Works matching AU Haller, Ronald G.

Results: 37

Effect of perfusion on exercised muscle: MR imaging evaluation.

Published in:

1992

By:

Archer, Branch T.;
Fleckenstein, James L.;
Bertocci, Loren A.;
Haller, Ronald G.;
Barker, Bruce;
Parkey, Robert W.;
Peshock, Ronald M.;
Archer, B T;
Fleckenstein, J L;
Bertocci, L A;
Haller, R G;
Barker, B;
Parkey, R W;
Peshock, R M

Publication type:

journal article

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry).

Published in:

2020

By:

Pinós, Tomàs;
Andreu, Antoni L.;
Bruno, Claudio;
Hadjigeorgiou, Georgios M.;
Haller, Ronald G.;
Laforêt, Pascal;
Lucía, Alejandro;
Martín, Miguel A.;
Martinuzzi, Andrea;
Navarro, Carmen;
Oflazer, Piraye;
Pouget, Jean;
Quinlivan, Ros;
Sacconi, Sabrina;
Scalco, Renata S.;
Toscano, Antonio;
Vissing, John;
Vorgerd, Matthias;
Wakelin, Andrew;
Martí, Ramon

Publication type:

journal article

A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 10, p. 1265, doi. 10.1038/ejhg.2008.65

By:

Swalwell, Helen;
Blakely, Emma L.;
Sutton, Ruth;
Tonska, Kasia;
Elstner, Matthias;
Langping He;
Taivassalo, Tanja;
Burns, Dennis K.;
Turnbull, Douglass M.;
Haller, Ronald G.;
Davidson, Mercy M.;
Taylor, Robert W.

Publication type:

Article

Aberrant iron homeostasis, oxidative fiber enrichment, and activation of ketogenesis in muscle tissue of ISCU Myopathy patients.

Published in:

2012

By:

Crooks, Daniel R.;
Natarajan, Thanemozhi G.;
Churning Chen;
Hongzhan Huang;
Ghosh, Manik C.;
Wing-Hang Tong;
Haller, Ronald G.;
Wu, Cathy;
Rouault, Tracey A.

Publication type:

Abstract

Experimental acute alcoholic myopathy-a histochemical study.

Published in:

Muscle & Nerve, 1985, v. 8, n. 3, p. 195, doi. 10.1002/mus.880080304

By:

Haller, Ronald G.

Publication type:

Article

Energy Contribution of Octanoate to Intact Rat Brain Metabolism Measured by [sup13]C Nuclear Magnetic Resonance Spectroscopy.

Published in:

Journal of Neuroscience, 2003, v. 23, n. 13, p. 5928, doi. 10.1523/JNEUROSCI.23-13-05928.2003

By:

Ebert, Douglas;
Haller, Ronald G.;
Walton, Marlei E.

Publication type:

Article

Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity.

Published in:

2021

By:

Sharma, Rohit;
Reinstadler, Bryn;
Engelstad, Kristin;
Skinner, Owen S.;
Stackowitz, Erin;
Haller, Ronald G.;
Clish, Clary B.;
Pierce, Kerry;
Walker, Melissa A.;
Fryer, Robert;
Oglesbee, Devin;
Xiangling Mao;
Shungu, Dikoma C.;
Khatri, Ashok;
Michio Hirano;
De Vivo, Darryl C.;
Mootha, Vamsi K.;
Mao, Xiangling;
Hirano, Michio

Publication type:

journal article

Energy deficit in Huntington disease: why it matters.

Published in:

2011

By:

Mochel, Fanny;
Haller, Ronald G.

Publication type:

journal article

Relative rates of anaplerotic flux in rested and contracted rat skeletal muscle measured by 13C NMR spectroscopy.

Published in:

Journal of Physiology, 2003, v. 548, n. 2, p. 541, doi. 10.1111/j.1469-7793.2003.00541.x

By:

Walton, Marlei E.;
Ebert, Douglas;
Haller, Ronald G.

Publication type:

Article

Role of 5′AMP-activated protein kinase in glycogen synthase activity and glucose utilization: insights from patients with McArdle's disease.

Published in:

Journal of Physiology, 2002, v. 541, n. 3, p. 979, doi. 10.1113/jphysiol.2002.018044

By:

Nielsen, Jakob N.;
Wojtaszewski, Jørgen F. P.;
Haller, Ronald G.;
Hardie, D. Grahame;
Kemp, Bruce E.;
Richter, Erik A.;
Vissing, John

Publication type:

Article

The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle's disease.

