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Cardiovascular Genetics and Genomics: Principles and Clinical Practice Softcover reprint of the original 1st ed. 2018 [Pehme köide]

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  • Formaat: Paperback / softback, 920 pages, kõrgus x laius: 235x155 mm, kaal: 1893 g, 110 Illustrations, color; 54 Illustrations, black and white; XIX, 920 p. 164 illus., 110 illus. in color., 1 Paperback / softback
  • Ilmumisaeg: 20-Mar-2019
  • Kirjastus: Springer International Publishing AG
  • ISBN-10: 3319881795
  • ISBN-13: 9783319881799
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  • Formaat: Paperback / softback, 920 pages, kõrgus x laius: 235x155 mm, kaal: 1893 g, 110 Illustrations, color; 54 Illustrations, black and white; XIX, 920 p. 164 illus., 110 illus. in color., 1 Paperback / softback
  • Ilmumisaeg: 20-Mar-2019
  • Kirjastus: Springer International Publishing AG
  • ISBN-10: 3319881795
  • ISBN-13: 9783319881799
Teised raamatud teemal:

This title reflects the exponential growth in the knowledge and information on this subject and defines the extensive clinical translation of cardiovascular genetics and genomics in clinical practice. This concise, clinically oriented text is targeted at a broad range of clinicians who manage patients and families with a wide range of heterogeneous inherited cardiovascular conditions.

Cardiovascular Genetics and Genomics: Principles and Clinical Practice includes a concise and clear account on selected topics written by a team of leading experts on clinical cardiovascular genetics. Each chapter include key information to assist the clinician and case histories have been incorporated to reflect contemporary practice in clinical cardiovascular genetics and genomics. Therefore this will be of key importance to all professionals working in the discipline, from clinicians and trainees in cardiology, cardiac surgery, electrophysiology, immunology through geneticists, nursing staff and those involved in precision medicine.

Arvustused

This compendium of 31 contributed chapters by recognized authorities in the field of cardiovascular genetics is a detailed, consultative resource for healthcare providers involved in the management of patients affected by genetic disorders of the cardiovascular system. This is eminently a clinical textbook. This is an outstanding contribution to the clinical world of genetic cardiovascular disorders, and clearly a unique resource. (Luis F Escobar, Doody's Book Reviews, February, 2019)

