Cushing Syndrome: History, Diagnosis and Treatment
Editat de Constantine A. Stratakisen Limba Engleză Paperback – 9 feb 2026
The book has a section dedicated to our patients with the patients’ experiences, which will add to the outcome research presented by the physicians. This is a must have reference for scientists and researchers with the latest information in diagnosing and treating this difficult-to-diagnose and difficult-to-treat condition and gives the clinician, a patient-centric approach to communicate with this particular group of patients.
- Provides comprehensive “how to” information for diagnosis and treatment
- Includes the latest information on genetics, all molecular advances, and new medical therapies
- Presents a patient-centric approach with an emphasis on patients’ perspectives and long-term effects of cortisol excess, well-being, and mental health
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Specificații
ISBN-13: 9780323961004
ISBN-10: 0323961002
Pagini: 426
Dimensiuni: 191 x 235 mm
Editura: ELSEVIER SCIENCE
ISBN-10: 0323961002
Pagini: 426
Dimensiuni: 191 x 235 mm
Editura: ELSEVIER SCIENCE
Cuprins
1. Identification of Cushing syndrome (CS) and its history from Harvey Cushing to today
2. Exogenous CS (iatrogenic): most frequent uses of glucocorticoids and outcomes, including recommendations for recovery (post-chemotherapy, asthma treatments, chronic use on rheumatoid and/or skeletal disorders)
3. Endogenous CS: causes and genetics
4. CS and malingering: Munchausen syndrome and Muncausen-by-proxy: cases, diagnosis, and outcomes
5. Non-tumorous functional hypercortisolemia (pseudo-CS): causes and long-term issues
6. Cushing disease: pituitary tumors causing CS: genetics, molecular advances, diagnosis, and treatment
7. Inferior Petrosal Sinus Sampling: to do or not to do
8. CRH test: to do or not to do
9. All about dexamethasone testing in CS
10. ACTH-independent CS: adrenal tumors causing CS: genetics, molecular advances, diagnosis, and treatment
11. Ectopic ACTH or CRH-producing tumors and CS: genetics, syndromes, molecular advances, diagnosis, and treatment
12. Animal models of CS: what do they teach us?
13. Medical therapies for CS
14. Surgical issues for a patient with CS: techniques, complications, and recovery
15. The patient with CS: perspectives written by patients; resources for patients
16. Cortisol exposure and mental health
17. CS and long-term effects on health, cognition, and function
2. Exogenous CS (iatrogenic): most frequent uses of glucocorticoids and outcomes, including recommendations for recovery (post-chemotherapy, asthma treatments, chronic use on rheumatoid and/or skeletal disorders)
3. Endogenous CS: causes and genetics
4. CS and malingering: Munchausen syndrome and Muncausen-by-proxy: cases, diagnosis, and outcomes
5. Non-tumorous functional hypercortisolemia (pseudo-CS): causes and long-term issues
6. Cushing disease: pituitary tumors causing CS: genetics, molecular advances, diagnosis, and treatment
7. Inferior Petrosal Sinus Sampling: to do or not to do
8. CRH test: to do or not to do
9. All about dexamethasone testing in CS
10. ACTH-independent CS: adrenal tumors causing CS: genetics, molecular advances, diagnosis, and treatment
11. Ectopic ACTH or CRH-producing tumors and CS: genetics, syndromes, molecular advances, diagnosis, and treatment
12. Animal models of CS: what do they teach us?
13. Medical therapies for CS
14. Surgical issues for a patient with CS: techniques, complications, and recovery
15. The patient with CS: perspectives written by patients; resources for patients
16. Cortisol exposure and mental health
17. CS and long-term effects on health, cognition, and function