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This digital document is an article from Nephrology Nursing Journal, published by Thomson Gale on July 1, 2007. The length of the article is 2388 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the author: 3. Develop an education plan for patients with a family history of Von Hippel-Lindau Disease.

Citation Details
Title: Von Hippel-Lindau disease: an overview.(Continuing Nuring Edcuation)(Disease/Disorder overview)
Author: Michele Inglese
Publication: Nephrology Nursing Journal (Magazine/Journal)
Date: July 1, 2007
Publisher: Thomson Gale
Volume: 34Issue: 4Page: 390(5)

Article Type: Disease/Disorder overview

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Targeted to patients, their families and allied health students, The Gale Encyclopedia of Neurological Disorders provides in-depth coverage of neurological diseases and disorders, including stroke, multiple sclerosis, Parkinson disease, Tourette Syndrome, Alzheimer's disease, cerebral palsy, vertigo, amnesia and epilepsy. Related topics include communication aids, electric personal assistive mobility devices, medications for treating neurological diseases and conditions, understanding the needs of Alzheimer patient caregivers and more. This two-volume set provides an alternative to resources that either fail to explore neurological disease in any depth and or do so at a level not appropriate for students and general readers.

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The article is excerpted fromGale Encyclopedia of Cancer
The resource students and researchers will turn to for reliable, up-to-date and clearly written information, the Gale Encyclopedia of Cancer is a comprehensive survey of 120 cancers, cancer drugs, traditional and alternative treatments and diagnostic procedures. The Encyclopediaincludes entries covering cancers, cancer drugs, treatments, side effects and diagnostic procedures. Entries typically include the following elements:

• Causes and Symptoms
• Definition
• Description
• Diagnosis
• Prevention
• Resources
• Risks
• Special Concerns
• And more

An appendix provides complete contact information for cancer centers, national support groups, government agencies and research groups. Features include anatomical illustrations of the major body systems, a subject index and approximately 200 photographs and drawings. ... Read more

Book Description
This book has been created for patients who have decided to make education and research an integral part of the treatment process. Although it also gives information useful to doctors, caregivers and other health professionals, it tells patients where and how to look for information covering virtually all topics related to von hippel-lindau disease (also Angioblastomatosis; Angiomatosis Retinae; Angiophakomatosis retinae et cerebelli; Cerebelloretinal hemangioblastomatosis; Cerebelloretinal hemangioblastomato-sis; Hippel Disease), 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 von hippel-lindau disease. Given patients' increasing sophistication in using the Internet, abundant references to reliable Internet-based resources are provided throughout this sourcebook. Where possible, guidance is provided on how to obtain free-of-charge, primary research results as well as more detailed information via the Internet. E-book and electronic versions of this sourcebook are fully interactive with each of the Internet sites mentioned (clicking on a hyperlink automatically opens your browser to the site indicated). Hard-copy users of this sourcebook can type cited Web addresses directly into their browsers to obtain access to the corresponding sites. In addition to extensive references accessible via the Internet, chapters include glossaries of technical or uncommon terms.Download Description
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 von hippel-lindau disease, 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 von hippel-lindau disease. Following an introductory chapter, the sourcebook is organized into three parts. PART I: THE ESSENTIALS; Chapter 1. The Essentials on Von Hippel-Lindau Disease: Guidelines; Chapter 2. Seeking Guidance; Chapter 3. Clinical Trials and Von Hippel-Lindau Disease; PART II: ADDITIONAL RESOURCES AND ADVANCED MATERIAL; Chapter 4. Studies on Von Hippel-Lindau Disease; Chapter 5. Books on Von Hippel-Lindau Disease; Chapter 6. Periodicals and News on Von Hippel-Lindau Disease; Chapter 7. Physician Guidelines and Databases; PART III. APPENDICES; Appendix A. Researching Your Medications; Appendix B. Researching Nutrition; Appendix C. Finding Medical Libraries; Appendix D. Your Rights and Insurance; ONLINE GLOSSARIES; VON HIPPEL-LINDAU DISEASE GLOSSARY; INDEX. Related topics include: Angioblastomatosis, Angiomatosis Retinae, Angiophakomatosis retinae et cerebelli, Cerebelloretinal hemangioblastomatosis, Cerebelloretinal hemangioblastomato-sis, Hippel Disease, Hippel-Lindau Syndrome, Lindau Disease, Retinocerebellar Angiomatosis. ... Read more

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Information on many genetic disorders, and the frequent new findings on them, has been extremely difficult to come byuntil now. The Gale Encyclopedia of Genetic Disorders addresses the need for current, hard-to-find facts on emerging discoveries. The two-volume Encyclopedia, presented in a single alphabetical sequence, provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand, in language accessible to laypersons. The articles are arranged in a standardized format for quick comparison and ease of use, while non-disorder topics are covered in detail with extended entries. Students will want to consult the Gale Encyclopedia of Genetic Disorders for useful information on a range of well known disorders, including Down Syndrome, Trisomy, Hemophilia and Tourette Syndrome, and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.

Product Description
In March 2001, the National Institutes of Health issued the following warning: "The number of Web sites offering health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading." Furthermore, because of the rapid increase in Internet-based information, many hours can be wasted searching, selecting, and printing. Since only the smallest fraction of information dealing with Von Hippel-Lindau syndrome is indexed in search engines, such as www.google.com or others, a non-systematic approach to Internet research can be not only time consuming, but also incomplete. This book was created for medical professionals, students, and members of the general public who want to conduct medical research using the most advanced tools available and spending the least amount of time doing so. ... Read more

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Students, researchers, and patients can find reliable, up-to-date and clearly written information in The Gale Encyclopedia of Cancer, a comprehensive survey of 120 cancers, cancer drugs, traditional and alternative treatments and diagnostic procedures.

Book Description
Neurocutaneous diseases are a wide group of conditions that affect the nervous system but appear as lesions of the skin. Some of the more common entities have variable forms of expression that can confuse the diagnosis; for the rare conditions it is difficult to find descriptions in the literature. Recent insights into their cellular, biochemical and molecular genetic bases have shown the essential need for a new nosology and updated genotype-phenotype correlations. The book provides an authoritative source ofknowledge about these difficult problems and bridges the gap between clinical recognition and the new molecular medicine.The editors, distinguished clinicians and geneticists, assembled an internationally renowned group of collaborators, many of them the experts who first described a particular disorder or established its present accepted definition. They have written a practical, comprehensive guide to the recognition, investigation and management of more than 60 recognised phakomatoses. ... Read more