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005			20231010110650.0
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008			230117s2018 enka fob 001|0|eng|d
020			_a9781910797891 (PDF ebook) : _cNo price
020			_z9781910797884 (pbk.) : _cNo price
020			_z9781910797891
040			_aStDuBDS _beng _cStDuBDS _erda _epn
060		4	_aWH 322
100	1		_aGlader, Bertil E., _d1939- _eauthor.
245	1	0	_aPyruvate kinase deficiency / _h[e-book]
250			_aFirst edition.
264		1	_aAbingdon, Oxford : _bKarger, _c2018.
300			_a1 online resource (64 pages) : _billustrations (colour).
490	1		_aFast facts
500			_aAlso issued in print: 2018.
504			_aIncludes bibliographical references and index.
520	8		_aYou may be unfamiliar with pyruvate kinase (PK) deficiency. It is a rare inherited enzyme disorder that affects the glycolytic pathway used by red blood cells to generate energy, manifesting as hemolytic anemia. The symptoms vary greatly between individuals, making diagnosis difficult, and management primarily comprises supportive treatments. Written by experts in the field, this book provides a comprehensive introduction to the condition.
521			_aSpecialized.
588			_aDescription based on online resource; title from PDF title page (viewed on January 17, 2023).
650		0	_aBlood _xDiseases.
650		0	_aMetabolism _xDisorders.
650		2	_aHematologic Diseases.
700	1		_aBarcellini, Wilma, _eauthor.
700	1		_aGrace, Rachael, _eauthor.
830		0	_aFast facts.
856	4	0	_uhttps://app.kortext.com/Shibboleth.sso/Login?entityID=https://idp.eng.nhs.uk/openathens&target=https://app.kortext.com/borrow/2133328 _yEligible NHS OpenAthens account holders click here for access
999			_c96842 _d96842