The Official Patient's Sourcebook on Charcot-Marie-Tooth Disorder

The Official Patient's Sourcebook on Charcot-Marie-Tooth Disorder

Author: James N. Parker

Publisher:

Published: 2002

Total Pages: 168

ISBN-13:

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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 charcot-marie-tooth disorder (also Charcot-Marie-Tooth Disease (Variant); Charcot-Marie-Tooth-Roussy-Levy Disease; Hereditary Areflexic Dystasia; Hereditary Motor and Sensory Neuropathy; Hereditary motor and sensory neu-ropathy; Hereditary Motor Sensory Neuropathy), 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 charcot-marie-tooth disorder. 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.


Consumer Sourcebook

Consumer Sourcebook

Author: Matthew Miskelly

Publisher: Gale Cengage

Published: 2007-06-20

Total Pages: 1610

ISBN-13: 9780787680930

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P IConsumer Sourcebook /I provides a comprehensive digest of accessible resources and advisory information for the American consumer. This new edition identifies and describes some 23,000 programs and services available to the general public at little or no cost. These services are provided by federal, state, county, and local governments and their agencies as well as by organizations and associations. PConsumer affairs and customer services departments for corporations are also listed as well as related publications, multimedia products, general tips and recommendations for consumers. The master index is arranged alphabetically by name and by subject term.


The Official Patient's Sourcebook on Behcet's Disease

The Official Patient's Sourcebook on Behcet's Disease

Author: James N. Parker

Publisher:

Published: 2002

Total Pages: 140

ISBN-13:

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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 behcet's disease (also Adamantiades-Behcet's Syndrome; Behcet's Disease; Franceschetti-Valerio syndrome; Halushi-Behcet's Syndrome; Mucocutaneous ocular syndrome; Oculo-Bucco-Genital Syndrome), 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 behcet's 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.


The Official Patient's Sourcebook on Scleroderma

The Official Patient's Sourcebook on Scleroderma

Author: James N. Parker

Publisher:

Published: 2002

Total Pages: 302

ISBN-13:

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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 scleroderma, 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 scleroderma. Following an introductory chapter, the sourcebook is organized into three parts. PART I: THE ESSENTIALS; Chapter 1. The Essentials on Scleroderma: Guidelines; Chapter 2. Seeking Guidance; Chapter 3. Clinical Trials and Scleroderma; PART II: ADDITIONAL RESOURCES AND ADVANCED MATERIAL; Chapter 4. Studies on Scleroderma; Chapter 5. Patents on Scleroderma; Chapter 6. Books on Scleroderma; Chapter 7. Multimedia on Scleroderma; Chapter 8. Periodicals and News on Scleroderma; Chapter 9. Physician Guidelines and Databases; Chapter 10. Dissertations on Scleroderma; 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; SCLERODERMA GLOSSARY; INDEX. Related topics include: Familial Progressive Systemic Sclerosis, Morphea, Progressive systemic sclerosis, Systemic Sclerosis.


Movement Disorders Sourcebook, 4th Ed.

Movement Disorders Sourcebook, 4th Ed.

Author: James Chambers

Publisher: Infobase Holdings, Inc

Published: 2021-08-01

Total Pages: 353

ISBN-13: 0780819144

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Consumer health information about diagnosis, treatment, and management of Parkinson disease and other hypokinetic and hyperkinetic movement disorders, along with advice for family members and caregivers.


The Official Patient's Sourcebook on Trigeminal Neuralgia

The Official Patient's Sourcebook on Trigeminal Neuralgia

Author: James N. Parker

Publisher:

Published: 2002

Total Pages: 248

ISBN-13:

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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 trigeminal neuralgia (also Fothergill Disease; Fothergill's neuralgia; Tic Douloureux; Trifacial neuralgia), 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 trigeminal neuralgia. 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.


Genetic Disorders Sourcebook, 7th Ed.

Genetic Disorders Sourcebook, 7th Ed.

Author: James Chambers

Publisher: Infobase Holdings, Inc

Published: 2019-04-01

Total Pages: 728

ISBN-13: 078081696X

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Provides basic consumer health information about disorders caused by gene and chromosome abnormalities and those with genetic and environmental components, along with facts about genetic testing and treatment research, and guidance for parents of children with special needs. Includes index, glossary of related terms, and other resources.