1 Introduction to Genes, Genome and Inheritance
1(34)
Dhavendra Kumar
2 Spectrum and Classification of Inherited Cardiovascular Disease
35(36)
Paul Brennan
3 Principles and Practice of Genetic Counselling for Inherited Cardiac Conditions
71(26)
Sharon Jenkins
Caroline Kirwan
4 Genetic and Genomic Technologies: Next Generation Sequencing for Inherited Cardiovascular Conditions
97(22)
Lorenzo Monserrat
5 Pharmacogenetics and Pharmacogenomics in Cardiovascular Medicine and Surgery
119(54)
Richard Myles Turner
Sir Munir Pirmohamed
6 Congenital Cardiovascular Disorders
173(16)
Dirk G. Wilson
7 Inherited Cardiovascular Metabolic Disorders
189(50)
Elaine Murphy
Oliver Watkinson
8 Mitochondrial Cardiovascular Diseases
239(20)
Michael J. Keogh
Hannah E. Steele
Patrick F. Chinnery
9 Inherited Cardiac Muscle Disorders: Hypertrophic and Restrictive Cardiomyopathies
259(60)
Mohammed Majid Akhtar
Juan Pablo Kaski
Perry Elliott
10 Inherited Cardiac Muscle Disease: Dilated Cardiomyopathy
319(48)
Eloisa Arbustini
Lorenzo Giuliani
Alessandro Di Toro
Valentina Favalli
11 Inherited Cardiac Muscle Disorders: Arrhythmogenic Right Ventricular Cardiomyopathy
367(22)
Kalliopi Pilichou
Barbara Bauce
Gaetano Thiene
Cristina Basso
12 Inherited Cardiac Muscle Disorders: Left Ventricular Noncom paction
389(24)
James Marangou
Michael Frenneaux
Girish Dwivedi
13 Inherited Arrhythmias: LQTS/SQTS/CPVT
413(24)
Andrea Mazzanti
Silvia G. Priori
14 Inherited Arrhythmias: Brugada Syndrome and Early Repolarisation Syndrome
437(44)
Pieter G. Postema
Krystien V.V. Lieve
Arthur A.M. Wilde
15 Inherited Conduction Disease and Atrial Fibrillation
481(42)
Claire Martin
Pier Lambiase
16 Cardiovascular Manifestations in Duchenne/Becker Muscular Dystrophy and Other Primary Myopathies
523(22)
Douglas A. Stoller
Pradeep P.A. Mammen
17 Familial Cardiac Amyloidoses
545(34)
Claudio Rapezzi
Christian Gagliardi
Fabrizio Salvi
Ilaria Bartolomei
Candida Cristina Quarta
Agnese Milandri
18 Cardiovascular Manifestations of Myotonic Dystrophy
579(10)
Umesh Vivekananda
Michael Hanna
Chris Turner
19 Marfan Syndrome and Related Disorders
589(28)
John C.S. Dean
Bart Loeys
20 Cardiovascular Manifestations in Inherited Connective Tissue Disorders
617(30)
Julie de Backer
Anne de Paepe
21 Thoracic Aortic Dilatation, Aneurysm and Dissection
647(14)
Michael Ibrahim
Nimesh D. Desai
22 Genetics and Genomics of Coronary Artery Disease
661(18)
Yoshiji Yamada
Yoshiki Yasukochi
23 Cardiovascular Manifestations of Immune-Mediated Inflammatory Disorders
679(16)
Anna Abou-Raya
Suzan Abou-Raya
24 Genetics and Genomics of Stroke
695(28)
Rhea Y.Y. Tan
Hugh S. Markus
25 Genetics and Genomics of Systemic Hypertension
723(18)
Patricia B. Munroe
Syeda N.S. Jahangir
Mark J. Caulfield
26 Inherited Pulmonary Arterial Hypertension
741(14)
Sophie Herbert
Robert M.R. Tulloh
27 Genetics and Genomics of Sudden Unexplained Cardiac Death----
755(26)
Efstathios Papatheodorou
Mary N. Sheppard
Elijah R. Behr
28 Specific Issues in Clinical Genetics and Genetic Counselling Practices Related to Inherited Cardiovascular Conditions
781(36)
Angus Clarke
Siv Fokstuen
29 Multi-Disciplinary Management of Inherited Cardiovascular Conditions
817(22)
Gerry Carr-White
Robert Leema
30 Interventions and Implantable Devices for Inherited Cardiac Conditions
839(30)
Zaheer Yousef
Mark Drury-Smith
31 Inherited Cardiovascular Conditions: Phenotype-Genotype Data Mining and Sharing, and Databases
869(10)
J. Peter van Tintelen
Paul A. van der Zwaag
Glossary: Commonly Used Terms and Phrases in Cardiovascular Genetics and Genomics 879(2)
Terms and Phrases 881(20)
Index 901
Professor Dhavendra Kumar is a Consultant in Clinical Genetics at the University Hospital of Wales, Cardiff University, United Kingdom. He is the lead Clinical Geneticist for Clinical Cardiovascular Genetics. He is the Visiting Professor to the Genomic Policy Unit at the University of South Wales, UK, the Adjunct Professor to the Public Health Genetics Unit at the Chinese Capital Medical University, Beijing (China) and Visiting Professor/ Chief Guest of the prestigious Ranbaxy Science Foundation, India.





Internationally renowned expert in cardiovascular genetics and genomics. Professor Perry Elliott is recognized for his lead contributions in different forms of inherited cardiomyopathies, particularly familial hypertrophic and dilated cardiomyopathy. His current roles include the Deputy Editor of the BMJ journal Heart and co-editor/author of Principles and Practice of Clinical Cardiovascular Genetics & Oxford Specialist Handbook Inherited Cardiac Disease.