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dc.contributor.authorMoore, D M
dc.contributor.authorNadarajan, P
dc.contributor.authorHawksworth, R
dc.contributor.authorLane, S J
dc.contributor.authorGraham, I M
dc.date.accessioned2011-07-25T13:35:01Z
dc.date.available2011-07-25T13:35:01Z
dc.date.issued2011-05
dc.identifier.citationExercise induced fatigue: unfit or unwell? 2011, 104 (5):151 Ir Med Jen
dc.identifier.issn0332-3102
dc.identifier.pmid21736093
dc.identifier.urihttp://hdl.handle.net/10147/136851
dc.description.abstractThis case report outlines the diagnoses of a rare myophosphorylase deficiency (McArdle Syndrome) in a unique way. A set of characteristic values from a Cardiopulmonary Exercise Test (CPET) combined with a typical patient history pointed to a failure of the glycolytic pathway in the skeletal muscle. McArdle Syndrome was confirmed with a skeletal muscle biopsy. There is no evidence of such a diagnostic method in the literature.
dc.language.isoenen
dc.titleExercise induced fatigue: unfit or unwell?en
dc.typeArticleen
dc.contributor.departmentAMNCH, Tallaght, Dublin 24. mooredm82@googlemail.comen
dc.identifier.journalIrish medical journalen
dc.description.provinceLeinster
refterms.dateFOA2018-08-22T13:14:44Z
html.description.abstractThis case report outlines the diagnoses of a rare myophosphorylase deficiency (McArdle Syndrome) in a unique way. A set of characteristic values from a Cardiopulmonary Exercise Test (CPET) combined with a typical patient history pointed to a failure of the glycolytic pathway in the skeletal muscle. McArdle Syndrome was confirmed with a skeletal muscle biopsy. There is no evidence of such a diagnostic method in the literature.


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