RonaldGeraldHallerMD

PubMed

• 10 citations
  Hyperpolarized 13C MR Spectroscopy Depicts in Vivo Effect of Exercise on Pyruvate Metabolism in Human Skeletal Muscle
  Jae Mo Park, Crystal Harrison, Junjie Ma, Jun Chen, James Ratnakar, Zungho Zun, Jeff Liticker, Galen D. Reed, Avneesh Chhabra, Ronald G. Haller, Thomas Jue, Craig R. M...> ;Radiology. 2021 Jun 22
• 72 citations
  Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity
  Rohit Sharma, Bryn Reinstadler, Kristin Engelstad, Owen S. Skinner, Erin Stackowitz, Ronald G. Haller, Clary B. Clish, Kerry A. Pierce, Melissa A. Walker, Robert Fryer...> ;The Journal of Clinical Investigation. 2021 Jan 19
• 2 citations
  Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
  Tomàs Pinós, Antoni L. Andreu, Claudio Bruno, Georgios M. Hadjigeorgiou, Ronald G. Haller, Pascal Laforêt, Alejandro Lucia, Miguel A. Martín, Andrea Martinuzzi, Carmen...> ;Orphanet Journal of Rare Diseases. 2020 Oct 15
• 3 citations
  Results of an open label feasibility study of sodium valproate in people with McArdle disease.
  Renata S Scalco, Mads Godtfeldt Stemmerik, Nicoline Løkken, Christoffer Rasmus Vissing, Karen Lindhardt Madsen, Zuzanna Michalak, Jatin Pattni, Richard Godfrey, George...> ;Neuromuscular Disorders. 2020 May 16
• 16 citations
  No effect of triheptanoin on exercise performance in McArdle disease.
  Karen Lindhardt Madsen, Pascal Laforêt, Astrid Emilie Buch, Mads Godtfeldt Stemmerik, Chris Ottolenghi, Stéphane N. Hatem, Daniel Raaschou-Pedersen, Nanna S. Poulsen, ...> ;Annals of Clinical and Translational Neurology. 2019 Oct 1
• 60 citations
  Acute loss of iron–sulfur clusters results in metabolic reprogramming and generation of lipid droplets in mammalian cells
  Daniel R. Crooks, Nunziata Maio, Andrew N. Lane, Michal Jarnik, Richard M. Higashi, Ronald G. Haller, Ye Yang, Teresa W.-M. Fan, W. Marston Linehan, Tracey A. Rouault> ;The Journal of Biological Chemistry. 2018 May 25
• 27 citations
  Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.
  Mariana C. Rocha, Hannah S. Rosa, John P. Grady, Emma L. Blakely, Langping He, Nadine Romain, Ronald G. Haller, Jane Newman, Robert McFarland, Yi Shiau Ng, Grainne S. ...> ;Annals of Neurology. 2018 Jan 1
• 18 citations
  Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency.
  Nicolai Preisler, Jonathan C. Cohen, Christoffer Rasmus Vissing, Karen Lindhardt Madsen, Katja Heinicke, Lydia Sharp, Lauren Phillips, Nadine Romain, Sun Young Park, M...> ;Molecular Genetics and Metabolism. 2017 Nov 1
• 27 citations
  Metabolic profiles of exercise in patients with McArdle disease or mitochondrial myopathy.
  Nigel F. Delaney, Rohit Sharma, Laura Tadvalkar, Clary B. Clish, Ronald G. Haller, Vamsi K. Mootha> ;Proceedings of the National Academy of Sciences of the United States of America. 2017 Aug 1
• 9 citations
  Use of antisense oligonucleotides to correct the splicing error in ISCU myopathy patient cell lines.
  Gregory P. Holmes-Hampton, Daniel R. Crooks, Ronald G. Haller, Shuling Guo, Susan M. Freier, Brett P. Monia, Tracey A. Rouault> ;Human Molecular Genetics. 2016 Dec 1
• 48 citations
  Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
  Charlotte L. Alston, Alison G. Compton, Luke E. Formosa, Valentina Strecker, Monika Oláhová, Tobias B. Haack, Joél Smet, Katrien Stouffs, Peter Diakumis, Elżbieta Ciar...> ;American Journal of Human Genetics. 2016 Jul 7
• 23 citations
  Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2A (calpainopathy)
  Irina Kramerova, Natalia Ermolova, Ascia Eskin, Andrea L. Hevener, Oswald Quehenberger, Aaron M. Armando, Ronald G. Haller, Nadine Romain, Stanley F. Nelson, Melissa J...> ;Human Molecular Genetics. 2016 Mar 22
• 69 citations
  TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies.
  Christopher A. Powell, Robert Kopajtich, Aaron R. D’Souza, Joanna Rorbach, Laura S. Kremer, Ralf A. Husain, Cristina Dallabona, Claudia Donnini, Charlotte L. Alston, H...> ;American Journal of Human Genetics. 2015 Aug 6
• 1 citations
  Glycogen storage disease type III: The phenotype branches out
  Ronald G. Haller> ;Neurology. 2015 Apr 28
• 46 citations
  Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle
  John P. Grady, J.L. Murphy, Emma L. Blakely, Ronald G. Haller, Robert W. Taylor, Douglass M. Turnbull, Helen A. L. Tuppen> ;Plos One. 2014 Dec 4
• 19 citations
  Reproducibility and absolute quantification of muscle glycogen in patients with glycogen storage disease by 13C NMR spectroscopy at 7 Tesla.
  Katja Heinicke, Ivan E. Dimitrov, Nadine Romain, S. Cheshkov, Jimin Ren, Craig R. Malloy, Ronald G. Haller> ;Plos One. 2014 Oct 8
• 20 citations
  Metabolic and mitochondrial myopathies.
  Lydia Sharp, Ronald G. Haller> ;Neurologic Clinics. 2014 Aug 1
• 112 citations
  Aerobic conditioning: an effective therapy in McArdle's disease.
  Ronald G. Haller, Phil Wyrick, Tanja Taivassalo, John Vissing> ;Annals of Neurology. 2006 Jun 1
• 51 citations
  No spontaneous second wind in muscle phosphofructokinase deficiency
  Ronald G. Haller, John Vissing> ;Neurology. 2004 Jan 13
• 107 citations
  Spontaneous "second wind" and glucose-induced second "second wind" in McArdle disease oxidative mechanisms
  Ronald G. Haller, John Vissing> ;Archives of Neurology. 2002 Sep 1
• Join now to see all