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001467641 001__ 1467641
001467641 003__ OCoLC
001467641 005__ 20230707003332.0
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001467641 008__ 110119s2011\\\\enka\\\\ob\\\\001\0\eng\d
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001467641 020__ $$a9781849964715$$q(electronic bk.)
001467641 020__ $$a1849964718$$q(electronic bk.)
001467641 020__ $$z9781849964708$$q(print)
001467641 020__ $$z184996470X$$q(print)
001467641 0247_ $$a10.1007/978-1-84996-471-5$$2doi
001467641 0248_ $$a9786613087430
001467641 035__ $$aSP(OCoLC)697508605
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001467641 049__ $$aISEA
001467641 050_4 $$aRC669$$b.B33 2011
001467641 08204 $$a616.1042$$222
001467641 24500 $$aClinical cardiogenetics /$$cH.F. Baars, J.J. van der Smagt, P.A.F.M. Doevandans (editors).
001467641 260__ $$aLondon :$$bSpringer,$$c©2011.
001467641 300__ $$a1 online resource (xv, 455 pages) :$$billustrations (some color)
001467641 336__ $$atext$$btxt$$2rdacontent
001467641 337__ $$acomputer$$bc$$2rdamedia
001467641 338__ $$aonline resource$$bcr$$2rdacarrier
001467641 347__ $$atext file$$bPDF$$2rda
001467641 504__ $$aIncludes bibliographical references and index.
001467641 5050_ $$aIntroduction to molecular genetics -- Clinical genetics -- Hypertrophic cardiomyopathy -- Familial dilated cardiomyopathy -- Arrhythmogenic right ventricular dysplasia/cardiomyopathy from desmosome to disease -- Noncompaction cardiomyopathy -- Mitochondrial cardiomyopathy -- Restrictive cardiomyopathy -- Congenital long QT-syndrome -- The Brugada syndrome -- Short QT syndrome -- Catecholaminergic polymorphic ventricular tachycardia -- A molecular genetic perspective on atrial fibrillation -- Idiopathic ventricular fibrillation -- The genetics of mitral valve prolapse -- Atrioventricular (AV) reentry tachycardia -- Hereditary cardiac conduction diseases -- Connective tissue disorders and smooth muscle disorders in cardiology -- Genetics of congenital heart defects -- Genetic disorders of the lipoprotein metabolism: diagnosis and management -- Novel insights into genetics of arterial thrombosis -- The pharmacogenetics of atherosclerosis -- Genetics of (premature) coronary artery disease -- Heredity neuromuscular diseases and cardiac involvement -- Sudden cardiac death in the young: epidemiology and cardiogenetic evaluation of victims and their relatives -- The outpatient clinics for cardiogenetics -- Abdominal aortic aneurysm -- Future of cardiogenetics.
001467641 506__ $$aAccess limited to authorized users.
001467641 520__ $$aClinical management and signs are the focus of this practical cardiogenetic reference for those who are involved in the care for cardiac patients with a genetic disease. With detailed discussion of the basic science of cardiogenetics in order to assist in the clinical understanding of the topic. The genetic causes of various cardiovascular diseases are explained in a concise clinical way that reinforces the current management doctrine in a practical manner. The authors will cover the principles of molecular genetics in general but also specific to cardiac diseases. They will discuss the etiolo.
001467641 588__ $$aDescription based on print version record.
001467641 650_0 $$aCardiovascular system$$xDiseases$$xGenetic aspects.
001467641 650_6 $$aAppareil cardiovasculaire$$xMaladies$$xAspect génétique.
001467641 655_0 $$aElectronic books.
001467641 7001_ $$aBaars, H. F.
001467641 7001_ $$aSmagt, J. J. van der.
001467641 7001_ $$aDoevendans, Pieter A.
001467641 7730_ $$tSpringer eBooks
001467641 77608 $$iPrint version:$$aBaars, H.F.$$tClinical cardiogenetics.$$dLondon : Springer, 2010$$z9781849964708$$w(OCoLC)646114767
001467641 852__ $$bebk
001467641 85640 $$3Springer Nature$$uhttps://univsouthin.idm.oclc.org/login?url=https://link.springer.com/10.1007/978-3-319-44203-7$$zOnline Access$$91397441.1
001467641 909CO $$ooai:library.usi.edu:1467641$$pGLOBAL_SET
001467641 980__ $$aBIB
001467641 980__ $$aEBOOK
001467641 982__ $$aEbook
001467641 983__ $$aOnline
001467641 994__ $$a92$$bISE