Results 261 to 270 of about 1,349,150 (316)
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Journal of Inherited Metabolic Disease, 1990
SummaryThis review describes clinical, biochemical and genetic features of the four inborn errors affecting muscle glycogen breakdown, namely deficiencies of phosphorylase, phosphorylase kinase, amylo‐1,6‐glucosidase and acid α‐glucosidase. They are characterized by a wide spectrum of clinical manifestation, affecting age of onset, clinical features ...
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SummaryThis review describes clinical, biochemical and genetic features of the four inborn errors affecting muscle glycogen breakdown, namely deficiencies of phosphorylase, phosphorylase kinase, amylo‐1,6‐glucosidase and acid α‐glucosidase. They are characterized by a wide spectrum of clinical manifestation, affecting age of onset, clinical features ...
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MUSCLE HISTOCHEMISTRY AND MUSCLE FUNCTION
Acta Paediatrica, 1980Abstract. Henriksson, K. G. (Neuromuscular Unit, Department of Neurology, Clinical Neurophysiology and Pathology I, University of Linköping, Linköping, Sweden). Muscle histochemistry and muscle function. Acta Paediatr Scand, Suppl. 283: 15, 1980.—A short review of the histochemical characteristics of the different muscle fibre types is given.
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Muscle conditioning and muscle injuries
Medicine & Science in Sports & Exercise, 1990Empirical and objective data suggest that muscle and connective tissue can undergo adaptations to physical training resulting in greater tissue mass and increased maximum tensile strength. These adaptations are especially apparent as a result of load bearing and resistive training.
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Continuum, 2022
This article describes the clinical features, diagnosis, pathophysiology, and management of nondystrophic myotonia and periodic paralysis.An increasing awareness exists about the genotype-phenotype overlap in skeletal muscle channelopathies, and thus genetic testing is needed to make a definitive diagnosis.
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This article describes the clinical features, diagnosis, pathophysiology, and management of nondystrophic myotonia and periodic paralysis.An increasing awareness exists about the genotype-phenotype overlap in skeletal muscle channelopathies, and thus genetic testing is needed to make a definitive diagnosis.
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Current Opinion in Rheumatology, 1995
Muscle biopsy remains a critical component in the evaluation of myopathies. Recent literature demonstrates that percutaneous biopsy instruments can effectively procure muscle tissue for analysis in clinical and research settings. We review issues of muscle biopsy technique and specimen processing in the context of available clinical methods for tissue ...
K S, O'Rourke, R W, Ike
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Muscle biopsy remains a critical component in the evaluation of myopathies. Recent literature demonstrates that percutaneous biopsy instruments can effectively procure muscle tissue for analysis in clinical and research settings. We review issues of muscle biopsy technique and specimen processing in the context of available clinical methods for tissue ...
K S, O'Rourke, R W, Ike
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MUSCLE ACTIVITY and MUSCLE PROTEINS
Biological Reviews, 1950Summary1. If it were experimentally possible to examine muscle extracts made during defined phases of the contraction cycle, the relation of muscular work to changes in the composition of such extracts might then be elucidated. The changes of normal muscle proteins in relation to muscular function, could then be considered from a truly physiological ...
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Muscle & Nerve, 2001
AbstractThere are 11 hereditary disorders of glycogen metabolism affecting muscle alone or together with other tissues, and they cause two main clinical syndromes: episodic, recurrent exercise intolerance with cramps, myalgia, and myoglobinuria; or fixed, often progressive weakness.
S, DiMauro, C, Lamperti
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AbstractThere are 11 hereditary disorders of glycogen metabolism affecting muscle alone or together with other tissues, and they cause two main clinical syndromes: episodic, recurrent exercise intolerance with cramps, myalgia, and myoglobinuria; or fixed, often progressive weakness.
S, DiMauro, C, Lamperti
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Best Practice & Research Clinical Anaesthesiology, 2003
Studies on the toxic effects of muscle relaxants are difficult to design because of the need for mechanical ventilation and, consequently, concomitant administration of anaesthetic drugs which may influence the results. The following overview shows that muscle relaxants are weak toxic agents with regard to their teratogenicity, carcinogenicity and ...
Sandra, Kampe +2 more
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Studies on the toxic effects of muscle relaxants are difficult to design because of the need for mechanical ventilation and, consequently, concomitant administration of anaesthetic drugs which may influence the results. The following overview shows that muscle relaxants are weak toxic agents with regard to their teratogenicity, carcinogenicity and ...
Sandra, Kampe +2 more
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Journal of Craniofacial Surgery, 2005
The aim of this study was to elucidate the precise anatomy of the zygomaticomandibularis muscle through cadaveric dissection and magnetic resonance imaging (MRI). Five fresh human cadavers and 10 fixed cadavers were dissected. Nine preserved human cadavers were used for the MRI study.
Kun, Hwang +4 more
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The aim of this study was to elucidate the precise anatomy of the zygomaticomandibularis muscle through cadaveric dissection and magnetic resonance imaging (MRI). Five fresh human cadavers and 10 fixed cadavers were dissected. Nine preserved human cadavers were used for the MRI study.
Kun, Hwang +4 more
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Canadian Journal of Applied Physiology, 1998
In this review, the term muscle fibre regionalization signifies the presence of regional intramuscular differences in fibre type composition. As is well known, highly regionalized muscles commonly have greater concentrations of slow fibres deep than superficially.
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In this review, the term muscle fibre regionalization signifies the presence of regional intramuscular differences in fibre type composition. As is well known, highly regionalized muscles commonly have greater concentrations of slow fibres deep than superficially.
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