Emery and Rimoin’s Principles and Practice of Medical Genetics and Genomics: Cardiovascular, Respiratory, and Gastrointestinal Disorders
Editat de Reed E. Pyeritz, Bruce R. Korf, Wayne W. Grodyen Limba Engleză Hardback – 3 sep 2019
In addition, genetic researchers, students and health professionals will find new and fully revised chapters on the molecular genetics of congenital heart defects, inherited cardiomyopathies, hypertension, cystic fibrosis, asthma, hereditary pulmonary emphysema, inflammatory bowel disease, and bile pigment metabolism disorders among other conditions.
- Offers pathways for diagnosis, prevention and disease management
- Includes color images supporting identification, concept illustration and method processing
- Features contributions by leading international researchers and practitioners of medical genetics
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Specificații
ISBN-13: 9780128125328
ISBN-10: 0128125322
Pagini: 594
Dimensiuni: 191 x 235 x 36 mm
Ediția:7
Editura: ELSEVIER SCIENCE
ISBN-10: 0128125322
Pagini: 594
Dimensiuni: 191 x 235 x 36 mm
Ediția:7
Editura: ELSEVIER SCIENCE
Public țintă
Students, physicians, and researchers in the field of medical genetics and personalized medicine; medical practitioners and researchers of cardiology, pulmonary medicine, gastrointestinal medicine, and nephrology, as well as genetic diagnostics and therapy in these and related disciplines; genetic counselors; genetic researchers in industry and pharmaCuprins
Section 1
1. Congenital Heart Defects
2. Inherited Cardiomyopathies
3. Heritable and Idiopathic Forms of Pulmonary Arterial Hypertension
4. Hereditary Hemorrhagic Telangiectasia (Osler–Weber–Rendu Syndrome)
5. Hereditary Disorders of the Lymphatic System and Varicose Veins
6. The Genetics of Cardiac Electrophysiology in Humans
7. Arteriopathy
8. Genetics of Blood Pressure Regulation
9. Common Genetic Determinants of Coagulation and Fibrinolysis
10. Genetics of Atherosclerotic Cardiovascular Disease
11. Disorders of the Venous System
12. Capillary Malformation/Arteriovenous Malformation
Section 2
13. Cystic Fibrosis
14. Genetic Underpinnings of Asthma and Related Traits
15. Hereditary Pulmonary Emphysema
16. LAM
17. Interstitial and Restrictive Pulmonary Disorders
Section 3
18. Congenital Anomalies of the Kidney and Urinary Tract
19. Cystic Diseases of the Kidney
20. Nephrotic Disorders
21. Renal Tubular Disorders
Section 4
22. Gastrointestinal Tract and Hepatobiliary Duct System
23. Inflammatory Bowel Disease
24. Bile Pigment Metabolism and Its Disorders
1. Congenital Heart Defects
2. Inherited Cardiomyopathies
3. Heritable and Idiopathic Forms of Pulmonary Arterial Hypertension
4. Hereditary Hemorrhagic Telangiectasia (Osler–Weber–Rendu Syndrome)
5. Hereditary Disorders of the Lymphatic System and Varicose Veins
6. The Genetics of Cardiac Electrophysiology in Humans
7. Arteriopathy
8. Genetics of Blood Pressure Regulation
9. Common Genetic Determinants of Coagulation and Fibrinolysis
10. Genetics of Atherosclerotic Cardiovascular Disease
11. Disorders of the Venous System
12. Capillary Malformation/Arteriovenous Malformation
Section 2
13. Cystic Fibrosis
14. Genetic Underpinnings of Asthma and Related Traits
15. Hereditary Pulmonary Emphysema
16. LAM
17. Interstitial and Restrictive Pulmonary Disorders
Section 3
18. Congenital Anomalies of the Kidney and Urinary Tract
19. Cystic Diseases of the Kidney
20. Nephrotic Disorders
21. Renal Tubular Disorders
Section 4
22. Gastrointestinal Tract and Hepatobiliary Duct System
23. Inflammatory Bowel Disease
24. Bile Pigment Metabolism and Its Disorders