Professor, Neurology, University of Texas Southwestern Medical Center
Neurology
Dr. Ronald G. Haller, MD
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Ronald G. Haller works in the field of Neurology. He researched medicine at University of Washington School of Medicine. Ronald G. Haller is a published doctor. He has 101 papers published. The most current publication "Oral branched-chain amino acids do not improve exercise capacity in McArdle disease."
Publications
- Metabolic and Mitochondrial Myopathies.
- The Effect of Rowing Ergometry and Resistive Exercise on Skeletal Muscle Structure and Function during Bed Rest.
- Elevated FGF21 secretion, PGC-1α and ketogenic enzyme expression are hallmarks of iron-sulfur cluster depletion in human skeletal muscle.
- Dynamic monitoring of carnitine and acetylcarnitine in the trimethylamine signal after exercise in human skeletal muscle by 7T 1H-MRS.
- Increased capillaries in mitochondrial myopathy: implications for the regulation of oxygen delivery.
- Exertional dyspnea in mitochondrial myopathy: clinical features and physiological mechanisms.
- Energy deficit in Huntington Disease: why it matters.
- Posttranslational stability of the heme biosynthetic enzyme ferrochelatase is dependent on iron availability and intact iron-sulfur cluster assembly machinery.
- A randomized clinical trial to assess the effect of statins on skeletal muscle function and performance: rationale and study design.
- A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions.
- Drilling for energy in mitochondrial Disease.
- Effect of changes in fat availability on exercise capacity in McArdle Disease.
- Fat metabolism during exercise in patients with mitochondrial Disease.
- Effect of oral sucrose shortly before exercise on work capacity in McArdle Disease.
- Fueling around with glycogen: the implications of muscle phosphorylase b kinase deficiency.
- Isolated cytochrome c oxidase deficiency in G93A SOD1 mice overexpressing CCS protein.
- Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intolerance.
- The effect of training on the expression of mitochondrial biogenesis- and apoptosis-related proteins in skeletal muscle of patients with mtDNA defects.
- Hypoxia-inducible factor 2alpha regulates expression of the mitochondrial aconitase chaperone protein frataxin.
- Aerobic conditioning: an effective therapy in McArdle's Disease.
- Exercise and training in mitochondrial myopathies.
- Effect of fuels on exercise capacity in muscle phosphoglycerate mutase deficiency.
- No spontaneous second wind in muscle phosphofructokinase deficiency.
- The effect of oral sucrose on exercise tolerance in patients with McArdle's Disease.
- Octanoate oxidation measured by 13C-NMR spectroscopy in rat skeletal muscle, heart, and liver.
- Identification and characterization of a common set of complex I assembly intermediates in mitochondria from patients with complex I deficiency.
- A diagnostic cycle test for McArdle's Disease.
- Energy contribution of octanoate to intact rat brain metabolism measured by 13C nuclear magnetic resonance spectroscopy.
- Spontaneous "second wind" and glucose-induced second "second wind" in McArdle Disease: oxidative mechanisms.
- A nonischemic forearm exercise test for McArdle Disease.
- Decreased insulin action in skeletal muscle from patients with McArdle's Disease.
- Venous oxygen levels during aerobic forearm exercise: An index of impaired oxidative metabolism in mitochondrial myopathy.
- Reproducibility and Absolute Quantification of Muscle Glycogen in Patients with Glycogen Storage Disease by 13C NMR Spectroscopy at 7 Tesla.
- [Multidisciplinary diagnostic approach to Fahr''s syndrome, a familial Disease (author''s transl)].
- [Stereochemistry of conversion of heterocyclic ketones with complex metal hydrides and Grignard-reagents].
- Selective phosphorus deficiency in the hyperalimented hypophosphatemic dog and phosphorylation potentials in the muscle cell.
- [Assignment of the configuration of piperidoneoximes by means of 1 H-NMR-spectroscopy].
- [Lithium alanate reduction of heterocyclic ketoximes].
- [Substituted 3,7-diaza-bicyclo-(3,3,1)-nonane-9-ols].
- [Nuclear resonance spectroscopy study of some tertiary 1-thiaand 1-oxa-cyclohexanols].
- [Results of a study of a family with aggregated occurrence of bilateral symmetrical basal ganglia calcinosis].
- Skeletal muscle Disorders and associated factors that limit exercise performance.
- Experimental acute alcoholic myopathy--a histochemical study.
- Hypophosphatemia and rhabdomyolysis.
- Alcoholic rhabdomyolysis: an experimental model in the rat.
- Pathophysiology of exercise performance in muscle Disease.
- Serum and muscle potassium in experimental alcoholic myopathy.
- MRI evaluation of amyloid myopathy.
