Metabolic myopathies: functional evaluation by different exercise testing approaches. - Wikidata - wikimedia - TriplyDB

Metabolic myopathies: functional evaluation by different exercise testing approaches.

Metabolic myopathies: functional evaluation by different exercise testing approaches.

http://www.wikidata.org/entity/Q37849644

about

Stepwise approach to myopathy in systemic disease Blood metabolite data in response to maximal exercise in healthy subjects.L-Arginine Affects Aerobic Capacity and Muscle Metabolism in MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes) Syndrome.Diagnostic Algorithm for Glycogenoses and Myoadenylate Deaminase Deficiency Based on Exercise Testing Parameters: A Prospective Study.Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease.Protein Stability, Folding and Misfolding in Human PGK1 Deficiency.Decreased Aerobic Capacity in ANO5-Muscular Dystrophy

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Metabolic myopathies: functional evaluation by different exercise testing approaches.

http://www.wikidata.org/entity/Q37849644

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 04 March 2011

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Metabolic myopathies: functional evaluation by different exercise testing approaches.

@en

Metabolic myopathies: functional evaluation by different exercise testing approaches.

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type

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Metabolic myopathies: functional evaluation by different exercise testing approaches.

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Metabolic myopathies: functional evaluation by different exercise testing approaches.

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Metabolic myopathies: functional evaluation by different exercise testing approaches.

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Metabolic myopathies: functional evaluation by different exercise testing approaches.

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S12306-011-0096-9

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Musculoskeletal surgery

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Metabolic myopathies: functional evaluation by different exercise testing approaches

@en

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D Orsucci

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G Siciliano

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L Volpi

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M Mancuso

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R Alessi

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S Piazza

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P2860

Molecular basis of AMP deaminase deficiency in skeletal muscle

Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria

Skeletal muscle metabolism during exercise in humans

Mitochondrial respiratory-chain diseases

Functional evaluation techniques in mitochondrial disorders.

Insights into muscle diseases gained by phosphorus magnetic resonance spectroscopy.

Glycogen storage diseases: new perspectives.

A nonischemic forearm exercise test for McArdle disease.

The ischaemic lactate-ammonia test.

Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.

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s12306-011-0096-9

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59-67

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scholarly article

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10.1007/S12306-011-0096-9

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2

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95

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Costanza Simoncini

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2011-03-04T00:00:00Z

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21373907

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