Published in:

Journal of Physiology, 2001, v. 537, n. 2, p. 641, doi. 10.1111/j.1469-7793.2001.00641.x

By:

Vissing, John;
MacLean, David A.;
Vissing, Susanne F.;
Sander, Mikael;
Saltin, Bengt;
Haller, Ronald G.

Publication type:

Article

The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.

Published in:

Brain: A Journal of Neurology, 2003, v. 126, n. 2, p. 413, doi. 10.1093/brain/awg028

By:

Taivassalo, Tanja;
Dysgaard Jensen, Tina;
Kennaway, Nancy;
DiMauro, Salvatore;
Vissing, John;
Haller, Ronald G.

Publication type:

Article

Aerobic conditioning: An effective therapy in McArdle's disease.

Published in:

Annals of Neurology, 2006, v. 59, n. 6, p. 922

By:

Ronald G. Haller;
Phil Wyrick;
Tanja Taivassalo;
John Vissing

Publication type:

Article

A diagnostic cycle test for McArdle's disease.

Published in:

Annals of Neurology, 2003, v. 54, n. 4, p. 539

By:

John Vissing;
Ronald G. Haller

Publication type:

Article

A nonischemic forearm exercise test for McArdle disease.

Published in:

2002

By:

Kazemi-Esfarjani, Pedram;
Skomorowska, Elwira;
Dysgaard Jensen, Tina;
Haller, Ronald G.;
Vissing, John;
Jensen, Tina Dysgaard

Publication type:

journal article

Venous oxygen levels during aerobic forearm exercise: An index of impaired oxidative metabolism in mitochondrial myopathy.

Published in:

2002

By:

Taivassalo, Tanja;
Abbott, Amy;
Wyrick, Phil;
Haller, Ronald G.

Publication type:

journal article

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects.

Published in:

2001

By:

Taivassalo, Tanja;
Shoubridge, Eric A.;
Chen, Jacqueline;
Kennaway, Nancy G.;
DiMauro, Salvatore;
Arnold, Douglas L.;
Haller, Ronald G.;
Taivassalo, T;
Shoubridge, E A;
Chen, J;
Kennaway, N G;
DiMauro, S;
Arnold, D L;
Haller, R G

Publication type:

journal article

Muscle phosphoglycerate mutase deficiency with tubular aggregates: effect of dantrolene.

Published in:

1999

By:

Vissing, John;
Schmalbruch, Henning;
Haller, Ronald G.;
Clausen, Torben;
Vissing, J;
Schmalbruch, H;
Haller, R G;
Clausen, T

Publication type:

journal article

Exercise fuel mobilization in mitochondrial myopathy: A metabolic dilemma.

Published in:

Annals of Neurology, 1996, v. 40, n. 4, p. 655, doi. 10.1002/ana.410400416

By:

Vissing, John;
Galbo, Henrik;
Haller, Ronald G.

Publication type:

Article

Oxygen Utilization and delivery in metabolic my opathies.

Published in:

Annals of Neurology, 1994, v. 36, n. 6, p. 811, doi. 10.1002/ana.410360603

By:

Haller, Ronald G.

Publication type:

Article

Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients.

Published in:

Annals of Neurology, 1994, v. 36, n. 4, p. 661, doi. 10.1002/ana.410360418

By:

Tsujino, Seiichi;
Shanske, Sara;
Brownell, A. Keith W.;
Haller, Ronald G.;
DiMauro, Salvatore

Publication type:

Article

Myophosphorylase deficiency impairs muscle oxidative metabolism.

Published in:

Annals of Neurology, 1985, v. 17, n. 2, p. 196, doi. 10.1002/ana.410170216

By:

Haller, Ronald G.;
Lewis, Steven F.;
Cook, J. D.;
Blomqvist, C. G.

Publication type:

Article

Increased capillaries in mitochondrial myopathy: implications for the regulation of oxygen delivery.

Published in:

Brain: A Journal of Neurology, 2012, v. 135, n. 1, p. 53, doi. 10.1093/brain/awr293

By:

Taivassalo, Tanja;
Ayyad, Karen;
Haller, Ronald G.

Publication type:

Article

Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease.

