Wilson Disease
Pathogenesis, Molecular Mechanisms, Diagnosis, Treatment and Monitoring
- 1 Edición - 21 de mayo de 2019
- Última edición
- Editores: Karl Heinz Weiss, Michael Schilsky
- Idioma: Inglés
Wilson Disease: Pathogenesis, Molecular Mechanisms, Diagnosis, Treatment and Monitoring translates both clinical and experimental findings into a comprehensive approach for anyon… Leer más
Descripción
Descripción
Wilson Disease: Pathogenesis, Molecular Mechanisms, Diagnosis, Treatment and Monitoring translates both clinical and experimental findings into a comprehensive approach for anyone involved in research and patient care. While the clinical variability of Wilson Disease poses a challenge from a diagnostic approach, the book uses the translational impact of new research findings to relate to new treatment concepts. Comprehensive chapters include common knowledge, guideline consensus statements, and discussions of clinical evidence. This is a must-have reference for researchers and clinicians in translational research.
Puntos claves
Puntos claves
- Delivers a substantial overview of evidence driven diagnostic pathways and treatment concepts for Wilson disease
- Provides an understanding of the translational impact of new research findings in Wilson Disease
- Reveals the current controversies in treatment decisions for Wilson disease, providing the best decisions for optimal patient care
De interès para
De interès para
Clinical and basic scientists with a research interest in Wilson Disease; Hepatology and Gastroenterology Clinicians
Índice
Índice
- History of WD
- Pathogenesis
2.1.) Normal copper metabolism
2.2.) ATP7B function
2.3.) Copper endpoints and cellular copper toxicity - Epidemiology and genetics
3.1.) Epidemiology and regional differences
3.2.) Genotype – Phenotype correlation and Phenotype definitions - Diagnosis
4.1.) Diagnostic work up
4.2.) Biochemical marker
3.3.) Hepatic Wilson Disease
4.4.) Neurologic Wilson Disease
4.5.) Liver pathology in WD and genetic testing - Treatment Decisions
5.1.) General considerations and the need for Liver transplantation
5.2.) Chelation therapy: D-penicilamine
5.3.) Chelation therapy: Trientine
5.4.) Zinc
5.5.) Other treatment regimens and emerging therapies
5.6.) Symptomatic treatment of residual neurologic or psychiatric disease
Monitoring
Detalles del producto
Detalles del producto
- Edición: 1
- Última edición
- Publicado: 21 de mayo de 2019
- Idioma: Inglés
Sobre los editores
Sobre los editores
KW
Karl Heinz Weiss
MS