The Official Patient's Sourcebook on Apraxia: A Revised and Updated Directory for the Internet Age

 
9780597830464: The Official Patient's Sourcebook on Apraxia: A Revised and Updated Directory for the Internet Age

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 apraxia, 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 apraxia. Following an introductory chapter, the sourcebook is organized into three parts. PART I: THE ESSENTIALS; Chapter 1. The Essentials on Apraxia: Guidelines; Chapter 2. Seeking Guidance; Chapter 3. Clinical Trials and Apraxia; PART II: ADDITIONAL RESOURCES AND ADVANCED MATERIAL; Chapter 4. Studies on Apraxia; Chapter 5. Books on Apraxia; Chapter 6. Multimedia on Apraxia; Chapter 7. Periodicals and News on Apraxia; Chapter 8. Physician Guidelines and Databases; Chapter 9. Dissertations on Apraxia; 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; APRAXIA GLOSSARY;INDEX. Related topics include: Cogan's Syndrome, Type II, Congenital Oculomotor Apraxia.

Le informazioni nella sezione "Riassunto" possono far riferimento a edizioni diverse di questo titolo.

From the Publisher:

This is a "must have" reference book for patients, parents, caregivers, and libraries with medical collections. This sourcebook is organized into three parts. Part I explores basic techniques to researching apraxia (e.g. finding guidelines on diagnosis, treatments, and prognosis), followed by a number of topics, including information on how to get in touch with organizations, associations, or other patient networks dedicated to apraxia. It also gives you sources of information that can help you find a doctor in your local area specializing in treating apraxia. Collectively, the material presented in Part I is a complete primer on basic research topics for patients with apraxia. Part II moves on to advanced research dedicated to apraxia. Part II is intended for those willing to invest many hours of hard work and study. It is here that we direct you to the latest scientific and applied research on apraxia. When possible, contact names, links via the Internet, and summaries are provided. In general, every attempt is made to recommend "free-to-use" options. Part III provides appendices of useful background reading for all patients with apraxia or related disorders. The appendices are dedicated to more pragmatic issues faced by many patients with apraxia. Accessing materials via medical libraries may be the only option for some readers, so a guide is provided for finding local medical libraries which are open to the public. Part III, therefore, focuses on advice that goes beyond the biological and scientific issues facing patients with apraxia.

Excerpt. © Reprinted by permission. All rights reserved.:

Though many physicians and public officials had thought that the emergence of the Internet would do much to assist patients in obtaining reliable information, 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." Since the late 1990s, physicians have seen a general increase in patient Internet usage rates. Patients frequently enter their doctor's offices with printed Web pages of home remedies in the guise of latest medical research. This scenario is so common that doctors often spend more time dispelling misleading information than guiding patients through sound therapies. ... This book has been created for patients who have decided to make education and research an integral part of the treatment process. ... While this sourcebook covers apraxia, your doctor, research publications, and specialists may refer to your condition using a variety of terms. Therefore, you should understand that apraxia is often considered a synonym or a condition closely related to the following: Cogan's Syndrome, Type II; Congenital Oculomotor Apraxia.

Le informazioni nella sezione "Su questo libro" possono far riferimento a edizioni diverse di questo titolo.

I migliori risultati di ricerca su AbeBooks

1.

Icon Health Publications
Editore: ICON Health Publications (2002)
ISBN 10: 0597830460 ISBN 13: 9780597830464
Nuovi Paperback Quantità: 1
Da
Ergodebooks
(RICHMOND, TX, U.S.A.)
Valutazione libreria
[?]

Descrizione libro ICON Health Publications, 2002. Paperback. Condizione libro: New. Codice libro della libreria DADAX0597830460

Maggiori informazioni su questa libreria | Fare una domanda alla libreria

Compra nuovo
EUR 37,76
Convertire valuta

Aggiungere al carrello

Spese di spedizione: EUR 3,43
In U.S.A.
Destinazione, tempi e costi

2.

Icon Health Publications
Editore: Icon Group Intl Inc (2002)
ISBN 10: 0597830460 ISBN 13: 9780597830464
Nuovi Paperback Quantità: 1
Da
Revaluation Books
(Exeter, Regno Unito)
Valutazione libreria
[?]

Descrizione libro Icon Group Intl Inc, 2002. Paperback. Condizione libro: Brand New. 188 pages. 11.00x8.25x0.50 inches. In Stock. Codice libro della libreria 0597830460

Maggiori informazioni su questa libreria | Fare una domanda alla libreria

Compra nuovo
EUR 51,87
Convertire valuta

Aggiungere al carrello

Spese di spedizione: EUR 6,71
Da: Regno Unito a: U.S.A.
Destinazione, tempi e costi