Published in:

Brain: A Journal of Neurology, 2009, v. 132, n. 6, p. 1545, doi. 10.1093/brain/awp065

By:

Vissing, John;
Duno, Morten;
Schwartz, Marianne;
Haller, Ronald G.

Publication type:

Article

Resistance training in patients with single, large-scale deletions of mitochondrial DNA.

Published in:

Brain: A Journal of Neurology, 2008, v. 131, n. 11, p. 2832, doi. 10.1093/brain/awn252

By:

Julie L. Murphy;
Emma L. Blakely;
Andrew M. Schaefer;
Langping He;
Phil Wyrick;
Ronald G. Haller;
Robert W. Taylor;
Douglass M. Turnbull;
Tanja Taivassalo

Publication type:

Article

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

Published in:

Brain: A Journal of Neurology, 2006, v. 129, n. 12, p. 3391, doi. 10.1093/brain/awl282

By:

Taivassalo, Tanja;
Gardner, Julie L.;
Taylor, Robert W.;
Schaefer, Andrew M.;
Newman, Jane;
Barron, Martin J.;
Haller, Ronald G.;
Turnbull, Douglass M.

Publication type:

Article

Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

Published in:

2018

By:

Rocha, Mariana C.;
Rosa, Hannah S.;
Grady, John P.;
Blakely, Emma L.;
He, Langping;
Romain, Nadine;
Haller, Ronald G.;
Newman, Jane;
McFarland, Robert;
Ng, Yi Shiau;
Gorman, Grainne S.;
Schaefer, Andrew M.;
Tuppen, Helen A.;
Taylor, Robert W.;
Turnbull, Doug M.

Publication type:

journal article

No effect of triheptanoin on exercise performance in McArdle disease.

Published in:

Annals of Clinical & Translational Neurology, 2019, v. 6, n. 10, p. 1949, doi. 10.1002/acn3.50863

By:

Madsen, Karen L.;
Laforêt, Pascal;
Buch, Astrid E.;
Stemmerik, Mads G.;
Ottolenghi, Chris;
Hatem, Stéphane N.;
Raaschou‐Pedersen, Daniel T.;
Poulsen, Nanna S.;
Atencio, Maria;
Luton, Marie‐Pierre;
Ceccaldi, Alexandre;
Haller, Ronald G.;
Quinlivan, Ros;
Mochel, Fanny;
Vissing, John

Publication type:

Article

Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle.

Published in:

PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0114462

By:

Grady, John P.;
Murphy, Julie L.;
Blakely, Emma L.;
Haller, Ronald G.;
Taylor, Robert W.;
Turnbull, Doug M.;
Tuppen, Helen A. L.

Publication type:

Article

Reproducibility and Absolute Quantification of Muscle Glycogen in Patients with Glycogen Storage Disease by 13C NMR Spectroscopy at 7 Tesla.

Published in:

PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0108706

By:

Heinicke, Katja;
Dimitrov, Ivan E.;
Romain, Nadine;
Cheshkov, Sergey;
Ren, Jimin;
Malloy, Craig R.;
Haller, Ronald G.

Publication type:

Article

Dynamic monitoring of carnitine and acetylcarnitine in the trimethylamine signal after exercise in human skeletal muscle by 7T 1H-MRS.

Published in:

Magnetic Resonance in Medicine, 2013, v. 69, n. 1, p. 7, doi. 10.1002/mrm.24249

By:

REN, Jimin;
Lakoski, Susan;
Haller, Ronald G.;
Sherry, A. Dean;
Malloy, Craig R.

Publication type:

Article

OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases.

Published in:

Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-022-04303-x

By:

Sturm, Gabriel;
Karan, Kalpita R.;
Monzel, Anna S.;
Santhanam, Balaji;
Taivassalo, Tanja;
Bris, Céline;
Ware, Sarah A.;
Cross, Marissa;
Towheed, Atif;
Higgins-Chen, Albert;
McManus, Meagan J.;
Cardenas, Andres;
Lin, Jue;
Epel, Elissa S.;
Rahman, Shamima;
Vissing, John;
Grassi, Bruno;
Levine, Morgan;
Horvath, Steve;
Haller, Ronald G.

Publication type:

Article

Use of antisense oligonucleotides to correct the splicing error in ISCU myopathy patient cell lines.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 23, p. 5178, doi. 10.1093/hmg/ddw338

By:

Holmes-Hampton, Gregory P.;
Crooks, Daniel R.;
Haller, Ronald G.;
Shuling Guo;
Freier, Susan M.;
Monia, Brett P.;
Rouault, Tracey A.

