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008			100301s2010 xxk| s |||| 0|eng d
020			_a9781848829275 _9978-1-84882-927-5
040			_cMX-MeUAM
050		4	_aRC681-688.2
082	0	4	_a616.12 _223
100	1		_aBrugada, Ramon. _eeditor.
245	1	0	_aClinical Approach to Sudden Cardiac Death Syndromes _h[recurso electrónico] / _cedited by Ramon Brugada.
264		1	_aLondon : _bSpringer London, _c2010.
300			_aXVI, 340 p. _bonline resource.
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
347			_atext file _bPDF _2rda
505	0		_aSudden Unexplained Death -- Sudden Unexplained Death in the Community -- Sudden Infant Death Syndrome: Gene-Environment Interactions -- Arrhythmias and sudden cardiac death. The initial investigation -- Unexplained Syncope -- Arrhythmias and Sudden Cardiac Death in Adult Congenital Heart Disease -- Endurance Sport Practice and Arrhythmias -- Electrocardiograms Not to Miss -- Sudden Cardiac Death in Forensic Pathology -- Cardiac genetic syndromes -- Genetic Studies -- The Long QT Syndrome -- Brugada Syndrome -- Short QT Syndrome -- Catecholaminergic Polymorphic Ventricular Tachycardia -- Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia -- Atrial Fibrillation -- Dilated Cardiomyopathy -- Hypertrophic Cardiomyopathy -- Genetic Lipoprotein Disorders and Cardiovascular Disease -- A Systematic Approach to Marfan Syndrome and Hereditary Forms of Aortic Dilatation and Dissection -- Inherited Metabolic Diseases: Emphasis on Myocardial Disease and Arrhythmogenesis -- Clinical Genetics in Congenital Heart Disease -- Polygenic cardiovascular genetics -- Pharmacogenomics -- Polygenic Studies in the Risk of Arrhythmias -- The Genetic Challenge of Coronary Artery Disease -- Ethical, legal and Social implications -- Psychological Implications of Genetic Investigations -- Participation in Recreational Sports for Young Patients with Genetic Cardiovascular Diseases -- Genetic Counseling in Cardiovascular Conditions.
520			_aClinical cardiologists are encountering an important challenge in the care of families with inherited cardiac diseases. The majority of the inherited cardiac diseases causing sudden death express themselves at variable ages in the form of altered muscle function – for instance hypertrophic or dilated cardiomyopathy – or in the form of arrhythmias, including Brugada syndrome and long QT syndrome. Clinical and genetic research is continuously ongoing not only to identify those at risk but also to better define their level of risk. Deciding on the most appropriate clinical tests is a challenge in inherited diseases. It is in this situation that specialized clinical-genetic clinics have appeared to provide a complete assessment of patients and family members. The clinicians in the community, faced with a growing number of questions and doubts in the caring of these individuals, are increasingly using the expertise of these centers to address the clinical decisions in their patients. Clinical Approach to Sudden Cardiac Death Syndromes details the main guidelines to clinicians on how to approach the patients and family members with an inherited disease. It also includes an in-depth review of what is currently available to assist in the diagnosis, prevention and risk stratification in sudden cardiac death. This book is therefore an essential reference for all cardiologists and electrophysiologists, but also this will be important reading for general practice physicians who may be responsible for the identification of families at risk.
650		0	_aMedicine.
650		0	_aEmergency medicine.
650		0	_aFamily medicine.
650		0	_aInternal medicine.
650		0	_aCardiology.
650		0	_aSports medicine.
650		0	_aEpidemiology.
650	1	4	_aMedicine & Public Health.
650	2	4	_aCardiology.
650	2	4	_aInternal Medicine.
650	2	4	_aEmergency Medicine.
650	2	4	_aGeneral Practice / Family Medicine.
650	2	4	_aSports Medicine.
650	2	4	_aEpidemiology.
710	2		_aSpringerLink (Online service)
773	0		_tSpringer eBooks
776	0	8	_iPrinted edition: _z9781848829268
856	4	0	_zLibro electrónico _uhttp://148.231.10.114:2048/login?url=http://link.springer.com/book/10.1007/978-1-84882-927-5
596			_a19
942			_cLIBRO_ELEC
999			_c200660 _d200660