- Muscle recruitment variations during wrist flexion exercise: MR evaluation.
- Skeletal muscle Disease in alcoholism.
- Oxygen utilization and delivery in metabolic myopathies.
- A "lipid myopathy" associated with a hyperkinetic circulatory response to exercise.
- Basal and insulin-mediated carbohydrate metabolism in human muscle deficient in phosphofructokinase 1.
- Locomotor system assessment by muscle magnetic resonance imaging.
- Physiologic measurement of exercise and fatigue with special reference to chronic fatigue Syndrome.
- Kinetics of carnitine-dependent fatty acid oxidation: implications for human carnitine deficiency.
- Low muscle levels of pyridoxine in McArdle's Syndrome.
- Mitochondrial myopathy presenting as exercise intolerance.
- Magnetic resonance imaging of muscle injury and atrophy in glycolytic myopathies.
- Hyperkinetic circulation during exercise in neuromuscular Disease.
- Effect of perfusion on exercised muscle: MR imaging evaluation.
- Neuromuscular Diseases as models of cardiovascular regulation during exercise.
- Tricarboxylic acid cycle intermediates during incremental exercise in healthy subjects and in patients with McArdle''s Disease.
- MRI-guided biopsy in inflammatory myopathy: initial results.
- Glycogenolysis, not perfusion, is the critical mediator of exercise-induced muscle modifications on MR images.
- Treatment of McArdle Disease.
- Impaired oxidative metabolism increases adenine nucleotide breakdown in McArdle's Disease.
- Metabolic control of cardiac output response to exercise in McArdle's Disease.
- Muscle fatigue in McArdle's Disease studied by 31P-NMR: effect of glucose infusion.
- The pathophysiology of McArdle's Disease: clues to regulation in exercise and fatigue.
- Abnormal ventilation during exercise in McArdle's Syndrome: modulation by substrate availability.
- Myophosphorylase deficiency impairs muscle oxidative metabolism.
- Submaximal delayed-onset muscle soreness: correlations between MR imaging findings and clinical measures.
- Abnormal high-energy phosphate metabolism in human muscle phosphofructokinase deficiency.
- Glucose-induced exertional fatigue in muscle phosphofructokinase deficiency.
- A modular NIRS system for clinical measurement of impaired skeletal muscle oxygenation.
- Muscle metabolism during lactate infusion in human phosphofructokinase deficiency.
- Impairment of sympathetic activation during static exercise in patients with muscle phosphorylase deficiency (McArdle's Disease).
- Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients.
- Absence of exercise-induced MRI enhancement of skeletal muscle in McArdle's Disease.
- McArdle's Disease presenting with asymmetric, late-onset arm weakness.
- Mitochondrial encephalomyopathy with coenzyme Q10 deficiency.
- Abnormal oxidative metabolism and O2 transport in muscle phosphofructokinase deficiency.
- Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.
- Effect of deficient Muscular glycogenolysis on extraMuscular fuel production in exercise.
- Paradoxically enhanced glucose production during exercise in humans with blocked glycolysis caused by muscle phosphofructokinase deficiency.
- Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.
- Exercise fuel mobilization in mitochondrial myopathy: a metabolic dilemma.
- Muscle phosphoglycerate mutase deficiency with tubular aggregates: effect of dantrolene.
- Fat metabolism during exercise in patients with McArdle Disease.
- Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect.
- The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle''s Disease.
- Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects.
- Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.
- Oral branched-chain amino acids do not improve exercise capacity in McArdle Disease.
- Sympathetic activation in exercise is not dependent on muscle acidosis. Direct evidence from studies in metabolic myopathies.
- Reduced levels of skeletal muscle Na+K+ -ATPase in McArdle Disease.
- Relative rates of anaplerotic flux in rested and contracted rat skeletal muscle measured by 13C NMR spectroscopy.
- The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.
- Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle Muscular dystrophy 2A (calpainopathy).
Schools
University of Washington
Baltimore City Hospital
Johns Hopkins Hospital
Conditions Treated
- Alzheimer's Disease
- Convulsions
- Dementia
- Dystonia
- View All
Doctors Specialties
- Internal Medicine
- Neurology
Accepted Insurances
- Aetna
- Blue Card PPO
- Blue Choice
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Commercial Insurance Company
- First Health (Coventry Health Care) PPO
- GEHA
- Choice Care PPO
- Preferred PPO
- Medicare MCR
- PHCS Network PPO
- Tricare
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Education
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Johns Hopkins University -
Johns Hopkins Bayview Medical Center -
University of Washington School of Medicine
Hospital
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University of Texas Southwestern Medical Center -
Veterans Affairs North Texas Health Care System
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