Publication type:

Article

Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron–sulfur cluster depletion in human skeletal muscle.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 1, p. 24, doi. 10.1093/hmg/ddt393

By:

Crooks, Daniel R.;
Natarajan, Thanemozhi G.;
Jeong, Suh Young;
Chen, Chuming;
Park, Sun Young;
Huang, Hongzhan;
Ghosh, Manik C.;
Tong, Wing-Hang;
Haller, Ronald G.;
Wu, Cathy;
Rouault, Tracey A.

Publication type:

Article

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 17, p. 3194, doi. 10.1093/hmg/ddp257

By:

Kramerova, Irina;
Kudryashova, Elena;
Wu, Benjamin;
Germain, Sean;
Vandenborne, Krista;
Romain, Nadine;
Haller, Ronald G.;
Verity, M. Anthony;
Spencer, Melissa J.

Publication type:

Article

McArdle's disease presenting with asymmetric, late-onset arm weakness.

Published in:

2000

By:

Wolfe, Gil I.;
Baker, Noel S.;
Haller, Ronald G.;
Burns, Dennis K.;
Barohn, Richard J.;
Wolfe, G I;
Baker, N S;
Haller, R G;
Burns, D K;
Barohn, R J

Publication type:

journal article

Magnetic resonance imaging of muscle injury and atrophy in glycolytic myopathies.

Published in:

Muscle & Nerve, 1989, v. 12, n. 10, p. 849, doi. 10.1002/mus.880121011

By:

Fleckenstein, James L.;
Peshock, Ronald M.;
Lewis, Steven F.;
Haller, Ronald G.

Publication type:

Article

Works matching AU Haller, Ronald G.

Effect of perfusion on exercised muscle: MR imaging evaluation.

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry).

A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?

Aberrant iron homeostasis, oxidative fiber enrichment, and activation of ketogenesis in muscle tissue of ISCU Myopathy patients.

Experimental acute alcoholic myopathy-a histochemical study.

Energy Contribution of Octanoate to Intact Rat Brain Metabolism Measured by [sup13]C Nuclear Magnetic Resonance Spectroscopy.

Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity.

Energy deficit in Huntington disease: why it matters.

Relative rates of anaplerotic flux in rested and contracted rat skeletal muscle measured by <sup>13</sup>C NMR spectroscopy.

Role of 5′AMP-activated protein kinase in glycogen synthase activity and glucose utilization: insights from patients with McArdle's disease.

The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle's disease.

The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.

Aerobic conditioning: An effective therapy in McArdle's disease.

A diagnostic cycle test for McArdle's disease.

A nonischemic forearm exercise test for McArdle disease.

Venous oxygen levels during aerobic forearm exercise: An index of impaired oxidative metabolism in mitochondrial myopathy.

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects.

Muscle phosphoglycerate mutase deficiency with tubular aggregates: effect of dantrolene.

Exercise fuel mobilization in mitochondrial myopathy: A metabolic dilemma.

Oxygen Utilization and delivery in metabolic my opathies.

Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients.

Myophosphorylase deficiency impairs muscle oxidative metabolism.

Increased capillaries in mitochondrial myopathy: implications for the regulation of oxygen delivery.

Splice mutations preserve myophosphorylase activity that ameliorates the phenotype in McArdle disease.

Resistance training in patients with single, large-scale deletions of mitochondrial DNA.

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

Pathological mechanisms underlying single large-scale mitochondrial DNA deletions.

No effect of triheptanoin on exercise performance in McArdle disease.

Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle.

Reproducibility and Absolute Quantification of Muscle Glycogen in Patients with Glycogen Storage Disease by <sup>13</sup>C NMR Spectroscopy at 7 Tesla.

Dynamic monitoring of carnitine and acetylcarnitine in the trimethylamine signal after exercise in human skeletal muscle by 7T <sup>1</sup>H-MRS.

OxPhos defects cause hypermetabolism and reduce lifespan in cells and in patients with mitochondrial diseases.

Use of antisense oligonucleotides to correct the splicing error in ISCU myopathy patient cell lines.

Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron–sulfur cluster depletion in human skeletal muscle.

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle.

McArdle's disease presenting with asymmetric, late-onset arm weakness.

Magnetic resonance imaging of muscle injury and atrophy in glycolytic myopathies.