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001			88163
003			ES-MaUEC
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008			161201s2016 gw | s |||| 0|eng d
020			_a9783319442037
024	7		_a10.1007/978-3-319-44203-7 _2doi
040			_aES-MaUEC
050		4	_aRC669 _b2016 EB
245	0	0	_aClinical Cardiogenetics _cedited by Hubert F. Baars, Pieter A. F. M. Doevendans, Arjan C. Houweling, J. Peter van Tintelen
250			_a2nd ed. 2017
260			_aCham, Switzerland _bSpringer _c2016
300			_a1 recurso en línea (VIII, 405 p.) _b93 ilustraciones, 55 ilustraciones en color
336			_aTexto (visual) _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
505	0		_aMolecular Genetics -- Clinical genetics -- Differential diagnosis of cardiomyopathies -- Hypertrophic Cardiomyopathy -- Dilated Cardiomyopathy -- Arrhythmogenic Cardiomyopathy -- Non-Compaction Cardiomyopathy -- Hereditary neuromuscular diseases and cardiac involvement -- Fabry disease -- Long QT Syndrome -- Brugada Syndrome -- Short QT Syndrome -- Cathecholaminergic Polymorphic VT -- Sudden death and Idiopathic Ventricular Fibrillation -- Thoracic Aortic Aneurysm Dissection -- Bicuspid aortic valve -- Premature coronary artery disease
520			_aThis extensively revised second edition provides a thorough basic knowledge on the genetic aspects of cardiovascular disorders. Many cardiologists have not been specifically trained in genetics, let alone in explaining genetics to their patients. While clinics for cardiogenetic disorders have been established in many academic teaching hospitals, it is neither desirable nor feasible that the care for this large group of patients and their relatives remains solely restricted to this small number of centers. This book reviews the expertise that all cardiologists, clinical and molecular geneticists, genetic nurses, and social workers need to provide optimal care for individuals with cardiac disease of probable genetic origin and their family members. Clinical Cardiogenetics, Second Edition, compiles the huge amount of information available in a single easy-to-read textbook. It does not require prior expert genetic knowledge and provides a practical clinical primer for cardiologists and other physicians involved in the management of these patients. With the continuing increase in genetic knowledge, and the expanding possibilities to prevent fatal arrhythmias in those individuals at high risk, a steady increase in questions regarding genetics from patients and their relatives in the years to come should be expected. This comprehensive textbook is a valuable tool in dealing with such questions
942			_2lcc _cLE
650	0	7	_aAparato circulatorio _xEnfermedades _0LocalZ _2embne _9169062
700	1		_aBaars, Hubert F. _eeditor literario _0Local _9101654
700	1		_aDoevendans, Pieter A. F. M. _eeditor literario _9101655 _0Local
700	1		_aHouweling, Arjan C. _eeditor literario _9101656 _0Local
700	1		_avan Tintelen, J. Peter. _eeditor literario _9101657 _0Local
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-44203-7zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
901			_ai9783319442037
907			_a.b12981679 _b10-10-17 _c08-03-17
988			_aSpringer_Medicine_2016
998			_am _a_alco _a_vill _b28-07-17 _cm _dz _eu _feng _ggw _h0
945			_aRC669 .C55 2016 EB _g1 _ieBOOK _j0 _lmae _o- _pEUR0.00 _q- _r- _sb _t15 _u0 _v0 _w0 _x0 _y.i11603513 _z06-04-17
999			_c88163 _d88163 _x1