Clinical and Translational Perspectives on WILSON DISEASE
Editat de Nanda Kerkar, Eve A Robertsen Limba Engleză Paperback – 24 sep 2018
- Delivers numerous, succinct, expert chapters with summaries designed for quick reference
- Includes a 'How-to appendix' for diagnosis and management tips
- Contains access to a companion website with a self-help teaching module, links to key resources, and an extended reference list
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Specificații
ISBN-13: 9780128105320
ISBN-10: 0128105321
Pagini: 502
Dimensiuni: 216 x 276 x 24 mm
Editura: ELSEVIER SCIENCE
ISBN-10: 0128105321
Pagini: 502
Dimensiuni: 216 x 276 x 24 mm
Editura: ELSEVIER SCIENCE
Public țintă
Clinical and basic scientists with a research interest in Wilson Disease; Clinicians including Gastroenterologists & Hepatologists.Cuprins
1. Introduction
2. History
Cellular physiology
3. Biological aspects of copper
4. Cu uptake (CTR1 etc)
5. Wilson ATPase structure
6. Wilson ATPase function
7. COMMD1
8. Cu in mitochondria
9. Ceruloplasmin
10. Metalloproteomics
11. Cu disposition in bacteria
12. Cu disposition in yeast
13. Animal models—KO mouse
ATP7B gene
14. Characteristics of gene; genetic diagnosis
15. Epigenetics
Clinical aspects
16. WD in adults
17. WD in children
18. Neuro-WD
19. Psychiatric-WD
20. Ophthalmological-WD
21. Biochemical diagnosis
22. Direct determination of NCB-Cu
23. Histopathology
24. Imaging--CNS
25. Role of scoring systems
26. Screening (population; kindreds)
27. Genetic counselling
WD around the world
28. Regional WD: northern Europe
29. Regional WD: Sardinia/ Mediterranean Europe
30. Regional WD: Israel
31. Regional WD: Brazil
32. Regional WD: India
33. Regional WD: China
Treatment
34. Treatment: D-penicillamine
35. Treatment: trientine
36. Treatment: zinc
37. Adherence to medications
38. Liver transplantation
39. New treatment modalities
Special issues related to Wilson disease
40. Wilsonian fulminant hepatic failure
41. Pregnancy
42. WD-mimics
43. ATP7B and Alzheimer disease
Related issues of copper disposition and disease
44. ATP7A disorders
45. Other disorders of copper-handling
2. History
Cellular physiology
3. Biological aspects of copper
4. Cu uptake (CTR1 etc)
5. Wilson ATPase structure
6. Wilson ATPase function
7. COMMD1
8. Cu in mitochondria
9. Ceruloplasmin
10. Metalloproteomics
11. Cu disposition in bacteria
12. Cu disposition in yeast
13. Animal models—KO mouse
ATP7B gene
14. Characteristics of gene; genetic diagnosis
15. Epigenetics
Clinical aspects
16. WD in adults
17. WD in children
18. Neuro-WD
19. Psychiatric-WD
20. Ophthalmological-WD
21. Biochemical diagnosis
22. Direct determination of NCB-Cu
23. Histopathology
24. Imaging--CNS
25. Role of scoring systems
26. Screening (population; kindreds)
27. Genetic counselling
WD around the world
28. Regional WD: northern Europe
29. Regional WD: Sardinia/ Mediterranean Europe
30. Regional WD: Israel
31. Regional WD: Brazil
32. Regional WD: India
33. Regional WD: China
Treatment
34. Treatment: D-penicillamine
35. Treatment: trientine
36. Treatment: zinc
37. Adherence to medications
38. Liver transplantation
39. New treatment modalities
Special issues related to Wilson disease
40. Wilsonian fulminant hepatic failure
41. Pregnancy
42. WD-mimics
43. ATP7B and Alzheimer disease
Related issues of copper disposition and disease
44. ATP7A disorders
45. Other disorders of copper-handling