000			03335nam a22003735i 4500
001			99841
003			DE-He213
005			20230110040153.0
007			cr nn 008mamaa
008			180725s2018 gw | s |||| 0|eng d
020			_a9783319767239 _9
024	7		_a10.1007/978-3-319-76723-9 _2doi
040			_aES-MaUEC _bspa
050		4	_aRC633 2018 EB
245	1	0	_aCongenital Bleeding Disorders: _bDiagnosis and Management _cedited by Akbar Dorgalaleh.
264		1	_aCham, Switzerland _bSpringer International Publishing _c2018
300			_a1 recurso en línea (XIV, 396 páginas 93 ilustraciones, 85 ilustraciones a color)
336			_2rdacontent _aTexto _btxt
337			_2rdamedia _aelectrónico _bc
338			_2rdacarrier _arecurso electrónico _bcr
347			_atext file _bPDF
505	0		_aPart I: Common bleeding disorders -- 1. Von Willebrand disease -- 2. Hemophilia A (congenital factor VIII deficiency) -- 3. Hemophilia B (congenital factor IX deficiency) Part II: Rare bleeding disorders -- 4. Congenital factor I (fibrinogen) disorders -- 5. Congenital factor II deficiency -- 6. Congenital factor V deficiency -- 7. Combined coagulation factor deficiencies -- 8. Congenital factor VII deficiency -- 9. Congenital factor X deficiency -- 10. Congenital factor XI deficiency -- 11. Congenital factor XIII deficiency Part III: Inherited platelet function disorders -- 12. Glanzmann thrombasthenia -- 13. Bernard-Soulier syndrome -- 14. Gray platelet syndrome -- 15. Quebec platelet disorder. .
520	3		_aThis book describes in detail the clinical presentation, diagnosis, and management of a wide range of congenital bleeding disorders. It will assist readers in overcoming the significant challenges involved in clinical and laboratory diagnosis and in providing effective clinical care that makes optimal use of new products, including recombinant factor concentrate. The coverage ranges from hemophilia A and B and von Willebrand disease to rare bleeding disorders such as congenital factor V, factor X, factor XI, and factor XIII deficiency and inherited platelet function disorders. The exceptional attention to rarer conditions is of particular importance given the considerable risk of overlooking them during diagnosis, with potential consequences for disease-related morbidity and mortality. The authors are acknowledged specialists in the field from across the world who have particular expertise in the disorder that they discuss. The book will be of value to hematologists, oncologists, pediatricians, laboratory specialists and technicians, general physicians, and trainees. .
650		7	_9140122 _aHematología _2embne
650		7	_9169169 _aSangre _xEnfermedades _2embne
700	1		_aDorgalaleh, Akbar. _eeditor literario
710	2		_aSpringerLink (Online service) _0http://id.loc.gov/authorities/names/no2005046756 _0http://viaf.org/viaf/148105729 _9106996
776	0	8	_iEdición impresa: _z9783319767222
776	0	8	_iEdición impresa: _z9783319767246
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-319-76723-9 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
490	0		_aMedicine (Springer-11650)
988			_aSpringer_Medicine_2018
998			_b01/2019 _dz _ea _feng _ggw _h0
999			_c99841 _d99841 _x1