Mol Genet Metab· December 2014

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Alterations of oxidative phosphorylation complexes in astrocytomas.
René Günther Feichtinger, Serge Weis, Johannes Adalbert Mayr, Franz Zimmermann, Reinhard Geilberger

Glia· April 2014

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Mitochondrial myopathy associated with a novel 5522G>A mutation in the mitochondrial tRNA(Trp) gene.
Ivo Barić, Ksenija Fumić, Danijela Petković Ramadža, Wolfgang Sperl, Franz A Zimmermann

Eur J Hum Genet· August 2013

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ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy.
Tobias B Haack, Robert Kopajtich, Peter Freisinger, Thomas Wieland, Joanna Rorbach, Franz A Zimmermann

Am J Hum Genet· August 2013

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Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings.
Tobias B Haack, Boris Rolinski, Birgit Haberberger, Franz Zimmermann, Jessica Schum

J Inherit Metab Dis· January 2013

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A 1.1 million base pair X-chromosomal deletion covering the PDHA1 and CDKL5 genes in a female patient with West syndrome and pyruvate oxidation deficiency.
Johannes A Mayr, Johannes Koch, Christine Fauth, Franz A Zimmermann, Christian Rauscher

Neuropediatrics· June 2012

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Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.
Johannes A Mayr, Tobias B Haack, Elisabeth Graf, Franz A Zimmermann, Thomas Wieland

Am J Hum Genet· February 2012

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Reduction of nuclear encoded enzymes of mitochondrial energy metabolism in cells devoid of mitochondrial DNA.
Edith E Mueller, Johannes A Mayr, Franz A Zimmermann, René G Feichtinger, Olaf Stanger

Biochem Biophys Res Commun· January 2012

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Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation.
Johannes A Mayr, Franz A Zimmermann, Christine Fauth, Christa Bergheim, David Meierhofer

Am J Hum Genet· December 2011

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Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway.
Johannes A Mayr, Peter Freisinger, Kurt Schlachter, Boris Rolinski, Franz A Zimmermann

Am J Hum Genet· December 2011

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