The Official Patient's Sourcebook on Hematuria

This sourcebook has been created for patients who have decided to make education and Internet-based research an integral part of the treatment process. Although it gives information useful to doctors, caregivers and other health professionals, it also tells patients where and how to look for information covering virtually all topics related to hematuria, from the essentials to the most advanced areas of research. The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research. Selected readings from various agencies are reproduced to give you some of the latest official information available to date on hematuria. Following an introductory chapter, the sourcebook is organized into three parts. PART I: THE ESSENTIALS; Chapter 1. The Essentials on Hematuria: Guidelines; Chapter 2. Seeking Guidance; PART II: ADDITIONAL RESOURCES AND ADVANCED MATERIAL; Chapter 3. Studies on Hematuria; Chapter 4. Books on Hematuria; Chapter 5. Multimedia on Hematuria; Chapter 6. Physician Guidelines and Databases; Chapter 7. Dissertations on Hematuria; PART III. APPENDICES; Appendix A. Researching Your Medications; Appendix B. Researching Alternative Medicine; Appendix C. Researching Nutrition; Appendix D. Finding Medical Libraries; Appendix E. Your Rights and Insurance; ONLINE GLOSSARIES; HEMATURIA GLOSSARY; INDEX. Related topics include: Berger's Disease, endemic hematuria, Hematuria - nephropathy - deafness, Hematuria, Benign, Recurrent, Hematuria, Essential, Hemorrhagic familial nephritis, Hereditary deafness and nephropathy, Hereditary nephritis, Idiopathic Renal Hematuria, Mesangial IGA Nephropathy, Nephropathy - IgA, Nephropathy, Thin-Basement-Membrane, urogenital schistosomiasis.