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Fat metabolism during exercise in patients with McArdle disease

Neurology, 2009-02, Vol.72 (8), p.718-724

2009

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Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA

Neurology, 2000-09, Vol.55 (5), p.644-649

2000

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The Effect of Oral Sucrose on Exercise Tolerance in Patients with McArdle's Disease

The New England journal of medicine, 2003-12, Vol.349 (26), p.2503-2509

2003

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

Human molecular genetics, 2009-09, Vol.18 (17), p.3194-3205

2009

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Exercise and training in mitochondrial myopathies

Medicine and science in sports and exercise, 2005-12, Vol.37 (12), p.2094-2101

2005

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Submaximal delayed-onset muscle soreness: correlations between MR imaging findings and clinical measures

Radiology, 1998-09, Vol.208 (3), p.815-820

1998

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Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency

The Journal of biological chemistry, 2003-10, Vol.278 (44), p.43081-43088

2003

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Reduced levels of skeletal muscle Na+K+ -ATPase in McArdle disease

Neurology, 1998-01, Vol.50 (1), p.37-40

1998

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

Annals of neurology, 2001-08, Vol.50 (2), p.133-141

2001

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Muscle phosphoglycerate mutase deficiency with tubular aggregates: Effect of dantrolene

Annals of neurology, 1999-08, Vol.46 (2), p.274-277

1999

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Sympathetic activation in exercise is not dependent on muscle acidosis. Direct evidence from studies in metabolic myopathies

The Journal of clinical investigation, 1998-04, Vol.101 (8), p.1654-1660

1998

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A modular NIRS system for clinical measurement of impaired skeletal muscle oxygenation

Journal of applied physiology (1985), 2000-01, Vol.88 (1), p.315-325

2000

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Oral branched-chain amino acids do not improve exercise capacity in McArdle disease

Neurology, 1998-11, Vol.51 (5), p.1456-1459

1998

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Exercise fuel mobilization in mitochondrial myopathy: A metabolic dilemma

Annals of neurology, 1996-10, Vol.40 (4), p.655-662

1996

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

Muscle & nerve, 2000-04, Vol.23 (4), p.641-645

2000

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Absence of exercise-induced MRI enhancement of skeletal muscle in McArdle's disease

Journal of applied physiology (1985), 1991-09, Vol.71 (3), p.961-969

1991

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Effect of deficient muscular glycogenolysis on extramuscular fuel production in exercise

Journal of applied physiology (1985), 1992-05, Vol.72 (5), p.1773-1779

1992

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Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency : abnormalities of several iron-sulfur proteins

The Journal of clinical investigation, 1993-12, Vol.92 (6), p.2660-2666

1993

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Mitochondrial encephalomyopathy with coenzyme Q10 deficiency

Neurology, 1997-05, Vol.48 (5), p.1238

1997

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Tricarboxylic acid cycle intermediates during incremental exercise in healthy subjects and in patients with McArdle's disease

Clinical science (1979), 1995-06, Vol.88 (6), p.687-693

1995

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Deficiency of skeletal muscle succinate dehydrogenase and aconitase : pathophysiology of exercise in a novel human muscle oxidative defect

The Journal of clinical investigation, 1991-10, Vol.88 (4), p.1197-1206

1991

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The pathophysiology of McArdle's disease: clues to regulation in exercise and fatigue

Journal of applied physiology (1985), 1986-08, Vol.61 (2), p.391-401

1986

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Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency

The Journal of clinical investigation, 1989-07, Vol.84 (1), p.155-161

1989

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Splice Mutation in the Iron-Sulfur Cluster Scaffold Protein ISCU Causes Myopathy with Exercise Intolerance

American journal of human genetics, 2008-03, Vol.82 (3), p.652-660

2008

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Paradoxically enhanced glucose production during exercise in humans with blocked glycolysis caused by muscle phosphofructokinase deficiency

Neurology, 1996-09, Vol.47 (3), p.766-771

1996

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Fat metabolism during exercise in patients with McArdle disease

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA

The Effect of Oral Sucrose on Exercise Tolerance in Patients with McArdle's Disease

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

Exercise and training in mitochondrial myopathies

Submaximal delayed-onset muscle soreness: correlations between MR imaging findings and clinical measures

Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency

Reduced levels of skeletal muscle Na+K+ -ATPase in McArdle disease

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

Muscle phosphoglycerate mutase deficiency with tubular aggregates: Effect of dantrolene

Sympathetic activation in exercise is not dependent on muscle acidosis. Direct evidence from studies in metabolic myopathies

A modular NIRS system for clinical measurement of impaired skeletal muscle oxygenation

Oral branched-chain amino acids do not improve exercise capacity in McArdle disease

Exercise fuel mobilization in mitochondrial myopathy: A metabolic dilemma

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

Absence of exercise-induced MRI enhancement of skeletal muscle in McArdle's disease

Effect of deficient muscular glycogenolysis on extramuscular fuel production in exercise

Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency : abnormalities of several iron-sulfur proteins

Mitochondrial encephalomyopathy with coenzyme Q10 deficiency

Tricarboxylic acid cycle intermediates during incremental exercise in healthy subjects and in patients with McArdle's disease

Deficiency of skeletal muscle succinate dehydrogenase and aconitase : pathophysiology of exercise in a novel human muscle oxidative defect

The pathophysiology of McArdle's disease: clues to regulation in exercise and fatigue

Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency

Splice Mutation in the Iron-Sulfur Cluster Scaffold Protein ISCU Causes Myopathy with Exercise Intolerance

Paradoxically enhanced glucose production during exercise in humans with blocked glycolysis caused by muscle phosphofructokinase deficiency

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